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List of works by Cornelia M. van Duijn

52 Genetic Loci Influencing Myocardial Mass

scientific article

A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study

scientific article published on 8 November 2016

A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings.

scientific article published on 30 April 2016

A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants.

scientific article

A Genome-Wide Scan for MicroRNA-Related Genetic Variants Associated With Primary Open-Angle Glaucoma

scientific article published on October 2017

A Genome-Wide Search for Genes Involved in Type 2 Diabetes in a Recently Genetically Isolated Population From the Netherlands

article

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila

scientific article

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

scientific article

A Large-Scale Population-Based Analysis of Common Genetic Variation in the Thyroid Hormone Receptor Alpha Locus and Bone

scholarly article by Marco Medici et al published February 2012 in Thyroid

A Mendelian Randomization Study of Metabolite Profiles, Fasting Glucose and Type 2 Diabetes

scientific article

A Method for Pooling Alleles from Different Genotyping Experiments

A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms

article

A case-control study of apolipoprotein E genotypes in Alzheimer's disease associated with Down's syndrome. Dutch Study Group on Down's Syndrome and Ageing

scientific article published in August 1995

A case-control study on the effect of p53 and p73 gene polymorphisms on gastric cancer risk and progression

scientific article published on 3 March 2009

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

scientific article published on 31 May 2019

A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy

scientific article published on 5 March 2018

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.

scientific article published on 19 June 2017

A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study

scientific article (publication date: 18 April 2006)

A critical appraisal of epidemiological studies comes from basic knowledge: a reader's guide to assess potential for biases

scientific article published on 15 March 2007

A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions

scientific article published on March 2008

A cross-omics integrative study of metabolic signatures of chronic obstructive pulmonary disease

scientific article published on 16 July 2020

A deletion in DJ-1 and the risk of dementia--a population-based survey

scientific article published in December 2004

A genetic association study of the IGF-1 gene and radiological osteoarthritis in a population-based cohort study (the Rotterdam Study).

scientific article published on June 1998

A genetic epidemiologic study of candidate genes involved in the optic nerve head morphology

scientific article

A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk

scientific article published on January 2014

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 identifies new childhood obesity loci

scientific article

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 scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project

scientific article

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

scientific article published on 4 January 2012

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

scientific article

A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.

scientific article

A genome-wide association study identifies genetic loci associated with specific lobar brain volumes

scientific article published on 02 August 2019

A genome-wide association study of aging

scientific article

A genome-wide association study of depressive symptoms

scientific journal article

A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation

scientific article

A genome-wide association study of optic disc parameters

scientific article

A genome-wide association study of sleep habits and insomnia

scientific article

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

scientific article

A genome-wide linkage study of individuals with high scores on NEO personality traits

scientific article published on 09 August 2011

A genome-wide screen for depression in two independent Dutch populations

scientific article published on 8 May 2010

A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol

scientific article

A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands

scientific article published on March 2002

A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population

scientific article

A genomic background based method for association analysis in related individuals

scientific article

A high-quality human reference panel reveals the complexity and distribution of genomic structural variants

scientific article published on 06 October 2016

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

scientific article published on 21 December 2015

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

scientific article

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

scientific article published on 14 August 2019

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

scientific article

A metabolic profile of all-cause mortality risk identified in an observational study of 44,168 individuals

scientific article published on 20 August 2019

A metabolomic profile is associated with the risk of incident coronary heart disease

scientific article published on 4 April 2014

A methodological perspective on genetic risk prediction studies in type 2 diabetes: recommendations for future research

scientific article published on December 2011

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

scientific article published on 10 April 2019

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

scientific article (publication date: July 2001)

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

scientific article

A novel common variant in DCST2 is associated with length in early life and height in adulthood

scientific article published on 3 October 2014

A novel method for serum lipoprotein profiling using high performance capillary isotachophoresis

scientific article

A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease

scientific article published on October 2002

A polymorphic CA repeat in the IGF-I gene is associated with gender-specific differences in body height, but has no effect on the secular trend in body height

scientific article

A polymorphic CA repeat in the promoter region of the insulin-like growth factor-I (IGF-I) gene

scientific article published on 01 January 2003

A polymorphism in the IGF-I gene influences the age-related decline in circulating total IGF-I levels

scientific article published on 01 February 2003

A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarction

scientific article published in March 2001

A polymorphism in the regulatory region of PRNP is associated with increased risk of sporadic Creutzfeldt-Jakob disease

scientific article

A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy

article

A population-based study of familial Alzheimer disease: linkage to chromosomes 14, 19, and 21.

scientific article published in October 1994

A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

scientific article published on 23 November 2016

A priori collaboration in population imaging: The Uniform Neuro-Imaging of Virchow-Robin Spaces Enlargement consortium

scientific article published on 31 October 2015

A promoter polymorphism of the insulin-like growth factor-I gene is associated with left ventricular hypertrophy

scientific article published on February 2005

A rare missense variant in RCL1 segregates with depression in extended families

scientific article published on 21 March 2017

A reference panel of 64,976 haplotypes for genotype imputation

scientific article

A study of familial aggregation of depression, dementia and Parkinson's disease

scientific article published in April 1998

A study of gene--environment interaction on the gene for angiotensin converting enzyme: a combined functional and population based approach

scientific article

A study of the SORL1 gene in Alzheimer's disease and cognitive function

scientific article published in January 2009

A systematic evaluation of 151 candidate genes for their association with osteoporosis and osteoporotic fracture in a meta-analysis of genome-wide association data

article

A systematic review of meta-analyses on gene polymorphisms and gastric cancer risk

scientific article published on September 2008

A unified approach to modelling linkage to quantitative and qualitative traits

scientific article published on September 2003

A variant of the IGF-I gene is associated with blood pressure but not with left heart dimensions at the age of 2 years: the Generation R Study

scientific article published on 10 June 2008

ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdala

scientific article

ACE polymorphisms

scientific article

APOE and the risk of PD with or without dementia in a population-based study

article

APOE genotyping in differential diagnosis of Alzheimer's disease

scientific article published in The Lancet

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

scientific article

ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure

scientific article published on 30 January 2015

ATP5H/KCTD2 locus is associated with Alzheimer's disease risk.

scientific article

Accuracy of self-reported family history is strongly influenced by the accuracy of self-reported personal health status of relatives

scientific article published in September 2011

Adherence to and dosing of beta-hydroxy-beta-methylglutaryl coenzyme A reductase inhibitors in the general population differs according to apolipoprotein E-genotypes

scientific article published in April 2003

Adherence to and dosing of statins differs according to apolipoprotein E-genotypes.

scientific article

Adiposity as a cause of cardiovascular disease: a Mendelian randomization study

scientific article

Adjacent genes, for COL2A1 and the vitamin D receptor, are associated with separate features of radiographic osteoarthritis of the knee

scientific article published in July 2000

Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the gene

article

Age- and sex-specific causal effects of adiposity on cardiovascular risk factors

scientific article published on 23 February 2015

Age-related accrual of methylomic variability is linked to fundamental ageing mechanisms

scientific article published on 22 September 2016

Agreement between oral contraceptive users and prescribers: Implications for case-control studies ⬇️

scientific article published on May 1, 1992

Alcohol and mortality. Results from the EPOZ (Epidemiologic Study of Cardiovascular Risk Indicators) follow-up study

scientific article

Alcohol and tobacco consumption as risk factors for Alzheimer's disease: a collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group

scientific article

Alcohol consumption and risk of dementia: the Rotterdam Study

scientific article published in January 2002

Alcohol intake in relation to brain magnetic resonance imaging findings in older persons without dementia

scientific article

Aldehyde dehydrogenase 2 and head and neck cancer: a meta-analysis implementing a Mendelian randomization approach

scientific article published in January 2009

Allelic variants of cytochrome P450 2C9 modify the interaction between nonsteroidal anti-inflammatory drugs and coumarin anticoagulants

scientific article published in June 2005

Alpha-adducin polymorphism, atherosclerosis, and cardiovascular and cerebrovascular risk

scientific article published on 2 November 2006

Altered bile acid profile associates with cognitive impairment in Alzheimer's disease-An emerging role for gut microbiome

