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Showing results 11 to 27 of 27 < previous

	Title	Author(s)	Issue Date	Views
	HaploShare: identification of extended haplotypes shared by cases and evaluation against controls Journal:Genome Biology (Online Edition)	Ying, D Sham, PC Smith, DK Zhang, L Lau, YL Yang, W	2015	162
	HLAreporter: a tool for HLA typing from next generation sequencing data Journal:Genome Medicine	Huang, Y Yang, J Ying, D Zhang, Y Shotelersuk, V Hirankarn, N Sham, PC Lau, YL Yang, W	2015	93
	Homozygosity mapping on a single patient-identification of homozygous regions of recent common ancestry by using population data Journal:Human Mutation	Zhang, L Yang, W Ying, D Cherny, SS Hildebrandt, F Sham, PC Lau, YL	2011	139
	Homozygous Missense Mutation in ABR Causes Cerebellar Hypoplasia with Early Lethality - A New Condition Identified by Exome Sequencing? Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Ying, D Shek, NWM Chu, WY Yeung, KS Leung, KC Tang, MHY Kan, SYA Chan, YK Chung, BHY	2014	67
	Homozygous missense mutation in ABR causes cerebellar hypoplasia with early lethality: a new condition identified by exome sequencing? Proceeding/Conference:American Journal of Medical Genetics Part A	Ying, D Shek, NWM Chu, YWY Yeung, KS Leung, KC Tang, MHY Kan, ASY Chan, YK Chung, BHY	2015	72
	Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, KC Ying, D Mak, CCY Chen, XY Xu, W Yeung, KS Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Lau, YL Lee, SL Chung, BHY	2016	30
	Identification of a novel homozygous missense mutation in ABR causing cerebellar hypoplasia with early lethality Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, GKC Ying, D Shek, NWM Chu, WY Yeung, KS Tang, MHY Kan, SYA Chan, YK Ip, JKJ Yang, W Lau, YL Chung, BHY	2016	52
	Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism Journal:Molecular Autism	Yeung, KS Tso, WYW Ip, JKJ MAK, CCY Leung, KC TSANG, HY Ying, D Pei, LCS Lee, SL Yang, W Chung, BHY	2017	98
	In-depth cDNA Library Sequencing Provides Quantitative Gene Expression Profiling in Cancer Biomarker Discovery Journal:Genomics, Proteomics and Bioinformatics	Yang, W Ying, D Lau, YL	2009
	Meta-analysis Followed by Replication Identifies Loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as Associated with Systemic Lupus Erythematosus in Asians Journal:The American Journal of Human Genetics	Yang, W Tang, H Zhang, Y Tang, X Zheng, J Sun, L Yang, J Cui, Y Zhang, L Hirankarn, N Cheng, H Pan, HF Gao, J Lee, TL Sheng, Y Lau, WCS Li, Y Chan, TM Yin, X Ying, D Lu, Q Leung, AMH Zuo, X Chen, X Tong, KL Zhou, F Diao, Q Tse, NKC Xie, H Mok, CC Hao, F Wong, SN Shi, B Lee, KW Hui, Y Ho, MHK Liang, B Lee, PPW Cui, H Guo, Q Chung, BHY Pu, X Liu, Q Zhang, X Zhang, C Chong, CY Fang, H Wong, RWS Sun, Y Mok, TMY Li, XP Avihingsanon, Y Zhi, Z Rianthavorn, P Deekajorndej, T Suphapeetiporn, K Gao, F Shotelersuk, V Kang, X Ying, SKY Zhang, L Wong, WHS Zhu, D Fung, SKS Zeng, F Lai, WM Wong, CM Ng, IOL Garcia-Barcelo, MM Cherny, SS Shen, N Tam, PKH Sham, PC Ye, DQ Yang, S Zhang, X Lau, YL	2013	158
	Molecular Diagnosis for Paediatric Genetic Disorders Using Whole Exome Sequencing of the Next Generation Sequencing Technology Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Yang, J Lee, PPW Ying, D Ho, MHK Lee, TL Yang, W Lau, YL	2014
	Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction Journal:Circulation: Genomic and Precision Medicine	Ma, ACH Mak, CCY Yeung, KS Pei, SLC Ying, D YU, MHC Hasan, KMM Chen, X Chow, PC Cheung, YF Chung, BHY	2020
	Novel damaging mutations in CC2D1A suggest a role in human heterotaxy and ciliary dysfunction Proceeding/Conference:American Society of Human Genetics (ASHG) Virtual Meeting, 2020	Chung, BHY Ma, ACH Mak, CCY Yeung, KS Ding, J Pei, LCS Ying, D Chow, PC Yu, HC Hasan, KMM Chen, X Cheung, YF	2020	20
	Policy-Based Primal-Dual Methods for Convex Constrained Markov Decision Processes Proceeding/Conference:The 37th AAAI Conference on Artificial Intelligence, AAAI 2023 (07/02/2023-14/02/2023, , , Washington, USA)	Ying, D Guo, MA Ding, Y Lavaei, J Shen, ZJ	7-Feb-2023
	Prenatal Tobacco Exposure Shortens Telomere Length in Children Journal:Nicotine & Tobacco Research	Ip, P Chung, BHY Ho, FKW Chan, GCF Deng, W Wong, WHS Lee, SL Chan, PYT Ying, D Wong, WL Tung, TS Lau, YL	2017
	PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data Journal:Bioinformatics	Zhang, L Zhang, J Yang, J Ying, D Lau, YL Yang, W	2013
	Three SARS-CoV-2 antibodies provide broad and synergistic neutralization against variants of concern, including Omicron Journal:Cell Reports	Wang, S Sun, H Zhang, Y Yuan, L Wang, Y Zhang, T Wang, S Zhang, J Yu, H Xiong, H Tang, Z Liu, L Huang, Y Chen, X Li, T Ying, D Liu, C Chen, Z Yuan, Q Zhang, J Cheng, T Li, S Guan, Y Zheng, Q Zheng, Z Xia, N	2022

Showing results 11 to 27 of 27 < previous