| Title | Author(s) | Year | View Count |  | Neurological deficits complicating thoracolumbar spinal pseudoarthrosis in ankylosing spondylitis: A report of four cases | Ho, EKW; Chan, FL; Upadhyay, SS; Chow, SP | 1992 | 38 |
| New restriction fragment length polymorphism (probe E9) reveals the highest linkage disequilibrium in Italian CF patients. | Devoto, M; De Benedetti, L; Ronchetto, P; Romano, L; Romeo, G; Tsui, LC; Dean, M; Collins, F; Seia, M; Piceni Sereni, L | 1990 | 89 |
 | No Evidence for a Major Gene Effect of the Dopamine D4 Receptor Gene in the Susceptibility to Gilles de la Tourette Syndrome in Five Canadian Families | Barr, CL; Wigg, KG; Zovko, E; Sandor, P; Tsui, LC | 1996 | 224 |
| No evidence for genetic heterogeneity in cystic fibrosis. | Tsui, LC; Buchwald, M | 1988 | 72 |
| 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 | 112 |
| Northland ophiolite, New Zealand, and implications for plate- tectonic evolution of the southwest Pacific | Malpas, J; Sporli, KB; Black, PM; Smith, IEM | 1992 | 44 |
| Novel cystic fibrosis mutation (2215insG) two adolescent Taiwanese siblings | Wu, CL; Shu, SG; Zielenski, J; Chiang, CD; Tsui, LC | 2000 | 259 |
 | A novel homozygous recessive mutation in the galactosyltransferase-I (B4GALT7) gene in individuals resembling the progeroid type of Ehlers-Danlos syndrome | Ul haque, MF; Teebi, AS; Al-ali, M; Al-mureikhi, MS; Kennedy, S; Al-thani, G; Zaidi, SHE; Tsui, L-C | 2003 | 301 |
| 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 | 1,663 |
| 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 | 372 |
| A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type | FaiyazUlHaque, M; Zaidi, SHE; AlAli, M; AlMureikhi, MS; Kennedy, S; AlThani, G; Tsui, LC; Teebi, AS | 2004 | 679 |
| Novel mutation in the gene encoding c-Abl-binding protein SH3BP2 causes cherubism | Lo, B; FaiyazUlHaque, M; Kennedy, S; Aviv, R; Tsui, LC; Teebi, AS | 2003 | 447 |
| Novel mutations in the EXT1 gene in two consanguineous families affected with multiple hereditary exostoses (familial osteochondromatosis) | FaiyazUlHaque, M; Ahmad, W; Zaidi, SHE; Hussain, S; Haque, S; Ahmad, M; Cohn, DH; Tsui, LC | 2004 | 689 |
| Nucleotide sequence for the cDNA of the bovine beta B2 crystallin and assignment of the orthologous human locus to chromosome 22. | Hogg, D; Gorin, MB; Heinzmann, C; Zollman, S; Mohandas, T; Klisak, I; Sparkes, RS; Breitman, M; Tsui, LC; Horwitz, J | 1987 | 206 |
| Oceanic lithosphere 1. The origin and evolution of oceanic lithosphere: Introduction | Malpas, J; Robinson, P | 1997 | 53 |
| Open treatment of fingertip injuries in adults | Chow, SP; Ho, E | 1982 | 52 |
| Organization of heterologous DNA inserts on the mouse meiotic chromosome core | Heng, HHQ; Tsui, LC; Moens, PB | 1994 | 225 |
| The origin of garnets in andesitic rocks from the Northland arc, New Zealand, and their implication for sub-arc processes | Bach, P; Smith, IEM; Malpas, JG | 2012 | 41 |
| Origin of oceanic phonolites by crystal fractionation and the problem of the Daly gap: An example from Rarotonga | Thompson, G; Smith, I; Malpas, J | 2001 | 56 |
| The origin of oceanic plagiogranites from the karmoy ophiolite, western Norway | Pedersen, RB; Malpas, J | 1984 | 48 |
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