Altered bile acid profile associates with cognitive impairment in Alzheimer's disease—An emerging role for gut microbiome

Altered bile acid profile in mild cognitive impairment and Alzheimer's disease: Relationship to neuroimaging and CSF biomarkers

scientific article published on 15 October 2018

Alzheimer's disease and glaucoma-reply

scholarly article by Sarah F Janssen et al published March 2014 in Progress in Retinal and Eye Research

Alzheimer's disease genes and cognition in the nondemented general population

scientific article published on 15 May 2012

Alzheimer's disease in Down syndrome: An overlooked population for prevention trials

scholarly article by Andre Strydom et al published 2018 in Alzheimer's & dementia (New York, N. Y.)

Amyloid precursor protein gene mutation in early-onset Alzheimer's disease

scientific article published in April 1991

Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease ⬇️

scientific article published on November 2, 2001

An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype

scientific article published on 8 December 2016

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

scientific article published on 27 May 2016

An R package "VariABEL" for genome-wide searching of potentially interacting loci by testing genotypic variance heterogeneity

scientific article

An approach for cutting large and complex pedigrees for linkage analysis

scientific article published on 27 February 2008

An empirical comparison of meta-analyses of published gene-disease associations versus consortium analyses

scientific article published in March 2009

An epidemiological perspective on the future of direct-to-consumer personal genome testing

scientific article

An igf-I gene polymorphism modifies the risk of diabetic retinopathy

scientific article published on 01 August 2006

An insulin-like growth factor-I gene polymorphism modifies the risk of microalbuminuria in subjects with an abnormal glucose tolerance

scientific article published in May 2006

An insulin-like growth factor-I promoter polymorphism is associated with increased mortality in subjects with myocardial infarction in an elderly Caucasian population

scientific article published on 10 March 2006

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

scientific article published on 13 June 2019

Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype

scientific article published on 10 June 2019

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

scientific article published on 29 September 2013

Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam Study

scientific article

Angiotensin converting enzyme gene, smoking and mortality in a population-based study

article

Angiotensin converting enzyme insertion/deletion polymorphism and the risk of heart failure in hypertensive subjects.

scientific article published in December 2004

Angiotensin-converting enzyme gene insertion/deletion polymorphism and breast cancer risk

scientific article published on 01 September 2005

Angiotensin-converting enzyme gene polymorphism and carotid artery wall thickness: a meta-analysis

scientific article

Angiotensin-converting enzyme gene polymorphism and common carotid stiffness. The Rotterdam study

scientific article published on 01 May 2004

Angiotensinogen M235T polymorphism and symptoms of depression in a population-based study and a family-based study

scientific article published in August 2008

Angiotensinogen M235T polymorphism and the risk of myocardial infarction and stroke among hypertensive patients on ACE-inhibitors or β-blockers

Angiotensinogen promoter B-haplotype associated with cerebral small vessel disease enhances basal transcriptional activity

scientific article

Antiepileptic drug regimens and major congenital abnormalities in the offspring

scientific article published on 01 November 1999

Antipsychotic-induced movement disorders in long-stay psychiatric patients and 45 tag SNPs in 7 candidate genes: a prospective study

scientific article

ApoE gene polymorphisms, BMD, and fracture risk in elderly men and women: the Rotterdam study

scientific article

Apolipoprotein E and carotid artery atherosclerosis: the Rotterdam study

scientific article published on September 2001

Apolipoprotein E epsilon4 allele is associated with left ventricular systolic dysfunction

scientific article published in April 2004

Apolipoprotein E epsilon4 and the risk of dementia with stroke. A population-based investigation

scientific article published in March 1997

Apolipoprotein E gene and sporadic frontal lobe dementia.

scientific article published in June 1997

Apolipoprotein E gene is related to mortality only in normal weight individuals: the Rotterdam Study

scientific article

Apolipoprotein E genotype and association between smoking and early onset Alzheimer's disease

scientific article published on March 1995

Apolipoprotein E genotype and concomitant clinical features in early-onset Alzheimer's disease

scientific article published in June 1996

Apolipoprotein E genotype and progression of Alzheimer's disease: the Rotterdam Study

scientific article published in April 1999

Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations

article

Apolipoprotein E genotype in patients with alzheimer's disease: Implications for the risk of dementia among relatives

article

Apolipoprotein E genotype, atherosclerosis, and cognitive decline: the Rotterdam Study

scientific article published in January 1998

Apolipoprotein E4 allele in a population–based study of early–onset Alzheimer's disease

scientific article published on 01 May 1994

Apolipoprotein E4 in the temporal variant of frontotemporal dementia

scientific article published in June 2002

Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes

scientific article

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

scientific article (publication date: November 2010)

Association analysis of bitter receptor genes in five isolated populations identifies a significant correlation between TAS2R43 variants and coffee liking

scientific article

Association analysis of ten candidate genes in a large multinational cohort of small for gestational age children and children with idiopathic short stature (NESTEGG study).

scientific article published on 23 November 2013

Association between an insulin-like growth factor I gene promoter polymorphism and bone mineral density in the elderly: the Rotterdam Study

scientific article

Association between apolipoprotein-epsilon4 and long-term outcome after traumatic brain injury

scientific article published on 30 October 2007

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

scientific article published on 23 December 2011

Association between genetic variation in the gene for insulin-like growth factor-I and low birthweight

scientific article published in March 2002

Association between type 2 diabetes loci and measures of fatness

scientific article

Association of 5' estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk

scientific article

Association of Altered Liver Enzymes With Alzheimer Disease Diagnosis, Cognition, Neuroimaging Measures, and Cerebrospinal Fluid Biomarkers

scientific article published on 03 July 2019

Association of Alzheimer's disease GWAS loci with MRI markers of brain aging

scientific article

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

scientific article published on 01 November 2019

Association of HSP70 and its co-chaperones with Alzheimer's disease

scientific article

Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants

scientific article

Association of adiposity genetic variants with menarche timing in 92,105 women of European descent

scientific article published on 04 April 2013

Association of an APOC3 promoter variant with type 2 diabetes risk and need for insulin treatment in lean persons

scientific article

Association of branched-chain amino acids and other circulating metabolites with risk of incident dementia and Alzheimer's disease: A prospective study in eight cohorts

scientific article published on 28 February 2018

Association of circulating metabolites in plasma or serum and risk of stroke: Meta-analysis from seven prospective cohorts

scientific article published on 02 December 2020

Association of cognitive functioning with retinal nerve fiber layer thickness.

