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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Disease and KDM5B[original query]
De novo damaging variants associated with congenital heart diseases contribute to the connectome.
Scientific reports 2020 Apr 10 (1): 7046.
Ji Weizhen, Ferdman Dina, Copel Joshua, Scheinost Dustin, Shabanova Veronika, Brueckner Martina, Khokha Mustafa K, Ment Laura
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
PLoS genetics 2021 Jul 17 (7): e1009679.
Audain Enrique, Wilsdon Anna, Breckpot Jeroen, Izarzugaza Jose M G, Fitzgerald Tomas W, Kahlert Anne-Karin, Sifrim Alejandro, Wünnemann Florian, Perez-Riverol Yasset, Abdul-Khaliq Hashim, Bak Mads, Bassett Anne S, Benson D Woodrow, Berger Felix, Daehnert Ingo, Devriendt Koenraad, Dittrich Sven, Daubeney Piers Ef, Garg Vidu, Hackmann Karl, Hoff Kirstin, Hofmann Philipp, Dombrowsky Gregor, Pickardt Thomas, Bauer Ulrike, Keavney Bernard D, Klaassen Sabine, Kramer Hans-Heiner, Marshall Christian R, Milewicz Dianna M, Lemaire Scott, Coselli Joseph S, Mitchell Michael E, Tomita-Mitchell Aoy, Prakash Siddharth K, Stamm Karl, Stewart Alexandre F R, Silversides Candice K, Siebert Reiner, Stiller Brigitte, Rosenfeld Jill A, Vater Inga, Postma Alex V, Caliebe Almuth, Brook J David, Andelfinger Gregor, Hurles Matthew E, Thienpont Bernard, Larsen Lars Allan, Hitz Marc-Phill
Rare genetic variants impact muscle strength.
Nature communications 2023 6 14 (1): 3449.
Yunfeng Huang, Dora Bodnar, Chia-Yen Chen, Gabriela Sanchez-Andrade, Mark Sanderson, , Jun Shi, Katherine G Meilleur, Matthew E Hurles, Sebastian S Gerety, Ellen A Tsai, Heiko Ru
Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk.
JAMA cardiology 2024 6 .
Oliver B Vad, Laia M Monfort, Christian Paludan-Müller, Konstantin Kahnert, Søren Z Diederichsen, Laura Andreasen, Luca A Lotta, Jonas B Nielsen, Alicia Lundby, Jesper H Svendsen, Morten S Olesen,
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