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	Title	Author(s)	Issue Date	Views
	Cost effective assay choice for rare disease study designs Proceeding/Conference:Human Heredity	Campbell, DD Porsch, RM Cherny, SS Capra, V Merello, E De Marco, P Sham, PC Garcia-Barcelo, MM	2015	70
	Cost effective assay choice for rare disease study designs Journal:Orphanet Journal of Rare Diseases	Campbell, DD PORSCH, RM Cherny, SS Capra, V Merello, E De Marco, P Sham, PC Garcia-Barcelo, MM	2015	84
	De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca Journal:Human Molecular Genetics	HSU, SJ So, MT Tang, SM Karim, A Porsch, RM Wong, CWY Yu, MON Yeung, F Xia, H ZHANG, R Cherny, SS Chung, HY Wong, KKY Sham, PC Ngo, ND Li, M Tam, PKH Lui, VCH Garcia-Barcelo, MM	2018	138
	Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese Journal:Nature Communications	Tang, CS Zhang, H Cheung, YY Xu, M Ho, JCY Zhou, W Cherny, SS Zhang, Y Holmen, O Au, KW Yu, H Xu, L Jia, J PORSCH, RM Sun, L Xu, W Zheng, H Wong, LY Mu, Y Dou, J Fong, HY Wang, S Hong, X Dong, L Liao, Y Wang, J Lam, SML Su, X Yan, H Yang, ML Chen, J Siu, DCW Xie, G Woo, YC Wu, Y Tan, KCB Hveem, K Cheung, BMY Zöllner, S Xu, A Eugene Chen, Y Jiamg, CQ Jiang, Y Lam, TH Ganesh, SK Huo, Y Sham, PC Lam, KSL Willer, CJ Tse, HF Gao, W	2015	165
	KS-Burden: Assessing distributional differences of rare variants in dichotomous traits	Porsch, RM Mak, SHT Tang, C Sham, PC	2018	96
	Longitudinal heritability of childhood aggression Journal:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics	PORSCH, RM Middeldorp, CM Cherny, SS Krapohl, E van Beijsterveldt, CEM Luokola, A Korhonen, T Pulkkinen, L Corley, R Rhee, S Kaprio, J Rose, RR Hewitt, JK Sham, PC Plomin, R Boomsma, DI Barteis, M	2016	65
	De novo mutations associated with sporadic cases of Caudal regresion syndrome Proceeding/Conference:European Journal of Human Genetics	Porsch, RM Merello, E De Marco, P So, MT Sham, PC Tam, PKH Cherny, SS Capra, V Garcia-Barcelo, MM Campbell, DD	2014	71
	Polygenic scores via penalized regression on summary statistics Journal:Genetic Epidemiology	Mak, SHT Porsch, RM Choi, SW Zhou, X Sham, PC	2017	107
	Sacral agenesis: a pilot whole exome sequencing and copy number study Journal:BMC Medical Genetics	Porsch, RM Merello, E De Marco, P Cheng, G Rodriguez, L So, MT Sham, PC Tam, PKH Capra, V Cherny, SS Garcia-Barcelo, MM Campbell, DD	2016	57
	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

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