Cristen J Willer


Ontology type: schema:Person     


Person Info

NAME

Cristen J

SURNAME

Willer

Publications in SciGraph latest 50 shown

  • 2019-02 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use in NATURE GENETICS
  • 2018-12 Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes in NATURE COMMUNICATIONS
  • 2018-12 Genome-wide analysis yields new loci associating with aortic valve stenosis in NATURE COMMUNICATIONS
  • 2018-12 Deep-coverage whole genome sequences and blood lipids among 16,324 individuals in NATURE COMMUNICATIONS
  • 2018-12 Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation in COMMUNICATIONS BIOLOGY
  • 2018-11 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program in NATURE GENETICS
  • 2018-09 Biobank-driven genomic discovery yields new insight into atrial fibrillation biology in NATURE GENETICS
  • 2018-09 Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies in NATURE GENETICS
  • 2018-07 A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers in HUMAN GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-05 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-04 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-01 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-12 Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology in NATURE GENETICS
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors in SCIENTIFIC REPORTS
  • 2017-12 Exome chip meta-analysis identifies novel loci and East Asian–specific coding variants that contribute to lipid levels and coronary artery disease in NATURE GENETICS
  • 2017-05-25 Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve in NATURE COMMUNICATIONS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2016-12 New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk in NATURE COMMUNICATIONS
  • 2016-10 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2016-10 A reference panel of 64,976 haplotypes for genotype imputation in NATURE GENETICS
  • 2016-10 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension in NATURE GENETICS
  • 2015-12 Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese in NATURE COMMUNICATIONS
  • 2015-02 Genetic studies of body mass index yield new insights for obesity biology in NATURE
  • 2015-02 New genetic loci link adipose and insulin biology to body fat distribution in NATURE
  • 2014-11 Defining the role of common variation in the genomic and biological architecture of adult human height in NATURE GENETICS
  • 2014-04 Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk in NATURE GENETICS
  • 2014-02 Meta-analysis of gene-level tests for rare variant association in NATURE GENETICS
  • 2013-11 Common variants associated with plasma triglycerides and risk for coronary artery disease in NATURE GENETICS
  • 2013-11 Discovery and refinement of loci associated with lipid levels in NATURE GENETICS
  • 2013-06 Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders in NATURE GENETICS
  • 2013-05 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture in NATURE GENETICS
  • 2013-04-15 Identification of heart rate-associated loci and genes in PROTOCOL EXCHANGE
  • 2013-04 WikiGWA: an open platform for collecting and using genome-wide association results in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-01 Large-scale association analysis identifies new risk loci for coronary artery disease in NATURE GENETICS
  • 2011-11 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution in NATURE GENETICS
  • 2011-07 Genomic inflation factors under polygenic inheritance in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-11 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index in NATURE GENETICS
  • 2010-11 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution in NATURE GENETICS
  • 2010-10 Hundreds of variants clustered in genomic loci and biological pathways affect human height in NATURE
  • 2010-08 Biological, clinical and population relevance of 95 loci for blood lipids in NATURE
  • 2010-07 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis in NATURE GENETICS
  • 2009-06 Genome-wide association study identifies eight loci associated with blood pressure in NATURE GENETICS
  • 2009-01 Common variants at 30 loci contribute to polygenic dyslipidemia in NATURE GENETICS
  • 2009-01 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation in NATURE GENETICS
  • 2008-06 Common variants near MC4R are associated with fat mass, weight and risk of obesity in NATURE GENETICS
  • 2008-03 Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations in DIABETOLOGIA
  • 2008-03 Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations in DIABETOLOGIA
  • 2008-02 Common variants in the GDF5-UQCC region are associated with variation in human height in NATURE GENETICS
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