Eric Boerwinkle


Ontology type: schema:Person     


Person Info

NAME

Eric

SURNAME

Boerwinkle

Publications in SciGraph latest 50 shown

  • 2019-12 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity in NATURE COMMUNICATIONS
  • 2019-04 Genetic architecture of laterality defects revealed by whole exome sequencing in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 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 Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels in NATURE COMMUNICATIONS
  • 2018-12 GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes in NATURE COMMUNICATIONS
  • 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
  • 2018-12 Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function in NATURE COMMUNICATIONS
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-09 Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis in HUMAN GENETICS
  • 2018-09 Multi-ethnic genome-wide association study for atrial fibrillation in NATURE 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
  • 2018-08 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
  • 2018-05 Serum metabolomic profile of incident diabetes in DIABETOLOGIA
  • 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
  • 2018-01 Genetic variants in microRNA genes and targets associated with cardiovascular disease risk factors in the African-American population in HUMAN GENETICS
  • 2017-12 Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism in SCIENTIFIC REPORTS
  • 2017-12 Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity in NATURE COMMUNICATIONS
  • 2017-12 Lessons learned from additional research analyses of unsolved clinical exome cases in GENOME MEDICINE
  • 2017-12 Exome-wide association study of plasma lipids in >300,000 individuals in NATURE GENETICS
  • 2017-12 Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos in LIPIDS IN HEALTH AND DISEASE
  • 2017-12 Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns in GENOME MEDICINE
  • 2017-12 Epigenome-wide association studies identify DNA methylation associated with kidney function in NATURE COMMUNICATIONS
  • 2017-12 Cerebral white matter hyperintensities on MRI and acceleration of epigenetic aging: the atherosclerosis risk in communities study in CLINICAL EPIGENETICS
  • 2017-12 Creating a data resource: what will it take to build a medical information commons? in GENOME MEDICINE
  • 2017-12 Whole Transcriptome Sequencing Analyses Reveal Molecular Markers of Blood Pressure Response to Thiazide Diuretics in SCIENTIFIC REPORTS
  • 2017-11 Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology in NATURE GENETICS
  • 2017-10 Trends in the incidence of dementia: design and methods in the Alzheimer Cohorts Consortium 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
  • 2017-07-18 Metabolomics and cognition in African American adults in midlife: the atherosclerosis risk in communities study in TRANSLATIONAL PSYCHIATRY
  • 2017-07 Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms in NATURE GENETICS
  • 2017-06 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation in NATURE GENETICS
  • 2017-06 Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk 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
  • 2017-02-01 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 POGZ truncating alleles cause syndromic intellectual disability in GENOME MEDICINE
  • 2016-12 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death in GENOME MEDICINE
  • 2016-12 A hybrid computational strategy to address WGS variant analysis in >5000 samples in BMC BIOINFORMATICS
  • 2016-12 Whole genome sequence analysis of serum amino acid levels in GENOME BIOLOGY
  • 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 An exome array study of the plasma metabolome in NATURE COMMUNICATIONS
  • 2016-12 DNA methylation signatures of chronic low-grade inflammation are associated with complex diseases in GENOME BIOLOGY
  • 2016-11-23 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape in NATURE COMMUNICATIONS
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