Search filters

List of works by Mark Lathrop

17q21 variants modify the association between early respiratory infections and asthma

scientific article published on 23 December 2009

17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression.

scientific article published on 13 December 2016

35th Annual Meeting of the European Association for the Study of Diabetes

article

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

article

6C.02: EXOME SEQUENCING IN SEVEN FAMILIES AND GENE-BASED ASSOCIATION STUDIES SUPPORT GENETIC HETEROGENEITY AND SUGGEST POSSIBLE CANDIDATES FOR FIBROMUSCULAR DYSPLASIA.

scientific article published on June 2015

A Distributed Whole Genome Sequencing Benchmark Study

scientific article published on 01 December 2020

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1

scholarly article by Pierre-Emmanuel Morange et al published April 2010 in American Journal of Human Genetics

A General Framework for Interrogation of mRNA Stability Programs Identifies RNA-Binding Proteins that Govern Cancer Transcriptomes ⬇️

scientific article published on 01 May 2018

A Genome Search for Genetic Determinants That Influence Plasma Fibrinogen Levels

scientific article published on 10 March 2005

A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma

scientific article published on 10 June 2011

A Novel Risk Locus at 6p21.3 for Epstein-Barr Virus-Positive Hodgkin Lymphoma

scientific article published on 24 September 2015

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

scientific article

A Quantitative Trait Locus Influencing Free Plasma Protein S Levels on Human Chromosome 1q

scientific article published on 09 January 2003

A Replicated, Genome-Wide Significant Association of Aortic Stenosis With a Genetic Variant for Lipoprotein(a): Meta-Analysis of Published and Novel Data

scientific article published in March 2017

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

scientific article

A comparison of two algorithms, MultiMap and gene mapping system, for automated construction of genetic linkage maps

scientific article published in January 1999

A comprehensive genetic map of the human genome based on 5,264 microsatellites

scientific article (publication date: 14 March 1996)

A comprehensive genome-wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants

scientific article published on 27 June 2016

A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines

scientific article published on 23 January 2013

A detailed genetic map of the long arm of chromosome 11

scientific article published on 01 July 1990

A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates ⬇️

scientific article published on May 1, 1991

A first high-density map of 981 biallelic markers on human chromosome 14.

scientific article published in December 2000

A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.

scientific article

A gene differentially expressed in the kidney of the spontaneously hypertensive rat cosegregates with increased blood pressure

scientific article

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q

scientific article

A gene-based genetic linkage and comparative map of the rat X chromosome

scientific article published in March 1997

A genetic linkage map of 41 restriction fragment length polymorphism markers for human chromosome 3

scientific article published on 01 November 1991

A genetic linkage map of markers for human chromosome 20

scientific article published on 01 November 1989

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 meta-analysis of plasma Aβ peptides concentrations in the elderly

scientific article published on 18 February 2014

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 confirms APOE as the major gene influencing survival in long-lived individuals

article

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 a novel susceptibility locus for renal cell carcinoma on 12p11.23

scientific article published on 18 October 2011

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis

scientific article published on 25 July 2013

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

scientific article

A genome-wide association study of global gene expression

scientific article (publication date: October 2007)

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

scientific article

A genome-wide association study of the Protein C anticoagulant pathway

scientific article

A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium

scientific article

A genome-wide exploration suggests an oligogenic model of inheritance for the TAFI activity and its antigen levels

scientific article published on 18 June 2008

A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis

scientific article

A genome-wide search for quantitative trait loci underlying asthma

scientific article

A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project

scientific article

A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate

scientific article published on 16 December 2008

A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL)

scientific article published on 01 September 2002

A high-resolution consensus linkage map of the rat, integrating radiation hybrid and genetic maps

scientific article published in July 2001

A high-resolution linkage map for the Z chromosome in chicken reveals hot spots for recombination

scientific article published in January 2007

A large-scale, consortium-based genomewide association study of asthma

scientific article

A linkage and physical map of chromosome 22, and some applications to gene mapping

scientific article

A linkage map of the rat genome derived from three F2 crosses

scientific article published in May 1997

A locus at 7p14.3 predisposes to refractory celiac disease progression from celiac disease

A major quantitative trait locus influences hyperactivity in the WKHA rat.

scientific article published in December 1996

A mapped set of DNA markers for human chromosome 15.

scientific article published in November 1988

A mapped set of DNA markers for human chromosome 17.

scientific article published in May 1988

A mapped set of genetic markers for human chromosome 9.

scientific article

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

scientific article

A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome

scientific article

A multi-stage multi-design strategy provides strong evidence that the BAI3 locus is associated with early-onset venous thromboembolism

scientific article published in December 2010

A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage

scientific article published on 27 November 2006

A neurobiological pathway to smoking in adolescence: TTC12-ANKK1-DRD2 variants and reward response.

scientific article published on 11 August 2018

A new locus on chromosome 18 that influences normal variation in activated protein C resistance phenotype and factor VIII activity and its relation to thrombosis susceptibility.

scientific article published on 15 August 2002

A new method to test genetic models in HLA associated diseases: the MASC method

scientific article

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

scientific article

A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.

scientific article

A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29

scientific article (publication date: 2003)

A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci

scientific article

A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions

scientific article published on 16 September 2017

A pharmacogenetic approach to blood pressure in Lyon hypertensive rats. A chromosome 2 locus influences the response to a calcium antagonist

scientific article published on October 1997

A phenotypic structure and neural correlates of compulsive behaviors in adolescents

scientific article

A polymorphism of the POLG2 gene is genetically associated with the invasiveness of urinary bladder cancer in Japanese males ⬇️

scientific article published on July 7, 2011

A primary genetic linkage map for human chromosome 12.

scientific article published in September 1987

A primary genetic map of chromosome 13q.

scientific article published in October 1986

A primary genetic map of markers of human chromosome 10

scientific article published on 01 February 1988

A primary map of 24 loci on human chromosome 16.

scientific article

A primary map of ten DNA markers and two serological markers for human chromosome 19

scientific article published on 01 July 1988

A quantitative-trait locus in the human factor XII gene influences both plasma factor XII levels and susceptibility to thrombotic disease

scientific article published on 22 January 2002

A radiation hybrid map of human chromosome 11q22-q23 containing the ataxia-telangiectasia disease locus

scientific article

A radiation hybrid map of the rat genome containing 5,255 markers

scientific article published on May 1999

A second-generation linkage map of the human genome

scientific article published on October 29, 1992

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

scientific article (publication date: 3 April 2008)

A systematic investigation of the contribution of genetic variation within the MHC region to HPV seropositivity

scientific article published on 23 January 2015

A test of the heterozygote-advantage hypothesis in cystic fibrosis carriers

scientific article published on June 1988

A tool for RNA sequencing sample identity check

scientific article published on 4 April 2013

A trans-ethnic genetic study of rheumatoid arthritis identified FCGR2A as a candidate common risk factor in Japanese and European populations ⬇️

scientific article published on May 24, 2011

A translational systems biology approach in both animals and humans identifies a functionally related module of accumbal genes involved in the regulation of reward processing and binge drinking in males.

