Cristen J Willer


Ontology type: schema:Person     


Person Info

NAME

Cristen J

SURNAME

Willer

Publications in SciGraph latest 50 shown

  • 2022-11-02 Using Genomic Structural Equation Modeling to Partition the Genetic Covariance Between Birthweight and Cardiometabolic Risk Factors into Maternal and Offspring Components in the Norwegian HUNT Study in BEHAVIOR GENETICS
  • 2022-10-27 A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies in NATURE METHODS
  • 2022-10-11 Whole genome sequence analysis of blood lipid levels in >66,000 individuals in NATURE COMMUNICATIONS
  • 2022-08-02 Author Correction: Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits in NATURE COMMUNICATIONS
  • 2022-06-20 Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease in NATURE GENETICS
  • 2022-06-16 Genome-wide meta-analysis of iron status biomarkers and the effect of iron on all-cause mortality in HUNT in COMMUNICATIONS BIOLOGY
  • 2022-06-13 Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals in COMMUNICATIONS BIOLOGY
  • 2022-05-11 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits in NATURE COMMUNICATIONS
  • 2022-05-09 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects in NATURE GENETICS
  • 2021-12-16 Author Correction: GWAS of thyroid stimulating hormone highlights the pleiotropic effects and inverse association with thyroid cancer in NATURE COMMUNICATIONS
  • 2021-12-09 The power of genetic diversity in genome-wide association studies of lipids in NATURE
  • 2021-11-12 Author Correction: A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease in NATURE GENETICS
  • 2021-09-07 A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease in NATURE GENETICS
  • 2021-07-16 Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals in NATURE COMMUNICATIONS
  • 2021-04-12 Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices in NATURE COMMUNICATIONS
  • 2021-03-16 Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals in NATURE GENETICS
  • 2021-03-01 Disclosure of clinically actionable genetic variants to thoracic aortic dissection biobank participants in BMC MEDICAL GENOMICS
  • 2021-02-19 Translating genetic association of lipid levels for biological and clinical application in CARDIOVASCULAR DRUGS AND THERAPY
  • 2020-12-22 Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors in NATURE GENETICS
  • 2020-12-18 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease in NATURE COMMUNICATIONS
  • 2020-11-23 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals in NATURE GENETICS
  • 2020-11-16 Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors in NATURE GENETICS
  • 2020-10-26 Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort in NATURE COMMUNICATIONS
  • 2020-10-23 MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk in NATURE COMMUNICATIONS
  • 2020-08-24 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale in NATURE GENETICS
  • 2020-08-07 GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer in NATURE COMMUNICATIONS
  • 2020-07-14 Avoiding dynastic, assortative mating, and population stratification biases in Mendelian randomization through within-family analyses in NATURE COMMUNICATIONS
  • 2020-06-05 Exploring and visualizing large-scale genetic associations by using PheWeb in NATURE GENETICS
  • 2020-05-18 Scalable generalized linear mixed model for region-based association tests in large biobanks and cohorts in NATURE GENETICS
  • 2020-03-13 Higher admission rates and in-hospital mortality for acute type A aortic dissection during Influenza season: a single center experience in SCIENTIFIC REPORTS
  • 2019-08-13 Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes in NATURE COMMUNICATIONS
  • 2019-04-23 Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis in NATURE COMMUNICATIONS
  • 2019-02-25 Biological and clinical insights from genetics of insomnia symptoms in NATURE GENETICS
  • 2019-02-18 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution in NATURE GENETICS
  • 2019-01-14 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use in NATURE GENETICS
  • 2018-10-01 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program in NATURE GENETICS
  • 2018-08-23 Deep-coverage whole genome sequences and blood lipids among 16,324 individuals in NATURE COMMUNICATIONS
  • 2018-08-13 Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies in NATURE GENETICS
  • 2018-07-30 Biobank-driven genomic discovery yields new insight into atrial fibrillation biology in NATURE GENETICS
  • 2018-07-14 A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers in HUMAN GENETICS
  • 2018-06-13 Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes in NATURE COMMUNICATIONS
  • 2018-06-12 Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation in COMMUNICATIONS BIOLOGY
  • 2018-04-09 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes in NATURE GENETICS
  • 2018-03-16 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-03-16 Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2018-03-07 Genome-wide analysis yields new loci associating with aortic valve stenosis in NATURE COMMUNICATIONS
  • 2017-12-22 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity in NATURE GENETICS
  • 2017-10-30 Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology in NATURE GENETICS
  • 2017-10-30 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-10-30 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
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