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Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

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Bibliographic Details
Published in:PLoS Genetics 2021, Vol.17 (7)
Main Authors: Audain, Enrique, Wilsdon, Anna, Breckpot, Jeroen, Izarzugaza, Jose MG, Fitzgerald, Tomas W, Kahlert, Anne-Karin, Sifrim, Alejandro, Wünnemann, Florian, Perez-Riverol, Yasset, Abdul-Khaliq, Hashim, Bak, Mads, Bassett, Anne S, Benson, Woodrow D, 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-Phillip
Format: Report
Language:English
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ISSN:1553-7390
DOI:10.1371/journal.pgen.1009679