List of works - Jerome I Rotter

40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 ⬇️

article

52 Genetic Loci Influencing Myocardial Mass

scientific article

73-OR: Clonal Hematopoiesis of Indeterminate Potential (CHIP), Glycemic Traits, and Type 2 Diabetes (T2D) Risk

scientific article published in 2021

A Comprehensive Analysis of Common and Rare Variants to Identify Adiposity Loci in Hispanic Americans: The IRAS Family Study (IRASFS).

scientific article published on 24 November 2015

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.

scientific article published on July 2016

A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter ⬇️

scientific article published on November 1, 1997

A Genetic Risk Score Associated with Chronic Obstructive Pulmonary Disease Susceptibility and Lung Structure on Computed Tomography

scientific article published on 01 September 2019

A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos

scientific article published on 18 June 2019

A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population

scientific article published on January 2017

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

scientific article

A Long Non-coding RNA, LOC157273, Is an Effector Transcript at the Chromosome 8p23.1-PPP1R3B Metabolic Traits and Type 2 Diabetes Risk Locus

scientific article published on 10 July 2020

A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait ⬇️

scientific article published on March 31, 2012

A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH

scientific article published on 03 November 2019

A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

scientific article published on 17 May 2022

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

scientific journal article

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis

scientific article published on 01 January 1993

A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes

scientific article

A generalized least-squares framework for rare-variant analysis in family data

scientific article

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

scientific article

A genome scan for fasting insulin and fasting glucose identifies a quantitative trait locus on chromosome 17p: the insulin resistance atherosclerosis study (IRAS) family study.

scientific article published on January 2005

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

scientific article published on 13 May 2012

A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS).

scientific article

A genome-wide association search for type 2 diabetes genes in African Americans

scientific article published on 4 January 2012

A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

scientific article published on 05 May 2013

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

scientific article

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries

scientific article published on 6 October 2011

A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3

scientific article

A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women

scientific article

A genome-wide association study of aging

scientific article

A genome-wide association study of central corneal thickness in Latinos

scientific article published on April 2013

A genome-wide association study of chronic obstructive pulmonary disease in Hispanics

scientific article

A genome-wide association study of depressive symptoms

scientific journal article

A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

article

A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium

scientific article published on 30 December 2016

A genome-wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study

scientific article published on 5 April 2017

A genome-wide scan for carotid artery intima-media thickness: the Mexican-American Coronary Artery Disease family study

scientific article published on 3 February 2005

A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci

scientific journal article

A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies

scientific article published on 21 March 2016

A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

scientific article published on June 2016

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

scientific article

A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

scientific article

A meta-analysis of genome-wide association studies identifies multiple longevity genes

scientific article published on 14 August 2019

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

scientific article

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

A new syndrome of Crohn's disease and pachydermoperiostosis in a family

scientific article published on 01 January 1997

A noncoding variant near PPP1R3B promotes liver glycogen storage and MetS, but protects against myocardial infarction

scientific article published on 24 November 2020

A novel Alzheimer disease locus located near the gene encoding tau protein.

scientific article

A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews

scientific article

A novel method for testing association of multiple genetic markers with a multinomial trait.

scientific article

A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains

scientific article

A prevalent caveolin-1 gene variant is associated with the metabolic syndrome in Caucasians and Hispanics

scientific article

A search for heterogeneity in insulin dependent diabetes mellitus (IDDM): HLA and autoimmune studies in simplex, multiplex and multigenerational families ⬇️

scientific article published on 01 May 1983

A statin-dependent QTL for GATM expression is associated with statin-induced myopathy

scientific article (publication date: 17 October 2013)

A structural variation reference for medical and population genetics

scientific article published on 27 May 2020

ANCA pattern and LTA haplotype relationship to clinical responses to anti-TNF antibody treatment in Crohn's disease

scientific article

APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema

journal article published in 2014

Abstract 14629: Rare Variants for Electrocardiographic Traits Identify Arrhythmia Susceptibility Genes

scientific article published in 2020

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

scientific article

Additional comments on the ulcer-multiple lentigines syndrome

scientific article published on 01 February 1982

Adiponectin Isoform Patterns in Ethnic-Specific ADIPOQ Mutation Carriers: The IRAS Family Study

scientific article published on 23 June 2017

Adiponectin, Insulin Sensitivity and Diabetic Retinopathy in Latinos With Type 2 Diabetes

scientific article

Adiposity-Independent Effects of Aging on Insulin Sensitivity and Clearance in Mice and Humans

scientific article published on 01 March 2019

Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies

scientific article published on April 2017

Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans

scientific article published on 01 February 2019

Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus

scientific article published on 11 December 2012

African Ancestry Analysis and Admixture Genetic Mapping for Proliferative Diabetic Retinopathy in African Americans

scientific article

African Ancestry Is Associated with Higher Intraocular Pressure in Latinos

scientific article

African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos

scientific article published on 20 September 2016

Air pollution and percent emphysema identified by computed tomography in the Multi-Ethnic study of Atherosclerosis

scientific article

Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci

scientific article published on 17 February 2020

Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

scientific article published on 26 December 2019

Alterations of a Cellular Cholesterol Metabolism Network Are a Molecular Feature of Obesity-Related Type 2 Diabetes and Cardiovascular Disease

scientific article

Alternative splicing of 3-hydroxy-3-methylglutaryl coenzyme A reductase is associated with plasma low-density lipoprotein cholesterol response to simvastatin

scientific article published on 16 June 2008

Amino acid position 37 of HLA-DRβ1 affects susceptibility to Crohn's disease in Asians

article

Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus

scientific article published on 01 November 1998

An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group

scientific article published on 27 May 2016

An Outbreak of Polygenic Scores for Coronary Artery Disease

scientific article published on 01 June 2020

An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.

scientific article published on 31 January 2008

An association between the calpastatin (CAST) gene and keratoconus

scientific article published on May 2013

An integrative cross-omics analysis of DNA methylation sites of glucose and insulin homeostasis.

scientific article published on 13 June 2019

An open resource of structural variation for medical and population genetics

scientific article

Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology

scientific article published in October 2017

Analysis of HLA-DQA1 and -DQB1 genes in Mexican Americans with insulin-dependent diabetes mellitus

scientific article published on 01 August 1993

Analysis of HLA-DQA1 and -DQB1 genes in Mexican Americans with insulin-dependent diabetes mellitus

article

Analysis of Whole Exome Sequencing with Cardiometabolic Traits Using Family-Based Linkage and Association in the IRAS Family Study

scientific article published on 9 January 2017

Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy

scientific article published on 07 May 2020

Analysis of family- and population-based samples in cohort genome-wide association studies

scientific article

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease

scientific article published on 24 April 2018

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

scientific article published in 2022

Ancestry and other genetic associations with plasma PCSK9 response to simvastatin

scientific article

Anti-flagellin (CBir1) phenotypic and genetic Crohn's disease associations.

scientific article published in May 2007

Application of Bayesian classification with singular value decomposition method in genome-wide association studies

scientific article

Application of Bayesian regression with singular value decomposition method in association studies for sequence data ⬇️

scientific article published on November 29, 2011

Application of synthetic oligonucleotides to detect DQ beta genes transmission within insulin-dependent diabetes families

scientific article published on 01 October 1989

Arthrogryposis multiplex congenita in an Arab kindred: update

scientific article published on 01 January 1995

Assessment of gene-by-sex interaction effect on bone mineral density

scientific article (publication date: October 2012)

