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Common Variants Increase Risk for Congenital Diaphragmatic Hernia Within the Context of De Novo Variants

Lu Qiao,Carrie L. Welch,Rebecca Hernan,Julia Wynn,Usha S. Krishnan,Jill M. Zalieckas,Terry Buchmiller,Julie Khlevner,Aliva De,Christiana Farkouh-Karoleski,Amy J. Wagner,Andreas Heydweiller,Andreas C. Mueller,Annelies de Klein,Brad W. Warner,Carlo Maj,Dai Chung,David J. McCulley,David Schindel,Douglas Potoka,Elizabeth Fialkowski,Felicitas Schulz,Florian Kipfmuller,Foong-Yen Lim,Frank Magielsen,George B. Mychaliska,Gudrun Aspelund,Heiko Martin Reutter,Howard Needelman,J. Marco Schnater,Jason C. Fisher,Kenneth Azarow,Mahmoud Elfiky,Markus M. Noethen,Melissa E. Danko,Mindy Li,Przemyslaw Kosinski,Rene M. H. Wijnen,Robert A. Cusick,Samuel Z. Soffer,Suzan C. M. Cochius-Den Otter,Thomas Schaible,Timothy Crombleholme,Vincent P. Duron,Patricia K. Donahoe,Xin Sun,Frances A. High,Charlotte Bendixen,Erwin Brosens,Yufeng Shen,Wendy K. Chung

AMERICAN JOURNAL OF HUMAN GENETICS（2024）

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关键词
congenital diaphragmatic hernia,de novo variants,common variants,genome-wide association study,single-nucleotide polymorphism,WNT5A
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