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Kari Stefansson

Showing results (21-30 of 687) with videos related to

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Scandinavian Journal of Urology and Nephrology|November 20, 2009
Familiality of kidney stone disease in IcelandVidar O Edvardsson, Runolfur Palsson, Olafur S Indridason, et al.
Annals of Medicine|March 6, 2004
Neuregulin 1 and schizophreniaHreinn Stefansson, Valgerdur Steinthorsdottir, Thorgeir E Thorgeirsson, et al.
Science Translational Medicine|December 1, 2021
Comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics"Hilma Hólm, Patrick Sulem, Vinicius Tragante, et al.
Plos Genetics|March 9, 2011
Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individualsAlkes L Price, Agnar Helgason, Gudmar Thorleifsson, et al.
European Journal of Human Genetics : EJHG|November 25, 2005
Segmental duplication density decrease with distance to human-mouse breaks of syntenyJesus Sainz, Pavol Rovensky, Sigurjon A Gudjonsson, et al.
American Journal of Respiratory and Critical Care Medicine|July 9, 2011
The CRP and GDNF genes do not contribute to apnea-hypopnea index or risk of obstructive sleep apneaThorarinn Gislason, Allan I Pack, Hafdis T Helgadottir, et al.
Journal of Learning Disabilities|March 5, 2013
The Adult Reading History Questionnaire (ARHQ) in Icelandic: Psychometric Properties and Factor StructureGyda Bjornsdottir, Jonas G Halldorsson, Stacy Steinberg, et al.
European Heart Journal|January 24, 2006
Familial aggregation of atrial fibrillation in IcelandDavid O Arnar, Sverrir Thorvaldsson, Teri A Manolio, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 14, 2022
Cartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank ResourceUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
Human Molecular Genetics|July 19, 2015
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's diseaseJohanna Huttenlocher, Hreinn Stefansson, Stacy Steinberg, et al.
Pageof 69

Showing results (21-30 of 687) with videos related to

Sort By:
Pageof 69
Scandinavian Journal of Urology and Nephrology|November 20, 2009
Familiality of kidney stone disease in IcelandVidar O Edvardsson, Runolfur Palsson, Olafur S Indridason, et al.
Annals of Medicine|March 6, 2004
Neuregulin 1 and schizophreniaHreinn Stefansson, Valgerdur Steinthorsdottir, Thorgeir E Thorgeirsson, et al.
Science Translational Medicine|December 1, 2021
Comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics"Hilma Hólm, Patrick Sulem, Vinicius Tragante, et al.
Plos Genetics|March 9, 2011
Single-tissue and cross-tissue heritability of gene expression via identity-by-descent in related or unrelated individualsAlkes L Price, Agnar Helgason, Gudmar Thorleifsson, et al.
European Journal of Human Genetics : EJHG|November 25, 2005
Segmental duplication density decrease with distance to human-mouse breaks of syntenyJesus Sainz, Pavol Rovensky, Sigurjon A Gudjonsson, et al.
American Journal of Respiratory and Critical Care Medicine|July 9, 2011
The CRP and GDNF genes do not contribute to apnea-hypopnea index or risk of obstructive sleep apneaThorarinn Gislason, Allan I Pack, Hafdis T Helgadottir, et al.
Journal of Learning Disabilities|March 5, 2013
The Adult Reading History Questionnaire (ARHQ) in Icelandic: Psychometric Properties and Factor StructureGyda Bjornsdottir, Jonas G Halldorsson, Stacy Steinberg, et al.
European Heart Journal|January 24, 2006
Familial aggregation of atrial fibrillation in IcelandDavid O Arnar, Sverrir Thorvaldsson, Teri A Manolio, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 14, 2022
Cartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank ResourceUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
Human Molecular Genetics|July 19, 2015
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's diseaseJohanna Huttenlocher, Hreinn Stefansson, Stacy Steinberg, et al.
Pageof 69