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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 15, 2024. (Total: 232521Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Hirschsprung Disease and PTCH1[original query]
Common genetic variations in Patched1 (PTCH1) gene and risk of hirschsprung disease in the Han Chinese population.
PloS one 2013 8 (9): e75407.
Wang Yang, Wang Jun, Pan Weihua, Zhou Ying, Xiao Yongtao, Zhou Kejun, Wen Jie, Yu Tingxi, Cai W
Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease.
Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2016 40 (3-4): 509-526.
Wang Yang, Wang Jun, Zhou Ying, Wei Zhiyun, Xiao Yongtao, Zhou Kejun, Wen Jie, Yan Junkai, Cai W
Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease.
Journal of cellular and molecular medicine 2018 Apr .
Wang Yang, Yan Weihui, Wang Jun, Zhou Ying, Chen Jie, Gu Beilin, Cai W
Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease.
Aging 2020 3 12 (5): 4379-4393.
Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W
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