scientific article

Association of common genetic variants with brain microbleeds: A Genome-wide Association Study

scientific article published on 10 September 2020

Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's disease

scientific article

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

scientific journal article

Association of heat shock proteins with Parkinson's disease

scientific article published on 26 November 2011

Association of heat shock proteins with all-cause mortality

scientific article published on 04 May 2012

Association of hypertension drug target genes with blood pressure and hypertension in 86,588 individuals

scientific article

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

scientific article

Association of lysophosphatidic acids with cerebrospinal fluid biomarkers and progression to Alzheimer's disease

scientific article published on 02 October 2020

Association of matrilin-3 polymorphisms with spinal disc degeneration and osteoarthritis of the first carpometacarpal joint of the hand

scientific article published on 5 January 2006

Association of metformin, sulfonylurea and insulin use with brain structure and function and risk of dementia and Alzheimer's disease: Pooled analysis from 5 cohorts

scholarly article by Galit Weinstein et al published 2019 in PLOS ONE

Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts

scientific article published on April 2009

Association of the IGF1 gene with fasting insulin levels

scientific article published on 10 February 2016

Association of the interleukin-1 gene cluster with radiographic signs of osteoarthritis of the hip.

scientific article published in April 2004

Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study

scientific article

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

Associations between the deletion polymorphism of the angiotensin 1-converting enzyme gene and ocular signs of primary open-angle glaucoma

scientific article

Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic Epidemiology (CHARGE) consortium

scientific article

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Associations with intraocular pressure across Europe: The European Eye Epidemiology (E3) Consortium

scientific article published on 09 September 2016

Attention-deficit/hyperactivity disorder (ADHD): parents' judgment about school, teachers' judgment about home

scientific article published on 01 October 2004

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

scientific article published in Nature Communications

Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

scientific article published on 01 December 2018

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

scientific article published on 01 September 2019

Author Correction: Heritability estimates for 361 blood metabolites across 40 genome-wide association studies

scientific article published on 31 March 2020

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

scientific article published on 01 May 2019

Automated workflow-based exploitation of pathway databases provides new insights into genetic associations of metabolite profiles

scientific article (publication date: 9 December 2013)

Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation

scientific article published in Nature Communications

Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7

scientific article (publication date: September 2002)

BSE and variant Creutzfeldt-Jakob disease: never say never

scientific article published on 13 April 2002

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

scientific article

Beyond public health genomics: proposals from an international working group

scientific article

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

scientific article

Bivariate Genome-Wide Association Study of Depressive Symptoms with Type 2 Diabetes and Quantitative Glycemic Traits

scientific article published on 27 December 2017

Blood lipids influence DNA methylation in circulating cells

scientific article published on 27 June 2016

Blood metabolomic measures associate with present and future glycemic control in type 2 diabetes

Blood-based metabolic signatures in Alzheimer's disease

scientific article published on 6 September 2017

Bone Mineral Density in Sjögren Syndrome Patients with and Without Distal Renal Tubular Acidosis

scientific article published on 12 February 2016

Breast-feeding modifies the association of PPARgamma2 polymorphism Pro12Ala with growth in early life: the Generation R Study

scientific article published on 02 February 2009

Burden of genetic risk variants in multiple sclerosis families in the Netherlands

scientific article

CDH6 and HAGH protein levels in plasma associate with Alzheimer's disease in APOE ε4 carriers

scientific article published on 19 May 2020

CHOLESTERYL ESTER TRANSFER PROTEIN GENE AND CORONARY HEART DISEASE MORTALITY: THE ROTTERDAM STUDY

article

COPD GWAS variant at 19q13.2 in relation with DNA methylation and gene expression

scientific article

CYP1A1, CYP2E1, GSTM1, GSTT1, EPHX1 exons 3 and 4, and NAT2 polymorphisms, smoking, consumption of alcohol and fruit and vegetables and risk of head and neck cancer

scientific article published on 05 July 2007

CYP1A2 and coffee intake and the modifying effect of sex, age, and smoking

scientific article

CYP2D6 polymorphism in Parkinson's disease: The Rotterdam study

scientific article published on 01 March 2001

CYP2E1PstI/RsaI polymorphism and interaction with tobacco, alcohol and GSTs in gastric cancer susceptibility: A meta-analysis of the literature

scientific article published on 11 July 2006

Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia.

scientific article published on 4 January 2018

Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective study

scientific article (publication date: 2012)

Candidate-gene association study searching for genetic factors involved in migraine chronification

scientific article published on 28 August 2014

Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993-95. European Union (EU) Collaborative Study Group of Creutzfeldt-Jakob disease (CJD).

scientific article published in April 1998

Cataract surgery and the risk of aging macula disorder: the rotterdam study

scientific article published on 3 July 2008

Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease

scientific article published in January 2010

Cathepsin D gene and the risk of Alzheimer's disease: a population-based study and meta-analysis.

scientific article published on 18 November 2009

Cdx-2 polymorphism in the promoter region of the human vitamin D receptor gene determines susceptibility to fracture in the elderly

scientific article published in September 2003

Cerebral small vessel disease genomics and its implications across the lifespan

scientific article published on 08 December 2020

Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias: a longitudinal multicentre study over 10 years

scientific article

Cerebrospinal fluid biomarkers in human genetic transmissible spongiform encephalopathies

scientific article

Cerebrovascular risk factors do not contribute to genetic variance of cognitive function: the ERF study

scientific article published on 12 May 2006

Characteristics of de novo structural changes in the human genome

scientific article

Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: a clinical interpretation strategy

scientific article published on 24 May 2017

Cholesterol and age-related macular degeneration: is there a link?

scientific article published in April 2004

Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies

scientific article

Circulating metabolites are associated with brain atrophy and white matter hyperintensities

scientific article published on 04 September 2020

Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals

scientific article

Clinical Implications of Old and New Genes for Open-Angle Glaucoma

article

Clinical features and mortality in patients with early-onset Alzheimer's disease

scientific article published in January 1996

Clinical features and neuroimaging of PARK7-linked parkinsonism

scientific article (publication date: July 2003)

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture

scientific article

Common DNA variants predict tall stature in Europeans

scientific article published on 20 November 2013

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

scientific article published on 10 June 2020

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common genetic determinants of intraocular pressure and primary open-angle glaucoma

scientific article

Common genetic variants associate with serum phosphorus concentration

scientific article

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

scientific article

Common genetic variants associated with open-angle glaucoma

scientific article published on 22 March 2011

Common genetic variants influence human subcortical brain structures

scientific article

Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium

scientific article published on 8 November 2011

Common polygenic variation enhances risk prediction for Alzheimer's disease

scientific article published on 21 October 2015

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

scientific article

Common variants at 12q14 and 12q24 are associated with hippocampal volume

scientific article

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

scientific article published on 15 April 2012

Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.

scientific article published on 11 December 2017

Common variants at 6q22 and 17q21 are associated with intracranial volume

scientific article published on 15 April 2012

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

scientific article (publication date: May 2011)

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

scientific article

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

scientific article published on 7 June 2021

Common variants in Mendelian kidney disease genes and their association with renal function

scientific article published on 12 September 2013

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

scientific article published on 24 October 2008

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration

scientific article

Comparison of participant information and informed consent forms of five European studies in genetic isolated populations

scientific article (publication date: March 2010)

Complement component C3 and risk of age-related macular degeneration

scientific article published on 24 January 2009

Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration

scientific article

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

scientific article published on September 2014

Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report

scientific article published in September 2011

Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countries

scientific article

Correction. Heritability and genome-wide association analyses of intracranial carotid artery calcification: The Rotterdam Study

scientific article

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

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: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

scientific article published on 23 August 2017

Correction: Susceptibility to chronic mucus hypersecretion, a genome wide association study

scientific article published on 29 May 2015

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

scientific article

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: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

scientific article published on November 2016

Corrigendum: Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

scientific article published on 30 March 2015

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scholarly article published in Nature Genetics

