| Title | Author(s) | Year | View Count |
 | Altered expression and deletion of RMO1 in osteosarcoma | Eppert, K; Wunder, JS; Aneliunas, V; Tsui, LC; Scherer, SW; Andrulis, IL | 2005 | 1,122 |
| Amplification of CFTR exon 9 sequences to multiple locations in the human genome | Rozmahel, R; Heng, HHQ; Duncan, AMV; Shi, XM; Rommens, JM; Tsui, LC | 1997 | 285 |
| Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621 + 1G → T and 711 + 1G → T mutations | Zielenski, J; Bozon, D; Markiewicz, D; Aubin, G; Simard, F; Rommens, JM; Tsui, LC | 1993 | 285 |
| Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland | Analiza mutacji w genie CFTR u pacjentów z rozpoznana mukowiscydoza w Polsce. | Aznarez, I; Bal, J; Casals, T; Estivill, X; Moral, N; Sands, D; Nunes, V; SobczyńskaTomaszewska, A; Tsui, LC; Zielenski, J | 2000 | 307 |
| Analysis of the CFTR gene in Turkish cystic fibrosis patients: Identification of three novel mutations (3172delAC, P1013L and M1028I) | Onay, T; Topaloglu, O; Zielenski, J; Gokgoz, N; Kayserili, H; Camcioglu, Y; Cokugras, H; Akcakaya, N; Apak, M; Tsui, LC; Kirdar, B | 1998 | 425 |
| Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly | Vargas, FR; Roessler, E; Gaudenz, K; Belloni, E; Whitehead, AS; Kirke, PN; Mills, JL; Hooper, G; Stevenson, RE; Cordeiro, I; Correia, P; Felix, T; Gereige, R; Cunningham, ML; Canún, S; Antonarakis, SE; Strachan, T; Tsui, LC; Scherer, SW; Muenke, M | 1998 | 424 |
| Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36 | Shiloh, Y; Donlon, T; Bruns, G; Breitman, ML; Tsui, L-C | 1986 | 279 |
| Assignment to human gamma crystallin multigene family to chromosome 2 | Willard, HF; Meakin, SO; Tsui, LC; Breitman, ML | 1985 | 249 |
| The BCL7 gene family: Deletion of BCL7B in Williams syndrome | Jadayel, DM; Osborne, LR; Coignet, LJA; Zani, VJ; Tsui, LC; Scherer, SW; Dyer, MJS | 1998 | 305 |
| Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphism | Mornet, E; Chateau, C; SimonBouy, B; Boue, J; Zielenski, J; Tsui, LC; Boue, A | 1992 | 230 |
| Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: A cystic fibrosis mutation of Slavic origin common in Central and East Europe | Dörk, T; Macek Jr, M; Mekus, F; Tümmler, B; Tzountzouris, J; Casals, T; Krebsová, A; Koudová, M; Sakmaryová, I; Macek Sr, M; Vávrová, V; Zemková, D; Ginter, E; Petrova, NV; Ivaschenko, T; Baranov, V; Witt, M; Pogorzelski, A; Bal, J; Zékanowsky, C; Wagner, K; Stuhrmann, M; Bauer, I; Seydewitz, HH; Neumann, T; Jakubiczka, S; Kraus, C; Thamm, B; Nechiporenko, M; Livshits, L; Mosse, N; Tsukerman, G; Kadási, L; RavnikGlavač, M; Glavač, D; Komel, R; Vouk, K; Kučinskas, V; Krumina, A; Teder, M; Kocheva, S; Efremov, GD; Onay, T; Kirdar, B; Malone, G; Schwarz, M; Zhou, Z; Friedman, KJ; Carles, S; Claustres, M; Bozon, D; Verlingue, C; Férec, C; Tzetis, M; Kanavakis, E; Cuppens, H; Bombieri, C; Pignatti, PF; Sangiuolo, F; Jordanova, A; Kusic, J; Radojkovič, D; Sertić, J; Richter, D; Rukavina, AS; Bjorck, E; Strandvik, B; Cardoso, H; Montgomery, M; Nakielna, B; Hughes, D; Estivill, X; Aznarez, I; Tullis, E; Tsui, LC; Zielenski, J | 2000 | 451 |
| Characterization of the segmental duplication LCR7-20 in the human genome | Liu, X; Li, X; Li, M; Acimovic, YJ; Li, Z; Scherer, SW; Estivill, X; Tsui, LC | 2004 | 907 |
| 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 | 311 |
| Chromosomal localization of the human gene encoding the 51-kDa subunit of mitochondrial complex I (NDUFV1) to 11q13 | Ali, ST; Duncan, AMV; Schappert, K; Heng, HHQ; Tsui, L-C; Chow, W; Robinson, BH | 1993 | 310 |
| Circling, deafness, and yellow coat displayed by yellow submarine (Ysb) and light coat and circling (Lcc) mice with mutations on chromosome 3 | Dong, S; Leung, KKH; Pelling, AL; Lee, PYT; Tang, ASP; Heng, HHQ; Tsui, LC; Tease, C; Fisher, G; Steel, KP; Cheah, KSE | 2002 | 375 |
| Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus | Kerem, E; Corey, M; Kerem, B; Durie, P; Tsui, LC; Levison, H | 1989 | 255 |
| Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and human | Crackower, MA; Snasac, DS; Xia, J; Motoyama, J; Prochazka, M; Rommens, JM; Sbherer, SW; Tsui, LC | 1999 | 222 |
| Cloning and chromosomal mapping of three novel genes, GPR9, GPR10, and GPR14, encoding receptors related to interleukin 8, neuropeptide Y, and somatostatin receptors | Marchese, A; Heiber, M; Nguyen, T; Heng, HHQ; Saldivia, VR; Cheng, R; Murphy, PM; Tsui, LC; Shi, X; Gregor, P; George, SR; O'Dowd, BF; Docherty, JM | 1995 | 238 |
| The cloning and chromosomal mapping of two novel human opioid- somatostatin-like receptor genes, GPR7 and GPR8, expressed in discrete areas of the brain | O'Dowd, BF; Scheideler, MA; Nguyen, T; Cheng, R; Rasmussen, JS; Marchese, A; Zastawny, R; Heng, HHQ; Tsui, LC; Shi, X; Asa, S; Puy, L; George, SR | 1995 | 256 |
| Cloning of human genes encoding novel G protein-coupled receptors | Marchese, A; Docherty, JM; Nguyen, T; Heiber, M; Cheng, R; Heng, HHQ; Tsui, LC; Shi, X; George, SR; O'Dowd, BF | 1994 | 253 |
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