| Title | Author(s) | Year | View Count |
 | 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 | 139 |
 | New HLBX9 mutations in Currarino patients | Garcia-Barcelo, MM; Lui, VCH; Fu, M; Li, L; Scherer, S; Herbrick, MA; Van Heurn, E; Tam, PKH | 2004 | 98 |
| Large-scale sequencing of two regions in human chromosome 7q22: Analysis of 650 kb of genomic sequence around the EPO and CUTL1 loci reveals 17 genes | Glockner, G; Scherer, S; Schattevoy, R; Boright, A; Weber, J; Tsui, LC; Rosenthal, A | 1998 | 226 |
| Identification of an amplified gene cluster in glioma including two novel amplified genes isolated by exon trapping | Mueller, HW; Michel, A; Heckel, D; Fischer, U; Tönnes, M; Tsui, LC; Scherer, S; Zang, KD; Meese, E | 1997 | 242 |
| Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: A possible contributor to the holoprosencephaly 3 phenotype | Mackay, M; Fantes, J; Scherer, S; Boyle, S; West, K; Tsui, LC; Belloni, E; Lutz, E; Van Heyningen, V; Harmar, AJ | 1996 | 313 |
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