Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung’s disease in Chinese Han population-Reference-Cited by-同舟云学术

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Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung’s disease in Chinese Han population

Published:2020-05-07 Issue:3 Volume:89 Page:694-700
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Yu Xian-Xian,Chu Xun,Wu Wen-Jie,Wei Zhi-Liang,Song Huan-Lei,Bai Mei-Rong,Lu Yan-Jiao,Gu Bei-Lin,Gong Yi-Ming,Cai Wei

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://www.nature.com/articles/s41390-020-0933-3.pdf

Reference31 articles.

1. Haricharan, R. N. & Georgeson, K. E. Hirschsprung disease. Semin. Pediatr. Surg. 17, 266–275 (2008).

2. Garcia-Barcelo, M.-M. et al. Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung’s disease. Proc. Natl Acad. Sci. USA 106, 2694–2699 (2009).

3. Jiang, Q. et al. Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability. Am. J. Hum. Genet. 96, 581–596 (2015).

4. Burkardt, D. D., Graham, J. M., Short, S. S. & Frykman, P. K. Advances in Hirschsprung disease genetics and treatment strategies: an update for the primary care pediatrician. Clin. Pediatr. 53, 71−81 (2014).

5. Lane, C., Milne, E. & Freeth, M. Cognition and behaviour in Sotos syndrome: a systematic review. PLoS ONE 11, e0149189 (2016).

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