Assessment of the Relationship Between Genetic Determinants of Thyroid Function and Atrial Fibrillation: A Mendelian Randomization Study

article published in 2019

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

scientific article published on 23 February 2017

Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels

scientific article

Association between ADIPOQ SNPs with plasma adiponectin and glucose homeostasis and adiposity phenotypes in the IRAS Family Study

scientific article

Association between Site-specific Bone Mineral Density and Glucose Homeostasis and Anthropometric Traits in Healthy Men and Women

scientific article published on 25 March 2018

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

scientific article

Association between angiotensinogen, angiotensin II receptor genes, and blood pressure response to an angiotensin-converting enzyme inhibitor

scientific article published on 29 January 2007

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies

scientific article published on 23 December 2011

Association between serum amyloid A proteins and coronary artery disease: evidence from two distinct arteriosclerotic processes

scientific article published on 01 November 1997

Association between sleep disordered breathing and epigenetic age acceleration: Evidence from the Multi-Ethnic Study of Atherosclerosis

scientific article published on 21 November 2019

Association of APOL1 Genotypes With Measures of Microvascular and Endothelial Function, and Blood Pressure in MESA

scientific article published on 27 August 2020

Association of Directly Measured Plasma Free 25(OH)D With Insulin Sensitivity and Secretion: The IRAS Family Study

scientific article published on 10 May 2017

Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis

scientific article published on 18 March 2020

Association of Genetic Variants with Primary Open-Angle Glaucoma among Individuals with African Ancestry

scientific article published on 01 November 2019

Association of Genetic Variation With Keratoconus

scientific article published on 19 December 2019

Association of HLA-DPB1*0301 with IDDM in Mexican-Americans

scientific article published on May 1996

Association of Mitochondrial DNA Copy Number With Cardiovascular Disease

scientific article published on 11 October 2017

Association of NOD2 and IL23R with inflammatory bowel disease in Puerto Rico

scientific article

Association of PNPLA3 with non-alcoholic fatty liver disease in a minority cohort: the Insulin Resistance Atherosclerosis Family Study ⬇️

scientific article published on January 13, 2011

Association of TCF7L2 gene polymorphisms with reduced acute insulin response in Hispanic Americans

scientific article

Association of Triglyceride-Related Genetic Variants With Mitral Annular Calcification

scientific article published on June 2017

Association of a 62 Variants Type 2 Diabetes Genetic Risk Score With Markers of Subclinical Atherosclerosis: A Transethnic, Multicenter Study.

scientific article

Association of antibody responses to microbial antigens and complications of small bowel Crohn's disease

scientific article published in February 2004

Association of fasting insulin and C peptide with diabetic retinopathy in Latinos with type 2 diabetes

scientific article

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

scientific article

Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies

scientific article published on 16 December 2012

Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

scientific journal article

Association of heat shock proteins with all-cause mortality

scientific article published on 04 May 2012

Association of insulin sensitivity and glucose tolerance with the c.825C>T variant of the G protein beta-3 subunit gene

scientific article published on 16 April 2008

Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study

scientific article (publication date: June 2014)

Association of low-density lipoprotein cholesterol-related genetic variants with aortic valve calcium and incident aortic stenosis

scientific article

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

scientific article

Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus

scientific article published on 31 October 2011

Association of severity of primary open-angle glaucoma with serum vitamin D levels in patients of African descent

scientific article published on 09 August 2019

Association of the IGF1 gene with fasting insulin levels

scientific article published on 10 February 2016

Association of the Kir6.2 E23K variant with reduced acute insulin response in African-Americans

scientific article published on 16 September 2008

Association of the diabetes gene calpain-10 with subclinical atherosclerosis: the Mexican-American Coronary Artery Disease Study

scientific article published in April 2005

Associations between SLC16A11 variants and diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL)

scientific article published in Scientific Reports

Associations between adherence to the dietary approaches to stop hypertension (DASH) diet and six glucose homeostasis traits in the Microbiome and Insulin Longitudinal Evaluation Study (MILES)

scientific article published in 2022

Associations between genetic variants in the ACE, AGT, AGTR1 and AGTR2 genes and renal function in the Multi-ethnic Study of Atherosclerosis

scientific article

Associations between two common polymorphisms in the ABCA1 gene and subclinical atherosclerosis: Multi-Ethnic Study of Atherosclerosis (MESA)

article

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

article

Associations of adiponectin with body fat distribution and insulin sensitivity in nondiabetic Hispanics and African-Americans

scientific article published on 10 April 2007

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Associations of candidate genes to age-related macular degeneration among racial/ethnic groups in the multi-ethnic study of atherosclerosis ⬇️

scientific article published on 12 August 2013

Associations of pentraxin 3 with cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis

scientific article

Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep

scientific article published on 16 April 2019

Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

scientific article published in Nature Communications

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 01 May 2019

Autoantibodies and human leucocyte antigen class II in first-degree family members of Mexican-American type 1 diabetic patients

scientific article

Benchmarking association analyses of continuous exposures with RNA-seq in observational studies

scientific article published on 01 November 2021

Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium

scientific article

Bidirectional Mendelian randomization to explore the causal relationships between body mass index and polycystic ovary syndrome

scientific article published on 01 January 2019

Biological, clinical and population relevance of 95 loci for blood lipids

scientific article

Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease

scientific article published on 19 August 2019

Blood monocyte transcriptome and epigenome analyses reveal loci associated with human atherosclerosis

scientific article published on 30 August 2017

Body Adiposity Index versus Body Mass Index and Other Anthropometric Traits as Correlates of Cardiometabolic Risk Factors ⬇️

scientific article published on June 11, 2013

Both preoperative perinuclear antineutrophil cytoplasmic antibody and anti-CBir1 expression in ulcerative colitis patients influence pouchitis development after ileal pouch-anal anastomosis

scientific article published on 18 April 2008

C-reactive protein gene polymorphism 1009A>G is associated with serum CRP levels in Chinese men: a TCVGHAGE study

scientific article published on 25 April 2007

CELF4 Variant and Anthracycline-Related Cardiomyopathy: A Children's Oncology Group Genome-Wide Association Study

scientific article published on 25 January 2016

CRTC3 links catecholamine signalling to energy balance

scientific journal article

CUBN is a gene locus for albuminuria

scientific article

Candidate gene association resource (CARe): design, methods, and proof of concept

scientific article

Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

scientific article

Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study

scientific article

Candidate locus for a nuclear modifier gene for maternally inherited deafness

scientific article

Carotid intima-media thickness (cIMT) cosegregates with blood pressure and renal function in hypertensive Hispanic families

scientific article published on 29 October 2007

Catechol-O-Methyltransferase and Cardiovascular Disease: MESA

scientific article published on 16 December 2019

Cerebral small vessel disease genomics and its implications across the lifespan

scientific article published on 08 December 2020

Cerivastatin, genetic variants, and the risk of rhabdomyolysis

scientific article

Challenges in elucidating the genetics of diabetic retinopathy

scientific article

Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans

scientific article

Characterization of statin dose response in electronic medical records

scientific article published on 04 October 2013

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

scientific article

Classification of Type 2 Diabetes Genetic Variants and a Novel Genetic Risk Score Association With Insulin Clearance

scientific article published on 01 April 2020

Clinical utility of pharmacogenetic biomarkers in cardiovascular therapeutics: a challenge for clinical implementation

scientific article

Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients

scientific article

Clonal hematopoiesis associated with epigenetic aging and clinical outcomes

scientific article published on 29 May 2021

Close genetic linkage between diabetes mellitus and kidd blood group ⬇️

scientific article published on October 24, 1981

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

scientific article (publication date: February 2009)

Coincident linkage of fasting plasma insulin and blood pressure to chromosome 7q in hypertensive hispanic families

scientific article

Combination of genetic and quantitative serological immune markers are associated with complicated Crohnʼs disease behavior ⬇️

scientific article published on March 9, 2011

Combination of innate and adaptive immune alterations increased the likelihood of fibrostenosis in Crohn's disease

scientific article published on August 2010

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

scientific article

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

scientific article

Combined influence of LDLR and HMGCR sequence variation on lipid-lowering response to simvastatin

scientific article

Common Coding Variants in Are Associated With the Nav1.8 Late Current and Cardiac Conduction

scientific article published on 01 May 2018

Common Variants in the Periostin Gene Influence Development of Atherosclerosis in Young Persons ⬇️

scientific article published on April 7, 2011

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common genetic variants and subclinical atherosclerosis: The Multi-Ethnic Study of Atherosclerosis (MESA).

scientific article

Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism

scientific article published on 29 October 2011

Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.

scientific article

Common genetic variation, residential proximity to traffic exposure, and left ventricular mass: the Multi-Ethnic Study of Atherosclerosis

journal article published in 2010

Common variants associated with plasma triglycerides and risk for coronary artery disease

scientific article

Common variants at five new loci associated with early-onset inflammatory bowel disease

scientific article

Common variants at ten loci influence QT interval duration in the QTGEN Study

scientific article published on 22 March 2009

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

scientific article

Common variants in KCNN3 are associated with lone atrial fibrillation

scientific article

Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest

scientific article published on 10 January 2014

Community Partnership in Precision Medicine: Themes from a Community Engagement Conference.

