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Showing results 1 to 14 of 14

	Title	Author(s)	Issue Date	Views
	A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway Journal:Molecular Human Reproduction	Li, L Zhou, X Wang, X Wang, J Zhang, W Wang, B Cao, Y Kee, K	2016	136
	A Practical Guide for Mapping Short Reads Book:Deep Sequencing Data Analysis	Zhou, X Bao, S Wang, B Zhang, X Song, Y	2013
	A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population Journal:Neurobiology of Aging	Wang, B Bao, S ZHANG, Z ZHOU, X WANG, J Fan, Y Zhang, Y Li, Y Chen, LP Jia, Y LI, J Li, M Zheng, W Mu, N Yang, W Yu, Z Lau, DSS Wong, SM ZHANG, Y Kwan, JSK Mak, HKF Ambalavanan, A Zhou, S Cai, W Zheng, J Huang, S Rouleau, GA Yang, W Rogaeva, E Ma, X St George-Hyslop, P Chu, LW Song, Y	2018	46
	Cell Culture System for Analysis of Genetic Heterogeneity Within Hepatocellular Carcinomas and Response to Pharmacologic Agents Journal:Gastroenterology	Gao, Q Wang, Z Duan, M Lin, Y Zhou, X Worthley, DL Wang, X Niu, G Xia, Y Deng, M Liu, L Shi, J Yang, L Zhang, S Ding, Z Zhou, J Liang, C Cao, Y Xiong, L Xi, R Shi, Y Fan, J	2017	140
	CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens Journal:Scientific Reports	Wang, B Ji, T Zhou, X Wang, J Wang, X Wang, JM Zhu, D Zhang, XJ Sham, PC Zhang, XG Ma, X Jiang, Y	2016	111
	Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy Journal:Scientific Reports	Chen, H Zhou, X Wang, J Wang, X Liu, L Wu, S Li, T Chen, S Yang, J Sham, PC Zhu, G Zhang, X Wang, B	2016	77
	Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family Journal:Annals of Human Genetics	Cheng, J Zhou, X Lu, Y Chen, J Han, B Zhu, Y Liu, Y Choy, KW Sham, PC Zhang, MQ Zhang, X Yuan, H Yuan, H	2014
	Hnrnpa1 Mutations Cause Congenital Heart Defects Proceeding/Conference:Hong Kong Inter-University Postgraduate Symposium in Biochemical Sciences, 2017	Yu, Z Tang, PLF Wang, J Bao, S Shieh, JT Leung, AWL Zhang, Z Gao, F Wong, SYY Hui, ALC Gao, Y Dung, NWF Zhang, ZG Fan, Y Zhou, X Zhang, Y Wong, DSM Sham, PC Azhar, A Kwok, PY Tam, PPL Lian, Q Cheah, KSE Wang, B Song, Y	2017	213
	Integrated analysis of mRNA-seq and miRNA-seq for host susceptibilities to influenza A (H7N9) infection in inbred mouse lines Journal:Functional & Integrative Genomics	Bao, S Jia, L Zhou, X ZHANG, Z Wu, WL Yu, Z NG, GCT Fan, Y Wong, SM Huang, S To, KKW Yuen, KY Yeung, ML Song, Y	2018
	Polygenic scores via penalized regression on summary statistics Journal:Genetic Epidemiology	Mak, SHT Porsch, RM Choi, SW Zhou, X Sham, PC	2017	107
	Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort Journal:Molecular Psychiatry	Toulopoulou, T Haren, NV Zhou, X Sham, PC Cherny, SS Campbell, DD Picchioni, M Murray, R Boomsma, DI Pol, HH	2015	84
	Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches. Journal:Journal of Human Genetics	Yu, L Zhou, X Jin, Z Cheng, J Shen, W Ji, F Liui, L Zhang, X Zhang, MQ Cao, Y Han, D Choy, KW Yuan, H	2014
	Systematic Characterization and Prediction of Post-Translational Modification Cross-Talk Journal:Molecular and Cellular Proteomics	Huang, Y Xu, B Zhou, X Li, Y Lu, M Jiang, R Li, T	2015
	Trans-ethnic polygenic analysis supports genetic overlaps of lumbar disc degeneration with height, body mass index, and bone mineral density Journal:Frontiers in Genetics	Zhou, X Cheung, CL Karasugi, T Karppinen, J Samartzis, D Hsu, YH Mak, SHT Song, Y Chiba, K Kawaguchi, Y LI, Y Chan, D Cheung, KMC Ikegawa, S Cheah, KSE Sham, PC	2018	104

Showing results 1 to 14 of 14