Hafdis T Helgadottir


Ontology type: schema:Person     


Person Info

NAME

Hafdis T

SURNAME

Helgadottir

Publications in SciGraph latest 50 shown

  • 2018-12 Somatic mutagenesis in satellite cells associates with human skeletal muscle aging in NATURE COMMUNICATIONS
  • 2016-05 A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences in MOLECULAR PSYCHIATRY
  • 2016-03 HLA class II sequence variants influence tuberculosis risk in populations of European ancestry in NATURE GENETICS
  • 2015-05 Large-scale whole-genome sequencing of the Icelandic population in NATURE GENETICS
  • 2014-05 Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31 in NATURE GENETICS
  • 2014-03 Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes in NATURE GENETICS
  • 2013-12 A common variant at 8q24.21 is associated with renal cell cancer in NATURE COMMUNICATIONS
  • 2013-05 Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits in NATURE
  • 2012-12 A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer in NATURE GENETICS
  • 2012-03 Discovery of common variants associated with low TSH levels and thyroid cancer risk in NATURE GENETICS
  • 2011-11 Mutations in BRIP1 confer high risk of ovarian cancer in NATURE GENETICS
  • 2011-11 Identification of low-frequency variants associated with gout and serum uric acid levels in NATURE GENETICS
  • 2011-11 A germline variant in the TP53 polyadenylation signal confers cancer susceptibility in NATURE GENETICS
  • 2011-03-06 A rare variant in MYH6 is associated with high risk of sick sinus syndrome in NATURE GENETICS
  • 2010-08 A sequence variant on 17q21 is associated with age at onset and severity of asthma in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-04 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations in NATURE GENETICS
  • 2009-03 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction in NATURE GENETICS
  • 2009-02 Sequence variants at the TERT-CLPTM1L locus associate with many cancer types in NATURE GENETICS
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