Current Position:
Research Assistant Professor
(appointed jointly by Dept of Paed and Dept of O&G)



1Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders
Szot JO, Campagnolo C, Cao Y, Iyer KR, Cuny H, Drysdale T, Flores-Daboub JA, Bi W, Westerfield L, Liu P, Leung TN, Choy KW, Chapman G, Xiao R, Siu VM, Dunwoodie SL
Am J Hum Genet. 2020 Jan 2;106(1):129-136
2Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis
Chau MHK, Cao Y, Kwok YKY, Chan S, Chan YM, Wang H, Yang Z, Wong HK, Leung TY, Choy KW
American Journal of Obstetrics and Gynecology 2019;221(5):493e1-e11.
3Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage
Dong Z, Yan J, Xu F, Yuan J, Jiang H, Wang H, Chen H, Zhang L, Ye L, Xu J, Shi Y, Yang Z, Cao Y, Chen L, Li Q, Zhao X, Li J, Chen A, Zhang W, Wong HG, Qin Y, Zhao H, Chen Y, Li P, Ma T, Wang WJ, Kwok YK, Jiang Y, Pursley AN, Chung JPW, Hong Yan, Kristiansen K, Yang H, PiƱa-Aguilar RE, Leung TY, Cheung SW, Morton CC, Choy KW, Chen ZJ
Am J Hum Genet. 2019 Dec 5;105(6):1102-1111
4Prenatal detection of 10q22q23 duplications: dilemmas in phenotype prediction
Kong Grace Wing Shan, Cao Ye, Huang Jin, Cheng Kwun Yue, Pursley Amber Nolen, Rosenfeld Jill Anne, Edwards Janice G., Chan Yiu Man, Cheung Sau Wai, Leung Tak Yeung, Choy Kwong Wai
Prenat Diagn. 2016 Dec;36(13):1211-1216
5SNaPshot Reveals High Mutation and Carrier Frequencies of 15 Common Hearing Loss Mutants in a Chinese Newborn Cohort.
Chen Y, Cao Ye, Li HB, Mao J, Liu MJ, Liu YH, Wang BJ, Jiang D, Zhu Q, Ding Y, Wang W, Li H, Choy KW
Clin Genet 2015;87(5): 467 - 472