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Title	Author(s)	Issue Date
A 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations Book:Biochemistry and Molecular Biology: The Complexity of Human Traits and Diseases	Baum, L Guo, Y Gui, H Sham, PC Cherny, SS Kwan, P	2015
Association of BDNF Polymorphisms with the Risk of Epilepsy: a Multicenter Study Journal:Molecular Neurobiology	Sha'ari, HM Haerian, BS Baum, L Tan, HJ Rafia, MH Kwan, P Cherny, SS Sham, PC GUI, H Raymond, AA Lim, KS Mohamed, Z	2016
Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset Journal:BMC Research Notes	Gui, H Li, M Sham, PC Cherny, SS	2011
Comprehensive comparison of copy number variations detection using Illumina Omni 2.5M and Affymetrix CytoScan® arrays Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Tang, SM Wong, EHM Gui, H Cherny, SS Sham, PC Tam, PKH Garcia-Barcelo, MM	2013
Correction of Hirschsprung-Associated Mutations in Human Induced Pluripotent Stem Cells Via Clustered Regularly Interspaced Short Palindromic Repeats/Cas9, Restores Neural Crest Cell Function Journal:Gastroenterology	Lai, FPL Lau, CST Wong, JKL Gui, H Wang, X Zhou, T Lai, KWH Tse, HF Tam, PKH Garcia-Barcelo, MM Ngan, ESW	2017
Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease Journal:Scientific Reports	Luzon-Toro, B GUI, H Ruiz-Ferrer, M Tang, SM Fernandez, RM Sham, PC Torroglosa, A Tam, PKH Espino-Paisan, L Cherny, SS Bleda, M Enguix-Riego, MDV Dopazo, J Antinolo, G Garcia-Barcelo, MM Borrego, S	2015
Exonic de novo mutations in sporadic Hirschsprung disease Proceeding/Conference:European Journal of Human Genetics	Hofstra, RMW Gui, H Schriemer, D Griseri, P Pelet, A Ruiz-Ferrer, M Berrios, C van Ijcken, W van den Hout, M Tam, PKH Cheng, W Tang, SM Eggen, BJL Matera, I Ceccherini, I Amiel, J Lyonnet, S Antinolo, G Borrego, S Chakravarti, A Garcia-Barcelo, MM	2014
Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population Journal:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics	Gui, H Li, M Sham, PC Baum, LW International League Against Epilepsy Consortium on Complex Epilepsies Kwan, P Cherny, SS	2018
Genome-wide gene-set analysis identifies different patterns of genetic sharing across complex phenotypes Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2015	Gui, H Kwan, J Sham, PC Cherny, SS Li, M	2015
A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits Journal:PLoS ONE	Guo, Y Tomlinson, B Chu, T Fang, YJ Gui, H Tang, CSM Yip, BH Cherny, SS Hur, YM Sham, PC Lam, TH Thomas, NG	2012
Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Cherny, SS Gui, H Xu, L Sham, PC Jiang, CQ Lam, TH Liu, B Jin, YL Zhu, T Zhang, WS Thomas, GN Cheng, KK	2013
Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study Journal:Neurobiology of Aging	Gui, H Jiang, C Cherny, SS Sham, PC Xu, L Liu, B Jin, YL Zhu, T Zhang, W Thomas, GN Cheng, KK Lam, TH	2014
Integrative genomic profile for a patient with Hirschsprung disease Proceeding/Conference:Conference of the International Rare Diseases Research Consortium, IRDiRC 2014	Gui, H Tang, SM Tam, PKH Garcia-Barcelo, MM	2014
Patterns and rates of exonic de novo mutations in sporadic Hirschsprung disease patients Proceeding/Conference:European Journal of Human Genetics	Gui, H Schriemer, D Eggen, BJL Hofstra, RMW van Ijcken, W van den Hout, M Griseri, P Matera, I Ceccherini, I Pelet, A Amiel, J Lyonnet, S Garcia-Barcelo, M Tam, PKH Ruiz-Ferrer, M Antinolo, G Borrego, S Berrios, C Chakravarti, A	2013
Patterns of epilepsy-schizophrenia genetic correlation and sharing revealed by secondary analyses of GWAS data Proceeding/Conference:Asian & Oceanian Epilepsy Congress, AOEC 2016	Gui, H Li, M Baum, L Kwan, P Cherny, SS	2016
Perturbed SUFU-GLI-SOX10 regulatory network underlies defective enteric nervous system development and Hirschsprung disease Proceeding/Conference:International Symposium on ENS Meeting	Ngan, E Liu, AJ Lai, PL Gui, H Sham, MH Garcia-Barcelo, MM Hui, CC	2015
Prenatal immune activation alters the adult neural epigenome but can be partly stabilised by a n-3 polyunsaturated fatty acid diet Journal:Translational Psychiatry	Basil, P Li, Q Gui, H Hui, TCK Ling, HM Wong, CY Mill, J McAlonan, GM Sham, PC	2018
Rare and common variants in sporadic Hirschsprung disease patients	Tang, SM Gui, H Garcia-Barcelo, MM HSCR, CONSORTIUM	2015
Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations Journal:Journal of Pediatric Surgery	Ngo, DN So, MT Gui, H Tran, AQ Bui, DH Cherny, S Tam, PKH Nguyen, TL Garcia-Barcelo, MM	2012
SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese Journal:The Pharmacogenomics Journal	Gui, H Kwok, M Baum, LW Sham, PC Kwan, P Cherny, SS	2018

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