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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 Krishnan, Jill M. Zalieckas, Terry L. Buchmiller, Julie Khlevner, Aliva De, Christiana Farkouh‐Karoleski, Amy J. Wagner, Andreas Heydweiller, Andreas Mueller, Annelies de Klein, Brad W. Warner, Carlo Maj, Dai H. Chung, David J. McCulley, David Schindel, Douglas A. Potoka, Elizabeth Fialkowski, Felicitas Schulz, Florian Kipfmüller, Foong‐Yen Lim, Frank Magielsen, George B. Mychaliska, Guðrún Aspelund, Heiko Reutter, Howard Needelman, J. Marco Schnater, Jason C. Fisher, Kenneth S. Azarow, Mahmoud Elfiky, Markus M. Nöthen, Melissa E. Danko, Mindy Li, Przemysław Kosiński, René Wijnen, Robert A. Cusick, Samuel Z. Soffer, Suzan C.M. Cochius-den Otter, Thomas Schaible, Timothy M. Crombleholme, Vincent Duron, Patricia K. Donahoe, Xin Sun, Frances A. High, Charlotte Bendixen, Erwin Brosens, Yufeng Shen, Wendy K. Chung

2024The American Journal of Human Genetics14 citationsDOIOpen Access PDF

Topics & Concepts

Congenital diaphragmatic herniaContext (archaeology)GeneticsGenetic variantsMedicineDiaphragmatic breathingBiologyGeneGenotypePathologyPregnancyAlternative medicineFetusPaleontologyCongenital Diaphragmatic Hernia StudiesNeurogenetic and Muscular Disorders ResearchRNA modifications and cancer
Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants | Litcius