Cornelia M Van Duijn


Ontology type: schema:Person     


Person Info

NAME

Cornelia M

SURNAME

Van Duijn

Publications in SciGraph latest 50 shown

  • 2019-12 Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases in NATURE COMMUNICATIONS
  • 2019-01-18 A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms in BEHAVIOR GENETICS
  • 2018-12 Genome-wide identification of directed gene networks using large-scale population genomics data in NATURE COMMUNICATIONS
  • 2018-12 From blood to lung tissue: effect of cigarette smoke on DNA methylation and lung function in RESPIRATORY RESEARCH
  • 2018-12 Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-12 DNA methylation signatures of educational attainment in NPJ SCIENCE OF LEARNING
  • 2018-12 Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases in NATURE COMMUNICATIONS
  • 2018-12 A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy in BMC MEDICAL GENOMICS
  • 2018-11-02 Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps in NATURE GENETICS
  • 2018-11 Meta-analysis of epigenome-wide association studies of cognitive abilities in MOLECULAR PSYCHIATRY
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-10 Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations in HUMAN GENETICS
  • 2018-08-14 Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation in MOLECULAR PSYCHIATRY
  • 2018-06 Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error in NATURE GENETICS
  • 2018-05 Understanding the role of the chromosome 15q25.1 in COPD through epigenetics and transcriptomics in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-05 Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability in NATURE GENETICS
  • 2018-05 Employed family-based genetic discovery combining linkage analysis and exome sequencing to identify RCL1 as a novel candidate gene for depression, with independent replication in a population-based cohort in MOLECULAR PSYCHIATRY
  • 2018-05 A rare missense variant in RCL1 segregates with depression in extended families in MOLECULAR PSYCHIATRY
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-03 Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology in THE PHARMACOGENOMICS JOURNAL
  • 2018-02 The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders in MOLECULAR PSYCHIATRY
  • 2018-01-04 Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia in MOLECULAR PSYCHIATRY
  • 2017-12 Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 2017-12 Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass in NATURE COMMUNICATIONS
  • 2017-12 Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders in TRANSLATIONAL PSYCHIATRY
  • 2017-12 Discovery and functional prioritization of Parkinson’s disease candidate genes from large-scale whole exome sequencing in GENOME BIOLOGY
  • 2017-09 The Rotterdam Study: 2018 update on objectives, design and main results in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2017-09 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease in NATURE GENETICS
  • 2017-09 Metabolomics based markers predict type 2 diabetes in a 14-year follow-up study in METABOLOMICS
  • 2017-08 Characterization of pathogenic SORL1 genetic variants for association with Alzheimer’s disease: a clinical interpretation strategy in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-08 Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-07 Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence in NATURE GENETICS
  • 2017-04-26 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits in NATURE COMMUNICATIONS
  • 2017-04-18 Short telomere length is associated with impaired cognitive performance in European ancestry cohorts in TRANSLATIONAL PSYCHIATRY
  • 2017-04 Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms in MOLECULAR PSYCHIATRY
  • 2017-01 Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity in NATURE
  • 2016-12-15 Heritability of the shape of subcortical brain structures in the general population in NATURE COMMUNICATIONS
  • 2016-12 New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk in NATURE COMMUNICATIONS
  • 2016-12 The Generation R Study: design and cohort update 2017 in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2016-12 HASE: Framework for efficient high-dimensional association analyses in SCIENTIFIC REPORTS
  • 2016-12 Molecular genetic aetiology of general cognitive function is enriched in evolutionarily conserved regions in TRANSLATIONAL PSYCHIATRY
  • 2016-12 Genome-wide analysis identifies 12 loci influencing human reproductive behavior in NATURE GENETICS
  • 2016-11-23 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape in NATURE COMMUNICATIONS
  • 2016-11 Associations with intraocular pressure across Europe: The European Eye Epidemiology (E3) Consortium in EUROPEAN JOURNAL OF EPIDEMIOLOGY
  • 2016-10 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2016-10 Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption in SCIENTIFIC REPORTS
  • 2016-10 Assessing the genetic overlap between BMI and cognitive function in MOLECULAR PSYCHIATRY
  • 2016-10 Genetic variants in RBFOX3 are associated with sleep latency in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-09-28 Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene in NATURE COMMUNICATIONS
  • 2016-09 Association of the IGF1 gene with fasting insulin levels in EUROPEAN JOURNAL OF HUMAN GENETICS
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