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Title	Author(s)	Issue Date
A significant inflation in TGM6 genetic risk casts doubt in its causation in spinocerebellar ataxia type 35 Journal:Parkinsonism & Related Disorders	Fung, LF TSANG, HY Leung, KC Yeung, KS MAK, CCY Fung, CW Chan, HSS YU, HC Chung, BHY	2019
ACBP4 and ACBP5, novel Arabidopsis acyl-CoA-binding proteins with kelch motifs that bind oleoyl-CoA Journal:Plant Molecular Biology	Leung, KC Li, HY Mishra, G Chye, ML	2004
Adiponectin isoform distribution in women-relationship to female sex steroids and insulin sensitivity Journal:Metabolism: Clinical and Experimental	Leung, KC Xu, A Craig, ME Martin, A Lam, KSL O'sullivan, AJ	2009
Aggregation-based QoS routing in the internet Journal:Journal of Communications	Hou, R Leung, KC Lui, KS Leung, KC Baker, F	2010
An Emission Line Analysis of MASH Galactic PNe Proceeding/Conference:The 8th Pacific Rim Conference on Stellar Astrophysics: A Tribute to Kam-Ching Leung ASP Conference Series	Kovacevic, A Parker, QA Komonjinda, S Cheng, KS Leung, KC Editor(s):Soonthornthum, B	2008
Application of whole exome sequencing in neuromuscular disorders patients in Hong Kong Proceeding/Conference:2nd Joint Annual Research & Scientific Meeting 2018 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association and Hong Kong College of Paediatric Nursing	TSANG, HY Kwong, BMH Pei, LCS Leung, KC Yeung, KS MAK, CCY YU, HC Fung, LF Liang, R Chung, BHY Chan, HSS	2018
The Application of Whole-Exome Sequencing in Diagnosis Pediatric Rare Disease in Hong Kong Journal:North American Journal of Medicine and Science	Mak, CCY Ying, D LEUNG, KC Lee, PPW Yang, J Yang, W Chung, BHY Lau, YL	2014
Arabidopsis ACBP3 is an extracellularly targeted acyl-CoA-binding protein Journal:Planta	Leung, KC Li, HY Xiao, S Tse, MH Chye, ML	2006
Before and after – Nutritional transformation of dysmorphism in a case of Costello syndrome Journal:European Journal of Medical Genetics	Chiu, TA Zhu, L Mok, TKG LEUNG, KC Chow, CB Chung, BHY	2016
BRCA mutation testing for ovarian cancer in the context of available targeted therapy: Survey and consensus of Hong Kong specialists Journal:Asia-Pacific Journal of Clinical Oncology	Kwong, A Cheng, DKL Hsue, CC Hui, SK Leung, RCY Leung, KC Ngan, KCR Soong, SI	2019
CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis Journal:Molecular Genetics & Genomic Medicine	LEUNG, KC Ying, D MAK, CCY Chen, XY Xu, W YEUNG, KS Wong, WL Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Sham, PC Lau, YL Chung, BHY Lee, SL	2017
CFTR: I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with cystic fibrosis Proceeding/Conference:Annual Scientific Meeting of the Hong Kong College of Paediatricians, HKCPaed 2014	Leung, KC Mak, CCY Chen, YX Chau, CSK Ying, D Chu, WY Li, AM Yang, W Lau, YL Chan, KYK Chen, JH Lee, SL Chung, BHY	2014
CFTR: p.I1023R is a rare but recurrent disease-causing mutation found in Chinese patients with Cystic Fibrosis Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2014	Chung, BHY Leung, KC Mak, CCY Chow, CSK Ying, JD Chu, YWY Yang, WL Lau, YL Chan, KYK Lee, SL	2014
Chinese patients with rasopathies: Detection of 29 known and novel variants using next-generation sequencing (NGS) Proceeding/Conference:36th Annual David W. Smith Workshop	Leung, KC Lo, I Luk, HM Tang, HMV Gao, W Wong, WL Chu, WY Lam, STS Ma, CH Jin, D Chan, YK Chung, BHY	2015
Contribution of gain-of-function mutations in R1T1 to the pathogenesis of Noonan syndrome: a report of 3 new Chinese patients in Hong Kong Proceeding/Conference:HKU Department of Paediatrics & Adolescent Medicine Golden Jubilee Scientific Meeting	Leung, KC Ma, CH Gao, W Chu, WY Wong, WL Jin, D Lo, IFM Luk, HM Chung, BHY	2014
Cyclometallated Gold(III) Complexes as Effective Catalysts for Synthesis of Propargylic Amines, Chiral Allenes and Isoxazoles Journal:Advanced Synthesis & Catalysis	Kung, KKY Lo, VKY Ko, HM Li, GL Chan, PY Leung, KC Zhou, Z Wang, M Che, CM Wong, MK	2013
De novo C-terminal truncating mutations in MN1 cause a neurodevelopmental syndrome with distinctive facial features Proceeding/Conference:European Human Genetics Conference, 2019	Gordon, CT Leung, KC Mak, CCY Doherty, D Lin, A Vegas, N Cho, M Dimartino, C Weisfeld-Adams, J Lessel, D Joss, S Li, C Gonzaga-Jauregui, C Zarate, Y Troyer, C Kant, S Leung, G Barone, A Yang, S Bend, E Roadhouse, C Zahir, F Stolerman, E Bienvenu, T Orenstein, N Dobyns, W Shieh, J Waggoner, D Gripp, K Parker, M Stoler, J Lyonnet, S Cormiere-Daire, V Viskochil, D Hoffman, T Amiel, J Chung, BHY	2019
De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients Journal:npj Genomic Medicine	MAK, CCY Chow, PC Liu, APY Chan, YK Chu, WY Mok, TKG LEUNG, KC YEUNG, KS Chau, AKT Lowther, C Scherer, SW Marshall, CR Bassett, AS Chung, BHY	2016
Dynamic discriminant functions with missing feature values Journal:Pattern Recognition Letters	Leung, KC Leung, CH	2013
Effectiveness of brachytherapy and fractionated stereotactic radiotherapy boost for persistent nasopharyngeal carcinoma Journal:Head Neck	Yau, TK Sze, WM Lee, WMA Yeung, MW Leung, KC Hung, WM Chan, WI	2004

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