scientific article published on 11 December 2015

A variant in FTO shows association with melanoma risk not due to BMI

scientific article

A variant in the CD209 promoter is associated with severity of dengue disease

scientific article

A whole-genome radiation hybrid panel and framework map of the rat genome

scientific article published in September 2000

ABCA7 rare variants and Alzheimer disease risk

scientific article published on April 2016

ADAM33, a new candidate for psoriasis susceptibility

scientific article

AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome).

scientific article published on 12 June 2013

ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP

article by A. Goel et al published November 2009 in Atherosclerosis

Aberration hubs in protein interaction networks highlight actionable targets in cancer. ⬇️

scientific article

Adolescent impulsivity phenotypes characterized by distinct brain networks

scientific article

Altered IFN-γ-mediated immunity and transcriptional expression patterns in N-Ethyl-N-nitrosourea-induced STAT4 mutants confer susceptibility to acute typhoid-like disease

scientific article published on 27 November 2013

An N-ethyl-N-nitrosourea (ENU)-induced dominant negative mutation in the JAK3 kinase protects against cerebral malaria

scientific article

An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders

scientific article published on 25 June 2009

An extended genetic linkage map of markers for human chromosome 10.

scientific article

Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations: Strongest Evidence for Association With a Variant in the Promoter Region of the Adiponectin Gene

article

Analysis of Distribution in the Human, Pig, and Rat Genomes Points toward a General Subtelomeric Origin of Minisatellite Structures

article

Analysis of Quantitative Trait Loci for Blood Pressure on Rat Chromosomes 2 and 13

scientific article published on 01 December 1996

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

scientific article published on 29 September 2013

Angiotensin II (type-1) receptor locus: CA repeat polymorphism and genetic mapping

scientific article published in May 1994

Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides

scientific article

Antibiotic Treatment of Venereal Disease and Reiter's Syndrome in a Greenland Population ⬇️

scientific article published on February 1, 1992

Are animal models of diabetes relevant to the study of the genetics of non-insulin-dependent diabetes in humans?

scientific article published on March 1997

Aristolochic acid exposure in Romania and implications for renal cell carcinoma ⬇️

scientific article

Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels

scientific article published on 26 May 2016

Association analysis indicates that a variant GATA-binding site in the PIK3CB promoter is a Cis-acting expression quantitative trait locus for this gene and attenuates insulin resistance in obese children

scientific article published on 31 October 2007

Association between Angiotensin-Converting Enzyme Gene Polymorphisms and Diabetic Nephropathy: Case-Control, Haplotype, and Family-Based Study in Three European Populations

article

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals

scientific article

Association between circadian genes, bipolar disorders and chronotypes

scientific article published on 9 April 2014

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

scientific article published on 18 March 2020

Association of LPA Variants With Aortic Stenosis: A Large-Scale Study Using Diagnostic and Procedural Codes From Electronic Health Records

scientific article

Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy.

scientific article

Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes

scientific article (publication date: 2012)

Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

scientific article

Associations between Nitric Oxide Synthase Genes and Exhaled NO-Related Phenotypes according to Asthma Status ⬇️

scientific article (publication date: 2012)

Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's disease

scientific article published in January 2001

Associations of the IL2Ralpha, IL4Ralpha, IL10Ralpha, and IFN (gamma) R1 cytokine receptor genes with AIDS progression in a French AIDS cohort

scientific article published on 21 February 2006

Associations of vitamin D pathway genes with circulating 25-hydroxyvitamin-D, 1,25-dihydroxyvitamin-D, and prostate cancer: a nested case-control study

scientific article

Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome

scientific article published on March 1, 1992

Automated identification of single nucleotide polymorphisms from sequencing data

scientific article

Automated identification of single nucleotide polymorphisms from sequencing data

scientific article published on 01 January 2002

Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing

scientific article published on 06 July 2015

Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD.

scientific article

Blood pressure loci identified with a gene-centric array

scientific article

C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies

scientific article

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

scientific article

CCDC88B is a novel regulator of maturation and effector functions of T cells during pathological inflammation

scientific journal article

CD14and Toll-like Receptor Gene Polymorphisms, Country Living, and Asthma in Adults

article

COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight

scientific article published in 2020

Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis

scientific article (publication date: 2012)

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

scientific article

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12

scientific article

Cerebral small vessel disease genomics and its implications across the lifespan

scientific article published on 08 December 2020

Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation

scientific article

Characterization of a set of variable number of tandem repeat markers conserved in bovidae

scientific article

Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants ⬇️

scientific article

Chromosomal mapping of genetic loci associated with non-insulin dependent diabetes in the GK rat

scientific article published on 01 January 1996

Chromosome 2p Shows Significant Linkage to Antihypertensive Response in the British Genetics of Hypertension Study

article

Chromosome 7p11.2 (EGFR) variation influences glioma risk

scientific journal article

Class II HLA-DC beta-chain DNA restriction fragments differentiate among HLA-DR2 individuals in insulin-dependent diabetes and multiple sclerosis ⬇️

scientific article published on March 1, 1984

Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families

scientific article published on 27 October 2004

Cohort profile: genomic data for 26 622 individuals from the Canadian Longitudinal Study on Aging (CLSA)

scientific article published in 2022

Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels

scientific article

Combined linkage and segregation analysis using regressive models

scientific article

Combined segregation and linkage analysis of genetic hemochromatosis using affection status, serum iron, and HLA.

scientific article

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats ⬇️

scientific article published on May 26, 2013

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

scientific article published on 10 December 2021

Common Polymorphisms in the CYP11B1 and CYP11B2 Genes: Evidence for a Digenic Influence on Hypertension

article

Common and rare variant analysis in early-onset bipolar disorder vulnerability

scientific article published on 11 August 2014

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

scientific article

Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach

scientific article published on 10 March 2009

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

scientific article

Common variants at 12q15 and 12q24 are associated with infant head circumference

scientific article published on 15 April 2012

Common variants at 30 loci contribute to polygenic dyslipidemia

scientific article

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

scientific article (publication date: May 2011)

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

scientific article

Common variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancer

scientific article

Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer

scientific journal article

Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.

scientific article

Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration

scientific article published on 30 July 2011

Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype

scientific article published on 13 January 2012

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

scientific article

Computing the genetic map.

scientific article published in April 1994

Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families

scientific article published in June 2007

Confirmation of genetic linkage between atopic IgE responses and chromosome 11q13

scientific article

Consequences of VHL Loss on Global DNA Methylome

scientific article published on 20 February 2018

Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome library

scientific article

Construction of human genetic linkage maps: I. Progress and perspectives

scientific article published on 01 January 1986

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis

scientific article published in January 1986

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

scientific article

Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls

scientific article published on 14 July 2017

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

scientific article published on October 2009

Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees

scientific article

Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's Disease

scientific article published on 01 January 2019

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

scientific article published on 07 May 2019

Correction: A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium.

scientific article published on 26 April 2011

Correction: Genetic Structure of Europeans: A View from the North–East.