Creutzfeldt-Jakob disease 38 years after diagnostic use of human growth hormone

scientific article published on June 2002

Creutzfeldt-Jakob disease: diagnosis, incidence, prevention and treatment

scientific article

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

scientific article

Cyclin-dependent kinase 5 is associated with risk for Alzheimer's disease in a Dutch population-based study

scientific article

DNA methylation is associated with lung function in never smokers

scientific article published on 02 December 2019

DNA methylation signatures of educational attainment

scientific article published on 23 March 2018

Decreased DNA repair capacity in familial, but not in sporadic Alzheimer's disease

scientific article published in July 1991

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

scientific article

Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency

scientific article

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Dense-core senile plaques in the Flemish variant of Alzheimer's disease are vasocentric

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Determining Possible Shared Genetic Architecture Between Myopia and Primary Open-Angle Glaucoma

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Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

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Direct-to-Consumer Personal Genome Testing for Age-Related Macular Degeneration

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Effects of the Renin-Angiotensin System Genes and Salt Sensitivity Genes on Blood Pressure and Atherosclerosis in the Total Population and Patients With Type 2 Diabetes

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

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Estrogen receptor alpha gene haplotype is associated with radiographic osteoarthritis of the knee in elderly men and women

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European lactase persistence genotype shows evidence of association with increase in body mass index

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Evaluation of Presumably Disease Causing SCN1A Variants in a Cohort of Common Epilepsy Syndromes

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Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia

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Evaluation of risk prediction updates from commercial genome-wide scans

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Evidence that the mitochondrial leucyl tRNA synthetase (LARS2) gene represents a novel type 2 diabetes susceptibility gene

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

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Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length

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Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old age.

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

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

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Exome-Wide Meta-Analysis Identifies Rare 3'-UTR Variant in ERCC1/CD3EAP Associated with Symptoms of Sleep Apnea

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

Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.

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

Expression and Gene Variation Studies Deny Association of Human HSD3B1 Gene With Aldosterone Production or Blood Pressure

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Fifteen Genetic Loci Associated With the Electrocardiographic P Wave

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

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Five genetic variants associated with prostate cancer

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Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

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

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

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GWAS of 126,559 individuals identifies genetic variants associated with educational attainment

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GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy

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GenABEL: an R library for genome-wide association analysis

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Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

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Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

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

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

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Genes predict village of origin in rural Europe

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Genes, pathways, and animal models in primary open-angle glaucoma

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Genetic African Ancestry Is Associated With Central Corneal Thickness and Intraocular Pressure in Primary Open-Angle Glaucoma

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

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

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

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Genetic Determinants of Unruptured Intracranial Aneurysms in the General Population

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Genetic Epidemiology of Alzheimer Disease ⬇️

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Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus

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

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Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project

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Genetic analysis for a shared biological basis between migraine and coronary artery disease

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

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

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

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Genetic architecture of circulating lipid levels

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Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

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Genetic architecture of plasma adiponectin overlaps with the genetics of metabolic syndrome-related traits

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Genetic architecture of subcortical brain structures in 38,851 individuals

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Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample

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Genetic association studies: genes in search of diseases

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

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Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

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Genetic contributions to glaucoma: heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphology

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

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

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Genetic determinants of circulating sphingolipid concentrations in European populations

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Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins

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Genetic evidence of assortative mating in humans

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Genetic factors and insulin secretion: gene variants in the IGF genes

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Genetic factors influence the clustering of depression among individuals with lower socioeconomic status

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

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Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration

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Genetic loci for coronary calcification and serum lipids relate to aortic and carotid calcification

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Genetic loci for retinal arteriolar microcirculation

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Genetic loci for serum lipid fractions and intracerebral hemorrhage

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

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Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus

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Genetic polymorphisms and heart failure

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Genetic prion disease: the EUROCJD experience

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Genetic risk of Parkinson's disease in the general population

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Genetic risk of age-related maculopathy. Population-based familial aggregation study

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Genetic risk of neurodegenerative diseases is associated with mild cognitive impairment and conversion to dementia

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Genetic risk profiles for depression and anxiety in adult and elderly cohorts

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Genetic scoring analysis: a way forward in genome wide association studies?

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Genetic screening for common mutations: lessons from hereditary hemochromatosis

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Genetic studies of body mass index yield new insights for obesity biology

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Genetic susceptibility to multiple sclerosis: Brain structure and cognitive function in the general population

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Genetic susceptibility, dietary antioxidants, and long-term incidence of age-related macular degeneration in two populations

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Genetic testing has no place as a routine diagnostic test in sporadic and familial cases of Alzheimer's disease

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Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia

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Genetic transmission of Alzheimer's disease among families in a Dutch population based study

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Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression

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

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Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

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Genetic variants in RBFOX3 are associated with sleep latency

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

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Genetic variants influencing circulating lipid levels and risk of coronary artery disease

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Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images

Genetic variation associated with circulating monocyte count in the eMERGE Network

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Genetic variation at the phospholipid transfer protein locus affects its activity and high-density lipoprotein size and is a novel marker of cardiovascular disease susceptibility

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

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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

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Genetic variation in the fibrinogen-alpha and fibrinogen-gamma genes in relation to arterial stiffness: the Rotterdam Study

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Genetic variation in the renin--angiotensin system, use of renin--angiotensin system inhibitors and the risk of myocardial infarction

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Genetic variation in the renin-angiotensin system and arterial stiffness. The Rotterdam Study

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Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile

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Genetic variation underlying cognition and its relation with neurological outcomes and brain imaging

Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach

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Genetics of the human metabolome, what is next?

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

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Genome-Wide Association Study of Vascular Dementia

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Genome-based prediction of breast cancer risk in the general population: a modeling study based on meta-analyses of genetic associations

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Genome-based prediction of common diseases: methodological considerations for future research

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Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length

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Genome-wide Association Study Links APOEϵ4 and BACE1 Variants with Plasma Amyloid β Levels

Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals

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

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Genome-wide analyses of borderline personality features

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Genome-wide analysis identifies 12 loci influencing human reproductive behavior

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Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course

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Genome-wide analysis of genetic loci associated with Alzheimer disease

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Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma

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

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

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Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention ⬇️

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

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Genome-wide association analysis identifies susceptibility loci for migraine without aura

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Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM

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Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking

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Genome-wide association and functional follow-up reveals new loci for kidney function

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Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

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Genome-wide association meta-analysis for total serum bilirubin levels

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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

scientific article published on 28 May 2018

Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits

scientific article published on 24 January 2019

Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence

scientific article published on 22 May 2017

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

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

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

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Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

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

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Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area

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

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

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Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels

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Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene

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

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Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

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Genome-wide association study identifies 48 common genetic variants associated with handedness

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Genome-wide association study identifies 74 loci associated with educational attainment

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Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited

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

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Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

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Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations

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

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Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region

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

scientific article published in Nature Communications

Genome-wide association study of PR interval

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Genome-wide association study of blood pressure and hypertension

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Genome-wide association study of intracranial aneurysm identifies three new risk loci

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Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

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

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Genome-wide association study of retinopathy in individuals without diabetes

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Genome-wide association study of smoking initiation and current smoking

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Genome-wide association study on the FEV1/FVC ratio in never-smokers identifies HHIP and FAM13A.

