| | Title | Author(s) | Year | View Count | | 1 |  | Arrhythmia and sudden death associated with elevated cardiac chloride channel activity | Ye, L; Zhu, W; Backx, PH; Cortez, MA; Wu, J; Chow, YH; Mckerlie, C; Wang, A; Tsui, LC; Gross, GJ; Hu, J | 2011 | 67 |
| 2 | | Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene? | Dorfman, R; Nalpathamkalam, T; Taylor, C; Gonska, T; Keenan, K; Yuan, XW; Corey, M; Tsui, LC; Zielenski, J; Durie, P | 2010 | 37 |
| 3 | | Modifier gene study of meconium ileus in cystic fibrosis: Statistical considerations and gene mapping results | Dorfman, R; Li, W; Sun, L; Lin, F; Wang, Y; Sandford, A; Paré, PD; McKay, K; Kayserova, H; Piskackova, T; MacEk, M; Czerska, K; Sands, D; Tiddens, H; Margarit, S; Repetto, G; Sontag, MK; Accurso, FJ; Blackman, S; Cutting, GR; Tsui, LC; Corey, M; Durie, P; Zielenski, J; Strug, LJ | 2009 | 121 |
| 4 | | A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome | FaiyazUlHaque, M; Zaidi, SHE; AlSanna, N; Alswaid, A; Momenah, T; Kaya, N; AlDayel, F; Bouhoaigah, I; Saliem, M; Tsui, LC; Teebi, AS | 2009 | 362 |
| 5 | | A systematic analysis of intronic sequences downstream of 5′ splice sites reveals a widespread role for U-rich motifs and TIA1/TIAL1 proteins in alternative splicing regulation | Aznarez, I; Barash, Y; Shai, O; He, D; Zielenski, J; Tsui, LC; Parkinson, J; Frey, BJ; Rommens, JM; Blencowe, BJ | 2008 | 359 |
| 6 | | 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 | 107 |
| 7 |  | Complex two-gene modulation of lung disease severity in children with cystic fibrosis | Dorfman, R; Sandford, A; Taylor, C; Huang, B; Frangolias, D; Wang, Y; Sang, R; Pereira, L; Sun, L; Berthiaume, Y; Tsui, LC; Paré, PD; Durie, P; Corey, M; Zielenski, J | 2008 | 147 |
| 8 | | Nonsteroidal anti-inflammatory drugs upregulate function of wild-type and mutant CFTR | Li, J; Xiang, YY; Ye, L; Tsui, LC; MacDonald, JF; Hu, J; Lu, WY | 2008 | 98 |
| 9 | | A second generation human haplotype map of over 3.1 million SNPs | Frazer, KA; Ballinger, DG; Cox, DR; Hinds, DA; Stuve, LL; Gibbs, RA; Belmont, JW; Boudreau, A; Hardenbol, P; Leal, SM; Pasternak, S; Wheeler, DA; Willis, TD; Yu, F; Yang, H; Zeng, C; Gao, Y; Hu, H; Hu, W; Li, C; Lin, W; Liu, S; Pan, H; Tang, X; Wang, J; Wang, W; Yu, J; Zhang, B; Zhang, Q; Zhao, H; Zhao, H; Zhou, J; Gabriel, SB; Barry, R; Blumenstiel, B; Camargo, A; Defelice, M; Faggart, M; Goyette, M; Gupta, S; Moore, J; Nguyen, H; Onofrio, RC; Parkin, M; Roy, J; Stahl, E; Winchester, E; Ziaugra, L; Altshuler, D; Shen, Y; Yao, Z; Huang, W; Chu, X; He, Y; Jin, L; Liu, Y; Shen, Y; Sun, W; Wang, H; Wang, Y; Wang, Y; Xiong, X; Xu, L; Waye, MMY; Tsui, SKW; Xue, H; Wong, JTF; Galver, LM; Fan, JB; Gunderson, K; Murray, SS; Oliphant, AR; Chee, MS; Montpetit, A; Chagnon, F; Ferretti, V; Leboeuf, M; Olivier, JF; Phillips, MS; Roumy, S; Sallée, C; Verner, A; Hudson, TJ; Kwok, PY; Cai, D; Koboldt, DC; Miller, RD; Pawlikowska, L; TaillonMiller, P; Xiao, M; Tsui, LC; Mak, W; You, QS; Tam, PKH; Nakamura, Y; Kawaguchi, T; Kitamoto, T; Morizono, T; Nagashima, A; Ohnishi, Y; Sekine, A; Tanaka, T; Tsunoda, T; Deloukas, P; Bird, CP; Delgado, M; Dermitzakis, ET; Gwilliam, R; Hunt, S; Morrison, J; Powell, D; Stranger, BE; Whittaker, P; Bentley, DR; Daly, MJ; De