scientific article

Correction: Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution.

scientific article published on 27 July 2009

Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans

scientific article published on 28 June 2013

Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation

scientific article published on 21 October 2019

Corrigendum re “Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma” [Eur Urol 2017;72:747–54]

scholarly article published in European Urology

Cytokine polymorphisms associated with carotid intima-media thickness in stroke patients

scientific article published on June 2006

D6S265*15 marks a DRB1*15, DQB1*0602 haplotype associated with attenuated protection from type 1 diabetes mellitus

scientific article published on 18 November 2005

DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23.

scientific article

DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.

scientific article

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.

scientific article published in October 2003

DNA markers for the cystic fibrosis locus.

scientific article published in January 1987

DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitis

scientific article published on 30 March 2016

Deciphering the 8q24.21 association for glioma

scientific article published on 11 February 2013

Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosa

scientific article

Detailed comparative gene map of rat chromosome 1 with mouse and human genomes and physical mapping of an evolutionary chromosomal breakpoint

scientific article published in February 2000

Detecting multi-way epistasis in family-based association studies

scientific article published on 13 May 2016

Detection of a recessive major gene for high IgE levels acting independently of specific response to allergens

article

Detection of genetic interference: simulation studies and mouse data

scientific article

Detection of linkage between a quantitative trait and a marker locus by the lod score method: sample size and sampling considerations

scientific article published in July 1988

Detection of putative functional angiotensinogen (AGT) gene variants controlling plasma AGT levels by combined segregation-linkage analysis

article

Determinants of early alcohol use in healthy adolescents: the differential contribution of neuroimaging and psychological factors

scientific article published on 23 November 2011

Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature

scientific article published on 18 May 2022

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

scientific article published on 14 March 2019

Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach

scientific article published in January 1996

Dissection of a quantitative trait locus for genetic hypertension on rat chromosome 10.

scientific article

Dominant gut Prevotella copri in gastrectomised non-obese diabetic Goto-Kakizaki rats improves glucose homeostasis through enhanced FXR signalling

scientific article published on 16 March 2020

Duplicating SNPs.

scientific article

Dysregulation at multiple points of the kynurenine pathway is a ubiquitous feature of renal cancer: implications for tumour immune evasion

scientific article published on 11 May 2020

EGEA (Epidemiological study on the Genetics and Environment of Asthma, bronchial hyperresponsiveness and atopy)-- descriptive characteristics

article

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome

scientific article (publication date: August 2000)

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Easy calculations of lod scores and genetic risks on small computers

scientific article (publication date: March 1984)

Effect of 17q21 variants and smoking exposure in early-onset asthma

scientific article

Effects of the circadian rhythm gene period 1 (per1) on psychosocial stress-induced alcohol drinking

scientific article published on 9 August 2011

Efficiency of recombination estimates using two-and three-point linkage data

scientific article published on January 1985

Efficiency of single-nucleotide polymorphism haplotype estimation from pooled DNA.

scientific article

Efficient computations in multilocus linkage analysis

scientific article

Epidemiologic study of the genetics and environment of asthma, bronchial hyperresponsiveness, and atopy.

scientific article published in March 2002

Epidemiological Study of the Genetics and Environment of Asthma, Bronchial Hyperresponsiveness, and Atopy ⬇️

scientific article published on October 1, 1997

Epidemiological study of genetic and environmental factors in asthma, bronchial hyperresponsiveness and atopy. Protocol and potential selection bias

scientific article published in September 2001

Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants

scientific article published in Nature Communications

Erratum: Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

scientific article published in Nature

Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference

scholarly article published in Nature Genetics

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

scientific article published in Nature

Erratum: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

scholarly article published in Nature Genetics

Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

article

Erratum: Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

scientific article published in November 2011

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

scientific article published in May 2010

Erratum: Susceptibility to lethal cerebral malaria is regulated by epistatic interaction between chromosome 4 (Berr6) and chromosome 1 (Berr7) loci in mice

article

Erratum: USP15 regulates type I interferon response and is required for pathogenesis of neuroinflammation.

scientific article published in November 2016

Establishment and characterization of a highly tumourigenic and cancer stem cell enriched pancreatic cancer cell line as a well defined model system

scientific article

Etiological heterogeneity in X-linked spastic paraplegia

scientific article

European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset

article

European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy

scientific article (publication date: 2008)

Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping

scientific article

Evaluating pedigree data. II. Identifying the cause of error in families with inconsistencies

scientific article

Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content

scientific article published on 01 December 2000

Evaluation of the SA locus in human hypertension

scientific article

Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA families

article

Evidence for gene × smoking exposure interactions in a genome-wide linkage screen of asthma and bronchial hyper-responsiveness in EGEA families

article

Evidence for linkage of a new region (11p14) to eczema and allergic diseases ⬇️

scientific article published on 18 October 2007

Evidence for the Presence of Insulin-Dependent Diabetes-Associated Alleles on the Distal Part of Mouse Chromosome 6 ⬇️

scientific article published on June 1, 1998

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

scientific article

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.

scientific article

Evolutionary trees and admixture: phylogenetic inference when some populations are hybridized

scientific article published on 01 July 1982

Exhaustive genotyping of the CEM15 (APOBEC3G) gene and absence of association with AIDS progression in a French cohort

scientific article published on 15 December 2004

Exhaustive genotyping of the interferon alpha receptor 1 (IFNAR1) gene and association of an IFNAR1 protein variant with AIDS progression or susceptibility to HIV-1 infection in a French AIDS cohort

scientific article published on 31 August 2006

Exhaustive genotyping of the interleukin-1 family genes and associations with AIDS progression in a French cohort

scientific article published on 26 October 2006

Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.

scientific article

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

scientific article published in November 2022

Exploring rare and low-frequency variants in the Saguenay-Lac-Saint-Jean population identified genes associated with asthma and allergy traits

scientific article published on 11 September 2018

Exposure to Polycyclic Aromatic Hydrocarbons and Accelerated DNA Methylation Aging.

scientific article

Expression of DRD2 Is Increased in Human Pancreatic Ductal Adenocarcinoma and Inhibitors Slow Tumor Growth in Mice

scientific article published on 28 August 2016

FTO, obesity and the adolescent brain

scientific article published on 30 November 2012

Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

scientific article published on 21 December 2020

Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16 ⬇️

scientific article published on October 1, 1997

Familial generalized epilepsy in Bulgarian Roma

scientific article

Family-based designs for genome-wide association studies ⬇️

scientific article published on June 1, 2011

Fibrinogen and coronary heart disease: test of causality by 'Mendelian randomization'

scientific article published on 26 July 2006

Fine mapping of eight psoriasis susceptibility loci

scientific article published on 3 September 2014

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions

scientific article

Frequent recombination is observed in the distal end of the long arm of chromosome 14

scientific article published on 01 January 1989

Functional annotations of diabetes nephropathy susceptibility loci through analysis of genome-wide renal gene expression in rat models of diabetes mellitus

scientific article published on 9 July 2009

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

scientific article published on 10 March 2017

Further data on linkage between cystic fibrosis and 7C22 (D7S16)

scientific article published on August 1987

Further linkage data on cystic fibrosis: the Utah Study

scientific article

G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes

scientific article published on 15 July 2008

Gene mapping

scientific article

Gene structure, polymorphism and mapping of the human endothelial nitric oxide synthase gene

scientific article published on February 1994

Gene-environment interaction for childhood asthma and exposure to farming in Central Europe ⬇️

scientific article published on January 1, 2011

Gene-environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study

scientific article

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

scientific article

Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma ⬇️

scientific article published on 7 August 2017

Genetic analysis combining path analysis with regressive models: the TAU model of multifactorial transmission

scientific article published in November 1994

Genetic analysis of an F(2) intercross between two chicken lines divergently selected for body-weight

scientific article

Genetic analysis of autoimmune type 1 diabetes mellitus in mice. 1991.

