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	Title	Author(s)	Issue Date
	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 Journal:Genome Research	Aznarez, I Barash, Y Shai, O He, D Zielenski, J Tsui, LC Parkinson, J Frey, BJ Rommens, JM Blencowe, BJ	2008
	Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Journal:Nature genetics	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
	Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy Journal:Nature Genetics	Minassian, BA Lee Jeffrey, R Herbrick, JA Huizenga, J Soder, S Mungall, AJ Dunham, I Gardner, R Fong, CYG Carpenter, S Jardim, L Satishchandra, P Andermann, E Carter Snead III, O LopesCendes, I Tsui, LC DelgadoEscueta, AV Rouleau, GA Scherer, SW	1998
	Combined blockade of angiotensin II and prorenin receptors ameliorates podocytic apoptosis induced by IgA-activated mesangial cells Journal:Apoptosis	Leung, JCK Chan, YY Saleem, MA Mathieson, PW Tang, SCW Lai, KN	2015
	Aging effects of vitamin C on a human lens protein produced in vitro Journal:FASEB Journal	Russell, P Garland, D Zigler Jr, JS Meakin, SO Tsui, LC Breitman, ML	1987
	Integrating ethics and science in the International HapMap Project Journal:Nature Reviews Genetics	The International HapMap Consortium Tam, PKH Tsui, L-C	2004
	FR167653 ameliorates intestinal allograft ischemic injury Journal:Transplantation Proceedings	Chan, KL Guo, WH Chan, KW Tam, PKH	2000
	Gastric electrical activity normalises in the first decade of life Journal:European Journal of Pediatric Surgery	Cheng, W Tam, PKH	2000
	Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprungs disease Journal:Human Molecular Genetics	Amiel, J Attie, T Jan, D Pelet, A Edery, P Bidaud, C Lacombe, D Tam, PKH Simeoni, J Flori, E Nihoul-Fekete, C Munnich, A Lyonnet, S	1996
	Isolation of P1 bacteriophage clones containing large contiguous segments of the human and mouse loci for the T-cell coreceptor molecule CD8 Journal:Genetic Analysis Techniques and Applications	Zhang, XL Kui Lai Lee Heng, HHQ Tsui, LC Parnes, JR Shepherd, NS Chamberlain, JW	1994
	The international HapMap project Journal:Nature	Belmont, JW Hardenbol, P Willis, TD Yu, F Yang, H Ch'ang, LY Huang, W Liu, B Shen, Y Tam, PKH Tsui, LC Waye, MMY Wong, JTF Zeng, C Zhang, Q Chee, MS Galver, LM Kruglyak, S Murray, SS Oliphant, AR Montpetit, A Chagnon, F Ferretti, V Leboeuf, M Phillips, MS Verner, A Duan, S Lind, DL Miller, RD Rice, J Saccone, NL TaillonMiller, P Xiao, M Sekine, A Sorimachi, K Tanaka, Y Tsunoda, T Yoshino, E Bentley, DR Hunt, S Powell, D Zhang, H Matsuda, I Fukushima, Y Macer, DR Suda, E Rotimi, C Adebamowo, CA Aniagwu, T Marshall, PA Matthew, O Nkwodimmah, C Royal, CDM Leppert, MF Dixon, M Cunningham, F Kanani, A Thorisson, GA Chen, PE Cutler, DJ Kashuk, CS Donnelly, P Marchini, J Mcvean, GAT Myers, SR Cardon, LR Morris, A Weir, BS Mullikin, JC Feolo, M Daly, MJ Qiu, R Kent, A Dunston, GM Kato, K Niikawa, N Watkin, J Gibbs, RA Sodergren, E Weinstock, GM Wilson, RK Fulton, LL Rogers, J Birren, BW Han, H Wang, H Godbout, M Wallenburg, JC L'archevêque, P Bellemare, G Todani, K Fujita, T Tanaka, S Holden, AL Collins, FS Brooks, LD Mcewen, JE Guyer, MS