Bakker, PIW; Barrett, J; Chretien, YR; Maller, J; McCarroll, S; Patterson, N; Pe'Er, I; Price, A; Purcell, S; Richter, DJ; Sabeti, P; Saxena, R; Schaffner, SF; Sham, PC; Varilly, P; Stein, LD; Krishnan, L; Smith, AV; TelloRuiz, MK; Thorisson, GA; Chakravarti, A; Chen, PE; Cutler, DJ; Kashuk, CS; Lin, S; Abecasis, GR; Guan, W; Li, Y; Munro, HM; Qin, ZS; Thomas, DJ; McVean, G; Auton, A; Bottolo, L; Cardin, N; Eyheramendy, S; Freeman, C; Marchini, J; Myers, S; Spencer, C; Stephens, M; Donnelly, P; Cardon, LR; Clarke, G; Evans, DM; Morris, AP; Weir, BS; Johnson, TA; Mullikin, JC; Sherry, ST; Feolo, M; Skol, A; Zhang, H; Matsuda, I; Fukushima, Y; MacEr, DR; Suda, E; Rotimi, CN; Adebamowo, CA; Ajayi, I; Aniagwu, T; Marshall, PA; Nkwodimmah, C; Royal, CDM; Leppert, MF; Dixon, M; Peiffer, A; Qiu, R; Kent, A; Kato, K; Niikawa, N; Adewole, IF; Knoppers, BM; Foster, MW; Clayton, EW; Watkin, J; Muzny, D; Nazareth, L; Sodergren, E; Weinstock, GM; Yakub, I; Birren, BW; Wilson, RK; Fulton, LL; Rogers, J; Burton, J; Carter, NP; Clee, CM; Griffiths, M; Jones, MC; McLay, K; Plumb, RW; Ross, MT; Sims, SK; Willey, DL; Chen, Z; Han, H; Kang, L; Godbout, M; Wallenburg, JC; L'Archevêque, P; Bellemare, G; Saeki, K; Wang, H; An, D; Fu, H; Li, Q; Wang, Z; Wang, R; Holden, AL; Brooks, LD; McEwen, JE; Guyer, MS; Wang, VO; Peterson, JL; Shi, M; Spiegel, J; Sung, LM; Zacharia, LF; Collins, FS; Kennedy, K; Jamieson, R; Stewart, J | 2007 | 10,910 |
| 10 | | Genome-wide detection and characterization of positive selection in human populations | Sabeti, PC; Varilly, P; Fry, B; Lohmueller, J; Hostetter, E; Cotsapas, C; Xie, X; Byrne, EH; McCarroll, SA; Gaudet, R; Schaffner, SF; Lander, ES; Frazer, KA; Ballinger, DG; Cox, DR; Hinds, DA; Stuve, LL; Gibbs, RA; Belmont, JW; Boudreau, A; Hardenbol, P; Leal, SM; Pasternak, S; Wheeler, DA; Willis, TD; Yu, F; Yang, H; Zeng, C; Gao, Y; Hu, H; Hu, W; Li, C; Lin, W; Liu, S; Pan, H; Tang, X; Wang, J; Wang, W; Yu, J; Zhang, B; Zhang, Q; Zhao, H; Zhao, H; Zhou, J; Gabriel, SB; Barry, R; Blumenstiel, B; Camargo, A; Defelice, M; Faggart, M; Goyette, M; Gupta, S; Moore, J; Nguyen, H; Onofrio, RC; Parkin, M; Roy, J; Stahl, E; Winchester, E; Ziaugra, L; Altshuler, D; Shen, Y; Yao, Z; Huang, W; Chu, X; He, Y; Jin, L; Liu, Y; Shen, Y; Sun, W; Wang, H; Wang, Y; Wang, Y; Xiong, X; Xu, L; Waye, MMY; Tsui, SKW; Xue, H; Wong, JTF; Galver, LM; Fan, JB; Gunderson, K; Murray, SS; Oliphant, AR; Chee, MS; Montpetit, A; Chagnon, F; Ferretti, V; Leboeuf, M; Olivier, JF; Phillips, MS; Roumy, S; Sallée, C; Verner, A; Hudson, TJ; Kwok, PY; Cai, D; Koboldt, DC; Miller, RD; Pawlikowska, L; TaillonMiller, P; Xiao, M; Tsui, LC; Mak, W; You, QS; Tam, PKH; Nakamura, Y; Kawaguchi, T; Kitamoto, T; Morizono, T; Nagashima, A; Ohnishi, Y; Sekine, A; Tanaka, T; Tsunoda, T; Deloukas, P; Bird, CP; Delgado, M; Dermitzakis, ET; Gwilliam, R; Hunt, S; Morrison, J; Powell, D; Stranger, BE; Whittaker, P; Bentley, DR; Daly, MJ; De