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Research Database

Health & Traits Publications

Explore scientific publications on genetic research, GWAS studies, and genomic discoveries.

7508 Publications
7508 GWAS Studies
905 Journals
3358 Replicated
21 of 7508 publications
Active: Eur Heart J Clear all
Title
Author
Journal
Disease/Trait
Date
Actions
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci.
Ishikawa T, Masuda T et al.
Eur Heart J
Brugada syndrome
2024-05-15
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study.
Yu Chen H, Dina C et al.
Eur Heart J
Aortic stenosis
2023-04-11
Genetic variants associated with syncope implicate neural and autonomic processes.
Aegisdottir HM, Thorolfsdottir RB et al.
Eur Heart J
Syncope
2023-02-07
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
Ghouse J, Tragante V et al.
Eur Heart J
ACE-inhibitor discontinuation
2022-06-25
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.
Roselli C, Yu M et al.
Eur Heart J
Mitral valve prolapse
2022-03-04
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
Ahlberg G, Andreasen L et al.
Eur Heart J
Left atrial maximum volume
2021-07-29
Genetic insight into sick sinus syndrome.
Thorolfsdottir RB, Sveinbjornsson G et al.
Eur Heart J
Sick sinus syndrome
2021-05-01
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.
Garnier S, Harakalova M et al.
Eur Heart J
Dilated cardiomyopathy
2021-03-03
Genetic insight into sick sinus syndrome.
Thorolfsdottir RB, Sveinbjornsson G et al.
Eur Heart J
Sick sinus syndrome
2021-02-13
Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.
Hartiala JA, Han Y et al.
Eur Heart J
Myocardial infarction
2021-02-03
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.
Ashar FN, Mitchell RN et al.
Eur Heart J
Sudden cardiac arrest
2018-08-28
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta.
Bjornsson T, Thorolfsdottir RB et al.
Eur Heart J
Aortic coarctation
2018-03-24
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