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Genome-wide associations for birth weight and correlations with adult disease

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Genome-wide identification of directed gene networks using large-scale population genomics data

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Genome-wide linkage analysis of serum creatinine in three isolated European populations.

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Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

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Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity

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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

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Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries

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

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Genome-wide meta-analysis identifies new susceptibility loci for migraine

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Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption

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Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

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

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Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels

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Genome-wide patterns and properties of de novo mutations in humans

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Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults

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Genome-wide profiling of blood pressure in adults and children

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Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.

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Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk

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Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

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Genomewide association studies of stroke

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

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Genomewide scan for affective disorder susceptibility Loci in families of a northern Swedish isolated population

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Genome‐wide meta‐analysis of late‐onset Alzheimer’s disease using rare variant imputation in 65,602 subjects identifies risk loci with roles in memory, neurodevelopment, and cardiometabolic traits: The international genomics of Alzheimer’s project (

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

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Glucocorticoid receptor gene-based SNP analysis in patients with recurrent major depression.

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Glucocorticoid receptor-9beta polymorphism is associated with systolic blood pressure and heart growth during early childhood. The Generation R Study

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Good prospects for genetic and molecular epidemiologic studies in the European Journal of Epidemiology

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Gray matter heritability in family-based and population-based studies using voxel-based morphometry

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Gut microbiome-wide association study of depressive symptoms

HFE gene mutations increase the risk of coronary heart disease in women.

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HFE variants, APOE and Alzheimer's disease: Findings from the population-based Rotterdam Study

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Haplotype analyses of the APOA5 gene in patients with familial combined hyperlipidemia

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Haplotype reference consortium panel: Practical implications of imputations with large reference panels

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Harmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank research

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Head trauma and risk of dementia and Alzheimer's disease: The Rotterdam Study

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Head trauma and the risk of Alzheimer's disease ⬇️

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Head trauma as a risk factor for Alzheimer's disease: a collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group

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Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families

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Heritabilities, apolipoprotein E, and effects of inbreeding on plasma lipids in a genetically isolated population: the Erasmus Rucphen Family Study

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Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants

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Heritability and Genome-Wide Association Analyses of Intracranial Carotid Artery Calcification: The Rotterdam Study

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Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes

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Heritability estimates for 361 blood metabolites across 40 genome-wide association studies

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Heritability of Serum Iron, Ferritin and Transferrin Saturation in a Genetically Isolated Population, the Erasmus Rucphen Family (ERF) Study

Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes

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Heritability of dietary food intake patterns

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Heritability of the Function and Structure of the Arterial Wall

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

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IGF-I gene promoter polymorphism is a predictor of survival after myocardial infarction in patients with type 2 diabetes

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Identification of a candidate gene for astigmatism

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Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

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Identification of seven loci affecting mean telomere length and their association with disease

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Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach

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Igf-I bioactivity in an elderly population: relation to insulin sensitivity, insulin levels, and the metabolic syndrome

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Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'.

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Improvement of Risk Prediction by Genomic Profiling: Reclassification Measures Versus the Area Under the Receiver Operating Characteristic Curve

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Increased High Density Lipoprotein-levels associated with Age-related Macular degeneration. Evidence from the EYE-RISK and E3 Consortia

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Increased High-Density Lipoprotein Levels Associated with Age-Related Macular Degeneration

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Increasing Prevalence of Myopia in Europe and the Impact of Education

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Independent Multiple Factor Association Analysis for Multiblock Data in Imaging Genetics

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Infectious mononucleosis-linked HLA class I single nucleotide polymorphism is associated with multiple sclerosis

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Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

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LPIN2 Is Associated With Type 2 Diabetes, Glucose Metabolism, and Body Composition

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Large common deletions associate with mortality at old age.

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Large meta-analysis establishes the ACE insertion-deletion polymorphism as a marker of Alzheimer's disease

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

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Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium

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

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Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness.

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Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

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

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Large-scale plasma metabolome analysis reveals alterations in HDL metabolism in migraine

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Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels

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Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population

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Loci influencing blood pressure identified using a cardiovascular gene-centric array.

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Long-term Air Pollution Exposure, Genome-wide DNA Methylation and Lung Function in the LifeLines Cohort Study

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Longevity candidate genes and their association with personality traits in the elderly

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

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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

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Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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Measurement and genetic architecture of lifetime depression in the Netherlands as assessed by LIDAS (Lifetime Depression Assessment Self-report)

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Mendelian randomization studies do not support a causal role for reduced circulating adiponectin levels in insulin resistance and type 2 diabetes

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Meta- and pooled analyses of the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and gastric cancer risk: a huge-GSEC review

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

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Meta-analyses of genetic studies on major depressive disorder

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

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Meta-analyses of the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and risk of head and neck and lung cancer

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

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

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Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

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

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

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Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

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Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

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Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder

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Meta-analysis of epigenome-wide association studies of cognitive abilities

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Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

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Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Meta-analysis of genome-wide association for migraine in six population-based European cohorts

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Meta-analysis of genome-wide association studies for personality.

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

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Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair

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Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.

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Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process

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

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

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Meta-analysis of telomere length in 19,713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect

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Metabolic Age Based on the BBMRI-NL 1H-NMR Metabolomics Repository as Biomarker of Age-related Disease

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Metabolic network failures in Alzheimer's disease: A biochemical road map.

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Metabolic profiling of intra- and extracranial carotid artery atherosclerosis

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Metabolomics Profile in Depression: A Pooled Analysis of 230 Metabolic Markers in 5283 Cases With Depression and 10,145 Controls

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Metabolomics based markers predict type 2 diabetes in a 14-year follow-up study

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Metabolomics reveals a link between homocysteine and lipid metabolism and leukocyte telomere length: the ENGAGE consortium

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Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and susceptibility to gastric adenocarcinoma in an Italian population

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Microbiomics, metabolomics, predicted metagenomics and hepatic steatosis in a population-based study of 1355 adults

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Micronutrients and the risk of lung cancer

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Migraine is not associated with enhanced atherosclerosis

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Migraine without aura: genome-wide association analysis identifies several novel susceptibility.

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Mild cognitive impairment--beyond controversies, towards a consensus: report of the International Working Group on Mild Cognitive Impairment

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Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels

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Modulation of genetic associations with serum urate levels by body-mass-index in humans

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Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada

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Mortality in patients with hypertension on angiotensin-I converting enzyme (ACE)-inhibitor treatment is influenced by the ACE insertion/deletion polymorphism

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

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

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

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

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

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

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Multi-trait genome-wide association study identifies new loci associated with optic disc parameters

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

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Multicenter cohort association study of SLC2A1 single nucleotide polymorphisms and age-related macular degeneration

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

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Multilocus genetic risk score associates with ischemic stroke in case-control and prospective cohort studies

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Multiomics integrative analysis identifies allele-specific blood biomarkers associated to Alzheimer's disease etiopathogenesis

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Multiple etiologies for Alzheimer disease are revealed by segregation analysis.

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Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors

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Multiple loci are associated with white blood cell phenotypes

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Multiple loci associated with indices of renal function and chronic kidney disease

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Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium

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Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression

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

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Mutation analysis of candidate genes within the 2q33.3 linkage area for familial early-onset generalised osteoarthritis.

