| Title | Author(s) | Year | View Count |
 | Genome-wide copy number variation study in anorectal malformations | Wong, EHM; Cui, L; Ng, CL; Tang, SM; Liu, X; So, MT; Yip, BHK; Cheng, G; Zhang, R; Tang, WK; Yang, W; Lau, YL; Baum, L; Kwan, P; Sun, LD; Zuo, ZB; 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, MM | 2013 | 4 |
 | Genome-wide copy number analysis uncovers a new HSCR gene: NRG3 | Tang, 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, MM | 2012 | 138 |
 | The role of circulating serotonin in the development of chronic obstructive pulmonary disease | Lau, WKW; Chan, MMW; Yip, BHK; Cheung, AHK; Ip, MSM; Mak, JCW; The COPD Study Group of the Hong Kong Thoracic Society | 2012 | 86 |
 | The role of circulating serotonin in the development of chronic obstructive pulmonary disease | Lau, WKW; Chan, MMW; Yip, BHK; Cheung, AHK; Ip, MSM; Mak, JCW | 2012 | 101 |
 | Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese | Guo, 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, P | 2012 | 112 |
 | Fine mapping of the NRG1 hirschsprung's disease locus | Tang, 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, MM | 2011 | 748 |
 | Hedgehog/notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans | Ngan, ESW; GarciaBarceló, MM; Yip, BHK; Poon, HC; Lau, ST; Kwok, CKM; Sat, E; Sham, MH; Wong, KKY; Wainwright, BJ; Cherny, SS; Hui, CC; Sham, PC; Lui, VCH; Tam, PKH | 2011 | 2,645 |
 | Estimating the total number of susceptibility variants underlying complex diseases from genome-wide association studies | So, HC; Yip, BHK; Sham, PC | 2010 | 94 |
 | A hierarchical frailty model applied to two-generation melanoma data | Moger, TA; Haugen, M; Yip, BHK; Gjessing, HK; Borgan, Ø | 2010 | 105 |
 | Hedgehog-notch induced premature gliogenesis of neural crest: a cause of Hirschsprung disease | Ngan, ESW; Garcia-Barcelo, MM; Yip, BHK; Sham, PC; Lui, VCH; Tam, PKH | 2010 | 219 |
 | Quantifying epistasis between two sets of signaling pathway genes by canonical correlation analysis | Yip, BHK; Tang, CSM; Cherny, SS; Tam, PKH; Ngan, ESW; Garcia-Barcelo, MM; Sham, PC | 2009 | 377 |
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