Huimin Wu

Heterozygosities and allelic frequencies of a set of microsatellite markers used for genome-wide scans in a Chinese population

E. Tan, L. Gan, E. Yap, 2002, Journal of Human Genetics.

Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31

D. Hunt, S. Bhattacharya, V. Vaclavik, 2008, Molecular vision.

Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.

D. Hunt, A. Bird, G. Holder, 2006, American journal of human genetics.

Haplotypes of the β2-adrenergic receptor gene are associated with essential hypertension in a Singaporean Chinese population

P. Munroe, M. Caulfield, E. Yap, 2004, Journal of hypertension.

Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31

D. Hunt, S. Bhattacharya, V. Vaclavik, 2008, Molecular vision.