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Mutation analysis of the chromosome 14q24.3 dihydrolipoyl succinyltransferase (DLST) gene in patients with early-onset Alzheimer disease

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Mutation screening of the tau gene in patients with early-onset Alzheimer's disease

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Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

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Mutations in the hemochromatosis gene (HFE) and stroke

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Mutations in the hemochromatosis gene (HFE), Parkinson's disease and parkinsonism

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Myocilin mutations in a population-based sample of cases with open-angle glaucoma: the Rotterdam Study

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N-acetyltransferase-2 polymorphism in Parkinson's disease: the Rotterdam study

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

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Neopterin and the risk of dementia in persons with Down syndrome.

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

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

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New genetic loci link adipose and insulin biology to body fat distribution

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New insights into the genetic etiology of Alzheimer's disease and related dementias

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New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

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New loci associated with kidney function and chronic kidney disease

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New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk ⬇️

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Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

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

No association between the angiotensin-converting enzyme gene and major depression: a case???control study and meta-analysis

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No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease

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No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob disease

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Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption

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Nonsteroidal Antiinflammatory Drugs and the Risk of Alzheimer's Disease

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Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations

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

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Novel Genetic Loci Associated With Retinal Microvascular Diameter

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Novel Rare Genetic Variants Associated with Airflow Obstruction in the General Population

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

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

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Novel genetic loci associated with hippocampal volume

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

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Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

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

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Novel parkin mutations detected in patients with early-onset Parkinson's disease

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Novel strategy to identify genetic risk factors for COPD severity: a genetic isolate

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Nucleotide excision DNA repair is associated with age-related vascular dysfunction

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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

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Occupational exposure to pesticides is associated with differential DNA methylation.

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Occupational exposures to solvents and lead as risk factors for Alzheimer's disease: a collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group

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Octapeptide repeat insertions in the prion protein gene and early onset dementia

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

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PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease

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Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

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Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

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Patients with an ApoE epsilon4 allele require lower doses of coumarin anticoagulants

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Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness

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Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children

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Plasma amino acids and neopterin in healthy persons with Down's syndrome

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Polymorphism in the promoter region of the insulin-like growth factor I gene is related to carotid intima-media thickness and aortic pulse wave velocity in subjects with hypertension

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Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease

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Prospects of genetic epidemiology in the 21st century

scientific article

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

article

Psychiatric history and related exposures as risk factors for Alzheimer's disease: a collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group

scientific article

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

scholarly article published in Nature Genetics

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

erratum

Publisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability

scientific article published on 01 July 2019

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

scientific article published on 01 July 2019

Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project

article

Quantifying prion disease penetrance using large population control cohorts

scientific article published on January 2016

Rapid variance components-based method for whole-genome association analysis

scientific article published on 16 September 2012

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

scientific article published on 11 December 2015

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

scientific article

Rare and low-frequency coding variants alter human adult height

scientific article (publication date: February 2017)

Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease

Rare variants in γ-aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes

scientific article

Rate of progression of Alzheimer's disease is associated with genetic risk

scientific article

Re: "Case-control studies of environmental influences in diseases with genetic determinants, with an application to Alzheimer's disease" ⬇️

scientific article published on June 1, 1992

Reasons for non-response in observational pharmacogenetic research

scientific article published in August 2009

Reducing the Genetic Risk of Age-Related Macular Degeneration With Dietary Antioxidants, Zinc, and ω-3 Fatty Acids

scientific article published on 01 June 2011

Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs

scientific article

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

article

Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions

scientific article published on 05 December 2012

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

scientific article published on 9 April 2018

Region-based association analysis of human quantitative traits in related individuals

scientific article

Relation between nicotine intake and Alzheimer's disease ⬇️

scientific article published on June 22, 1991

Relation between smoking and risk of dementia and Alzheimer disease: The Rotterdam Study

scholarly article by C. Reitz et al published 4 September 2007 in Neurology

Relationship between gut microbiota and circulating metabolites in population-based cohorts

scientific article published on 20 December 2019

Relationship of the Ubiquilin 1 gene with Alzheimer's and Parkinson's disease and cognitive function

scientific article published in August 2007

Renin-angiotensin system inhibitors, angiotensin I-converting enzyme gene insertion/deletion polymorphism, and cancer: the Rotterdam Study

scientific article published on 01 February 2008

Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease

scientific article published on 23 August 2009

Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis

scientific article

Reply to Stephan et al.

scientific article published on 3 July 2008

Reply to “Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis”

Reproductive period and risk of dementia in postmenopausal women

scientific article published in March 2001

Retinal vessel diameters and risk of impaired fasting glucose or diabetes: the Rotterdam study

scientific article published in February 2006

Revisiting the Role of Insulin-Like Growth Factor-I Receptor Stimulating Activity and the Apolipoprotein E in Alzheimer's Disease

scholarly article by Sara A Galle et al published 2019 in Frontiers in Aging Neuroscience

Revisiting the clinical validity of multiplex genetic testing in complex diseases

scientific article published on March 2004

Risk Factors for Alzheimer's Disease: The EURODEM Collaborative Re-Analysis of Case-Control Studies ⬇️

scientific article published on January 1, 1992

Risk estimates of dementia by apolipoprotein E genotypes from a population-based incidence study: the Rotterdam Study

scientific article published in July 1998

Risk factors for Alzheimer's disease: overview of the EURODEM collaborative re-analysis of case-control studies. EURODEM Risk Factors Research Group

scientific article published on 01 January 1991

Risk factors for Creutzfeldt-Jakob disease: a reanalysis of case-control studies

scientific article published on May 1996

Risk factors for childhood acute non-lymphocytic leukemia: an association with maternal alcohol consumption during pregnancy?

scientific article (publication date: September 1994)

Risk genes associated with pediatric-onset MS but not with monophasic acquired CNS demyelination.

scientific article

Risk of left ventricular dysfunction in patients with probable Alzheimer's disease with APOE*4 allele.

scientific article

Risk scores of common genetic variants for lipid levels influence atherosclerosis and incident coronary heart disease

scientific article published on 13 June 2013

Roaming through methodology. XXXVII. Unintentional population stratification in genetic case-control studies

scientific article published in January 2002

Role of APOE in dementia: A critical reappraisal

scientific article

Role of shared genetic and environmental factors in symptoms of depression and body composition

article

Runs of homozygosity do not influence survival to old age.

scientific article

SIRT1 genetic variation and mortality in type 2 diabetes: interaction with smoking and dietary niacin

scientific article published on 10 January 2009

SIRT1 genetic variation is related to BMI and risk of obesity

scientific article published on 09 September 2009

STROBE-ME too! ⬇️

scientific article published on October 1, 2011

STrengthening the REporting of Genetic Association Studies (STREGA)-an extension of the STROBE statement

article

STrengthening the REporting of Genetic Association Studies (STREGA): An Extension of the STROBE Statement

article

STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement

scientific article

STrengthening the REporting of Genetic Association studies (STREGA)--an extension of the STROBE statement

scientific article published on April 2009

STrengthening the REporting of Genetic Association studies (STREGA)—an extension of the STROBE statement

article

Scientific reporting is suboptimal for aspects that characterize genetic risk prediction studies: a review of published articles based on the Genetic RIsk Prediction Studies statement

scientific article published on 08 January 2014

Score statistic to test for genetic correlation for proband-family design

scientific article published on July 2005

Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics

scientific article published on 01 July 2019

Second probable case of vCJD in the Netherlands

scientific article published on 29 June 2006

Separating the mechanism-based and off-target actions of cholesteryl ester transfer protein inhibitors with CETP gene polymorphisms

scientific article

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

scientific article

Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits

scientific article published on 3 August 2011

Serum MHPG strongly predicts conversion to Alzheimer's disease in behaviorally characterized subjects with Down syndrome.

