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	Title	Author(s)	Issue Date
	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
	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
	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
	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
	KS-Burden: Assessing distributional differences of rare variants in dichotomous traits	Porsch, RM Mak, SHT Tang, C Sham, PC	2018
	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
	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
	Polygenic scores via penalized regression on summary statistics Journal:Genetic Epidemiology	Mak, SHT Porsch, RM Choi, SW Zhou, X Sham, PC	2017
	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
	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

Showing results 1 to 10 of 10