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Nature Genetics
|
January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Human Molecular Genetics
|
December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibition
Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
Communications Biology
|
October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillation
Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Stroke
|
November 23, 2013
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
Martin Dichgans, Rainer Malik, Inke R König, et al.
Human Molecular Genetics
|
March 29, 2013
A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm
Gregory T Jones, Matthew J Bown, Solveig Gretarsdottir, et al.
JAMA Cardiology
|
September 4, 2024
Genome-Wide Association Study of Accessory Atrioventricular Pathways
Hildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, et al.
European Heart Journal
|
July 24, 2020
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease
Anna Helgadottir, Gudmar Thorleifsson, Kristjan F Alexandersson, et al.
Nature Communications
|
March 8, 2018
Genome-wide analysis yields new loci associating with aortic valve stenosis
Anna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir, et al.
Nature
|
July 3, 2007
Variants conferring risk of atrial fibrillation on chromosome 4q25
Daniel F Gudbjartsson, David O Arnar, Anna Helgadottir, et al.
Nature Genetics
|
July 15, 2009
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
Daniel F Gudbjartsson, Hilma Holm, Solveig Gretarsdottir, et al.
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Search research articles
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Showing results (31-40 of 67) with videos related to
Sort By:
Page
of 7
Nature Genetics
|
January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
Jonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Human Molecular Genetics
|
December 1, 2025
Observational and Mendelian randomization studies of plasma sclerostin levels do not provide evidence of cardiovascular adverse effects of sclerostin inhibition
Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Grimur Hjorleifsson Eldjarn, et al.
Communications Biology
|
October 2, 2018
Coding variants in <i>RPL3L</i> and <i>MYZAP</i> increase risk of atrial fibrillation
Rosa B Thorolfsdottir, Gardar Sveinbjornsson, Patrick Sulem, et al.
Stroke
|
November 23, 2013
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
Martin Dichgans, Rainer Malik, Inke R König, et al.
Human Molecular Genetics
|
March 29, 2013
A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm
Gregory T Jones, Matthew J Bown, Solveig Gretarsdottir, et al.
JAMA Cardiology
|
September 4, 2024
Genome-Wide Association Study of Accessory Atrioventricular Pathways
Hildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, et al.
European Heart Journal
|
July 24, 2020
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease
Anna Helgadottir, Gudmar Thorleifsson, Kristjan F Alexandersson, et al.
Nature Communications
|
March 8, 2018
Genome-wide analysis yields new loci associating with aortic valve stenosis
Anna Helgadottir, Gudmar Thorleifsson, Solveig Gretarsdottir, et al.
Nature
|
July 3, 2007
Variants conferring risk of atrial fibrillation on chromosome 4q25
Daniel F Gudbjartsson, David O Arnar, Anna Helgadottir, et al.
Nature Genetics
|
July 15, 2009
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
Daniel F Gudbjartsson, Hilma Holm, Solveig Gretarsdottir, et al.
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of 7