scientific article

Serum NGAL is Associated with Distinct Plasma Amyloid-β Peptides According to the Clinical Diagnosis of Dementia in Down Syndrome

scientific article published in January 2015

Serum apolipoprotein E is associated with long-term risk of Alzheimer's disease: The Rotterdam Study

scientific article

Serum apolipoprotein E level is not increased in Alzheimer's disease: the Rotterdam study

scientific article

Serum levels of interleukin-6 are not elevated in patients with Alzheimer's disease

scientific article published in January 1990

Seven new loci associated with age-related macular degeneration

scientific article

Sex-specific genetic effects influence variation in body composition

article

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

scientific article

Shared constitutional risks for maternal vascular-related pregnancy complications and future cardiovascular disease

scientific article published on 7 February 2008

Shared genetic factors in migraine and depression: evidence from a genetic isolate

scientific article

Shared genetic factors in the co-occurrence of symptoms of depression and cardiovascular risk factors

scientific article

Short telomere length is associated with impaired cognitive performance in European ancestry cohorts.

scientific article

Single nucleotide polymorphisms in genes that are associated with a modified response to statin therapy: the Rotterdam Study

scientific article published on 2 March 2010

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

scientific article

Smoking and risk of dementia and Alzheimer's disease in a population-based cohort study: the Rotterdam Study

scientific article published in June 1998

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

scientific article published on 07 May 2020

Smoking-dependent effects of the angiotensin-converting enzyme gene insertion/deletion polymorphism on blood pressure

scientific article published in February 2004

Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies

scientific article

Source of variant Creutzfeldt-Jakob disease outside United Kingdom

scientific article

Space-time clustering patterns of gliomas in The Netherlands suggest an infectious aetiology

scientific article published on 7 November 2005

Standard process-oriented workflow introduces pre-analytical error when used in large study sample batches

scientific article published on 01 November 2018

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

scientific article

Strengthening the Reporting of Genetic Risk Prediction Studies: The GRIPS Statement

scientific article published on 15 March 2011

Strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS): explanation and elaboration

scientific article published on 16 March 2011

Strengthening the reporting of Genetic RIsk Prediction Studies: the GRIPS Statement

scientific article

Strengthening the reporting of Genetic RIsk Prediction Studies: the GRIPS Statement

scientific article published on 16 March 2011

Strengthening the reporting of Genetic Risk Prediction Studies: The GRIPS statement

scientific article published on 01 May 2011

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE Statement

article

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement

article

Strengthening the reporting of genetic association studies (STREGA): an extension of the strengthening the reporting of observational studies in epidemiology (STROBE) statement

scientific article published on 12 February 2009

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

scientific article

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

scientific article (publication date: April 2011)

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

Strengthening the reporting of genetic risk prediction studies: The GRIPS Statement

scientific article published in March 2011

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

scientific article published on 16 March 2011

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

scientific article published on 15 March 2011

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement.

scientific article

Strong linkage on 2q33.3 to familial early-onset generalized osteoarthritis and a consideration of two positional candidate genes

scientific article

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

scientific article published on 29 May 2018

Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population

scientific article

Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease

scientific article published on November 2003

Survival in elderly persons with Down syndrome

scientific article published in December 2008

Susceptibility loci for intracranial aneurysm in European and Japanese populations

scientific article

Susceptibility to chronic mucus hypersecretion, a genome wide association study

scientific article

TGF-β1 Polymorphisms and Risk of Myocardial Infarction and Stroke

THE ASSOCIATION BETWEEN INSULIN-LIKE GROWTH FACTOR I BIOACTIVITY, PHYSICAL ACTIVITY AND DEMENTIA

scholarly article published 1 November 2018

TMEM106B influences volume of left-sided temporal lobe and interhemispheric structures in the general population

article by Hieab H.H. Adams et al published 15 September 2014 in Biological Psychiatry

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

scientific article published on 02 October 2019

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

scientific article published in January 2002

Telomere length in circulating leukocytes is associated with lung function and disease.

scientific article published on 5 December 2013

The -1997 G/T and Sp1 polymorphisms in the collagen type I alpha1 (COLIA1) gene in relation to changes in femoral neck bone mineral density and the risk of fracture in the elderly: the Rotterdam study

scientific article published on 7 June 2007

The -514 C->T hepatic lipase promoter region polymorphism and plasma lipids: a meta-analysis

scientific article published in August 2004

The -Adducin Gene Is Associated With Macrovascular Complications and Mortality in Patients With Type 2 Diabetes

article

The ACE insertion/deletion polymorphism and risk of cancer, a review and meta-analysis of the literature

scientific article published on May 2011

The Alzheimer's Disease Sequencing Project: Study design and sample selection

scientific article published on 13 October 2017

The Association Between H63D Mutations in HFE and Amyotrophic Lateral Sclerosis in a Dutch Population

article

The Consortium on Health and Ageing: Network of Cohorts in Europe and the United States (CHANCES) project--design, population and data harmonization of a large-scale, international study

scientific article

The ERCC6 gene and age-related macular degeneration

scientific article (publication date: November 2010)

The Effect of Genetic Drift in a Young Genetically Isolated Population

The Effect of Genetic Drift in a Young Genetically Isolated Population

The Epistasis Project: A Multi-Cohort Study of the Effects of BDNF, DBH, and SORT1 Epistasis on Alzheimer's Disease Risk

scientific article published on 01 January 2019

The GAB2 gene and the risk of Alzheimer's disease: replication and meta-analysis

scientific article published on 31 December 2008

The GenABEL Project for statistical genomics

scientific article

The Generation R Study: Biobank update 2015.

scientific article published on 21 December 2014

The Generation R Study: design and cohort update 2012.

scientific article

The Generation R Study: design and cohort update 2017

scientific article published on 09 January 2017

The Generation R Study: design and cohort update until the age of 4 years

article

The Genome of the Netherlands: design, and project goals

scientific article (publication date: February 2014)

The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease

scientific article published in January 1999

The H63D variant in the HFE gene predisposes to arthralgia, chondrocalcinosis and osteoarthritis

scientific article

The Impact of Partial and Complete Loss-of-Function Mutations in Endothelial Lipase on High-Density Lipoprotein Levels and Functionality in Humans

article

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

scientific article

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

scholarly article published 13 July 2017

The PCLO gene and depressive disorders: replication in a population-based study

article

The Rotterdam Study: 2010 objectives and design update

scientific article

The Rotterdam Study: 2012 objectives and design update

scientific article

The Rotterdam Study: 2014 objectives and design update

scientific article

The Rotterdam Study: 2016 objectives and design update

scientific article

The Rotterdam Study: 2018 update on objectives, design and main results

scientific article published on 24 October 2017

The Rotterdam Study: objectives and design update

scientific article

The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease

scientific article

The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years

scientific article published on 6 October 2005

The Well-Known Gene HHIP and Novel Gene MECR Are Implicated in Small Airway Obstruction

scientific article published in November 2016

The apolipoprotein E epsilon 2 allele is associated with an increased risk of early-onset Alzheimer's disease and a reduced survival.

