Accès ouvert
2026
article
OpenAlex
Minna Kraatari‐Tiri, Hina Ishtiaq, Jaakko Tyrmi, Siying Lin et autres
Importance: Substantial unexplained heritability remains for pathogenic inherited retinal disease (IRD) variants. Application of genome-wide association studies (GWAS) could help identify causal genes in rare diseases. Objective: To leverage a GWAS for the discovery of IRD-associated genes. Design, Setting, and Participants: This …
fi, ph, gb, us
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2025
article
OpenAlex
Katja Pahkala, Suvi Rovio, Noora Kartiosuo, Kari Auranen et autres
The longstanding national multicenter Cardiovascular Risk in Young Finns Study (YFS) was originally designed to provide information on cardiovascular risk factors and their determinants in children and adolescents of various ages in different parts of Finland [1, 2]. The first examination in …
fi, au
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
S. Rajić, Saara Marttila, P. Mishra, N. Mononen et autres
fi, de
(code pays fourni par la source)
Accès ouvert
2022
article
OpenAlex
D.O. Arnar, E.A. Whitsel, J.W. Jukema, A.P. Reiner et autres
The electrocardiographic PR interval reflects atrioventricular conduction, and is associated with conduction abnormalities, pacemaker implantation, atrial fibrillation (AF), and cardiovascular mortality. Here we report a multi-ancestry (N = 293,051) genome-wide association meta-analysis for the PR interval, discovering 202 loci of which 141 …
us
(code pays fourni par la source)