| Title | Author(s) | Year | View Count |
 | Identification and characterization of human genes encoding Hprp3p and Hprp4p, interacting components of the spliceosome | Wang, A; FormanKay, J; Luo, Y; Luo, M; Chow, YH; Plumb, J; Friesen, JD; Tsui, LC; Heng, HHQ; Woolford Jr, JL; Hu, J | 1997 | 365 |
 | Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis gene | Rommens, JM; Zengerling, S; Burns, J; Melmer, G; Kerem, B; Plavsic, N; Zsiga, M; Kennedy, D; Markiewicz, D; Rozmahel, R; Riordan, JR; Buchwald, M; Tsui, L | 1988 | 256 |
| Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas | Edelson, MI; Scherer, SW; Tsui, LC; Welch, WR; Bell, DA; Berkowitz, RS; Mok, SC | 1997 | 110 |
| Identification of a human LIM-Hox gene, hLH-2, aberrantly expressed in chronic myelogenous leukaemia and located on 9q33-34.1 | Wu, HK; Heng, HHQ; Siderovski, DP; Dong, WF; Okuno, Y; Shi, XM; Tsui, LC; Minden, MD | 1996 | 124 |
| Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans | Wen, XY; Hegele, RA; Wang, J; Yan Wang, D; Cheung, J; Wilson, M; Yahyapour, M; Bai, Y; Zhuang, L; Skaug, J; Young, TK; Connelly, PW; Koop, BF; Tsui, LC; Stewart, AK | 2003 | 712 |
| Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families | FaiyazulHaque, M; Zaidi, SHE; Wahab, AA; Eltohami, A; AlMureikhi, MS; AlThani, G; Peltekova, VD; Tsui, LC; Teebi, AS | 2008 | 110 |
| Identification of a polymorphic DNA marker pDL32B (D12S7) and its localization to the long arm of chromosome 12, region q14.3-qter | Tsui, LC; Buchwald, M; Markiewicz, D; Kao, FT; Cai, GY; Law, ML | 1985 | 307 |
 | Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome | Osborne, LR; Campbell, T; Daradich, A; Scherer, SW; Tsui, LC | 1999 | 208 |
| Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient | Alley, TL; Gray, BA; Lee, SH; Scherer, SW; Tsui, LC; Tint, GS; Williams, CA; Zori, R; Wallace, MR | 1995 | 280 |
| 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 |
| Identification of four new mutations in the cystic fibrosis transmembrane conductance regulator gene: I148T, L1077P, Y1092X, 2183AA→G | Bozon, D; Zielenski, J; Rininsland, F; Tsui, LC | 1994 | 96 |
| Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients | Osborne, LR; Martindale, D; Scherer, SW; Shi, XM; Huizenga, J; Heng, HHQ; Costa, T; Pober, B; Lew, L; Brinkman, J; Rommens, J; Koop, B; Tsui, LC | 1996 | 288 |
| Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene | Zielenski, J; Bozon, D; Kerem, BS; Markiewicz, D; Durie, P; Rommens, JM; Tsui, LC | 1991 | 337 |
| Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene | Kerem, B; Zielenski, J; Markiewicz, D; Bozon, D; Gazit, E; Yahav, J; Kennedy, D; Riordan, JR; Collins, FS; Rommens, JM; Tsui, LC | 1990 | 300 |
| Identification of revertants for the cystic fibrosis ΔF508 mutation using STE6-CFTR chimeras in yeast | Teem, JL; Berger, HA; Ostedgaard, LS; Rich, DP; Tsui, LC; Welsh, MJ | 1993 | 262 |
| Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene | Zielenski, J; Markiewicz, D; Chen, HS; Schappert, K; Seller, A; Durie, P; Corey, M; Tsui, LC | 1995 | 268 |
| Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. | Belloni, E; Muenke, M; Roessler, E; Traverso, G; SiegelBartelt, J; Frumkin, A; Mitchell, HF; DonisKeller, H; Helms, C; Hing, AV; Heng, HH; Koop, B; Martindale, D; Rommens, JM; Tsui, LC; Scherer, SW | 1996 | 286 |
| Identification of the cystic fibrosis gene: Chromosome walking and jumping | Rommens, JM; Iannuzzi, MC; Kerem, BS; Drumm, ML; Melmer, G; Dean, M; Rozmahel, R; Cole, JL; Kennedy, D; Hidaka, N; Zsiga, M; Buchwald, M; Riordan, JR; Tsui, LC; Collins, FS | 1989 | 414 |
| Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA | Riordan, JR; Rommens, JM; Kerem, BS; Alon, N; Rozmahel, R; Grzelczak, Z; Zielinski, J; Lok, S; Plavsic, N; Chou, JL; Drumm, ML; Iannuzzi, MC; Collins, FS; Tsui, LC | 1989 | 389 |
| Identification of the cystic fibrosis gene: Genetic analysis | Kerem, BS; Rommens, JM; Buchanan, JA; Markiewicz, D; Cox, TK; Chakravarti, A; Buchwald, M; Tsui, LC | 1989 | 285 |
|
