Gardar Sveinbjornsson


Ontology type: schema:Person     


Person Info

NAME

Gardar

SURNAME

Sveinbjornsson

Publications in SciGraph latest 50 shown

  • 2018-12 Genome-wide association meta-analysis yields 20 loci associated with gallstone disease in NATURE COMMUNICATIONS
  • 2018-12 Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6 in GENOME BIOLOGY
  • 2018-12 Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis in NATURE GENETICS
  • 2018-12 A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin in COMMUNICATIONS BIOLOGY
  • 2018-12 Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits in NATURE COMMUNICATIONS
  • 2018-12 MAP1B mutations cause intellectual disability and extensive white matter deficit 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 Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis in NATURE GENETICS
  • 2018-08 Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis in NATURE GENETICS
  • 2017-08 Truncating mutations in RBM12 are associated with psychosis in NATURE GENETICS
  • 2017-08 Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-08 Identification of sequence variants influencing immunoglobulin levels in NATURE GENETICS
  • 2017-05 Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-02-22 Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation in NATURE COMMUNICATIONS
  • 2016-11-16 Epigenetic and genetic components of height regulation in NATURE COMMUNICATIONS
  • 2016-06 Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease in NATURE GENETICS
  • 2016-03 HLA class II sequence variants influence tuberculosis risk in populations of European ancestry in NATURE GENETICS
  • 2016-03 Weighting sequence variants based on their annotation increases power of whole-genome association studies in NATURE GENETICS
  • 2016-02-03 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase in NATURE COMMUNICATIONS
  • 2015-12 Common and rare variants associated with kidney stones and biochemical traits in NATURE COMMUNICATIONS
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