Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms

Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung disease

(2014) Gunadi et al.   JOURNAL OF PEDIATRIC SURGERY

Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model

(2013) Maria M. Alves et al.   DEVELOPMENTAL BIOLOGY

Mutational Spectrum of Semaphorin 3A and Semaphorin 3D Genes in Spanish Hirschsprung patients

(2013) Berta Luzón-Toro et al.   PLoS One

Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients

(2012) Theerawut Phusantisampan et al.   JOURNAL OF HUMAN GENETICS

Comprehensive Analysis of NRG1 Common and Rare Variants in Hirschsprung Patients

(2012) Berta Luzón-Toro et al.   PLoS One

Semaphorin 3A expression in the colon of Hirschsprung disease

(2011) Li-Li Wang et al.   BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY

Rapid and efficient human mutation detection using a bench-top next-generation DNA sequencer

(2011) Qian Jiang et al.   HUMAN MUTATION

Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability

(2010) Eileen Sproat Emison et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genome-wide association study identifiesNRG1as a susceptibility locus for Hirschsprung's disease

(2009) Maria-Mercè Garcia-Barcelo et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA