Results 1 to 19 of 19
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TypeTitleAuthor(s)YearViews
Genome-wide copy number variation study in anorectal malformationsWong, EHM; Cui, L; Ng, CL; Tang, CSM; Liu, X; So, MT; Yip, BHK; Cheng, G; Zhang, R; Tang, WK; Yang, W; Lau, YL; Baum, L; Kwan, P; Sun, LD; Zuo, XB; Ren, YQ; Yin, XY; Miao, X; Liu, JJ; Lui, VCH; Ngan, ESW; Yuan, ZW; Zhang, SW; Xia, JL; Wang, HL; Sun, XB; Wang, RY; Chang, T; Chan, IHY; Chung, HY; Zhang, XJ; Wong, KKY; Cherny, SS; Sham, PC; Tam, PKH; Garcia-Barcelo, MM2013142
 
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in ChineseGuo, Y; Baum, LW; Sham, PC; Wong, V; Ng, PW; Lui, CHT; Sin, NC; Tsoi, TH; Tang, CSM; Kwan, JSH; Yip, BHK; Xiao, SM; Thomas, GN; Lau, YL; Yang, W; Cherny, SS; Kwan, P2012146
 
Mutations in the NRG1 gene are associated with Hirschsprung diseaseTang, 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, MM2012244
 
Fine mapping on chromosome 10q24.2 implicates ADD3 in biliary atresiaGarcia-Barcelo, MM; Cheng, G; Tang, CSM; Liu, X; Zhang, R; So, MT; Wong, EHM; Chung, PHY; Chan, IHY; Liu, J; Zhong, W; Xia, H; Yu, J; Wong, KKY; Cherny, SS; Sham, PC; Tam, PKH201265
 
Genome-wide copy number variation in anorectal malformationsCherny, SS; Wong, EHM; Cui, L; Ng, CL; Tang, CSM; So, MT; Yip, BHK; Cheng, G; Lui, VCH; Sham, PC; Tam, PKH; Garcia-Barcelo, MM201239
 
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3Tang, CSM; Cheng, G; So, MT; Yip, BHK; Miao, XP; Wong, EHM; Ngan, ESW; Lui, VCH; Song, YQ; Chan, D; Cheung, K; Yuan, ZW; Lei, L; Chung, PHY; Liu, XL; Wong, KKY; Marshall, CR; Scherer, S; Cherny, SS; Sham, PC; Tam, PKH; GarciaBarceló, MM2012207
 
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, PKH2011157
 
Fine mapping of the NRG1 hirschsprung's disease locusTang, CSM; Tang, WK; So, MT; Miao, XP; Leung, BMC; Yip, BHK; Leon, TYY; Ngan, ESW; Lui, VCH; Chen, Y; Chan, IHY; Chung, PHY; Liu, XL; Wu, XZ; Wong, KKY; Sham, PC; Cherny, SS; Tam, PKH; GarciaBarceló, MM2011817
 
Genome-wide copy number analysis uncovers a new HSCR gene: NRG3Garcia-Barcelo, M; Tang, CSM; So, MT; Marshall, CR; Scherer, S; Cherny, S; Sham, P; Tam, P2011113
 
Genomi-wide association study on anorectal malformations in the Chinese populationWong, EHM; Tang, CSM; Barcelo, MG; Zhang, XJ; Liu, JJ; Cherny, SS; Sham, PC; Tam, PKH2010133
 
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2GarciaBarceló, 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, PKH2010751
 
Identification of rare variants in the NRG1 gene of Hirschsprung's patientsGarcia-Barcelo, MM; Tang, WK; Miao, XP; Tang, CSM; So, MT; Leon, YY; Sham, PC; Cherny, SS; Tam, PKH2009153
 
A RET founder mutation in Chinese hirschsprung's patientsCornes, BK; Tang, CSM; Leon, TYY; So, MT; Sham, PC; Tam, PKH; Garcia-Barcelo, MM200991
 
Quantifying epistasis between two sets of signaling pathway genes by canonical correlation analysisYip, BHK; Tang, CSM; Cherny, SS; Tam, PKH; Ngan, ESW; Garcia-Barcelo, MM; Sham, PC2009352
 
Genome-wide profile of copy number variants for Hirschsprung diseaseTang, CSM; Garcia-Barcelo, MM; Cherny, SS; Sham, PC; Tam, PKH2009150
 
Fine mapping of Hirschsprung’s disease loci in 9q31Cherny, SS; Tang, CSM; Sribudiani, Y; Miao, XP; So, MT; Sham, PC; Tam, PKH; Garcia-Barcelo, MM; Hofstra, R2009220
 
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's diseaseGarcia-Barcelo, MM; Tang, CSM; Ngan, ESW; Lui, VCH; Chen, Y; So, MT; Leon, TYY; Miao, XP; Shum, CKY; Liu, FQ; Yeung, MY; Yuan, ZW; Guo, WH; Liu, L; Sun, XB; Huang, LM; Tou, JF; Song, YQ; Chan, D; Cheung, KMC; Wong, KKY; Cherny, SS; Sham, PC; Tam, PKH2009538
 
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's diseaseTam, PKH; Tang, CSM; Ngan, ESW; Lui, VCH; Chen, Y; So, MT; Leon, TYY; Miao, XP; Shum, CKY; Liu, FQ; Yeung, MY; Yuan, ZW; Guo, WH; Liu, L; Sun, XB; Huang, LM; Tou, JF; Song, YQ; Chan, D; Cheung, KMC; Wong, KKY; Cherny, SS; Sham, PC; Garcia-Barcelo, MM2009114
 
A Structural Split in the Human GenomeTang, CSM; Epstein, RJ200798
 
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