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Solveig Gretarsdottir

Showing results (1-10 of 67) with videos related to

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Trends in Molecular Medicine|May 11, 2005
Genes contributing to risk for common forms of strokeJeffrey R Gulcher, Solveig Gretarsdottir, Anna Helgadottir, et al.
Plos Genetics|June 21, 2008
A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuriesAstridur Palsdottir, Agnar Helgason, Snaebjorn Palsson, et al.
Journal of the Neurological Sciences|July 28, 2007
PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in SwedenKonstantinos Kostulas, Solveig Gretarsdottir, Vasilios Kostulas, et al.
European Heart Journal|March 30, 2018
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery diseaseAnna Helgadottir, Patrick Sulem, Gudmundur Thorgeirsson, et al.
The New England Journal of Medicine|May 1, 2008
Multiple genetic loci for bone mineral density and fracturesUnnur Styrkarsdottir, Bjarni V Halldorsson, Solveig Gretarsdottir, et al.
Journal of the American College of Cardiology|October 21, 2017
A Missense Variant in PLEC Increases Risk of Atrial FibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Nature Genetics|December 17, 2008
New sequence variants associated with bone mineral densityUnnur Styrkarsdottir, Bjarni V Halldorsson, Solveig Gretarsdottir, et al.
European Heart Journal|March 29, 2018
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aortaThorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, et al.
Nature Communications|October 24, 2019
Sequence variants with large effects on cardiac electrophysiology and diseaseKristjan Norland, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Trends in Molecular Medicine|May 11, 2005
Genes contributing to risk for common forms of strokeJeffrey R Gulcher, Solveig Gretarsdottir, Anna Helgadottir, et al.
Plos Genetics|June 21, 2008
A drastic reduction in the life span of cystatin C L68Q carriers due to life-style changes during the last two centuriesAstridur Palsdottir, Agnar Helgason, Snaebjorn Palsson, et al.
Journal of the Neurological Sciences|July 28, 2007
PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in SwedenKonstantinos Kostulas, Solveig Gretarsdottir, Vasilios Kostulas, et al.
European Heart Journal|March 30, 2018
Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery diseaseAnna Helgadottir, Patrick Sulem, Gudmundur Thorgeirsson, et al.
The New England Journal of Medicine|May 1, 2008
Multiple genetic loci for bone mineral density and fracturesUnnur Styrkarsdottir, Bjarni V Halldorsson, Solveig Gretarsdottir, et al.
Journal of the American College of Cardiology|October 21, 2017
A Missense Variant in PLEC Increases Risk of Atrial FibrillationRosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Nature Genetics|December 17, 2008
New sequence variants associated with bone mineral densityUnnur Styrkarsdottir, Bjarni V Halldorsson, Solveig Gretarsdottir, et al.
European Heart Journal|March 29, 2018
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aortaThorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
European Heart Journal|October 16, 2016
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillationDaniel F Gudbjartsson, Hilma Holm, Patrick Sulem, et al.
Nature Communications|October 24, 2019
Sequence variants with large effects on cardiac electrophysiology and diseaseKristjan Norland, Gardar Sveinbjornsson, Rosa B Thorolfsdottir, et al.
Pageof 7