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Showing results 278 to 286 of 286 < previous

	Title	Author(s)	Issue Date	Views
	UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population Journal:BioMed Research International	Wisnumurti, DW Sribudiani, YS Porsch, RM Maskoen, AM Rahayuningsih, LA Rahayuningsih, SR Asni, EA Sleutels, FS Kockx, CK van Ijcken, WI Sukadi, AS Achmad, TA	2018	90
	Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals Journal:The American Journal of Human Genetics	Baum, LW Sham, PC Epi25 Collaborative,	2019	68
	Uncovering Resistant Genes in EGFR-mutated Lung Adenocarcinomas Prior to Targeted Therapy Proceeding/Conference:Health Research Symposium 2017	Gao, X Xu, H Ho, JCM Chan, SH Sham, PC Xiao, Z Xu, F Tin, VPC Lee, VHF Au, JSK Wang, J Wang, S Yam, JWP Wong, MP	2017	106
	Understanding the genetic contribution to endogenous self-protective potentials of intervertebral disc Proceeding/Conference:Gordon-Kenan Research Seminar on Cartilage Biology & Pathology (GRS)	Xiong, C Li, Y Muhammad, FR Sandell, L Chan, WCW Tam, V Zhang, Y Song, Y Cheah, KSE Sham, PC Chan, D	2015	46
	Validation of association signals identified from genome-wide association studies of diabetic retinopathy in Chinese patients with type 2 diabetes Proceeding/Conference:13th International Symposium on Healthy Aging, Hong Kong	NG, KK Lee, CHP Woo, YC Chow, WS Wong, LC Fong, HY Xu, A Sham, PC Lam, KSL Cheung, YY	2018	99
	Validation, and refinement of a RUNX1 mutation-associated gene expression signature in blast crisis chronic myeloid leukemia Journal:Leukemia	Lee, KL Ko, TK Saw, YL Javed, A Hillmer, AM Chuah, C Krishnan, V Ong, ST	2022
	Whole Exome Sequencing versus Target Gene Panels for Evaluation of Isolated CaseProbands with Dilated and Hypertrophic Cardiomyopathy Journal:Heart Rhythm	Mak, SHT Lee, YK Tang, SM Hai, SHJJ Ran, X Sham, PC Tse, HF	2017	73
	wKGGSeq: A Comprehensive Strategy-Based and Disease-Targeted Online Framework to Facilitate Exome Sequencing Studies of Inherited Disorders Journal:Human Mutation	Li, MJ Deng, SJ Wang, P Yang, W Ho, SL Sham, PC Wang, JJ Li, M	2015	85
	X-linked tspyi2deficit mouse is associated with a phenotype of schizophrenia Proceeding/Conference:Schizophrenia Research	Li, Q Wong, KK Wei, R Lam, SSY Zhang, X Sham, PC Chua, SE Chan, SY McAlonan, GM	2012	164

Showing results 278 to 286 of 286 < previous