scientific article

Genetic analysis of diabetes and insulitis in an interspecific cross of the nonobese diabetic mouse with Mus spretus

scientific article

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers

scientific article published on February 1986

Genetic and environmental influences on left ventricular mass. A family study

scientific article published on 01 November 2000

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

scientific article

Genetic and functional evaluation of MITF as a candidate gene for cutaneous melanoma predisposition in pigs

scientific article published on 28 May 2011

Genetic and haplotypic structure in 14 European and African cattle breeds

scientific article

Genetic approaches to common diseases

scientific article published on December 1993

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

scientific article published on 24 August 2015

Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension

scientific article published on 8 June 2007

Genetic basis of hypertension

scientific article published on March 1994

Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity

scientific article

Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats

article by Christopher Dubay et al published April 1993 in Nature Genetics

Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain

scientific article

Genetic effect on specific human immune responses to tetanus anatoxin

scientific article published on January 1983

Genetic evidence of assortative mating in humans

article

Genetic heterogeneity according to age at onset in bipolar disorder: a combined positional cloning and candidate gene approach

scientific article

Genetic heterogeneity of asthma phenotypes identified by a clustering approach

scientific article published on 5 December 2013

Genetic influences on the end-stage effector phase of arthritis

scientific article

Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree

scientific article published on March 1, 1992

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene

scientific article published in September 1992

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

scientific article published in Nature

Genetic mapping through the use of synthetic tandem repeats in the mouse genome

scientific article published in January 1993

Genetic polymorphisms in 85 DNA repair genes and bladder cancer risk

scientific article published on 23 February 2009

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

scientific article

Genetic risk profiles identify different molecular etiologies for glioma

scientific article

Genetic structure of Europeans: a view from the North-East

scientific article

Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10.

scientific article published in November 1997

Genetic variants associated with Lp(a) lipoprotein level and coronary disease

scientific article published in December 2009

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

scientific article published on 6 October 2011

Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions.

scientific article

Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies

scientific journal article

Genetics of emotional reactivity in bipolar disorders

scientific article

Genetics of insulin-dependent diabetes mellitus

scientific article published on June 1996

Genetics of rheumatoid arthritis contributes to biology and drug discovery

scientific article

Genetics of the thrombomodulin-endothelial cell protein C receptor system and the risk of early-onset ischemic stroke

scientific article published in PLoS ONE

Genetics of venous thrombosis: insights from a new genome wide association study

scientific article (publication date: 2011)

Genome Screen for Asthma and Related Phenotypes in the French EGEA Study

article

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project

article

Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2

scientific article

Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder

scientific article published in March 2011

Genome-wide analysis of genetic loci associated with Alzheimer disease

scientific article

Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension

scientific article published on 17 March 2013

Genome-wide association analysis identifies three new breast cancer susceptibility loci

scientific article published on 22 January 2012

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

scientific article

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

scientific article published on 27 April 2020

Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.

scientific article

Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution

scientific article published in June 2009

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population

scientific article published on 17 November 2010

Genome-wide association study identifies eight loci associated with blood pressure

scientific article (publication date: June 2009)

Genome-wide association study identifies five susceptibility loci for glioma

scientific article (publication date: August 2009)

Genome-wide association study identifies four loci associated with eruption of permanent teeth

scientific article

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

scientific article

Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder

scientific article

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

scientific article published on 16 October 2011

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

scientific journal article

Genome-wide association study identifies multiple risk loci for renal cell carcinoma ⬇️

scientific article

Genome-wide association study identifies multiple susceptibility loci for glioma ⬇️

scientific article

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

scientific journal article

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

scientific article

Genome-wide association study identifies three loci associated with melanoma risk

scientific article published on 05 July 2009

Genome-wide association study identifies three new melanoma susceptibility loci

scientific article

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

scientific article (publication date: October 2009)

Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

scientific article

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

scientific article

Genome-wide association study of HPV seropositivity

scientific article

Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3

scientific article

Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups

scientific journal article

Genome-wide association study of glioma and meta-analysis

journal article published in 2012

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors

scientific article published on 27 March 2017

Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project

scientific article published on 28 September 2010

Genome-wide association study of lung function decline in adults with and without asthma

scientific article published on 16 March 2012

Genome-wide association study of major recurrent depression in the U.K. population

scientific article published in June 2010

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

scientific article published on 26 May 2013

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

scientific journal article

Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.

scientific article published on 30 November 2010

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

scientific article published on 20 March 2012

Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia

scientific article

Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood

scientific article published on 01 October 2019

Genome-wide linkage analysis for human longevity: Genetics of Healthy Aging Study

scientific article published on 06 February 2013

Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels

scientific article published on 18 June 2008

Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project

scientific article published on 01 March 2003

Genome-wide mapping of human loci for essential hypertension

scientific article

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma ⬇️

scientific article

Genome-wide pharmacogenetics of antidepressant response in the GENDEP project

scientific article

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

scientific article (publication date: 2011)

Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14

scientific article

Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways

scientific article

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

scientific article published in March 2011

Genomewide linkage analysis of soluble transferrin receptor plasma levels

scientific article published on 23 August 2005

Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS.

scientific article published on 23 March 2004

Genomic approach of AIDS pathogenesis: exhaustive genotyping of the TNFR1 gene in a French AIDS cohort

scientific article published on 01 September 2005

Genomic binding of Pol III transcription machinery and relationship with TFIIS transcription factor distribution in mouse embryonic stem cells

scientific article published on 12 September 2011

Genomic regulation of type 2 diabetes endophenotypes: Contribution from genetic studies in the Goto-Kakizaki rat.

scientific article published on 23 August 2017

Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein

scientific article

Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

scientific article

Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements.

scientific article published in December 2013

Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements

scientific article published on 31 October 2013

Global genetic architecture of an erythroid quantitative trait locus, HMIP-2

scientific article

Global genetic variations predict brain response to faces

scientific article

Goodness-of-fit tests for locus order in three-point mapping

scientific article published in January 1987

HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families

scientific article published on 30 June 2016

HLA antigens and seronegative rheumatoid arthritis

scientific article

HLA haplotypes in non-familial rheumatoid arthritis

scientific article published on May 1987

HLA has strongest association with IgA nephropathy in genome-wide analysis

scientific article

HLA heterozygosity contributes to susceptibility to rheumatoid arthritis ⬇️

scientific article published on September 1, 1992

HLA-DR genotype risks in seropositive rheumatoid arthritis.

