Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects-Reference-Cited by-同舟云学术

Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects

Published:2021-12 Issue:12 Volume:56 Page:2286-2294
ISSN:0022-3468
Container-title:Journal of Pediatric Surgery
language:en
Short-container-title:Journal of Pediatric Surgery

Author:

Kapoor Ashish,Nandakumar Priyanka,Auer Dallas R.^ORCID,Sosa Maria X.,Ross Holly,Bollinger Juli,Yan Jia^ORCID,Berrios Courtney^ORCID,Chakravarti Aravinda^ORCID

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

General Medicine,Pediatrics, Perinatology and Child Health,Surgery

Reference28 articles.

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

Cited by 4 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. The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung’s disease;Frontiers in Cell and Developmental Biology;2023-07-07

2. Genetic Background Influences Severity of Colonic Aganglionosis and Response to GDNF Enemas in the Holstein Mouse Model of Hirschsprung Disease;International Journal of Molecular Sciences;2021-12-05

3. A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease;Genome Research;2021-11-15

4. Magnitude of Mendelian versus complex inheritance of rare disorders;American Journal of Medical Genetics Part A;2021-08-21