Bakker, PIW; Barrett, J; Chretien, YR; Maller, J; McCarroll, S; Patterson, N; Pe'Er, I; Price, A; Purcell, S; Richter, DJ; Saxena, R; Sham, PC; Stein, LD; Krishnan, L; Smith, AV; TelloRuiz, MK; Thorisson, GA; Chakravarti, A; Chen, PE; Cutler, DJ; Kashuk, CS; Lin, S; Abecasis, GR; Guan, W; Li, Y; Munro, HM; Qin, ZS; Thomas, DJ; McVean, G; Auton, A; Bottolo, L; Cardin, N; Eyheramendy, S; Freeman, C; Marchini, J; Myers, S; Spencer, C; Stephens, M; Donnelly, P; Cardon, LR; Clarke, G; Evans, DM; Morris, AP; Weir, BS; Johnson, TA; Mullikin, JC; Sherry, ST; Feolo, M; Skol, A; Zhang, H; Matsuda, I; Fukushima, Y; MacEr, DR; Suda, E; Rotimi, CN; Adebamowo, CA; Ajayi, I; Aniagwu, T; Marshall, PA; Nkwodimmah, C; Royal, CDM; Leppert, MF; Dixon, M; Peiffer, A; Qiu, R; Kent, A; Kato, K; Niikawa, N; Adewole, IF; Knoppers, BM; Foster, MW; Clayton, EW; Watkin, J; Muzny, D; Nazareth, L; Sodergren, E; Weinstock, GM; Yakub, I; Birren, BW; Wilson, RK; Fulton, LL; Rogers, J; Burton, J; Carter, NP; Clee, CM; Griffiths, M; Jones, MC; McLay, K; Plumb, RW; Ross, MT; Sims, SK; Willey, DL; Chen, Z; Han, H; Kang, L; Godbout, M; Wallenburg, JC; L'Archevêque, P; Bellemare, G; Saeki, K; Wang, H; An, D; Fu, H; Li, Q; Wang, Z; Wang, R; Holden, AL; Brooks, LD; McEwen, JE; Guyer, MS; Wang, VO; Peterson, JL; Shi, M; Spiegel, J; Sung, LM; Zacharia, LF; Collins, FS; Kennedy, K; Jamieson, R; Stewart, J | 2007 | 724 |
| 11 | | Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar [5] | FaiyazUlHaque, M; Zaidi, SHE; AlMureikhi, MS; Peltekova, I; Tsui, LC; Teebi, AS | 2007 | 111 |
| 12 | | Citrin/mitochondrial glycerol-3-phosphate dehydrogenase double knock-out mice recapitulate features of human citrin deficiency | Saheki, T; Iijima, M; Meng, XL; Kobayashi, K; Horiuchi, M; Ushikai, M; Okumura, F; Xiao, JM; Inoue, I; Tajima, A; Moriyama, M; Eto, K; Kadowaki, T; Sinasac, DS; Tsui, LC; Tsuji, M; Okano, A; Kobayashi, T | 2007 | 198 |
| 13 | | Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X | Aznarez, I; Zielenski, J; Rommens, JM; Blencowe, BJ; Tsui, LC | 2007 | 176 |
| 14 | | Pyruvate ameliorates the defect in ureogenesis from ammonia in citrin-deficient mice | Moriyama, M; Li, MX; Kobayashi, K; Sinasac, DS; Kannan, Y; Iijima, M; Horiuchi, M; Tsui, LC; Tanaka, M; Nakamura, Y; Saheki, T | 2006 | 98 |
| 15 | | Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials | Wilschanski, M; Dupuis, A; Ellis, L; Jarvi, K; Zielenski, J; Tullis, E; Martin, S; Corey, M; Tsui, LC; Durie, P | 2006 | 1,399 |
