| Title | Author(s) | Year | View Count |
 | Molecular characterization of the 2011 Hong Kong scarlet fever outbreak | Tse, H; Bao, JYJ; Davies, MR; Maamary, P; Tsoi, HW; Tong, AHY; Ho, TCC; Lin, CH; Gillen, CM; Barnett, TC; Chen, JHK; Lee, M; Yam, WC; Wong, CK; Ong, CLY; Chan, YW; Wu, CW; Ng, T; Lim, WWL; Tsang, THF; Tse, CWS; Dougan, G; Walker, MJ; Lok, S; Yuen, KY | 2012 | 80 |
| Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: Susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment | Lau, KC; Lam, CW; Law, CY; Lai, ST; Tsang, TY; Siu, CWK; To, WK; Leung, KF; Mak, CM; Poon, WT; Chan, PKS; Chan, YW | 2011 | 165 |
| Circulating fluorocytes at the first attack of acute intermittent porphyria: A missing link in the pathogenesis | Lam, CW; Lau, KC; Mak, CM; Tsang, MW; Chan, YW | 2011 | 183 |
| Young-onset Parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndrome | Mak, CM; Sheng, B; Lee, HHC; Lau, KK; Chan, WT; Lam, CW; Chan, YW | 2011 | 132 |
| Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese | Mak, CM; Lam, CW; Siu, TS; Chan, KY; Siu, WK; Yeung, WL; Hui, J; Wong, VCN; Low, LCK; Ko, CH; Fung, CW; Chen, SP; Yuen, YP; Lee, HC; Yau, E; Chan, B; Tong, SF; Tam, S; Chan, YW | 2010 | 236 |
| Maternally inherited leigh syndrome: An unusual cause of infantile apnea | Chau, CSK; Kwok, KL; Ng, DK; Lam, CW; Tong, SF; Chan, YW; Siu, WK; Yuen, YP | 2010 | 201 |
 | Pectoralis major flap | Wei, WI; Chan, YW | 2009 | 139 |
| Prospective randomized study of selective neck dissection versus observation for N0 neck of early tongue carcinoma | Yuen, PW; Ho, CM; Chow, TL; Tang, LC; Cheung, WY; Ng, WM; Wei, WI; Kong, CK; Book, KS; Yuen, WC; Lam, AK; Yuen, NW; Trendell-Smith, NJ; Chan, YW; Wong, BYH; Li, GKH; Ho, ACW; Ho, WK; Wong, SY; Yao, TJ | 2009 | 395 |
| Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity | Mak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, JY; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW | 2008 | 213 |
| Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity (Journal of Human Genetics (2008) 53 (55-63) DOI: 10.1007/s10038-007-0218-2) | Mak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, ST; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW | 2008 | 77 |
| Germline epimutation of MLH1 in early-onset colorectal cancer | Chan, TL; Tsui, WY; Chan, YW; Chan, ASY; Lee, TYH; Yuen, ST; Leung, SY | 2008 | 194 |
| DNA-based diagnosis of methylmalonic aciduria and homocystinuria, cblC type in a Chinese patient presenting with mild developmental delay | Yuen, YP; Lam, CW; Chan, KY; Lai, CK; Tong, SF; Chan, YW | 2007 | 57 |
| Immunohistochemical staining on tissue microarray of colorectal cancers constitutes a convenient means to rapidly screen for MMR deficiency | Chan, TL; Guo, D; Yuen, ST; Chan, YW; Chan, ASY; Leung, SY | 2007 | 166 |
| Study of the mechanisms underlying heritable germline epimutation of MSH2 in a Hereditary Nonpolyposis Colorectal Cancer family | Chan, TL; Yuen, ST; Lo, MWS; Lee, TYH; Kong, CK; Chan, YW; Tsui, WY; Li, VSW; Chan, ASY; Leung, SY | 2007 | 177 |
| Heritable germline epimutation of MSH2 in a hereditary nonpolyposis colorectal cancer family | Chan, TL; Yuen, ST; Kong, CK; Chan, YW; Chan, ASY; Leung, SY | 2007 | 202 |
| Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer | Chan, TL; Yuen, ST; Kong, CK; Chan, YW; Chan, ASY; Ng, WF; Tsui, WY; Lo, MWS; Tam, WY; Li, VSW; Leung, SY | 2006 | 135 |
| Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer. | Sheng, JQ; Chan, TL; Chan, YW; Huang, JS; Chen, JG; Zhang, MZ; Guo, XL; Mu, H; Chan, AS; Li, SR; Yuen, ST; Leung, SY | 2006 | 106 |
| Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria | Yuen, YP; Lam, CW; Lai, CK; Tong, SF; Li, PS; Tam, S; Kwan, EYW; Chan, SY; Tsang, WK; Chan, KY; Mak, WL; Cheng, CW; Chan, YW | 2006 | 64 |
| Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome | Lam, CW; Yuen, YP; Cheng, WF; Chan, YW; Tong, SF | 2006 | 61 |
| Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia [2] | Poon, WT; Au, KM; Chan, YW; Chan, KY; Chow, CB; Tong, SF; Lam, CW | 2006 | 46 |
|