scientific article published on 6 September 2018

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

scientific article

Comparison of Genome-Wide and Gene-Specific DNA Methylation Profiling in First-Trimester Chorionic Villi From Pregnancies Conceived With Infertility Treatments

scientific article published on January 2016

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

scientific article

Comparison of Proteomic Assessment Methods in Multiple Cohort Studies

scientific article published on 09 May 2020

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes

scientific article published on March 1997

Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8

scientific article

Consanguinity and common adult diseases in Israeli Arab communities

scientific article published on 01 June 1997

Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.

scientific article published on May 1997

Consumption of meat is associated with higher fasting glucose and insulin concentrations regardless of glucose and insulin genetic risk scores: a meta-analysis of 50,345 Caucasians

scientific article

Coronary Heart Disease Genetic Risk Score Predicts Cardiovascular Disease Risk in Men, Not Women

scientific article published on 01 October 2018

Correction: Four Novel Loci (19q13, 6q24, 12q24, and 5q14) Influence the Microcirculation In Vivo.

scientific article

Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

scientific article

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

scientific article

Correlates and heritability of nonalcoholic fatty liver disease in a minority cohort

scientific article published on 19 February 2009

Cosegregation of albuminuria and blood pressure: the Insulin Resistance Atherosclerosis (IRAS) family study

scientific article published in June 2005

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

scientific article

D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study

scientific article published on 14 September 2017

DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation

scientific article published on 30 November 2017

DPB1 alleles are associated with type 1 diabetes susceptibility in multiple ethnic groups

scientific article published in August 2004

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

scientific article

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

scientific article published in Nature Communications

Deep-coverage whole genome sequences and blood lipids among 16,324 individuals

Defining the role of common variation in the genomic and biological architecture of adult human height

scientific article

Deleterious Effect of Butyrylcholinesterase K-Variant in Donepezil Treatment of Mild Cognitive Impairment

scientific article published on 29 November 2016

Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis

scientific article

Detection of genetic loci associated with plasma fetuin-A: a meta-analysis of genome-wide association studies from the CHARGE Consortium

scientific article published on 3 April 2017

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

scientific article

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Determination and use of haplotypes: ethnic comparison and association of the lipoprotein lipase gene and coronary artery disease in Mexican-Americans

scientific article published in July 2003

Diabetes Mellitus: The Search for Genetic Markers ⬇️

scientific article published on March 1, 1979

Dietary fatty acids modulate associations between genetic variants and circulating fatty acids in plasma and erythrocyte membranes: Meta-analysis of nine studies in the CHARGE consortium

scientific article

Differences in First-Trimester Maternal Metabolomic Profiles in Pregnancies Conceived From Fertility Treatments

scientific article published on 01 April 2019

Different HLA haplotypes in Mexican Americans with IDDM.

scientific article published in July 1989

Differential effects of ramipril on ambulatory blood pressure in African Americans and Caucasians

scientific article published in August 2007

Differential gene expression during placentation in pregnancies conceived with different fertility treatments compared with spontaneous pregnancies

scientific article published on 02 January 2019

Differential gene expression of blood-derived cell lines in familial combined hyperlipidemia

scientific article

Differentially expressed genes in adipocytokine signaling pathway of adipose tissue in pregnancy

scientific article published on May 2013

Directional dominance on stature and cognition in diverse human populations

scientific article published in July 2015

Discovery and fine mapping of serum protein loci through transethnic meta-analysis

scientific article

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

scientific article

Discovery and refinement of loci associated with lipid levels

scientific article

Discovery of novel heart rate-associated loci using the Exome Chip

scientific article

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

scientific article published on 23 November 2020

Disentangling the genetics of lean mass

article

Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium

scientific article

Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval

scientific article published on 05 March 2013

Duodenal-ulcer disease associated with elevated serum pepsinogen I: an inherited autosomal dominant disorder

scientific article published on January 11, 1979

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

scientific article published on 24 August 2020

Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals

scientific article published on 01 June 2019

Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations

scientific article

Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies

scientific article published on 10 January 2019

Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies

scientific article published on 14 October 2011

Electrocardiographic abnormalities associated with the metabolic syndrome and its components: the multi-ethnic study of atherosclerosis

scientific article published on 4 November 2011

Elevated plasma free fatty acids are associated with sudden death: a prospective community-based evaluation at the time of cardiac arrest

scientific article

Empirical characteristics of family-based linkage to a complex trait: the ADIPOQ region and adiponectin levels

scientific article

Epigenome-wide association analysis of daytime sleepiness in the Multi-Ethnic Study of Atherosclerosis reveals African-American-specific associations

scientific article published on 01 August 2019

Erratum. Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetes 2019;68:441-456

scientific article published on 27 April 2020

Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

scholarly article published in Nature Genetics

Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

scholarly article published in Nature Genetics

Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk

scientific article published on 2 August 2017

Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci

scholarly article published in Nature Genetics

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

scientific article

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

scientific article published in July 2017

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

scientific article published in May 2010

Estimating the Contributions of Rare and Common Genetic Variations and Clinical Measures to a Model Trait: Adiponectin ⬇️

scientific article published on 02 October 2012

Estimating the recombination frequency for the MN and the Ss loci

scientific article published on 01 January 1984

Evaluating gene x gene and gene x smoking interaction in rheumatoid arthritis using candidate genes in GAW15.

scientific article

Evaluation of mitochondrial DNA copy number estimation techniques

scientific article published on 31 January 2020

Evidence for a major dominance component in the variation of serum pepsinogen I levels

scientific article

Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation ⬇️

scientific article published on June 5, 1998

Evidence for joint genetic control of insulin sensitivity and systolic blood pressure in hispanic families with a hypertensive proband

scientific article

Evidence for linkage of a candidate chromosome 1 region to human systemic lupus erythematosus

scientific article published on February 1997

Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6.

scientific article

Evidence of insulin resistant lipid metabolism in adipose tissue in familial combined hyperlipidemia, but not type 2 diabetes mellitus

scientific article published in October 2002

Exome Chip Analysis Identifies Low-Frequency a on Brain Magnetic Imaging

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

scientific article

Exome Sequencing Identifies Genetic Variants Associated with Circulating Lipid Levels in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study (IRASFS).

scientific article

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

article by Jason Flannick et al published 22 May 2019 in Nature

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

scientific article published on 06 June 2019

Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology

scientific article published on 01 September 2019

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

Exome-wide association study of plasma lipids in >300,000 individuals

scientific article published on 30 October 2017

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Familial Mediterranean fever in Armenians: autosomal recessive inheritance with high gene frequency

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Familial Mediterranean fever--linkage studies with genetic markers on chromosome 6.

scientific article

Familial Mediterranean fever: analysis of inheritance and current linkage data

scientific article published on September 15, 1992

Familial Mediterranean fever: effects of genotype and ethnicity on inflammatory attacks and amyloidosis

scientific article published on May 2000

Familial empiric risk estimates of inflammatory bowel disease in Ashkenazi Jews

scientific article published in April 1989

Familial empirical risks for inflammatory bowel disease: differences between Jews and non-Jews

scientific article

Familial expression of anti-Escherichia coli outer membrane porin C in relatives of patients with Crohn's disease

scientific article

Familial expression of anti-Saccharomyces cerevisiae mannan antibodies in affected and unaffected relatives of patients with Crohn's disease

scientific article

Families with Familial Combined Hyperlipidemia and Families Enriched for Coronary Artery Disease Share Genetic Determinants for the Atherogenic Lipoprotein Phenotype ⬇️

scientific article published on August 1, 1998

Family history and serology predict Crohn's disease after ileal pouch-anal anastomosis for ulcerative colitis

scientific article published on 18 December 2007

Family history: A comprehensive genetic risk assessment method for the chronic conditions of adulthood ⬇️

scientific article published on August 22, 1997

Fasting insulin reflects heterogeneous physiological processes: role of insulin clearance ⬇️

scientific article published on May 31, 2011

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave

scientific article

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

scientific article published on 22 May 2017

Fine mapping of QT interval regions in global populations refines previously identified QT interval loci and identifies signals unique to African and Hispanic descent populations

scientific article

Fine mapping the CETP region reveals a common intronic insertion associated to HDL-C

scientific article

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

scientific article

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

scientific article published on 08 October 2018

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

scientific article

Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo

scientific article published in October 2010

Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease

scientific article

Further investigation in europeans of susceptibility variants for polycystic ovary syndrome discovered in genome-wide association studies of Chinese individuals

