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Showing results 1 to 18 of 18

	Title	Author(s)	Issue Date
	Analysis of shared heritability in common disorders of the brain Journal:Science	Baum, LW	2018
	Association Between the Apolipoprotein E Gene Polymorphism and Atherosclerotic Middle Cerebral Artery Stenosis Journal:The Neurologist	Baum, LW	2018
	Effects of Deferasirox in Alzheimer’s Disease and Tauopathy Animal Models Journal:Biomolecules	Kwan, P Ho, A Baum, LW	2022
	Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects Journal:Brain	Niestroj, LM Perez-Palma, E Howrigan, DP Zhou, Y Cheng, F Saarentaus, E Nürnberg, P Stevelink, R Daly, MJ Palotie, A Lal, D Baum, LW Sham, PC The Epi25 Collaborative	2020
	Exome sequencing of mesial temporal lobe epilepsy with hippocampal sclerosis in parent-offspring trios Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2015	Cherny, SS Wong, KL Sham, PC Baum, LW Kwan, P	2015
	Exome sequencing of mesial temporal lobe epilepsy with hippocampal sclerosis in parent-offspring trios Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2014	Cherny, SS Wong, JKL Sham, PC Baum, LW Kwan, P	2014
	Genetic association studies Proceeding/Conference:Invited Lecture, Affiliated Hospital of Jining Medical University	Baum, LW	2018
	Genetic association studies Proceeding/Conference:2019 International Symposium of Ophthalmology (ISO), Shantou, China	Baum, LW	2019
	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
	Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients Journal:Neurology	Baum, LW	2018
	Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti‐seizure medications Journal:Epilepsia	Mullan, KA Anderson, A Shi, YW Ding, JH Ng, CC Chen, Z Baum, LW Cherny, SS Petrovski, S Sham, PC Lim, KS Liao, WP Kwan, P	2022
	Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis Journal:Neurology Genetics	Baum, LW	2018
	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
	SNP-based HLA tagging, imputation, and association in adverse drug reaction of epilepsy patients from Hong Kong Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2015	Cherny, SS Gui, H Kwok, M Sham, PC Baum, LW Kwan, P	2015
	Systemic neuro-dysregulation in depression: Evidence from genome-wide association Journal:European Neuropsychopharmacology	TUBBS, JD DING, J Baum, LW Sham, PC	2020
	Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese Journal:Human Molecular Genetics	Guo, Y Baum, LW Sham, PC Wong, V Ng, PW Lui, CHT Sin, NC Tsoi, TH Tang, CSM Kwan, JSH Yip, BHK Xiao, SM Thomas, GN Lau, YL Yang, W Cherny, SS Kwan, P	2012
	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
	Whole genome sequencing identified novel common risk and protective variants of antiseizure medication-induced Stevens-Johnson syndrome in Han Chinese Proceeding/Conference:41st Lorne Genome Conference	Mullan, K Anderson, A Mifsud, NA Illing, PT Purcell, AW Baum, LW Cherny, S Ng, CC Shi, YW Petrovski, S Sham, PC Lim, KS Liao, WP Kwap, P	2020

Showing results 1 to 18 of 18