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Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome study.
Audain, Enrique, Wilsdon, Anna, Dombrowsky, Gregor, Sifrim, Alejandro, Breckpot, Jeroen, Perez-Riverol, Yasset, Loughna, Siobhan, Daly, Allan, Antoniou, Pavlos, Hofmann, Philipp, Perez-Riverol, Amilcar, Kahlert, Anne-Karin, Bauer, Ulrike, Pickardt, Thomas, Klaassen, Sabine ORCID logoORCID: https://orcid.org/0000-0001-5925-9912, Berger, Felix, Daehnert, Ingo, Dittrich, Sven, Stiller, Brigitte, Abdul-Khaliq, Hashim, Bu'lock, Frances, Uebing, Anselm, Kramer, Hans-Heiner, Iyer, Vivek, Larsen, Lars Allan, Brook, J. David and Hitz, Marc-Phillip
NPJ Genomic Medicine 11 (1): 30. 2 June 2026

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