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GENOME-WIDE INTERACTION WITH SELECTED TYPE 2 DIABETES LOCI REVEALS NOVEL LOCI FOR TYPE 2 DIABETES IN AFRICAN AMERICANS.

scientific article

GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium

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GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes

scientific article published in Nature Communications

GWAS for executive function and processing speed suggests involvement of the CADM2 gene.

scientific article

GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations

scientific article published on 28 June 2019

GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy

scientific article

GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals

scientific article published on 6 December 2017

Gain-of-function lipoprotein lipase variant rs13702 modulates lipid traits through disruption of a microRNA-410 seed site

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Gene expression in thiazide diuretic or statin users in relation to incident type 2 diabetes

scientific article published on 17 February 2014

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia

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Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations

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Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

scientific article published on 05 May 2020

Gene-gene Interaction Analyses for Atrial Fibrillation

scientific article

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

scientific article

General Framework for Meta-Analysis of Haplotype Association Tests

scientific article published on 8 March 2016

Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations

scientific article published on 21 November 2016

Generalized correlation measure using count statistics for gene expression data with ordered samples.

scientific article published on 12 October 2017

Genes associated with risk of type 2 diabetes identified by a candidate-wide association scan: as a trickle becomes a flood

scientific article

Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men ⬇️

scientific article published on December 1, 2011

Genetic Architecture of Primary Open Angle Glaucoma in Individuals of African Descent: The African Descent & Glaucoma Evaluation Study (ADAGES) III

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Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans

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Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

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Genetic Determinants of Electrocardiographic P-wave Duration and Relation to Atrial Fibrillation

scientific article published on 21 August 2020

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

scientific article

Genetic Heterogeneity of Hyperpepsinogenemic I and Normopepsinogenemic I Duodenal Ulcer Disease

scientific article published on 01 September 1979

Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium

scientific article published on 12 September 2017

Genetic Marker Associations With Proliferative Retinopathy in Persons Diagnosed With Diabetes Before 30 yr of age ⬇️

scientific article published on 01 July 1992

Genetic Risk Prediction of Atrial Fibrillation

scientific article published on 28 October 2016

Genetic Risk Score in Diabetes Associated With Chronic Pancreatitis Versus Type 2 Diabetes Mellitus

scientific article published on 01 July 2019

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

scientific article published on 11 September 2020

Genetic Variants Associated With Obesity and Insulin Resistance in Hispanic Boys With Nonalcoholic Fatty Liver Disease

scientific article published on 21 February 2018

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium

scientific article

Genetic Variants Associated with Circulating Fibroblast Growth Factor 23

Genetic Variants Associated with Circulating Parathyroid Hormone

scientific article published on 07 December 2016

Genetic Variation in the Human SORBS1 Gene is Associated With Blood Pressure Regulation and Age at Onset of Hypertension: A SAPPHIRe Cohort Study

scientific article published in March 2016

Genetic analysis of adiponectin variation and its association with type 2 diabetes in African Americans

scientific article published on 11 June 2013

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Genetic ancestry and the relationship of cigarette smoking to lung function and per cent emphysema in four race/ethnic groups: a cross-sectional study

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Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

scientific article published on 24 May 2017

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting

Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33

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Genetic architecture of gene expression traits across diverse populations

scholarly article published 10 January 2018

Genetic architecture of gene expression traits across diverse populations

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Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus

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Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

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Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).

scientific article

Genetic associations with valvular calcification and aortic stenosis

scientific article published on February 2013

Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949).

scientific article

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

scientific article published on 22 September 2020

Genetic determinants of osteoporosis susceptibility in a female Ashkenazi Jewish population

scientific article published in January 2004

Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium

scientific article published on 2 February 2012

Genetic effects on obesity assessed by bivariate genome scan: the Mexican-American coronary artery disease study

scientific article published on 01 July 2006

Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease

scientific article published on June 2009

Genetic heterogeneity in common disease

scientific article published on 01 January 1982

Genetic heterogeneity in diabetes mellitus and diabetic microangiopathy

scientific article published on 01 January 1981

Genetic heterogeneity in peptic ulcer ⬇️

scientific article published on May 19, 1979

Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.

scientific article published on 13 June 2018

Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits

scientific article published in 2022

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

scientific article published in 2022

Genetic loci associated with heart rate variability and their effects on cardiac disease risk

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Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies

scientific article published on 23 January 2016

Genetic loci associated with nonobstructive coronary artery disease in Caucasian women

scientific article published on 3 November 2015

Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication

scientific article published on October 2008

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

scientific article published on 13 November 2020

Genetic loci for retinal arteriolar microcirculation

scientific article

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome llq

scientific article published in Nature

Genetic mapping of disposition index and acute insulin response loci on chromosome 11q. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study

scientific article published in April 2006

Genetic marker family studies in familial Mediterranean fever (FMF) in Armenians

scientific article published on November 1990

Genetic markers: progress and potential for cardiovascular disease

scientific article published in June 2004

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 28 February 2019

Genetic predictors of medically refractory ulcerative colitis

scientific journal article

Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity

scientific article

Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

scientific article

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

scientific article published on 6 October 2011

Genetic variants modulate gene expression statin response in human lymphoblastoid cell lines

scientific article published on 12 August 2020

Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease

scientific article

Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis

scientific article

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

scientific journal article

Genetic variation in lipoprotein (a) levels in families enriched for coronary artery disease is determined almost entirely by the apolipoprotein (a) gene locus.

scientific article published on January 1995

Genetic variation of SORBS1 gene is associated with glucose homeostasis and age at onset of diabetes: A SAPPHIRe Cohort Study.

scientific article published on 12 July 2018

Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization Study

scientific article

Genetics of Coronary Artery Disease in Taiwan: A Cardiometabochip Study by the Taichi Consortium

scientific article

Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).

scientific article published on 02 March 2017

Genetics of coronary artery calcification among African Americans, a meta-analysis

scientific article

Genetics of diabetes

scientific article published on September 1983

Genetics of inflammatory bowel disease

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Genetics, diabetes mellitus heterogeneity, and coronary heart disease.

scientific article published on January 1984

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

scientific article published in November 2018

Genome Scan for Blood Pressure in Dutch Dyslipidemic Families Reveals Linkage to a Locus on Chromosome 4p ⬇️

scientific article published on October 1, 2001

Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

scientific article

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A

scientific article published on 01 November 2000

Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease

scientific article

Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated With Cardiac Morphogenesis and Heart Failure Development

scientific article published on 25 September 2019

Genome-Wide Association Studies

scientific article published on 01 November 2019

Genome-Wide Association Study Highlights APOH as a Novel Locus for Lipoprotein(a) Levels

scientific article published on 29 October 2020

Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium

scientific article published on 20 June 2019

Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.

scientific article published on April 2017

Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium

scientific article

Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group

scientific article published on 01 November 2019

Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci

scientific article published on 14 July 2016

Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

scientific article published on 25 August 2015

Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys

scientific article published on 14 September 2017

Genome-Wide Interaction with Insulin Secretion Loci Reveals Novel Loci for Type 2 Diabetes in African Americans

scientific article

Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent

scientific article published on 21 September 2017

Genome-Wide Linkage of Plasma Adiponectin Reveals a Major Locus on Chromosome 3q Distinct From the Adiponectin Structural Gene: The IRAS Family Study

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Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans

scientific article published on 27 November 2017

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans

scientific article

Genome-wide Meta-analysis of 158,000 Individuals of European Ancestry Identifies Three Loci Associated with Chronic Back Pain

Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis

scientific article published on 19 December 2016

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

scientific article published in Nature Communications

Genome-wide analysis of genetic loci associated with Alzheimer disease

scientific article

Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia

scientific article published on 24 April 2013

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

scientific article published in February 2013

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

scientific article published on 06 January 2013

Genome-wide association analysis identifies multiple loci related to resting heart rate

scientific article

Genome-wide association analysis identifies six new loci associated with forced vital capacity

scientific article

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

scientific article

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

scientific article published on 09 January 2020

Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.

scientific article

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

scientific article

Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology

scientific article

Genome-wide association identifies multiple ulcerative colitis susceptibility loci

scientific article

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

scientific article published on 11 September 2019

Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

Genome-wide association meta-analysis of fish and EPA+DHA consumption in 17 US and European cohorts.