scientific article

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study

article

Heterozygosity mapping for human dominant trait variants

scientific article published on 24 April 2019

Homocysteine and Coronary Heart Disease: Meta-analysis of MTHFR Case-Control Studies, Avoiding Publication Bias ⬇️

scientific article (publication date: February 2012)

Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease

scientific article published in March 2005

Human Variable Number of Tandem Repeat Probes As a Source of Polymorphic Markers in Experimental Animals ⬇️

scientific article published on January 1, 1991

Human islets of Langerhans express the delta(C) isoform of calcium/calmodulin-dependent protein kinase II.

scientific article

Human leukocyte antigen class II variants and adult-onset asthma: does occupational allergen exposure play a role?

scientific article published on 17 July 2014

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

scientific article

IBD risk loci are enriched in multigenic regulatory modules encompassing putative causative genes.

scientific article

Identification and mapping of RFLPs for human tissue factor (HTF) to chromosome 1p.

scientific article

Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasis

scientific article published on May 1997

Identification of a new locus at 16q12 associated with time to asthma onset

scientific article

Identification of distinct quantitative trait Loci affecting length or weight variability at birth in humans

scientific article published on 18 July 2006

Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia

scientific article

Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome

scientific article

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

scientific article

Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells

scientific article

Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study

scientific article published on 24 October 2012

Impact of common variation in bone-related genes on type 2 diabetes and related traits

scientific article

Implication of the Immune System in Alzheimer's Disease: Evidence from Genome-Wide Pathway Analysis

article

Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

journal article published in 2014

Imputation of KIR Types from SNP Variation Data

scientific article

Incidence of Breast Cancer and Its Subtypes in Relation to Individual and Multiple Low-Penetrance Genetic Susceptibility Loci ⬇️

scientific article published on July 28, 2010

Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study

article

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

scientific article

Independent risk factors for simvastatin-related myopathy and relevance to different types of muscle symptom

scientific article published on 23 July 2020

Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.

scientific article

Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred

scientific article

Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls

scientific article

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

scientific article published in Nature

Integrated genomics point to immune vulnerabilities in pleural mesothelioma

scientific article published on 27 September 2021

Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma risk

scientific article

Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinoma ⬇️

scientific article published on October 18, 2011

Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene

scientific article

Integration of the rat recombination and EST maps in the rat genomic sequence and comparative mapping analysis with the mouse genome

scientific article published on April 2004

Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsiveness

scientific article published on 21 January 2016

Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained families

article

Interferon gamma receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection

scientific article published on 29 June 2010

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

scholarly article

International network of cancer genome projects

scientific article

Investigation of the fine structure of European populations with applications to disease association studies

scientific article published in December 2008

Isolation and mapping of a polymorphic DNA sequence (2CJ52.208M2) on chromosome 11 [D11S351]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.1) on chromosome 16 [D16S152]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.10) on chromosome 16 [D16S153]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.105) on chromosome 16 [D16S154]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.112) on chromosome 16 [D16S158]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.15) on chromosome 11 [D11S383]

scientific article published on December 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.161) on chromosome 16 [D16S150]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.193) on chromosome 11 [D11S384]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.197) on chromosome 16 [D16S156]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.199) on chromosome 16 [D16S155]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.27) on chromosome 16 [D16S149]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.4) on chromosome 11 [D11S388]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.5) on chromosome 11 [D11S386]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (CJ52.96) on chromosome 16 [D16S157]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (HBI18P1) on chromosome 11 [D11S147]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (MCT117) on chromosome 11 [D11S145]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (cKKA39) on chromosome 14 [D14S23].

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (cMCOC46) on chromosome 13 [D13S54]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (cMCOD13) on chromosome 3 [D3S44]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (cMCOE32) on chromosome 2 [D2S53]

scientific article published on July 1988

Isolation and mapping of a polymorphic DNA sequence (cMHZ47) on chromosome 13 [D13S52].

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (cYNA12) on chromosome 13 [D13S53]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (cYNA4) on chromosome 2 [D2S50]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (p1CJ52.208M2) on chromosome 11 [D11S351]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.102T1) on chromosome 11 [D11S387]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.196M1) on chromosome 16 [D16S160]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.209M1) on chromosome 16 [D16S151]

scientific article published on September 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.209M2) on chromosome 16 [D16S151]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.75M1) on chromosome 11 [D11S385]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.94T1) on chromosome 16 [D16S159]

scientific article published on September 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.95M1) on chromosome 16 [D16S148]

scientific article published on October 1989

Isolation and mapping of a polymorphic DNA sequence (pCJ52.99M2) on chromosome 11 [D11S389]

scientific article published on November 1989

Isolation and mapping of a polymorphic DNA sequence (pCMI37) on chromosome 7 [D7S368]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pCMI40) on chromosome 13 [D13S49]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM1.2) on chromosome 12q [D12S15]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM17.1) on chromosome 10 [D10S16].

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM17.4) on chromosome 10 [D10S23]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM6) on chromosome 20 [D20S19]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM62) on chromosome 14 [D14S21]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM63) on chromosome 2 [D2S51]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM65) on chromosome 16 [D16S84]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM66) on chromosome 14 [D14S22]

scientific article published on July 1988

Isolation and mapping of a polymorphic DNA sequence (pCMM86) on chromosome 17q [D17S74]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD134.7) on chromosome 3 [D3S45]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD145) on chromosome 3 [D3S32]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD49.2) on chromosome 15

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD49.3) on chromosome 15

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD52.1) on chromosome 15.

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD53.2) on chromosome 1 [D1S73]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD6) chromosome 6 [D6S41]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD64.1) on chromosome 3.

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD64.2) on chromosome 3 [D3S46]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD70.3) on chromosome 18 [D18S23]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pEFD85.7) on chromosome 15 [D15S37]

scientific article published on July 1988

Isolation and mapping of a polymorphic DNA sequence (pEFZ13) on chromosome 1p [D1S64].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pEFZ31) on chromosome 22 [D22S32]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pEFZ33) on chromosome 15

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pEFZ38) on chromosome 2 [D2S60]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pEKMDA2-I) on chromosome 16 [D16S83]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pHBI59) on chromosome 11 [D11S146].

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pHHH106) on chromosome 1 [D1S67]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pHHH119) on chromosome 1 [D1S59]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pHHH157) on chromosome 6p [D6S29]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pHHH163) on chromosome 18 [D18S21]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pHHH171) on chromosome 6p [D6S38]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pHHH208) on chromosome 14 [D14S19].

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pJCZ30) on chromosome 6 [D6S37]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pJCZ67) on chromosome 7 [D7S396]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pKKA12) on chromosome 7 [D7S398]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pKKA35) on chromosome 17 [D17S75].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pKKA40) on chromosome 9q [D9S31].

