Agnar Helgason


Ontology type: schema:Person     


Person Info

NAME

Agnar

SURNAME

Helgason

Publications in SciGraph latest 50 shown

  • 2018-11-05 Multiple transmissions of de novo mutations in families in NATURE GENETICS
  • 2018-11 Author Correction: The rate of meiotic gene conversion varies by sex and age in NATURE GENETICS
  • 2018-02 Reconstructing an African haploid genome from the 18th century in NATURE GENETICS
  • 2017-12 COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA in BMC MEDICAL GENETICS
  • 2017-09-21 Whole genome characterization of sequence diversity of 15,220 Icelanders in SCIENTIFIC DATA
  • 2017-09 Parental influence on human germline de novo mutations in 1,548 trios from Iceland in NATURE
  • 2017-08 Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-06-13 Reproductive fitness and genetic risk of psychiatric disorders in the general population in NATURE COMMUNICATIONS
  • 2017-05 Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis in NATURE GENETICS
  • 2017-05 Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility in NATURE GENETICS
  • 2017-04 Diversity in non-repetitive human sequences not found in the reference genome in NATURE GENETICS
  • 2016-11-16 Epigenetic and genetic components of height regulation in NATURE COMMUNICATIONS
  • 2016-11 The rate of meiotic gene conversion varies by sex and age in NATURE GENETICS
  • 2016-06 Physical and neurobehavioral determinants of reproductive onset and success in NATURE GENETICS
  • 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
  • 2015-05 Identification of a large set of rare complete human knockouts in NATURE GENETICS
  • 2015-05 The Y-chromosome point mutation rate in humans in NATURE GENETICS
  • 2015-03-25 Sequence variants from whole genome sequencing a large group of Icelanders in SCIENTIFIC DATA
  • 2014-03 Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes in NATURE GENETICS
  • 2013-05 Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits in NATURE
  • 2012-10 A direct characterization of human mutation based on microsatellites in NATURE GENETICS
  • 2012-08 Rate of de novo mutations and the importance of father’s age to disease risk in NATURE
  • 2011-11 Identification of low-frequency variants associated with gout and serum uric acid levels in NATURE GENETICS
  • 2011-03-06 A rare variant in MYH6 is associated with high risk of sick sinus syndrome in NATURE GENETICS
  • 2010-10-28 Fine-scale recombination rate differences between sexes, populations and individuals in NATURE
  • 2010-10 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma in NATURE GENETICS
  • 2008-11 Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits in NATURE GENETICS
  • 2008-08 Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma in NATURE GENETICS
  • 2008-07 ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma in NATURE GENETICS
  • 2008-07 Two newly identified genetic determinants of pigmentation in Europeans in NATURE GENETICS
  • 2008-03 Genetics of gene expression and its effect on disease in NATURE
  • 2007-12 Genetic determinants of hair, eye and skin pigmentation in Europeans in NATURE GENETICS
  • 2007-08 Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes in NATURE GENETICS
  • 2007-07 Variants conferring risk of atrial fibrillation on chromosome 4q25 in NATURE
  • 2007-07 Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer in NATURE GENETICS
  • 2007-07 A Statistical Approach to Identify Ancient Template DNA in JOURNAL OF MOLECULAR EVOLUTION
  • 2007-05 Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 in NATURE GENETICS
  • 2007-02 Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution in NATURE GENETICS
  • 2006-06 A common variant associated with prostate cancer in European and African populations in NATURE GENETICS
  • 2006-03 Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes in NATURE GENETICS
  • 2006-01 A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction in NATURE GENETICS
  • 2005-08 Genetic evidence for a family-based Scandinavian settlement of Shetland and Orkney during the Viking periods in HEREDITY
  • 2005-02 A common inversion under selection in Europeans in NATURE GENETICS
  • 2005-01 An Icelandic example of the impact of population structure on association studies in NATURE GENETICS
  • 2000-12 Genetic homogeneity of Icelanders in NATURE GENETICS
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