Jordan, E Peterson, JL Spiegel, J Sung, LM Zacharia, LF Kennedy, K Dunn, MG Seabrook, R Shillito, M Skene, B Stewart, JG Valle, DL Clayton, EW Jorde, LB Chakravarti, A Cho, MK Duster, T Foster, MW Jasperse, M Knoppers, BM Kwok, PY Licinio, J Long, JC Ossorio, P Wang, VO Rotimi, CN Spallone, P Terry, SF Lander, ES Lai, EH Nickerson, DA Abecasis, GR Altshuler, D Boehnke, M Deloukas, P Douglas, JA Gabriel, SB Hudson, RR Hudson, TJ Kruglyak, L Nakamura, Y Nussbaum, RL Schaffner, SF Sherry, ST Stein, LD Tanaka, T	2003
	Assignment of the human homolog of mouse Dlx3 to Chromosome 17q21.3-q22 by analysis of somatic cell hybrids and fluorescence in situ hybridization Journal:Mammalian Genome	Scherer, SW Heng, HHQ Robinson, GW Mahon, KA Evans, JP Tsui, LC	1995
	Two novel frameshift deletions (1924del7, 2055del9→A) in the CFTR gene in Mexican cystic fibrosis patients Journal:Human Mutation	Orozco, L Zielenski, J Markiewicz, D Villarreal, T Tsui, LC Lezana, JL Del Angel, RM	1997
	Screening for genetic mutations [1] Journal:Nature	Carlsson, C Jonsson, M Norden, B Dulay, MT Zare, RN Noolandi, J Nielsen, PE Tsui, LC Zielenski, J	1996
	Utilization of cultured epithelial cells from the sweat gland in studies of the CF defect. Journal:Progress in clinical and biological research	Riordan, J Burns, J Tsui, LC Reddy, MM Quinton, P Buchwald, M	1987
	MspI RFLP at CRYB1 locus (17q11.2 → 17q12) Journal:Nucleic Acids Research	Barker, DF Fain, PR Wright, EC Nguyen, K Tsui, LC	1989
	Paraoxonase-2 gene (PON2) G148 variant associated with elevated fasting plasma glucose in noninsulin-dependent diabetes mellitus Journal:Journal of Clinical Endocrinology and Metabolism	Hegele, RA Connelly, PW Scherer, SW Hanley, AJG Harris, SB Tsui, LC Zinman, B	1997
	Modifier gene study of meconium ileus in cystic fibrosis: Statistical considerations and gene mapping results Journal:Human Genetics	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
	Tracing the mutations in cystic fibrosis by means of closely linked DNA markers Journal:American Journal of Human Genetics	Tsui, LC	1989
	Differential expression of a basic helix-loop-helix phosphoprotein gene, G0S8, in acute leukemia and localization to human chromosome 1q31 Journal:Leukemia	Wu, HK Heng, HHQ Shi, XM Forsdyke, DR Tsui, LC Mak, TW Minden, MD Siderovski, DP	1995
	Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621 + 1G → T and 711 + 1G → T mutations Journal:Human Molecular Genetics	Zielenski, J Bozon, D Markiewicz, D Aubin, G Simard, F Rommens, JM Tsui, LC	1993
	A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein Journal:Nature	Cutting, GR Kasch, LM Rosenstein, BJ Zielenski, J Tsui, LC Antonarakis, SE Kazazian Jr, HH	1990
	Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA Journal:Science	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
	A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7 Journal:Nature	Knowlton, RG Cohen-Haguenauer, O Nguyen, Van Frezal, J Brown, V Barker, D Braman, JC Schumm, JW Tsui, L-C Buchwald, M Donis-Keller, H	1985
	Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36 Journal:Human Genetics	Shiloh, Y Donlon, T Bruns, G Breitman, ML Tsui, L-C	1986