Eric Boerwinkle


Ontology type: schema:Person     


Person Info

NAME

Eric

SURNAME

Boerwinkle

Publications in SciGraph latest 50 shown

  • 2019-04 Insights into genetics, human biology and disease gleaned from family based genomic studies in GENETICS IN MEDICINE
  • 2019-02 Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data in HUMAN GENETICS
  • 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 PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity in NATURE COMMUNICATIONS
  • 2018-12 Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies in BMC MEDICAL GENOMICS
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-08 Comprehensive genomic analysis of patients with disorders of cerebral cortical development in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2018-08 Maternal Exposures Associated with Autism Spectrum Disorder in Jamaican Children in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 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
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 Lessons learned from additional research analyses of unsolved clinical exome cases in GENOME MEDICINE
  • 2017-12 Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity in NATURE COMMUNICATIONS
  • 2017-12 Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos in LIPIDS IN HEALTH AND DISEASE
  • 2017-11 Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology in NATURE GENETICS
  • 2017-09 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease in NATURE GENETICS
  • 2017-06 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation in NATURE GENETICS
  • 2017-02-01 Rare and low-frequency coding variants alter human adult height in NATURE
  • 2017-02 Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations in INTERNATIONAL JOURNAL OF OBESITY
  • 2016-12 Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate in BMC MEDICAL GENOMICS
  • 2016-12 Whole genome sequence analysis of serum amino acid levels in GENOME BIOLOGY
  • 2016-12 An exome array study of the plasma metabolome in NATURE COMMUNICATIONS
  • 2016-10 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci in NATURE GENETICS
  • 2016-10 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals in NATURE GENETICS
  • 2016-09 Association of the IGF1 gene with fasting insulin levels in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-09 Rare coding TTN variants are associated with electrocardiographic QT interval in the general population in SCIENTIFIC REPORTS
  • 2016-07 Molecular diagnostic experience of whole-exome sequencing in adult patients in GENETICS IN MEDICINE
  • 2016-06 A causal network analysis in an observational study identifies metabolomics pathways influencing plasma triglyceride levels in METABOLOMICS
  • 2016-06 Human genome meeting 2016 in HUMAN GENOMICS
  • 2016-02-18 Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis in NATURE COMMUNICATIONS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 Sequence variation in telomerase reverse transcriptase (TERT) as a determinant of risk of cardiovascular disease: the Atherosclerosis Risk in Communities (ARIC) study in BMC MEDICAL GENETICS
  • 2015-12 Rare variants analysis using penalization methods for whole genome sequence data in BMC BIOINFORMATICS
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Rare coding variants and X-linked loci associated with age at menarche in NATURE COMMUNICATIONS
  • 2015-11 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair in NATURE GENETICS
  • 2015-10 A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease in NATURE GENETICS
  • 2015-07-01 Directional dominance on stature and cognition in diverse human populations in NATURE
  • 2015-04 Transethnic meta-analysis suggests genetic variation in the HEME pathway influences potassium response in patients treated with hydrochlorothiazide in THE PHARMACOGENOMICS JOURNAL
  • 2014-12 Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins in NATURE COMMUNICATIONS
  • 2014-09 A framework for the interpretation of de novo mutation in human disease in NATURE GENETICS
  • 2014-02 Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans in THE PHARMACOGENOMICS JOURNAL
  • 2013-12 Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease in NATURE GENETICS
  • 2013-11 Discovery and refinement of loci associated with lipid levels in NATURE GENETICS
  • 2013-08 Whole-genome sequence-based analysis of high-density lipoprotein cholesterol in NATURE GENETICS
  • 2013-06 Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin in HUMAN GENETICS
  • 2013-05 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture in NATURE GENETICS
  • 2013-02 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations in NATURE GENETICS
  • 2013-01 Seafood Consumption and Blood Mercury Concentrations in Jamaican Children With and Without Autism Spectrum Disorders in NEUROTOXICITY RESEARCH
  • 2013-01 Large-scale association analysis identifies new risk loci for coronary artery disease in NATURE GENETICS
  • 2012-10 Common variants at 6p21.1 are associated with large artery atherosclerotic stroke in NATURE GENETICS
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