Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese-Reference-Cited by-同舟云学术

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Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese

Published:2017-03 Issue:3 Volume:64 Page:385-390
ISSN:0277-2116
Container-title:Journal of Pediatric Gastroenterology & Nutrition
language:en
Short-container-title:

Author:

Li Qi,Zhang Zhen,Diao Mei,Gan Liang,Cheng Wei,Xiao Ping,Su Lin,Shangguan Shaofang,Jiang Qian,Li Long

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology,Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Hirschsprung disease, associated syndromes and genetics: a review;Amiel;J Med Genet,2008

2. A genetic study of Hirschsprung disease;Badner;Am J Hum Genet,1990

3. Genetics of Hirschsprung disease;Parisi;Curr Opin Pediatr,2000

4. Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model;Alves;Dev Biol,2013

5. Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer;Jiang;Hum Mutat,2012

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Transcriptome profiling of intact bowel wall reveals that PDE1A and SEMA3D are possible markers with roles in enteric smooth muscle apoptosis, proliferative disorders, and dysautonomia in Crohn’s disease;Frontiers in Genetics;2023-08-31

2. Association of rs2435357 and rs2506030 polymorphisms in RET with susceptibility to hirschsprung disease: A systematic review and meta-analysis;Frontiers in Pediatrics;2022-10-17

3. Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects;Journal of Pediatric Surgery;2021-12

4. Effect of semaphorin 3C gene variants in multifactorial Hirschsprung disease;Journal of International Medical Research;2021-02

5. Multiple, independent, common variants overlapping known and putative gut enhancers at RET, SEMA3 and NRG1 underlie Hirschsprung disease risk in European ancestry subjects;2020-06-08

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