scientific article published on 13 December 2017

Genome-wide association of body fat distribution in African ancestry populations suggests new loci

scientific article

Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.

scientific article

Genome-wide association of lipid-lowering response to statins in combined study populations

scientific article

Genome-wide association of pericardial fat identifies a unique locus for ectopic fat

scientific article

Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

scientific article

Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction

scientific article

Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference

scientific article published on 20 January 2016

Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium

scientific article

Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium

scientific article

Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy.

scientific article published on 4 April 2018

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction

scientific article

Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos

scientific article

Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis

scientific article

Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans

Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease

scientific article

Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels

scientific article published on 17 January 2018

Genome-wide association study in a Chinese population with diabetic retinopathy ⬇️

scientific article published on 04 April 2013

Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume

scientific article published in Nature Communications

Genome-wide association study of PR interval

scientific article

Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2.

scientific article published on 10 November 2017

Genome-wide association study of blood pressure and hypertension

scientific journal article

Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL

scientific article published in 2021

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

scientific article

Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of Latinos

scientific article published on 16 December 2017

Genome-wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos

scientific article published on 9 May 2016

Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts.

scientific article

Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation?

scientific article published on 7 March 2017

Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations

scientific article published on 13 October 2018

Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

scientific article

Genome-wide association study of retinopathy in individuals without diabetes

scientific article

Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study

scientific article

Genome-wide association: which do you want first: the good news, the bad news, or the good news?

scientific article published in December 2007

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

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Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk

scientific article

Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans.

scientific article

Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function

scientific article

Genome-wide linkage and association analysis of cardiometabolic phenotypes in Hispanic Americans

scientific article published on 18 August 2016

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

scientific article

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

scientific article

Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain

scientific article published on 27 September 2018

Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry

scientific article published on 01 June 2018

Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium

scientific article published on 09 July 2018

Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci

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Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake

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Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry

scientific article published on 06 December 2019

Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans

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Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).

scientific article

Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium

scientific article

Genomewide association studies of stroke

scientific article published on 15 April 2009

Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits ⬇️

scientific article published on 21 June 2016

Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium

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Genotype Imputation for Latinos Using the HapMap and 1000 Genomes Project Reference Panels ⬇️

scientific article published on June 27, 2012

Geographic origins of Jewish patients with inflammatory bowel disease

scientific article published on 01 October 1989

Glucose, insulin, and incident hypertension in the multi-ethnic study of atherosclerosis

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Growth curves in achondroplasia

scientific article published on 01 January 1977

HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

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HLA class II haplotype associations with inflammatory bowel disease in Jewish (Ashkenazi) and non-Jewish caucasian populations

scientific article (publication date: March 2000)

HLA genotypic study of insulin-dependent diabetes the excess of DR3/DR4 heterozygotes allows rejection of the recessive hypothesis

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HLA haplotype sharing and proband genotype in IDDM

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HLA on chromosome 6: the story gets longer and longer

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HLA-B5 associated with duodenal ulcer

scientific article published on 01 September 1977

HLA-DR and the 5' insulin gene polymorphism in insulin-dependent diabetes

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HLA-DR3 and DR4 and their relation to the incidence and progression of diabetic retinopathy1 1The authors have no proprietary interest in any of the products mentioned in this study

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Habitual sleep duration is associated with BMI and macronutrient intake and may be modified by CLOCK genetic variants

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Haplotypes in the lipoprotein lipase gene influence fasting insulin and discovery of a new risk haplotype

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Haplotypes in the lipoprotein lipase gene influence high-density lipoprotein cholesterol response to statin therapy and progression of atherosclerosis in coronary artery bypass grafts

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Harnessing expression data to identify novel candidate genes in polycystic ovary syndrome

scientific article (publication date: 2011)

Hemodynamic fluid shear stress response genes and carotid intima-media thickness: a candidate gene association analysis in the cardiovascular health study ⬇️

scientific article published on May 21, 2012

Heritability of dehydroepiandrosterone sulfate in women with polycystic ovary syndrome and their sisters

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Heritability of subclinical atherosclerosis in Latino families ascertained through a hypertensive parent

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Heritability of the severity of diabetic retinopathy: the FIND-Eye study

scientific article published on September 2008

Heritability patterns in hand osteoarthritis: the role of osteophytes ⬇️

scientific article published on September 28, 2010

Hermansky-Pudlak syndrome: an immunologic assessment of 15 cases

scientific article published on December 1988

Heterogeneity in Diabetes Mellitus—Update, 1978: Evidence for Further Genetic Heterogeneity within Juvenile-onset Insulin-dependent Diabetes Mellitus ⬇️

scientific article published on May 1, 1978

High-frequency haplotypes in the X chromosome locus TLR8 are associated with both CD and UC in females

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High-resolution linkage mapping for susceptibility genes in human polygenic disease: insulin-dependent diabetes mellitus and chromosome 11q.

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Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies

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Home use of a compact, 12‑lead ECG recording system for newborns

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Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

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Human genetic variation in VAC14 regulates Salmonella invasion and typhoid fever through modulation of cholesterol.

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Hundreds of variants clustered in genomic loci and biological pathways affect human height

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Hypertension genes are genetic markers for insulin sensitivity and resistance

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Hypothesis: familial Mediterranean fever--a genetic disorder of the lipocortin family?

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IBD-associated TL1A gene (TNFSF15) haplotypes determine increased expression of TL1A protein

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IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease

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IL23R haplotypes provide a large population attributable risk for Crohn's disease

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Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

scientific article published on 23 March 2015

Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene

scientific article published on 4 January 2016

Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia

scientific article published on 01 September 2000

Identification of candidate genes and pathways in retinopathy of prematurity by whole exome sequencing of preterm infants enriched in phenotypic extremes

scientific article published on 02 March 2021

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

scientific article published on 14 April 2013

Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

scientific article published on 4 September 2017

Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease

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Identification of quantitative trait loci for glucose homeostasis: the Insulin Resistance Atherosclerosis Study (IRAS) Family Study

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Identification of type 2 diabetes loci in 433,540 East Asian individuals

scientific article published on 06 May 2020

Identifying association under a previous linkage peak on chromosome 16 for body mass index using cross-sectional and longitudinal data of the Framingham Heart Study

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Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans

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Immunochip meta-analysis of inflammatory bowel disease identifies three novel loci and four novel associations in previously reported loci.

scientific article published on 23 March 2018

Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

scientific article published on 26 September 2019

Impact of ancestry and common genetic variants on QT interval in African Americans

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Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.

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Improved Performance of Dynamic Measures of Insulin Response Over Surrogate Indices to Identify Genetic Contributors of Type 2 Diabetes: The GUARDIAN Consortium

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Improved imputation accuracy in Hispanic/Latino populations with larger and more diverse reference panels: applications in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).

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Inactivating mutations in NPC1L1 and protection from coronary heart disease

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Incidence of Age-Related Macular Degeneration in a Multi-Ethnic United States Population: The Multi-Ethnic Study of Atherosclerosis

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Increased immune reactivity predicts aggressive complicating Crohn's disease in children

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Increased intestinal permeability in patients with Crohn's disease and their relatives. A possible etiologic factor

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Increased risk for type I (insulin-dependent) diabetes in relatives of patients with alopecia areata (AA).

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Individualizing therapies in type 2 diabetes mellitus based on patient characteristics: what we know and what we need to know

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Inflammation and the incidence of type 2 diabetes: the Multi-Ethnic Study of Atherosclerosis (MESA).

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Inherited causes of clonal haematopoiesis in 97,691 whole genomes

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Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis

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Insulin Clearance Is Associated with Hepatic Lipase Activity and Lipid and Adiposity Traits in Mexican Americans

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Insulin Resistance Exacerbates Genetic Predisposition to Nonalcoholic Fatty Liver Disease in Individuals Without Diabetes

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Insulin and islet cell autoantibodies as time-dependent covariates in the development of insulin-dependent diabetes: a prospective study in relatives

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Insulin clearance and the incidence of type 2 diabetes in Hispanics and African Americans: the IRAS Family Study

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Insulin clearance: confirmation as a highly heritable trait, and genome-wide linkage analysis ⬇️

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Insulin sensitivity and insulin clearance are heritable and have strong genetic correlation in Mexican Americans

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Insulin sensitivity, body fat distribution, and family diabetes history: the IRAS Family Study.