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pMCA1-1) on chromosome 15 [D15S33]

scientific article published on February 1988

Isolation and mapping of a polymorphic DNA sequence (pMCOA12) on chromosome 9q [D9S28]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pMCOC12) on chromosome 14 [D14S20]

scientific article published on July 1988

Isolation and mapping of a polymorphic DNA sequence (pMCOC14) on chromosome 4p [D4S124]

scientific article published on July 1988

Isolation and mapping of a polymorphic DNA sequence (pMCT106) on chromosome 2 [D2S61]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pMCT108.2) on chromosome 18 [D18S24]

scientific article

Isolation and mapping of a polymorphic DNA sequence (pMCT128.2) on chromosome 8 [D8S39]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pMCT149.2) on chromosome 15.

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pMCT15) on chromosome 21 [D21S113]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pMCT32.1) on chromosome 3 [D3S31]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pMCT96.1 and pMCT96.2) on chromosome 9q [D9S14]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pMHZ13) on chromosome 9q [D9S13].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pMHZ17) on chromosome 13 [D13S51].

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pMHZ21) on chromosome 9q [D9S30].

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pRMR6) on chromosome 20 [D20S20]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pRMU7.4) on chromosome 7p [D7S370]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pTB10.163) on chromosome 10 [D10S22]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pTB10.171) on chromosome 10 [D10S19]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH14) on chromosome 12p [D12S16]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH22) on chromosome 9 [D9S12]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH26) on chromosome 11 [D11S149]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH28) on chromosome 7p [D7S371]

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH28) on chromosome 7p [D7S371]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH37) on chromosome 14 [D14S16]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH55) on chromosome

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH55) on chromosome 15 [D15S27].

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pTHH59) on chromosome 17q [D17S4]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pTHI54) on chromosome 1p [D1S62].

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pTHIZ53) on chromosome 12 [D12S18].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pYNA15.2) on chromosome 15 [D15S36]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pYNH20) on chromosome 13 [D13S50].

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence (pYNH3) on chromosome X [DXS287].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pYNM18.1) on chromosome 15 [D15S35]

scientific article published on April 1988

Isolation and mapping of a polymorphic DNA sequence (pYNZ132) on chromosome 6 [D6S40]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence (pYNZ132) on chromosome 6 [D6S40].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pYNZ15) on chromosome 2 [D2S50].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pYNZ2) on chromosome 1p [D1S57]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pYNZ22) on chromosome 17p [D17S30].

scientific article published on June 1988

Isolation and mapping of a polymorphic DNA sequence (pYNZ32) on chromosome 4p [D4S125]

scientific article published on May 1988

Isolation and mapping of a polymorphic DNA sequence (pYNZ94) on chromosome 17 [D17S80]

scientific article published on October 1988

Isolation and mapping of a polymorphic DNA sequence MCT128.1 on chromosome 11 [D11S285]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence cEFD52 on chromosome 17q [D17S26]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence for NRAS pMCR3 on chromosome 1.

scientific article

Isolation and mapping of a polymorphic DNA sequence for human muscle glycogen phosphorylase (pMCMP1) on chromosome II [PYGM]

scientific article published on November 1988

Isolation and mapping of a polymorphic DNA sequence pEFD122 on chromosome 2 (D2S48).

scientific article

Isolation and mapping of a polymorphic DNA sequence pEFD126.3 on chromosome 9q (D9S7).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pEFD33.2 on chromosome 12 [D12S14]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pEFD4.2 on chromosome 19 [D19S22]

scientific article published on February 1988

Isolation and mapping of a polymorphic DNA sequence pEFD40.3 on chromosome 9 (D9S8).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pEFZ18.2 on chromosome 14 [D14S17]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pEKH7.4 to chromosome 1 (D1S65).

scientific article

Isolation and mapping of a polymorphic DNA sequence pEKZ104.1 on chromosome 15 [D15S30]

scientific article published on February 1988

Isolation and mapping of a polymorphic DNA sequence pEKZ105 on chromosome 2 (D2S55).

scientific article

Isolation and mapping of a polymorphic DNA sequence pEKZ130 on chromosome 9 (D9S9).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pEKZ19.3 on chromosome 9q (D9S17).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pHBI18P2 on chromosome 11 [D11S147]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pHBI40 on chromosome 1 (D1S66).

scientific article

Isolation and mapping of a polymorphic DNA sequence pHBI59 on chromosome 11 [D11S146]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pHHH115.2 on chromosome 2 (D2S54).

scientific article

Isolation and mapping of a polymorphic DNA sequence pHHH133 on chromosome 2 (D2S45).

scientific article

Isolation and mapping of a polymorphic DNA sequence pHHH152 on chromosome 17q [D17S32]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pHHH202 on chromosome 17 [D17S33]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pHHH220 on chromosome 9p (D9S27).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pJCZ3.1 on chromosome 19 [D19S20]

scientific article published on February 1988

Isolation and mapping of a polymorphic DNA sequence pMCK2 on chromosome 10 [D10S15]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pMCT136 on chromosome 9q (D9S10).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pMCT35.1 on chromosome 17p [D17S31]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pMCT46.2 on chromosome 15 [D15S26]

scientific article published on February 1988

Isolation and mapping of a polymorphic DNA sequence pMHZ10 on chromosome 9q (D9S11).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pMHZ14 on chromosome 1p (D1S60).

scientific article

Isolation and mapping of a polymorphic DNA sequence pMHZ15 on chromosome 10 [D10S17]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pMHZ9 on chromosome 14 [D14S18]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pMLJ14 on chromosome 14 [D14S13]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pRMU1 on chromosome 17q [D17S27]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pRMU3 on chromosome 17q [D17S24]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pTBAB5.7 on chromosome 2 (D2S47).

scientific article

Isolation and mapping of a polymorphic DNA sequence pTHH54 on chromosome 10 [D10S13]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pYNH15 on chromosome 12q [D12S17]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44).

scientific article

Isolation and mapping of a polymorphic DNA sequence pYNH37.3 on chromosome 17p [D17S28]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pYNM17 on chromosome 9q (D9S6).

scientific article published on December 1987

Isolation and mapping of a polymorphic DNA sequence pYNM3 on chromosome 8 (D8S38).

scientific article

Isolation and mapping of a polymorphic DNA sequence pYNZ156 on chromosome 10 [D10S18]

scientific article published on January 1988

Isolation and mapping of a polymorphic DNA sequence pYNZ23 to chromosome 1 (DIS58).

scientific article

Isolation and mapping of a polymorphic DNA sequence pYNZ86.1 on chromosome 3 (D3S30).

