中大職務
- 醫學院副院長 (發展)
- 化學病理學系教授
- 李嘉誠健康科學研究所教授
專業範疇
- 化學病理學
- 分子診斷學
- 分子病理學
- 遺傳學
- 基因組學
教育及資歷
MBBS(Qld), PhD(CUHK), FRCPA, FHKCPath, FHKAM (Pathology), FRCPA
專注研究
- 發展非侵入性產前診斷方法
- 發展非侵入性癌症診斷方法
- 循環核酸分析的臨床應用
- 了解循環核酸的特性
- 發展創新的分子診斷策略和分子分析工具
更多資訊
專業服務
- 國際產前診斷學會董事會秘書
- 國際產前診斷學會董事
- Clinical Chemistry 副編輯
- Prenatal Diagnosis 編輯委員會成員
- Clinical Biochemistry 編輯委員會成員
- Clinical Chemistry and Laboratory Medicine 編輯委員會成員
中大教學職務
- 內外全科醫學士課程環球醫學領袖培訓專修組別(MBChB-GPS)導師
- 醫學教育處統籌委員會成員
部分論文 (只有英文版本)
- Hudecova I, Jiang P, Davies J, Lo YMD, Kadir RA, Chiu RWK (2017).Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers. Blood 130:340-7.
- Hui WW, Jiang P, Tong YK, Lee WS, Cheng YK, New MI, Kadir RA, Chan KCA, Leung TY, Lo YMD and Chiu RWK (2017). Universal haplotype-based noninvasive prenatal testing for single gene diseases. Clin Chem 63: 513-24.
- Benn P, Borrell A, Chiu RWK, Cuckle H, Dugoff L, Faas B, Gross S, Huang T, Johnson J, Maymon R, Norton M, Odibo A, Schielen P, Spencer K, Wright D and Yaron Y (2015). Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis. Prenat Diagn 35: 725-34.
- Yu SCYJ, Chan KCA, Zheng YW, Jiang P, Liao GJW, Sun H, Akolekar R, Leung TY, Go AT, van Vugt JM, Minekawa R, Oudejans CBM, Nicolaides KH, Chiu RWK, Lo YMD (2014). Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing. Proc Natl Acad Sci U S A 111, 8583-8.
- *Lun FMF, *Chiu RWK, Sun K, Leung TY, Jiang P, Chan KCA, Sun H and Lo YMD (2013). Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA. Clin Chem. 59, 1583-94 (*Equal first authors).
- Yu SCYJ, Jiang P, Choy KW, Chan KCA, Won HS, Leung WC, Lau ET, Tang MH, Leung TY, Lo YMD and Chiu RWK (2013). Noninvasive prenatal molecular karyotyping from maternal plasma. PLoS One 8, e60968
- Chiu RWK, Akolekar R, Zheng YW, Leung TY, Sun H, Chan KCA, Lun FMF, Go AT, Lau ET, To WW, Leung WC, Tang RY, Au-Yeung SK, Lam H, Kung YY, Zhang X, van Vugt JM, Minekawa R, Tang MH, Wang J, Oudejans CB, Lau TK, Nicolaides KH, Lo YMD (2011). Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study. BMJ 342, c7401.
- Lo YMD, Chan KCA, Sun H, Chen EZ, Jiang P, Lun FMF, Zheng YW, Leung TY, Lau TK, Cantor CR, Chiu RWK (2010). Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus. Sci Transl Med 2, 61ra91.
- Chiu RWK, Chan KCA, Gao Y, Lau VYM, Zheng W, Leung TY, Foo CH, Xie B, Tsui NBY, Lun FMF, Zee BC, Lau TK, Cantor CR, Lo YMD (2008). Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma. Proc Natl Acad Sci U S A 105, 20458-63.
- Chiu RWK, Lau TK, Leung TN, Chow KCK, Chui DHK and Lo YMD (2002). Prenatal exclusion of beta thalassaemia major by examination of maternal plasma. Lancet 360, 998-1000.