| Title | Author(s) | Year | View Count |  | Mutations in the NRG1 gene are associated with Hirschsprung disease | Tang, CSM; Ngan, ESW; Tang, WK; So, MT; Cheng, G; Miao, XP; Leon, TYY; Leung, BMC; Hui, KJWS; Lui, VHC; Chen, Y; Chan, IHY; Chung, PHY; Liu, XL; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH; GarciaBarcelo, MM | 2012 | 204 |
| Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 (vol 19, pg 2917, 2010) | Garcia-Barcelo, MM; Yeung, MY; Miao, XP; Tang, CSM; Cheng, G; So, MT; Ngan, EW; Lui, VCH; Chen, Y; Liu, XL; Hui, KJWS; Li, L; Guo, WH; Sun, XB; Tou, JF; Chan, KW; Wu, XZ; Song, YQ; Chan, D; Cheung, K; Chung, PHY; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH | 2011 | 156 |
 | Fine mapping of the 9q31 Hirschsprung's disease locus | Tang, CS; Sribudiani, Y; Miao, XP; De Vries, AR; Burzynski, G; So, MT; Leon, YY; Yip, BH; Osinga, J; Hui, KJWS; Verheij, JBGM; Cherny, SS; Tam, PKH; Sham, PC; Hofstra, RMW; GarciaBarceló, MM | 2010 | 141 |
| Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population | Cornes, BK; Tang, CS; Leon, TYY; Hui, KJWS; So, MT; Miao, X; Cherny, SS; Sham, PC; Tam, PKH; GarciaBarcelo, MM | 2010 | 692 |
| Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 | GarciaBarceló, MM; Yeung, MY; Miao, XP; Tang, CSM; Cheng, G; So, MT; Ngan, ES; Lui, VCH; Chen, Y; Liu, XL; Hui, KJWS; Li, L; Guo, WH; Sun, XB; Tou, JF; Chan, KW; Wu, XZ; Song, YQ; Chan, D; Cheung, K; Chung, PHY; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH | 2010 | 728 |
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