scientific article published in May 1995

The apolipoprotein E epsilon 4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations

scientific article published in September 1994

The apolipoprotein E gene and its age-specific effects on cognitive function

scientific article

The association between angiotensin-converting enzyme gene polymorphism and coronary calcification. The Rotterdam Coronary Calcification Study

scientific article published on 01 September 2005

The association between antihypertensive drugs and glioma

scientific article published on March 2006

The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels

scientific article

The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer's disease

scientific article

The cholesteryl ester transfer protein I405V polymorphism is associated with increased high-density lipoprotein levels and decreased risk of myocardial infarction: the Rotterdam Study

scientific article published on 01 June 2007

The complement component 5 gene and age-related macular degeneration

scientific article

The dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders: a meta-analysis

scientific article

The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project

scientific article

The dystrophin gene and cognitive function in the general population

scientific article published on 17 September 2014

The effect of APOE and other common genetic variants on the onset of Alzheimer's disease and dementia: a community-based cohort study

scientific article published on 16 March 2018

The effect of APOE on dementia is not through atherosclerosis: the Rotterdam Study

scientific article published on 01 October 1999

The effect of catechol-O-methyltransferase Met/Val functional polymorphism on smoking cessation: retrospective and prospective analyses in a cohort study

scientific article published in January 2009

The effectiveness of HMG-CoA reductase inhibitors in an elderly population is independent of apolipoprotein E-genotypes.

scientific article published in May 2002

The effectiveness of hydroxy-methylglutaryl coenzyme A reductase inhibitors (statins) in the elderly is not influenced by apolipoprotein E genotype

scientific article published in November 2002

The expression of type III hyperlipoproteinemia: involvement of lipolysis genes

scientific article

The first case of variant Creutzfeldt-Jakob disease in The Netherlands

scientific article published on 21 April 2007

The first patient with the new variant of Creutzfeldt-Jakob's disease in The Netherlands

scientific article published in December 2005

The first two patients with dura mater associated Creutzfeldt-Jakob disease in the Netherlands ⬇️

scientific article published on October 1, 2001

The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample

scientific article

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

scientific article

The genetic epidemiology of glioma ⬇️

scientific article published on November 27, 2001

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

scientific article published on 12 September 2016

The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetes

scientific article published on 01 March 2002

The impact of APOE on myocardial infarction, stroke, and dementia: the Rotterdam Study

scientific article published in April 2004

The impact of genotype frequencies on the clinical validity of genomic profiling for predicting common chronic diseases

scientific article published on August 2007

The impact of low-frequency and rare variants on lipid levels

scientific article published on 11 May 2015

The influence of an insulin-like growth factor I gene promoter polymorphism on hip bone geometry and the risk of nonvertebral fracture in the elderly: the Rotterdam Study

scientific article published on 12 April 2004

The influence of the alpha-adducin G460W polymorphism and angiotensinogen M235T polymorphism on antihypertensive medication and blood pressure

scientific article published on 17 May 2006

The interleukin-6-174 G/C promoter polymorphism and arterial stiffness; the Rotterdam Study

scientific article published on January 2008

The involvement of upstream stimulatory factor 1 in Dutch patients with familial combined hyperlipidemia

scientific article published on 25 October 2006

The molecular genetic architecture of self-employment

scientific article

The neuronal transporter gene SLC6A15 confers risk to major depression

scientific article

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

scientific article published on 10 January 2017

The rationale and design of the PERindopril GENEtic association study (PERGENE): a pharmacogenetic analysis of angiotensin-converting enzyme inhibitor therapy in patients with stable coronary artery disease

scientific article

The relationship between fertility and lifespan in humans

scientific article published on 11 January 2011

The risk of bleeding complications in patients with cytochrome P450 CYP2C9*2 or CYP2C9*3 alleles on acenocoumarol or phenprocoumon

scientific article (publication date: July 2004)

The risk of myocardial infarction in patients with reduced activity of cytochrome P450 2C9.

scientific article

The risk of overanticoagulation in patients with cytochrome P450 CYP2C9*2 or CYP2C9*3 alleles on acenocoumarol or phenprocoumon

scientific article

The role of adiposity in cardiometabolic traits: a Mendelian randomization analysis

scientific article (publication date: 2013)

The role of body mass index, insulin, and adiponectin in the relation between fat distribution and bone mineral density

scientific article

The role of hemochromatosis C282Y and H63D gene mutations in type 2 diabetes: findings from the Rotterdam Study and meta-analysis

scientific article published on 01 November 2002

The sex-specific associations of the aromatase gene with Alzheimer's disease and its interaction with IL10 in the Epistasis Project

scientific article published on 05 June 2013

The vast complexity of primary open angle glaucoma: disease genes, risks, molecular mechanisms and pathobiology

scientific article

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

scientific article

Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene

scientific article

Three VCP Mutations in Patients with Frontotemporal Dementia

scientific article published on 01 January 2018

Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene

scientific article

Total zinc intake may modify the glucose-raising effect of a zinc transporter (SLC30A8) variant: a 14-cohort meta-analysis

scientific article

Towards predictive genetic testing of complex diseases

scientific article published on 08 December 2006

Trans-ethnic meta-analysis of white blood cell phenotypes

scientific article

Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project

scientific article

Translational research in genomics of Alzheimer's disease: a review of current practice and future perspectives

scientific article published on January 2010

Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck

scientific article published on 25 February 2016

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scientific article

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

scientific article

Twenty loci associated with bone mineral density identified by large-scale meta-analysis of genome-wide association datasets

Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram

scientific article published on 08 March 2016

Two MTHFR polymorphisms, maternal B-vitamin intake, and CHDs

scientific article published in June 2008

Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies

scientific article

Understanding the role of the chromosome 15q25.1 in COPD through epigenetics and transcriptomics

scientific article published on 8 February 2018

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

scientific article published on 22 September 2009

Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes

scientific article

VEGF polymorphisms are associated with endocardial cushion defects: a family-based case-control study

scientific article published on 01 January 2010

Value of the HLA-DRB1 shared epitope for predicting radiographic damage in rheumatoid arthritis depends on the individual patient risk profile

scientific article published on September 2006

Variance heterogeneity analysis for detection of potentially interacting genetic loci: method and its limitations

scientific article

Variant Creutzfeldt-Jakob disease

scientific article published on 01 January 2003

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

scientific article

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

scientific article

Variants in MTNR1B influence fasting glucose levels

scientific article

Variants in STAT5B Associate with Serum TC and LDL-C Levels

article published in 2011

Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.

scientific article published on 17 May 2017

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

scientific article published on 13 July 2009

Variation in the IGF-1 gene is associated with lymphocyte subset counts in neonates: the Generation R Study

scientific article published on 8 May 2008

Variation in the IGF1 gene and growth in foetal life and infancy. The Generation R Study

scientific article published on 19 September 2007

Variation in the von Willebrand factor gene is associated with von Willebrand factor levels and with the risk for cardiovascular disease

scientific article published on 12 October 2010

Variations in estrogen receptor alpha gene and risk of dementia, and brain volumes on MRI.

scientific article

WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness

scientific article published on 5 June 2015

White Matter Lesion Progression: Genome-Wide Search for Genetic Influences

scientific article

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

article

Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.

scientific article published on 13 March 2018

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

article

Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane

Whole-Genome Linkage Scan Combined With Exome Sequencing Identifies Novel Candidate Genes for Carotid Intima-Media Thickness

article

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

scientific article

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

scientific article

[Gliomas: the role of environmental risk factors and genetic predisposition]

scientific article published in October 2005

[The role of apolipoproteins E genotyping in the differential diagnosis of dementia]

scientific article published on 01 October 1996

miLD and booLD programs for calculation and analysis of corrected linkage disequilibrium

scientific article published in July 2003

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