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Showing results 7 to 18 of 18 < previous

	Title	Author(s)	Issue Date	Views
	Genetic association studies Proceeding/Conference:2019 International Symposium of Ophthalmology (ISO), Shantou, China	Baum, LW	2019
	Genetic association studies Proceeding/Conference:Invited Lecture, Affiliated Hospital of Jining Medical University	Baum, LW	2018	11
	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	51
	Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients Journal:Neurology	Baum, LW	2018	67
	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	60
	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	87
	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	168
	Systemic neuro-dysregulation in depression: Evidence from genome-wide association Journal:European Neuropsychopharmacology	TUBBS, JD DING, J Baum, LW Sham, PC	2020	35
	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	208
	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
	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 7 to 18 of 18 < previous