scientific article

Isolation and mapping of a polymorphic DNA sequence pYNZ9.1 on chromosome 2 (D2S46)

scientific article

Isolation and mapping of a polymorphic DNA sequence pYNZ90.1 on chromosome 15 [D15S28]

scientific article published on January 1988

Isolation of mapping of a polymorphic DNA sequence pEFZ10 on chromosome 18 [D18S22]

scientific article published on February 1988

Jean B Dausset, 19 October 1916-6 June 2009

scientific article

KCNJ6 is associated with adult alcohol dependence and involved in gene × early life stress interactions in adolescent alcohol drinking

scientific article

KNG1 Ile581Thr and susceptibility to venous thrombosis

scientific article published on 26 January 2011

L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1

scientific article

Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E epsilon2/epsilon3/epsilon4 genotype

scientific article published on 01 February 2003

Large-scale genotyping by mass spectrometry: experience, advances and obstacles

scientific article

Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators

scientific article published on 01 February 2000

Leveling the Playing Field in Homozygosity Mapping Using Map Distances

scientific article

Linkage Analysis and Construction of a Congenic Strain for a Blood Pressure QTL on Rat Chromosome 9 ⬇️

scientific article published on July 15, 1998

Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5

scientific article

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension

scientific article

Linkage and physical mapping of rat microsatellites derived from minisatellite loci

scientific article published in April 1999

Linkage maps of human chromosomes

scientific article

Linkage of DNA probe B79a (D7S13) to cystic fibrosis

scientific article

Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes

scientific article published in November 1987

Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease risk

scientific article published on 15 July 2004

Lipoprotein(a) genetic variants associated with coronary and peripheral vascular disease but not with stroke risk in the Heart Protection Study

scientific article published on 20 January 2011

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1 ⬇️

scientific article published on January 1, 2002

Localisation of atopy and beta subunit of high-affinity IgE receptor (Fc epsilon RI) on chromosome 11q.

scientific article

Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5

scientific article

Localization of the rat stimulatory G-protein alpha subunit (GNPAS) gene to rat chromosome 3 by linkage analysis

scientific article

Localization of tub and uncoupling proteins (Ucp) 2 and 3 to a region of rat chromosome 1 linked to glucose intolerance and adiposity in the Goto-Kakizaki (GK) type 2 diabetic rat.

scientific article published in November 1998

Localization, cDNA sequence and genomic organization of the rat seipin gene (Bscl2) and sequence analysis in inbred rat models of Type 2 diabetes mellitus

scientific article

Loss of chromosome Y leads to down regulation of KDM5D and KDM6C epigenetic modifiers in clear cell renal cell carcinoma ⬇️

scientific article published on 23 March 2017

Low frequency and rare coding variation contributes to multiple sclerosis risk

Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222.

scientific article published on 9 April 2013

Lower ventral striatal activation during reward anticipation in adolescent smokers

scientific article

Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium

scientific article published in March 2012

Lung cancer susceptibility locus at 5p15.33

scientific article

Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study

scientific article (publication date: July 2006)

Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 Deficiency

scientific article

Manual dexterity correlating with right lobule VI volume in right-handed 14-year-olds

scientific article published on 8 September 2011

Mapping approaches to gene identification in humans

scientific article

Mapping complex disease traits with global gene expression

scientific article

Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.

scientific article

Mapping of familial thoracic aortic aneurysm/dissection with patent ductus arteriosus to 16p12.2-p13.13.

scientific article published on 5 July 2005

MeQA: a pipeline for MeDIP-seq data quality assessment and analysis

scientific article

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

scientific article

Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population

scientific journal article

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

scientific article

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

scientific article

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments

scientific article

Minisatellite linkage maps in the mouse by cross-hybridization with human probes containing tandem repeats

scientific article

Missense mutation in sterile alpha motif of novel protein SamCystin is associated with polycystic kidney disease in (cy/+) rat.

scientific article

Modulation of Malaria Phenotypes by Pyruvate Kinase (PKLR) Variants in a Thai Population

scientific article published on 14 December 2015

Mold allergen sensitization in adult asthma according to integrin β3 polymorphisms and Toll-like receptor 2/+596 genotype

Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci

scientific article published on 01 April 2002

Molecular genetics of the transcription factor GLIS3 identifies its dual function in beta cells and neurons

scientific article published on 11 September 2017

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

scientific article published on 22 December 2017

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

scientific article (publication date: May 1985)

Mutational analysis of GLUT1 (SLC2A1) in glut-1 deficiency syndrome; dong wang; pamela kranz-eble; darryl C. De vivo; (Article was originally published in human mutation 16:224-231, 2000)

scientific article published on 01 December 2000

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease

scientific article

Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus

scientific article published on September 2013

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

scientific article

Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome

scientific article

Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans

scientific article published on June 2017

Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3.

scientific article

Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

scientific article

Mutations in the gene encoding SLURP-1 in Mal de Meleda

scientific article

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

scientific journal article

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)

scientific article published in December 1996

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

scientific article

Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analyses

scientific article

Neural basis of reward anticipation and its genetic determinants

scientific article published on 21 March 2016

Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trial

scientific article published on 8 July 2015

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

scientific article

New susceptibility loci for cutaneous melanoma risk and progression revealed using a porcine model.

scientific article published on 12 June 2018

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

scientific article

No impact of KIF6 genotype on vascular risk and statin response among 18,348 randomized patients in the heart protection study

scientific article published on 31 March 2011

Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations

scientific article published in June 2002

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

scientific article

Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study

scientific article published on 24 January 2011

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

scientific article

Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13.

scientific article

Nucleotide sequence variation within the PI3K p85 alpha gene associates with alcohol risk drinking behaviour in adolescents

scientific article

On the use of DNA fingerprints for linkage studies in cattle

scientific article

Oppositional COMT Val158Met effects on resting state functional connectivity in adolescents and adults

scientific article

PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans

scientific article

Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene ⬇️

scientific article published on December 1, 1991

Perilipin deficiency and autosomal dominant partial lipodystrophy

scientific article published on February 2011

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

scientific article

Polygenic Control of Idiopathic Generalized Epilepsy Phenotypes in the Genetic Absence Rats from Strasbourg (GAERS)

scientific article published in April 2004

Polygenic control of autoimmune diabetes in nonobese diabetic mice

scientific article

Polygenic disease: methods for mapping complex disease traits

scientific article published on December 1995

Polymorphism discovery in 62 DNA repair genes and haplotype associations with risks for lung and head and neck cancers

scientific article

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion

scientific article

Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome

scientific article

Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation

scientific article

Positional cloning of a novel gene influencing asthma from chromosome 2q14.

