Jonas B Nielsen


Ontology type: schema:Person     


Person Info

NAME

Jonas B

SURNAME

Nielsen

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 Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation in NATURE COMMUNICATIONS
  • 2018-12 Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation in COMMUNICATIONS BIOLOGY
  • 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
  • 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 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
  • 2017-05 Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality in GENETICS IN MEDICINE
  • 2014-12 New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome in BMC GENETICS
  • 2014-12 Brugada syndrome risk loci seem protective against atrial fibrillation in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-09 New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-12 Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation in BMC MEDICAL GENETICS
  • 2012-08 High prevalence of genetic variants previously associated with LQT syndrome in new exome data in EUROPEAN JOURNAL OF HUMAN GENETICS
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