G Bragi Walters


Ontology type: schema:Person     


Person Info

NAME

G Bragi

SURNAME

Walters

Publications in SciGraph latest 50 shown

  • 2019-01 Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder in NATURE GENETICS
  • 2018-12 MAP1B mutations cause intellectual disability and extensive white matter deficit in NATURE COMMUNICATIONS
  • 2017-12 Sequence variant at 4q25 near PITX2 associates with appendicitis in SCIENTIFIC REPORTS
  • 2017-06-13 Reproductive fitness and genetic risk of psychiatric disorders in the general population in NATURE COMMUNICATIONS
  • 2017-04-25 15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia in TRANSLATIONAL PSYCHIATRY
  • 2017-02-22 Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation in NATURE COMMUNICATIONS
  • 2017-01-09 Genetic evidence of assortative mating in humans in NATURE HUMAN BEHAVIOUR
  • 2016-11-16 Epigenetic and genetic components of height regulation in NATURE COMMUNICATIONS
  • 2016-02-03 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase in NATURE COMMUNICATIONS
  • 2015-07 Polygenic risk scores for schizophrenia and bipolar disorder predict creativity in NATURE NEUROSCIENCE
  • 2015-05 Large-scale whole-genome sequencing of the Icelandic population in NATURE GENETICS
  • 2014-01 CNVs conferring risk of autism or schizophrenia affect cognition in controls in NATURE
  • 2013-11 A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration in NATURE GENETICS
  • 2013-10 A common biological basis of obesity and nicotine addiction in TRANSLATIONAL PSYCHIATRY
  • 2013-05 Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits in NATURE
  • 2012-08 Rate of de novo mutations and the importance of father’s age to disease risk in NATURE
  • 2012-03 Discovery of common variants associated with low TSH levels and thyroid cancer risk in NATURE GENETICS
  • 2011-11 Identification of low-frequency variants associated with gout and serum uric acid levels 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
  • 2011-03-29 Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis in NATURE GENETICS
  • 2011-03-06 A rare variant in MYH6 is associated with high risk of sick sinus syndrome in NATURE 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
  • 2010-10-28 Fine-scale recombination rate differences between sexes, populations and individuals in NATURE
  • 2010-10 Hundreds of variants clustered in genomic loci and biological pathways affect human height in NATURE
  • 2010-10 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in NATURE GENETICS
  • 2010-08 Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm in NATURE GENETICS
  • 2010-07 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis in NATURE GENETICS
  • 2010-05 Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk in NATURE GENETICS
  • 2010-02 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk in NATURE GENETICS
  • 2009-12 Parental origin of sequence variants associated with complex diseases in NATURE
  • 2009-08 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density in NATURE GENETICS
  • 2009-08 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke in NATURE GENETICS
  • 2009-01 New sequence variants associated with bone mineral density in NATURE GENETICS
  • 2009-01 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity in NATURE GENETICS
  • 2008-05 Many sequence variants affecting diversity of adult human height in NATURE GENETICS
  • 2008-03 Genetics of gene expression and its effect on disease in NATURE
  • 2008-02 The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm in NATURE GENETICS
  • 2007-06 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes in NATURE GENETICS
  • 2006-03 Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes in NATURE GENETICS
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