Tsui, Lap-Chee

Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

Riordan, J. R., Rommens, J. M., Kerem, B.-S., Alon, N., Rozmahel, R., Grzelczak, Z., Zielenski, J., Lok, S., Plavsic, N., Chou, J.-L., et al. (1989) · Science

Cystic Fibrosis Research AdvancesIon Transport and Channel Regulation

Cited by 7,418

Identification of the Cystic Fibrosis Gene: Genetic Analysis

Kerem, B.-S., Rommens, J. M., Buchanan, J. A., Markiewicz, D., Cox, T. K., Chakravarti, A., Buchwald, M., & Tsui, L.-C. (1989) · Science

Cystic Fibrosis Research AdvancesGenetic and Kidney Cyst Diseases

Cited by 4,142

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

Roessler, E., Belloni, E., Gaudenz, K., Jay, P., Berta, P., Scherer, S. W., Tsui, L.-C., & Muenke, M. (1996) · Nature Genetics

Fetal and Pediatric Neurological DisordersHedgehog Signaling Pathway Studies

Cited by 1,152

An embryoprotective role for glucose‐6‐phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis

NICOL, C. J., ZIELENSKI, J., TSUI, L., & WELLS, P. G. (2000) · The FASEB Journal

Neonatal Health and BiochemistryRedox biology and oxidative stress

Cited by 180

A novel missense mutation in the galactosyltransferase‐I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers–Danlos syndrome resembling the progeroid type

Faiyaz‐Ul‐Haque, M., Zaidi, S. H. E., Al‐Ali, M., Al‐Mureikhi, M. S., Kennedy, S., Al‐Thani, G., Tsui, L., & Teebi, A. S. (2004) · American Journal of Medical Genetics Part A

Connective tissue disorders researchGenomics and Rare Diseases

Cited by 111

A Novel Locus of Ectodermal Dysplasia Maps to Chromosome 10q24.32–q25.1

Rafiq, M. A., Faiyaz-ul-Haque, M., Amin ud Din, M., Malik, S., Sohail, M., Anwar, M., Haque, S., Paterson, A. D., Tsui, L.-C., & Ahmad, W. (2005) · Journal of Investigative Dermatology

dental development and anomaliesHair Growth and Disorders

Cited by 10