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Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

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Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups ⬇️

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Integrative predictive model of coronary artery calcification in atherosclerosis

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Interaction of HLA and immunoglobulin antigens in Type 1 (insulin-dependent) diabetes ⬇️

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Interactions between candidate cardiovascular disease genes, traffic proximity, and left ventricular mass: the Multi-Ethnic Study of Atherosclerosis (MESA)

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Interactions between commensal fungi and the C-type lectin receptor Dectin-1 influence colitis

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Interactions of dietary whole-grain intake with fasting glucose- and insulin-related genetic loci in individuals of European descent: a meta-analysis of 14 cohort studies

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Intercellular adhesion molecule 1 gene associations with immunologic subsets of inflammatory bowel disease

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Intestinal permeability in patients with Crohn's disease and their healthy relatives

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Investigation of the Interplay between Circulating Lipids and IGF-I and Relevance to Breast Cancer Risk: An Observational and Mendelian Randomization Study

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Israel-Gaza conflict

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KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference

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LDL Cholesterol and Dysglycemia: an Intriguing Physiological Relationship

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LPA Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins

Lack of an association between polymorphisms of the T-cell receptor alpha-chain and ulcerative colitis

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Large Meta-Analysis in the CHARGE Consortium Provides Evidence For an Association of Serum Vitamin D With Pulmonary Function

Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

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Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

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Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

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Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

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Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

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Large-scale candidate gene analysis in whites and African Americans identifies IL6R polymorphism in relation to atrial fibrillation: the National Heart, Lung, and Blood Institute's Candidate Gene Association Resource (CARe) project

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Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

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Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

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Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function

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Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function ⬇️

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Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

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Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.

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Leptin-mediated increases in catecholamine signaling reduce adipose tissue inflammation via activation of macrophage HDAC4

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Levels of Free Fatty Acids (FFA) Are Associated with Insulin Resistance But Do Not Explain the Relationship between Adiposity and Insulin Resistance in Hispanic Americans: The IRAS Family Study ⬇️

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Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

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Linkage Analysis of High-density SNPs Confirms Keratoconus Locus at 5q Chromosomal Region

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Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.

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Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple non-parametric analyses

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Linkage of Crohn's disease-related serological phenotypes: NFKB1 haplotypes are associated with anti-CBir1 and ASCA, and show reduced NF-kappaB activation

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Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study

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Lipoprotein lipase is a gene for insulin resistance in Mexican Americans

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Lipoprotein lipase locus and progression of atherosclerosis in coronary-artery bypass grafts

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Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies

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Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia

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Long-range LD can confound genome scans in admixed populations

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Low oxygen saturation during sleep reduces CD1D and RAB20 expressions that are reversed by CPAP therapy

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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

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Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis

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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

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Lysine-specific demethylase 1: an epigenetic regulator of salt-sensitive hypertension

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MAGI2 genetic variation and inflammatory bowel disease

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Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community

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Mendelian Randomization Analysis of Hemoglobin A1c as a Risk Factor for Coronary Artery Disease

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Mendelian randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

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Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways

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Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function

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Meta-analysis across Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium provides evidence for an association of serum vitamin D with pulmonary function

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Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

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Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

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Meta-analysis identifies six new susceptibility loci for atrial fibrillation

scientific article published on 29 April 2012

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

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Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

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Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels

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Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

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Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index

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Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error

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Meta-analysis of genome-wide association studies of HDL cholesterol response to statins

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Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs

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Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

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Metabolic Syndrome Derived from Principal Component Analysis and Incident Cardiovascular Events: The Multi Ethnic Study of Atherosclerosis (MESA) and Health, Aging, and Body Composition (Health ABC).

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Metabolic and cardiovascular genes in polycystic ovary syndrome: a candidate-wide association study (CWAS).

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Metabolomics Identifies Distinctive Metabolite Signatures for Measures of Glucose Homeostasis: The Insulin Resistance Atherosclerosis Family Study (IRAS-FS).

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Minimal model-based insulin sensitivity has greater heritability and a different genetic basis than homeostasis model assessment or fasting insulin

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Mitochondrial DNA copy number and incident atrial fibrillation

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Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study ⬇️

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Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

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Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

scientific article published in 2021

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

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Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

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Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

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Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study

scientific article published in 2021

Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits

scientific article published on 30 June 2020

Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men.

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Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project

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Multi-ethnic genome-wide association study for atrial fibrillation

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Multi-ethnic genome-wide association study of decomposed cardioelectric phenotypes illustrates strategies to identify and characterize evidence of shared genetic effects for complex traits

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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

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Multidimensional Prognostic Risk Assessment Identifies Association Between IL12B Variation and Surgery in Crohn’s Disease ⬇️

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Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.

scientific article published on 21 November 2016

Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control

scientific article published on 28 November 2018

Multiethnic Meta-analysis Identifies New Loci for Pulmonary Function

Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI

scientific article published on 7 February 2015

Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

scientific article published on 05 December 2016

Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function

scientific article published in Nature Communications

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease

scientific article (publication date: 17 September 2013)

Multilocus genetic determinants of LDL particle size in coronary artery disease families

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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

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Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians

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Multi‐phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations

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Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's disease

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NOD2 variants and antibody response to microbial antigens in Crohn's disease patients and their unaffected relatives.

scientific article published on 10 November 2006

NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium

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Native American ancestry is associated with severe diabetic retinopathy in Latinos.

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Natural Selection on Genes Related to Cardiovascular Health in High-Altitude Adapted Andeans

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Neutrophil autoantibodies in ulcerative colitis: Familial aggregation and genetic heterogeneity ⬇️

scholarly article by F Shanahan et al published August 1992 in Gastroenterology

New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475 000 Individuals

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New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders

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New gene functions in megakaryopoiesis and platelet formation

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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

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Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360)

No association of 9p21 with arterial elasticity and retinal microvascular findings

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No interactions between previously associated 2-hour glucose gene variants and physical activity or BMI on 2-hour glucose levels

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Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

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Novel Genetic Loci Associated With Retinal Microvascular Diameter

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Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium

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Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

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Novel genetic loci associated with hippocampal volume

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Novel genetic loci underlying human intracranial volume identified through genome-wide association

scientific article (publication date: 3 October 2016)

Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese

scientific article published on 30 January 2014

Novel human alpha1a-adrenoceptor single nucleotide polymorphisms alter receptor pharmacology and biological function

scientific article published on 10 March 2005

Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts

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Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease

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Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study

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Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

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OR15-6 Epigenetic Differences in First Trimester Pregnancies Conceived with Infertility.

scientific article published on 30 April 2019

Ocular Manifestations in Inflammatory Bowel Disease Are Associated with Other Extra-intestinal Manifestations, Gender, and Genes Implicated in Other Immune-related Traits.

scientific article published on 8 October 2015

Omega-3 Fatty Acids and Genome-Wide Interaction Analyses Reveal DPP10-Pulmonary Function Association

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Optimization of techniques for multiple platform testing in small, precious samples such as human chorionic villus sampling

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Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium

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Outdoor air pollution and mosaic loss of chromosome Y in older men from the Cardiovascular Health Study

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Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis

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PCSK9 Loss-of-Function Variants, Low-Density Lipoprotein Cholesterol, and Risk of Coronary Heart Disease and Stroke: Data From 9 Studies of Blacks and Whites

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PLD3 variants in population studies

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PPIP5K2 and PCSK1 are Candidate Genetic Contributors to Familial Keratoconus

scientific article published on 18 December 2019

PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity

scientific article published in Nature Communications

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

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Parent-of-Origin Effects of the APOB Gene on Adiposity in Young Adults

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Pathological acid secretion not due to gastrinoma

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Pattern recognition receptor and autophagy gene variants are associated with development of antimicrobial antibodies in Crohn's disease

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Peptic Ulcer Disease-A Heterogeneous Group of Disorders? ⬇️

scientific article published on September 1, 1977

Perinuclear antineutrophil cytoplasmic antibodies in patients with Crohn's disease define a clinical subgroup

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Personalized Medicine in Ophthalmology: From Pharmacogenetic Biomarkers to Therapeutic and Dosage Optimization

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Personalized medicine and pharmacogenetic biomarkers: progress in molecular oncology testing

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Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

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Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology

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Pharmacometabolomic signature links simvastatin therapy and insulin resistance

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Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

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Phenotypic predictors of response to simvastatin therapy among African-Americans and Caucasians: the Cholesterol and Pharmacogenetics (CAP) Study

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Physical Activity Associations with Bone Mineral Density and Modification by Metabolic Traits

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Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

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Pleiotropic genes for metabolic syndrome and inflammation

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Pleiotropy and heterogeneity in the expression of atherogenic lipoproteins: the IRAS Family Study

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Polycystic ovary syndrome in Mexican-Americans: prevalence and association with the severity of insulin resistance

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Polymorphic gene markers in Mexican-Americans residing in southern California

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Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein

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Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin

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Population structure of Hispanics in the United States: the multi-ethnic study of atherosclerosis

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Precise gene dosage determination by polymerase chain reaction: theory, methodology, and statistical approach ⬇️

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Predicting stroke through genetic risk functions: the CHARGE Risk Score Project

scientific article (publication date: February 2014)

Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease

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Predictors of mortality in hospitalized COVID-19 patients: A systematic review and meta-analysis

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Preferential transmission of diabetic alleles within the HLA gene complex

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Prognostic Significance of Large Airway Dimensions on Computed Tomography in the General Population: The Multi-Ethnic Study of Atherosclerosis (MESA) Lung Study

scientific article published on 12 March 2018

Progress in understanding the genetics of diabetes mellitus.