| 16 | | A haplotype map of the human genome | Belmont, JW; Boudreau, A; Leal, SM; Hardenbol, P; Pasternak, S; Wheeler, DA; Willis, TD; Yu, F; Yang, H; Gao, Y; Hu, H; Wang, Y; Wang, Y; Xiong, X; Xu, L; Waye, MMY; Tsui, SKW; Xue, H; Wong, JTF; Galver, LM; Barrett, J; Sodergren, E; Fan, JB; Murray, SS; Oliphant, AR; Chee, MS; Montpetit, A; Chagnon, F; Ferretti, V; Leboeuf, M; Olivier, JF; Phillips, MS; Weinstock, GM; Fry, B; Roumy, S; Sallée, C; Verner, A; Hudson, TJ; Frazer, KA; Ballinger, DG; Cox, DR; Hinds, DA; Stuve, LL; Yakub, I; Kwok, PY; Hu, W; Cai, D; Koboldt, DC; Miller, RD; Pawlikowska, L; TaillonMiller, P; Xiao, M; Tsui, LC; Mak, W; Gabriel, SB; Sham, PC; Song, YQ; Maller, J; Tam, PKH; Nakamura, Y; Kawaguchi, T; Kitamoto, T; Morizono, T; Nagashima, A; Ohnishi, Y; Onofrio, RC; Sekine, A; Tanaka, T; Deloukas, P; McCarroll, S; Bird, CP; Delgado, M; Dermitzakis, ET; Patterson, N; Pe'er, I; Purcell, S; Ziaugra, L; Richter, DJ; Sabeti, P; Saxena, R; Schaffner, SF; Varilly, P; Li, C; Stein, LD; Krishnan, L; Smith, AV; Thorisson, GA; Birren, BW; Chakravarti, A; Chen, PE; Cutler, DJ; Kashuk, CS; Lin, S; Abecasis, GR; Lin, W; Guan, W; Munro, HM; Qin, ZS; Daly, MJ; Thomas, DJ; McVean, G; Bottolo, L; Eyheramendy, S; Freeman, C; Marchini, J; Myers, S; Liu, S; Spencer, C; Stephens, M; Wilson, RK; Donnelly, P; Cardon, LR; Clarke, G; Evans, DM; Morris, AP; Weir, BS; Tsunoda, T; Mullikin, JC; Pan, H; Sherry, ST; Yu, J; Feolo, M; Zhang, H; Zeng, C; Zhao, H; Matsuda, I; Fukushima, Y; Macer, DR; Suda, E; Rotimi, CN; Tang, X; Gwilliam, R; Adebamowo, CA; Ajayi, I; Aniagwu, T; Marshall, PA; Nkwodimmah, C; Royal, CDM; Leppert, MF; Dixon, M; Peiffer, A; Qiu, R; Fulton, LL; Wang, J; Kent, A; Kato, K; Niikawa, N; Adewole, IF; Knoppers, BM; Foster, MW; Clayton, EW; Watkin, J; Gibbs, RA; Rogers, J; Muzny, D; Wang, W; Nazareth, L; Burton, J; Carter, NP; Clee, CM; Griffiths, M; Jones, MC; McLay, K; Plumb, RW; Ross, MT; Hunt, S; Zhang, B; Sims, SK; Willey, DL; Chen, Z; Han, H; Kang, L; Godbout, M; Wallenburg, JC; L'Archevêque, P; Bellemare, G; Morrison, J; Saeki, K; Zhang, Q; Wang, H; An, D; Fu, H; Li, Q; Wang, Z; Wang, R; Holden, AL; Brooks, LD; Powell, D; McEwen, JE; Bird, CR; Zhao, H; Guyer, MS; Nailer, PJ; Wang, VO; Peterson, JL; Shi, M; Spiegel, J; Sung, LM; Stranger, BE; Witonsky, J; Zacharia, LF; Collins, FS; Zhou, J; Kennedy, K; Jamieson, R; Stewart, J; Barry, R; Blumenstiel, B; Camargo, A; Whittaker, P; Defelice, M; Faggart, M; Goyette, M; Gupta, S; Moore, J; Nguyen, H; Parkin, M; Roy, J; Stahl, E; Winchester, E; Bentley, DR; Altshuler, D; Shen, Y; Yao, Z; Huang, W; Chu, X; He, Y; Jin, L; Liu, Y; Shen, Y; Sun, W; De Bakker, PIW; Wang, H | 2005 | 1,519 |
| 17 | | A novel locus of ectodermal dysplasia maps to chromosome 10q24.32-q25.1 | Rafiq, MA; FaiyazulHaque, M; Ud Din, MA; Malik, S; Sohail, M; Anwar, M; Haque, S; Paterson, AD; Tsui, LC; Ahmad, W | 2005 | 1,649 |
| 18 | | A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13 | Zaidi, SHE; Peltekova, V; Meyer, S; Lindinger, A; Paterson, AD; Tsui, LC; FaiyazUlHaque, M; Teebi, AS | 2005 | 543 |
| 19 | | High-resolution FISH analysis. | Heng, HH; Windle, B; Tsui, LC | 2005 | 99 |
| 20 |  | Altered expression and deletion of RMO1 in osteosarcoma | Eppert, K; Wunder, JS; Aneliunas, V; Tsui, LC; Scherer, SW; Andrulis, IL | 2005 | 1,122 |
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