Integrative Analysis of Genomic Variants Reveals New Associations of Candidate Haploinsufficient Genes with Congenital Heart Disease
Enrique Audain,Anna Wilsdon,Jeroen Breckpot,Jose M. G. Izarzugaza,Tomas W. Fitzgerald,Anne-Karin Kahlert,Alejandro Sifrim,Florian Wunnemann,Yasset Perez-Riverol,Hashim Abdul-Khaliq,Mads Bak,Anne S. Bassett,D. Woodrow Benson,Felix Berger,Ingo Daehnert,Koenraad Devriendt,Sven Dittrich,Piers E. F. Daubeney,Vidu Garg,Karl Hackmann,Kirstin Hoff,Philipp Hofmann,Gregor Dombrowsky,Thomas Pickardt,Ulrike Bauer, Bernard D. Keavney,Sabine Klaassen,Hans-Heiner Kramer,Christian R. Marshall,Dianna M. Milewicz,Scott Lemaire,Joseph S. Coselli,Michael E. Mitchell,Aoy Tomita-Mitchell,Siddharth K. Prakash,Karl Stamm, Alexandre F. R. Stewart,Candice K. Silversides,Reiner Siebert,Brigitte Stiller,Jill A. Rosenfeld,Inga Vater,Alex V. Postma,Almuth Caliebe, J. David Brook,Gregor Andelfinger, Matthew E. Hurles,Bernard Thienpont,Lars Allan Larsen,Marc-Phillip Hitz PLOS GENETICS（2021）
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Congenital Heart Defects,Congenital Heart Disease
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