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	Title	Author(s)	Issue Date	Views
	Patient-specific 3D-pinted helmet for post-craniectomy defect – a case report Journal:3D Printing in Medicine	Pang, SYSFang, EChen, KWLeung, MWYChow, LYVFang, C	2022
	Mitochondrial DHODH regulates hypoxia-inducible factor 1 expression in OTSCC Journal:The American Journal of Cancer Research	Gao, WHu, LZhang, MLiu, SXu, SChow, LYVChan, YWWong, TS	2022
	Long-term results of robotic-assisted nasopharyngectomy for recurrent nasopharyngeal carcinoma Journal:Head and Neck	Tsang, RKYChan, WCHolsinger, FCChung, CKJChow, LYVChan, YWHo, WKWei, WI	2022
	Relevance of the MHC region for breast cancer susceptibility in Asians Journal:Breast Cancer	Ho, PJKhng, AJTan, BKTTan, EYTan, SMTan, VKMLim, GHAronson, KJChan, TLChoi, JYDennis, JHo, WKHou, MFIto, HIwasaki, MJohn, EMKang, DKim, SWKurian, AWKwong, ALophatanaono, AMatsuo, KMohd-Taib, NAMuir, KMurphy, RAPark, SKShen, CYShu, XOTeo, SHWang, QYamaji, TZheng, WBolla, MKDunning, AMEaston, DFPaharoah, PDPHartman, MLi, JM	2022
	How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer? Journal:BMC Medical Genomics	Kwong, AHo, CYSShin, VYAu, CHChan, TLMa, ESK	2022
	Vitamin D enhances hematoma clearance and neurologic recovery in intracerebral hemorrhage Journal:Stroke	LIU, JLI, NZHU, ZKiang, MYKNG, CKADONG, MLeung, GKK	2022
	Germline mutations in Chinese ovarian cancer with or without breast cancer Journal:Molecular Genetics & Genomic Medicine	Kwong, AHo, CYSShin, VYAu, CHLuk, WPFung, LHChan, TLChan, KKLNgan, HYSMa, ESK	2022
	New insights empowered by single-cell sequencing: From neural crest to enteric nervous system Journal:Computational and Structural Biotechnology Journal	LI, ZNgan, ESW	2022
	Transapical transcatheter J-valve for aortic regurgitation in dextrocardia situs inversus (Case Study) Journal:Asian Cardiovascular and Thoracic Annals	Chan, DTLBhatia, ILam, SCCAu, TWK	2022
	Ablating a benign thyroid nodule with an ultrasound-guided high-intensity focused ultrasound ablation device Journal:Video Endocrinology	Lang, HHB	2022
	Gastrostomy tube migration causing gastric outlet obstruction and gastric perforation in children—two case reports Journal:Translational Pediatrics	Wong, CWYChung, HY	2021
	In silico identification of transcription end sites in eukaryotes Journal:International Journal of Pharmacy and Biological Sciences	Sivasankaran Menon, S	2021
	Current understanding in the clinical characteristics and molecular mechanisms in different subtypes of biliary atresia Journal:International Journal of Molecular Sciences	He, LChung, HYLui, VCHTang, SMTam, PKH	2022
	Developing biliary atresia-like model by treating human liver organoids with Polyinosinic:Polycytidylic Acid (Poly (I:C)) Journal:Current Issues in Molecular Biology	Chung, HYBabu, ROWu, ZWong, KKYTam, PKHLui, VCH	2022
	Optimal timing for Soave primary pull-through in short-segment Hirschsprung disease: A meta-analysis Journal:Journal of Pediatric Surgery	Westfal, MLOkiemy, OChung, HYFeng, JLu, CMiyano, GTam, PKHTang, WBWong, KKYYamataka, AGuyer, RADoody, DPGoldstein, AM	2022
	Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors Journal:JCI Insight	Tang, SMMononen, MLam, WYJin, SCZHUANG, XGarcia-Barcelo, MMLin, QYang, YSahara, MEroglu, EChien, KRHong, HTam, PKHGruber, PJ	2022
	BACE2 variant identified from HSCR patient causes AD-like phenotypes in hPSC-derived brain organoids Journal:Cell Death Discovery	Luo, JZou, HGuo, YHuang, KNgan, ESWLi, P	2022
	Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese Journal:npj Genomic Medicine	Chau, FTJYU, HCChui, MCMYeung, CCWKwok, AWCZHUANG, XLee, RFung, LFLEE, MMak, CCYNg, YTNChung, CYChung, CYTSANG, HYChan, JCKChan, YKKan, ASYChung, HYYang, WLee, SLChan, GCFTam, PKHLau, YLYeung, KSChung, BHYTang, SM	2022	1
	Statistical approach for predicting genome architecture and the major challenges Journal:World Journal of Advanced Research and Reviews	Sivasankaran Menon, SLui, VCHTam, PKH	2022
	Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases Journal:Nucleic Acids Research	Jiang, LJiang, HDai, SChen, YSong, YTang, SMPang, SYYHo, SLWang, BGarcia-Barcelo, MMTam, PKHCherny, SSLi, MJSham, PCLi, M	2022