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Prospective study of particulate air pollution exposures, subclinical atherosclerosis, and clinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis and Air Pollution (MESA Air)

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Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease

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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

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Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

scientific article published in Nature Communications

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

scientific article published on 01 April 2020

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes

scientific article published on 01 July 2019

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 16 March 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

scientific article published on 01 July 2019

Quality of dietary fat and genetic risk of type 2 diabetes: individual participant data meta-analysis

scientific article published on 25 July 2019

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

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Quantifying the health benefits of genetic tests: a clinical perspective

scientific article published on 01 March 2006

Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent

scientific article published on 4 April 2015

Quantitative serum pepsinogen: genetics and relationship to urinary and gastric phenotypes

scientific article published on 01 January 1985

Quantitative trait analysis of type 2 diabetes susceptibility loci identified from whole genome association studies in the Insulin Resistance Atherosclerosis Family Study

scientific article published on 5 February 2008

Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22.

scientific article published on May 1996

Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk

scientific article published on 11 December 2015

Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease

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Rare Genetic Variants Associated With Sudden Cardiac Death in Adults

scientific article published on 11 November 2019

Rare and low-frequency coding variants alter human adult height

scientific article (publication date: February 2017)

Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF

scientific article

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

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Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project

scientific article published on 13 January 2016

Rationale, Design, and Baseline Characteristics of the Microbiome and Insulin Longitudinal Evaluation Study (MILES)

scientific article published on 20 July 2020

Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease

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Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

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Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13.

scientific article published on July 1993

Relationship of sex to diabetes risk in statin trials

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Relationships among serum pepsinogen I, serum pepsinogen II, and gastric mucosal histology. A study in relatives of patients with pernicious anemia

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Relationships between the human pepsinogen DNA and protein polymorphisms

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Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis

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Replication of association of DENND1A and THADA variants with polycystic ovary syndrome in European cohorts

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Replication of calpain-10 genetic association with carotid intima-media thickness

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Restriction fragment length polymorphism (RFLP) heterogeneity of HLA-DQ beta genes associated with DNA fragment identical to the DR1-beta DNA structure

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Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels

scientific article published on 08 June 2020

Rooted in risk: genetic predisposition for low-density lipoprotein cholesterol level associates with diminished low-density lipoprotein cholesterol response to statin treatment

scientific article published on 20 September 2016

SORCS1: a novel human type 2 diabetes susceptibility gene suggested by the mouse

scientific article published on 10 April 2007

Sample-size calculations in segregation analysis.

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Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders.

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Saturated fat intake modulates the association between an obesity genetic risk score and body mass index in two US populations

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Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).

scientific article

Sensorineural deafness inherited as a tissue specific mitochondrial disorder ⬇️

scientific article published on February 1, 1992

Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level

scientific article published on 24 October 2019

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

scientific article published on 6 March 2019

Sequencing of SCN5A identifies rare and common variants associated with cardiac conduction: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

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Serum amyloid A and P protein genes in familial Mediterranean fever

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Serum immune responses predict rapid disease progression among children with Crohn's disease: immune responses predict disease progression

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Serum metabolic signatures of coronary and carotid atherosclerosis and subsequent cardiovascular disease

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Sex differences in the late first trimester human placenta transcriptome

scientific article published on 15 January 2018

Single nucleotide polymorphisms in the apolipoprotein M gene are associated with percent emphysema, HDL and HDL subfractions among European- And African-Americans: the MESA Lung and SNP Health Association Resource (SHARe) studies

abstract published in 2012

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

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Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

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Standard growth curves for achondroplasia

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Statin-induced LDL cholesterol response and type 2 diabetes: a bidirectional two-sample Mendelian randomization study

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Statin-induced changes in gene expression in EBV-transformed and native B-cells

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Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner

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Statin-induced expression change of INSIG1 in lymphoblastoid cell lines correlates with plasma triglyceride statin response in a sex-specific manner.

scientific article published on March 2016

Steroidogenic regulatory factor FOS is underexpressed in polycystic ovary syndrome (PCOS) adipose tissue and genetically associated with PCOS susceptibility

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Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function ⬇️

scientific article published on 29 May 2018

Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitis

scientific article published in October 1996

Susceptibility to Crohn's disease is mediated by KIR2DL2/KIR2DL3 heterozygosity and the HLA-C ligand

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Systematic evaluation of validated type 2 diabetes and glycaemic trait loci for association with insulin clearance ⬇️

scientific article published on March 14, 2013

Systemic Soluble Tumor Necrosis Factor Receptors 1 and 2 Are Associated with Severity of Diabetic Retinopathy in Hispanics ⬇️

scientific article published on February 11, 2012

TNFRSF1B Is Associated with ANCA in IBD.

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TNFSF15 is an ethnic-specific IBD gene

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Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study

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Testing the gene or testing a variant? The case of TCF7L2

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The 3' untranslated region of the lipoprotein lipase gene: haplotype structure and association with post-heparin plasma lipase activity

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The 5' insulin gene polymorphism and the genetics of vascular complications in type 1 (insulin-dependent) diabetes mellitus

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The African Descent and Glaucoma Evaluation Study (ADAGES) III: Contribution of Genotype to Glaucoma Phenotype in African Americans: Study Design and Baseline Data

scientific article published on 17 January 2018

The Association of Estrogen Receptor-β Gene Variation With Salt-Sensitive Blood Pressure

scientific article published on 5 September 2017

The GENNID Study. A resource for mapping the genes that cause NIDDM.

scientific article published in August 1996

The GLP-1 response to glucose does not mediate beta and alpha cell dysfunction in Hispanics with abnormal glucose metabolism

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The HMG-CoA reductase gene and lipid and lipoprotein levels: the multi-ethnic study of atherosclerosis

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The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

scientific article

The M694V mutation in Armenian-Americans: a 10-year retrospective study of MEFV mutation testing for familial Mediterranean fever at UCLA.

scientific article published on 7 November 2012

The Polygenic and Monogenic Basis of Blood Traits and Diseases

scientific article published on 01 September 2020

The aggregation of the 5' insulin gene polymorphism in insulin dependent (type I) diabetes mellitus families ⬇️

scientific article published on July 1, 1992

The chromosome 9p21 variant not predicting long-term cardiovascular mortality in Chinese with established coronary artery disease: an eleven-year follow-up study

scientific article published on 02 April 2014

The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity

scientific article

The gene for familial Mediterranean fever is mapped to 16p 13.3- p13.1 with evidence for homogeneity.

scientific article published on January 1995

The genetic syndromology of peptic ulcer ⬇️

scientific article published on 01 January 1981

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

scientific article published in PLoS ONE

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

scientific article published on 12 September 2016

The genetics of diabetes

scientific article published on 01 May 1987

The genetics of retinopathy of prematurity: a model for neovascular retinal disease

article

The genetics of the glucose intolerance disorders

scientific article published on 01 January 1981

The landscape of recombination in African Americans

scientific article

The lipoprotein lipase (LPL) S447X gain of function variant involves increased mRNA translation

scientific article published on 27 December 2011

The role of the Toll receptor pathway in susceptibility to inflammatory bowel diseases

article

The transcriptional landscape of age in human peripheral blood

scientific article

The triglyceride to high-density lipoprotein cholesterol (TG/HDL-C) ratio as a predictor of insulin resistance, β-cell function, and diabetes in Hispanics and African Americans

scientific article published on 03 November 2018

Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations.

