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Journal of the American Heart Association|July 14, 2023
Screening for Rare Coding Variants That Associate With the QTc Interval in IcelandGardar Sveinbjornsson, Bara D Benediktsdottir, Gunnlaugur Sigfusson, et al.Nature Genetics|July 20, 2021
Distinction between the effects of parental and fetal genomes on fetal growthThorhildur Juliusdottir, Valgerdur Steinthorsdottir, Lilja Stefansdottir, 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.JAMA|May 12, 2005
Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trialHakon Hakonarson, Sverrir Thorvaldsson, Anna Helgadottir, et al.Circulation. Genomic and Precision Medicine|October 26, 2018
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac DeathGardar Sveinbjornsson, Eva F Olafsdottir, Rosa B Thorolfsdottir, et al.Scientific Reports|June 10, 2017
Sequence variant at 4q25 near PITX2 associates with appendicitisRagnar P Kristjansson, Stefania Benonisdottir, Asmundur Oddsson, et al.Annals of Neurology|November 11, 2008
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic strokeSolveig Gretarsdottir, Gudmar Thorleifsson, Andrei Manolescu, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|August 19, 2021
Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in IcelandEythór Björnsson, Guðmundur Thorgeirsson, Anna Helgadóttir, et al.Nature Genetics|March 8, 2011
A rare variant in MYH6 is associated with high risk of sick sinus syndromeHilma Holm, Daniel F Gudbjartsson, Patrick Sulem, et al.Pageof 11