scientific article

Practicable approaches to targeted comparative mapping of rat chromosome regions: linkage mapping of five genes on rat chromosome 13 ⬇️

scientific article published on January 1, 1998

Precision medicine from the renal cancer genome

scientific article

Prevalence of mutations in AGPAT2 among human lipodystrophies

scientific article

Protein C levels are regulated by a quantitative trait locus on chromosome 16: results from the Genetic Analysis of Idiopathic Thrombophilia (GAIT) Project

scientific article

Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort

scientific article published on 4 April 2016

Quantifying the heritability of glioma using genome-wide complex trait analysis

scientific article

Quantitative phenotype analysis for localization and identification of disease-related genes in a complex genetic background

scientific article published on January 1996

Quantitative trait loci for fasting glucose in young Europeans replicate previous findings for type 2 diabetes in 2q23-24 and other locations

scientific article published on 6 April 2007

Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus

scientific article published on 13 August 2013

RASGRF2 regulates alcohol-induced reinforcement by influencing mesolimbic dopamine neuron activity and dopamine release

scientific article

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration

scientific article

Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19

scientific article

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

scientific article

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

scientific journal article

Rat gene mapping using PCR-analyzed microsatellites ⬇️

scientific article published on July 1, 1992

Recovery in Patients With Dilated Cardiomyopathy With Loss-of-Function Mutations in the Titin Gene

scientific article

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

scientific journal article

Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region

scientific article

Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene

scientific article

Regulation of insulin gene expression by the IDDM associated, insulin locus haplotype

scientific article published on April 1995

Reiter's syndrome in Greenland. A clinical and epidermiological study of two communities

scientific article published in January 1985

Reiter's syndrome in the Inuit population of Greenland. A clinical, immunogenetic and epidemiological study

scientific article published in June 1987

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

scientific article

Risk taking and the adolescent reward system: a potential common link to substance abuse

scientific article

Robustness and power of the unified model in the analysis of quantitative measurements

scientific article published on February 1986

Rsu1 regulates ethanol consumption in Drosophila and humans

scientific article published on 13 July 2015

SHANK1 Deletions in Males with Autism Spectrum Disorder

scientific article

SLC2A9 is a high-capacity urate transporter in humans

scientific article

SLCO1B1 variants and statin-induced myopathy--a genomewide study

scientific article (publication date: 21 August 2008)

SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease.

scientific article published on 25 August 2015

SRPX2 mutations in disorders of language cortex and cognition

scientific article

Scores of asthma and asthma severity reveal new regions of linkage in EGEA study families

scientific article published on 25 April 2007

Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons

scientific article published on 05 August 2015

Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis ⬇️

scientific article

Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies

scientific article

Serial translocation by means of circular intermediates underlies colour sidedness in cattle

scientific article published in February 2012

Serum IgE Concentration and Other Immune Manifestations of Treatment with Gold Salts Are Linked to the MHC and IL4 Regions in the Rat

scientific article published on 01 January 1996

Seven new loci associated with age-related macular degeneration

scientific article

Sex specific associations in genome wide association analysis of renal cell carcinoma

scientific article published on 23 June 2019

Sex-specific effect of IL9 polymorphisms on lung function and polysensitization

scientific article published on 18 June 2009

Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci

scientific article

Sex-specific role for adenylyl cyclase type 7 in alcohol dependence

scientific article

Shared genomic segment analysis with equivalence testing

scientific article published on 16 July 2020

Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents

scientific article (publication date: February 2015)

Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease

scientific article

Specific immune responses after booster immunization with tetanus toxoid in man: study of kinetics, family segregation, and linkage to HLA of in vitro lymphocyte proliferative responses and serum-antibody responses

scientific article published on January 1983

Strategies for multilocus linkage analysis in humans

scientific article (publication date: June 1984)

Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR.

scientific article

Susceptibility to lethal cerebral malaria is regulated by epistatic interaction between chromosome 4 (Berr6) and chromosome 1 (Berr7) loci in mice

scientific article published on 18 April 2013

Systematic Analysis of Candidate Genes for Alzheimer's Disease in a French, Genome-Wide Association Study

article

Systematic analysis of glutamatergic neurotransmission genes in alcohol dependence and adolescent risky drinking behavior

scientific article

Systems Genetics of Hepatic Metabolome Reveals Octopamine as a Target for Non-Alcoholic Fatty Liver Disease Treatment

article

TCF12 is mutated in anaplastic oligodendroglioma

scientific article published on 12 June 2015

THEMIS is required for pathogenesis of cerebral malaria and protection against pulmonary tuberculosis

scientific article

Tests of gene order from three-locus linkage data

scientific article

The 1993-94 Généthon human genetic linkage map

scientific article

The ANO3/MUC15 locus is associated with eczema in families ascertained through asthma

article

The Arf6 activator Efa6/PSD3 confers regional specificity and modulates ethanol consumption in Drosophila and humans

scientific article published on 13 June 2017

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study

scientific article

The European dimension for the mouse genome mutagenesis program

scientific article

The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.

scientific article published on 29 March 2010

The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells

scientific article published on 15 June 2009

The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans

scientific article published on 21 August 2007

The IMAGEN study: reinforcement-related behaviour in normal brain function and psychopathology ⬇️

scientific article published on December 1, 2010

The Microbial Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell Function

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

scholarly article published 13 July 2017

The Natural Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell Function

scientific article published on 01 February 2020

The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption

scientific article

The effect on melanoma risk of genes previously associated with telomere length

scientific article

The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

scientific article

The exon 1–8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom population

article

The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy

scientific article

The genetic basis of hypertension ⬇️

scientific article published on March 1, 1995

The human "interferon-beta 2/hepatocyte stimulating factor/interleukin-6" gene: DNA polymorphism studies and localization to chromosome 7p21.

scientific article published in July 1988

The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population

scientific article published on 19 April 2011

The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study ⬇️

scientific article published on 03 January 2019

The nuclear factor I/A (NFIA) gene is associated with the asthma plus rhinitis phenotype

article

The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence

scientific article

Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice

scientific article published on 17 May 2013

Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression

scientific article

Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activity

scientific article published on July 1, 1997

Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE).

scientific article published on May 2001

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

scientific article published on 20 May 2020

Transient receptor potential genes, smoking, occupational exposures and cough in adults

scientific article published on 23 March 2012

Twenty-eight loci form a continuous linkage map of markers for human chromosome 1.

scientific article published on January 1989

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension

article

USP15 regulates type I interferon response and is required for pathogenesis of neuroinflammation

scientific article published on 10 October 2016

Unifying candidate gene and GWAS Approaches in Asthma

scientific article

Untargeted Mass Spectrometry Lipidomics identifies correlation between serum sphingomyelins and plasma cholesterol

scientific article published on 02 February 2019

Use of the regressive models in linkage analysis of quantitative traits

article

Using genetic proxies for lifecourse sun exposure to assess the causal relationship of sun exposure with circulating vitamin d and prostate cancer risk

scientific article published on 25 February 2013

Using prior information from the medical literature in GWAS of oral cancer identifies novel susceptibility variant on chromosome 4--the AdAPT method

scientific article

Using spatio-temporal surveillance data to test the infectious environment of children before type 1 diabetes diagnosis

scientific article (publication date: 2017)

Variants in DNA double-strand break repair and DNA damage-response genes and susceptibility to lung and head and neck cancers

scientific article published in July 2008

Variation in IL-1beta gene expression is a major determinant of genetic differences in arthritis aggressivity in mice

scientific article

Variation in genomic landscape of clear cell renal cell carcinoma across Europe

scientific article published on 29 October 2014

Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome

scientific article

Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.

scientific article

Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

article

Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity

scientific article

ZBTB7B (ThPOK) Is Required for Pathogenesis of Cerebral Malaria and Protection against Pulmonary Tuberculosis

scientific article published on 22 January 2020

eQTL mapping identifies insertion- and deletion-specific eQTLs in multiple tissues

scientific article published on 08 May 2015

Paulina is supported by:

About Paulina

Help