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The Journal of Clinical Investigation|August 16, 2011
Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humansElly Sau-Wai Ngan, Maria-Mercè Garcia-Barceló, Benjamin Hon-Kei Yip, et al.
Ebiomedicine|April 4, 2025
Multi-ancestry genome-wide association meta-analysis identifies novel associations and informs genetic risk prediction for Hirschsprung diseaseYuanxin Zhong, Man-Ting So, Zuyi Ma, et al.
Clinical Chemistry|October 29, 2005
Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndromeMercè Garcia-Barceló, Man-Ting So, Danny Ko-Chun Lau, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 26, 2008
Mutational analysis of SHH and GLI3 in anorectal malformationsMaria-Mercè Garcia-Barceló, Vincent Chi-Hang Lui, Xiaoping Miao, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Mapping of a Hirschsprung's disease locus in 3p21Maria-Mercè Garcia-Barceló, Pui-yee Fong, Clara S Tang, et al.
Ebiomedicine|August 29, 2021
Identification of a wide spectrum of ciliary gene mutations in nonsyndromic biliary atresia patients implicates ciliary dysfunction as a novel disease mechanismWai-Yee Lam, Clara Sze-Man Tang, Man-Ting So, et al.
Plos One|February 2, 2011
Fine mapping of the NRG1 Hirschsprung's disease locusClara Sze-Man Tang, Wai-Kiu Tang, Man-Ting So, et al.
Plos Genetics|May 17, 2012
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3Clara Sze-Man Tang, Guo Cheng, Man-Ting So, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2009
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's diseaseMaria-Mercè Garcia-Barcelo, Clara Sze-Man Tang, Elly Sau-Wai Ngan, et al.
Human Molecular Genetics|May 13, 2010
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2Maria-Mercè Garcia-Barceló, Ming-Yiu Yeung, Xiao-Ping Miao, et al.
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