Kids First: Pediatric Research Project on the Genomic Analysis of Congenital Diaphragmatic Hernia

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Outcomes of congenital diaphragmatic hernia in the modern era of management.

J. Wynn, U. Krishnan, G. Aspelund, et al.. (2013). The Journal of pediatrics. Cited 205 times. https://doi.org/10.1016/j.jpeds.2012.12.036

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Hongjian Qi, Lan Yu, Xueya Zhou, et al.. (2018). PLoS Genetics. Cited 102 times. https://doi.org/10.1371/journal.pgen.1007822

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

Lan Yu, J. Wynn, Y. Cheung, et al.. (2013). Human Genetics. Cited 91 times. https://doi.org/10.1007/s00439-012-1249-0

De novo copy number variants are associated with congenital diaphragmatic hernia

Lan Yu, J. Wynn, Lijiang Ma, et al.. (2012). Journal of Medical Genetics. Cited 77 times. https://doi.org/10.1136/jmedgenet-2012-101135

Developmental outcomes of children with congenital diaphragmatic hernia: a multicenter prospective study.

J. Wynn, G. Aspelund, A. Zygmunt, et al.. (2013). Journal of pediatric surgery. Cited 74 times. https://doi.org/10.1016/j.jpedsurg.2013.02.041

Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia.

Lan Yu, A. Sawle, J. Wynn, et al.. (2015). Human molecular genetics. Cited 68 times. https://doi.org/10.1093/hmg/ddv196

Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

Lan Yu, James T. Bennett, J. Wynn, et al.. (2014). Journal of Medical Genetics. Cited 59 times. https://doi.org/10.1136/jmedgenet-2013-101989
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