Brian H.Y. Chung
Brian H.Y. Chung
The University of Hong Kong, Department of Paediatrics & