Brian H.Y. Chung
Brian H.Y. Chung
The University of Hong Kong, Department of Paediatrics & Adolescent Medicine
Verified email at - Homepage
Cited by
Cited by
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...
Cell 180 (3), 568-584. e23, 2020
Genome-Wide Association Study in Asian Populations Identifies Variants in ETS1 and WDFY4 Associated with Systemic Lupus Erythematosus
W Yang, N Shen, DQ Ye, Q Liu, Y Zhang, XX Qian, N Hirankarn, D Ying, ...
PLoS genetics 6 (2), e1000841, 2010
Phenotypic Spectrum Associated with De Novo and Inherited Deletions and Duplications at 16p11.2 in Individuals Ascertained for Diagnosis of Autism Spectrum Disorder
Journal of Medical Genetics 47, 195-203, 2010
Practical guidelines for managing adults with 22q11. 2 deletion syndrome
WLA Fung, NJ Butcher, G Costain, DM Andrade, E Boot, EWC Chow, ...
Genetics in Medicine 17 (8), 599-609, 2015
Autism spectrum disorders and epigenetics
D Grafodatskaya, B Chung, P Szatmari, R Weksberg
Journal of the American Academy of Child & Adolescent Psychiatry 49 (8), 794-809, 2010
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
ET Lim, M Uddin, S De Rubeis, Y Chan, AS Kamumbu, X Zhang, ...
Nature neuroscience 20 (9), 1217-1224, 2017
Pediatric stroke among hong kong chinese subjects
B Chung, V Wong
Pediatrics 114 (2), e206-e212, 2004
Association of MTOR mutations with developmental brain disorders, including megalencephaly, focal cortical dysplasia, and pigmentary mosaicism
GM Mirzaa, CD Campbell, N Solovieff, CP Goold, LA Jansen, S Menon, ...
JAMA neurology 73 (7), 836-845, 2016
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians
W Yang, H Tang, Y Zhang, X Tang, J Zhang, L Sun, J Yang, Y Cui, ...
The American Journal of Human Genetics 92 (1), 41-51, 2013
A modified screening tool for autism (Checklist for Autism in Toddlers [CHAT-23]) for Chinese children
V Wong, LHS Hui, WC Lee, LSJ Leung, PKP Ho, WLC Lau, CW Fung, ...
Pediatrics 114 (2), e166-e176, 2004
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ...
Nature genetics 54 (9), 1320-1331, 2022
Spinal muscular atrophy: survival pattern and functional status
BHY Chung, VCN Wong, P Ip
Pediatrics 114 (5), e548-e553, 2004
Relationship between five common viruses and febrile seizure in children
B Chung, V Wong
Archives of disease in childhood 92 (7), 589-593, 2007
NSD1 mutations generate a genome-wide DNA methylation signature
S Choufani, C Cytrynbaum, BHY Chung, AL Turinsky, D Grafodatskaya, ...
Nature communications 6 (1), 10207, 2015
GRIN2A-related disorders: genotype and functional consequence predict phenotype
V Strehlow, HO Heyne, DRM Vlaskamp, KFM Marwick, G Rudolf, ...
Brain 142 (1), 80-92, 2019
Neuroimaging in stroke recovery: a position paper from the First International Workshop on Neuroimaging and Stroke Recovery
H Christensen, L Derex, JB Pialat, M Wiart, N Nighoghossian, M Hermier, ...
Cerebrovascular diseases 18 (3), 260-267, 2004
Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development
AL Lennox, ML Hoye, R Jiang, BL Johnson-Kerner, LA Suit, ...
Neuron 106 (3), 404-420. e8, 2020
Recessive gene disruptions in autism spectrum disorder
RN Doan, ET Lim, S De Rubeis, C Betancur, DJ Cutler, AG Chiocchetti, ...
Nature genetics 51 (7), 1092-1098, 2019
22q11. 2 deletion syndrome in diverse populations
P Kruszka, YA Addissie, DE McGinn, AR Porras, E Biggs, M Share, ...
American Journal of Medical Genetics Part A 173 (4), 879-888, 2017
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