scientific article published on 9 January 2018

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

scientific article

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

scientific article published on 01 September 2020

Trans-ethnic fine mapping identifies a novel independent locus at the 3' end of CDKAL1 and novel variants of several susceptibility loci for type 2 diabetes in a Han Chinese population

scientific article published on 08 September 2013

Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci

scientific article published on 8 April 2017

Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained

scientific article

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

scientific article published in Nature Communications

Trans-ethnic meta-analysis of white blood cell phenotypes

scientific article

Transcriptome-Wide Analysis Identifies Novel Associations With Blood Pressure

scientific article published on 07 August 2017

Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations

scientific article published in 2021

Transethnic Transferability of a Genome-wide Polygenic Score for Coronary Artery Disease

scientific article published on 07 December 2020

Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study

scientific article published on 27 November 2012

Transferability and fine-mapping of glucose and insulin quantitative trait loci across populations: CARe, the Candidate Gene Association Resource

scientific article

Tumor necrosis factor microsatellites define a Crohn's disease-associated haplotype on chromosome 6.

scientific article

Two-locus mitochondrial and nuclear gene models for mitochondrial disorders ⬇️

scientific article published on 01 January 1992

Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis

scientific article published in December 2023

Ulcerative colitis and total alopecia in a mother and her son

scientific article published on 01 April 1993

Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study

scientific article

Ulcerative colitis: a genetically heterogeneous disorder defined by genetic (HLA class II) and subclinical (antineutrophil cytoplasmic antibodies) markers

scientific article

Ultraconserved elements in the human genome: association and transmission analyses of highly constrained single-nucleotide polymorphisms

scientific article

Unusual congenital anomalies

scientific article published on January 1, 1975

Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study

scientific article published on 27 January 2022

Uridine monophosphate kinase and susceptibility to invasive Haemophilus influenzae type B disease

scientific article published on 01 January 1986

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

scientific article published on 23 December 2019

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

scientific article

Variants identified in a GWAS meta-analysis for blood lipids are associated with the lipid response to fenofibrate

scientific article

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry ⬇️

scientific article published on 13 July 2009

Variants in ZNF365 isoform D are associated with Crohn's disease ⬇️

scientific article published on January 21, 2011

Variants in angiopoietin-2 (ANGPT2) contribute to variation in nocturnal oxyhaemoglobin saturation level

scientific article

Variants of the caveolin-1 gene: a translational investigation linking insulin resistance and hypertension

scientific article

Variation in the 3-hydroxyl-3-methylglutaryl coenzyme a reductase gene is associated with racial differences in low-density lipoprotein cholesterol response to simvastatin treatment

scientific article published on 10 March 2008

Variation in the gene for muscle-specific AMP deaminase is associated with insulin clearance, a highly heritable trait

scientific article published in April 2005

Variation in the lysyl oxidase (LOX) gene is associated with keratoconus in family-based and case-control studies

scientific article published on 28 June 2012

Visceral fat and prevalence of hypertension among African Americans and Hispanic Americans: findings from the IRAS family study

scientific article published on 19 June 2008

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

scientific article published on 05 January 2021

Whole genome sequence analysis of pulmonary function and COPD in 19,996 multi-ethnic participants

scientific article published on 14 October 2020

Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction

scientific article published on 01 March 2019

Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.

scientific article

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

scientific article

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

scientific article

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

scientific article published in 2021

Workshop on genetics of diabetes

scientific article published on 01 January 1982

X chromosome dosage of histone demethylase KDM5C determines sex differences in adiposity

scientific article published on 23 July 2020

rs641738C>T near MBOAT7 is associated with liver fat, ALT, and fibrosis in NAFLD: a meta-analysis

scientific article published on 31 August 2020

List of works by Jerome I Rotter

40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 ⬇️

52 Genetic Loci Influencing Myocardial Mass

73-OR: Clonal Hematopoiesis of Indeterminate Potential (CHIP), Glycemic Traits, and Type 2 Diabetes (T2D) Risk

A Comprehensive Analysis of Common and Rare Variants to Identify Adiposity Loci in Hispanic Americans: The IRAS Family Study (IRASFS).

A Comprehensive Evaluation of the Genetic Architecture of Sudden Cardiac Arrest

A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.

A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter ⬇️

A Genetic Risk Score Associated with Chronic Obstructive Pulmonary Disease Susceptibility and Lung Structure on Computed Tomography

A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos

A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

A Long Non-coding RNA, LOC157273, Is an Effector Transcript at the Chromosome 8p23.1-PPP1R3B Metabolic Traits and Type 2 Diabetes Risk Locus

A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait ⬇️

A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH

A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium

A catalog of genetic loci associated with kidney function from analyses of a million individuals

A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis

A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes

A generalized least-squares framework for rare-variant analysis in family data

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

A genome scan for fasting insulin and fasting glucose identifies a quantitative trait locus on chromosome 17p: the insulin resistance atherosclerosis study (IRAS) family study.

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS).

A genome-wide association search for type 2 diabetes genes in African Americans

A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries

A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3

A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women

A genome-wide association study of aging

A genome-wide association study of central corneal thickness in Latinos

A genome-wide association study of chronic obstructive pulmonary disease in Hispanics

A genome-wide association study of depressive symptoms

A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes

A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium

A genome-wide linkage and association analysis of imputed insertions and deletions with cardiometabolic phenotypes in Mexican Americans: The Insulin Resistance Atherosclerosis Family Study

A genome-wide scan for carotid artery intima-media thickness: the Mexican-American Coronary Artery Disease family study

A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci

A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies

A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

A meta-analysis of genome-wide association studies identifies multiple longevity genes

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

A new syndrome of Crohn's disease and pachydermoperiostosis in a family

A noncoding variant near PPP1R3B promotes liver glycogen storage and MetS, but protects against myocardial infarction

A novel Alzheimer disease locus located near the gene encoding tau protein.

A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews

A novel method for testing association of multiple genetic markers with a multinomial trait.

A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains

A prevalent caveolin-1 gene variant is associated with the metabolic syndrome in Caucasians and Hispanics

A search for heterogeneity in insulin dependent diabetes mellitus (IDDM): HLA and autoimmune studies in simplex, multiplex and multigenerational families ⬇️

A statin-dependent QTL for GATM expression is associated with statin-induced myopathy

A structural variation reference for medical and population genetics

ANCA pattern and LTA haplotype relationship to clinical responses to anti-TNF antibody treatment in Crohn's disease

APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema

Abstract 14629: Rare Variants for Electrocardiographic Traits Identify Arrhythmia Susceptibility Genes

Actionable exomic incidental findings in 6503 participants: challenges of variant classification

Additional comments on the ulcer-multiple lentigines syndrome

Adiponectin Isoform Patterns in Ethnic-Specific ADIPOQ Mutation Carriers: The IRAS Family Study

Adiponectin, Insulin Sensitivity and Diabetic Retinopathy in Latinos With Type 2 Diabetes

Adiposity-Independent Effects of Aging on Insulin Sensitivity and Clearance in Mice and Humans

Admixture Mapping of Subclinical Atherosclerosis and Subsequent Clinical Events Among African Americans in 2 Large Cohort Studies

Admixture mapping identifies novel loci for obstructive sleep apnea in hispanic/latino americans

Admixture mapping of coronary artery calcified plaque in African Americans with type 2 diabetes mellitus

African Ancestry Analysis and Admixture Genetic Mapping for Proliferative Diabetic Retinopathy in African Americans

African Ancestry Is Associated with Higher Intraocular Pressure in Latinos

African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos

Air pollution and percent emphysema identified by computed tomography in the Multi-Ethnic study of Atherosclerosis

Allele-specific expression changes dynamically during T cell activation in HLA and other autoimmune loci

Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts

Alterations of a Cellular Cholesterol Metabolism Network Are a Molecular Feature of Obesity-Related Type 2 Diabetes and Cardiovascular Disease

Alternative splicing of 3-hydroxy-3-methylglutaryl coenzyme A reductase is associated with plasma low-density lipoprotein cholesterol response to simvastatin

Amino acid position 37 of HLA-DRβ1 affects susceptibility to Crohn's disease in Asians

Amyloidosis in familial mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus

An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group

An Outbreak of Polygenic Scores for Coronary Artery Disease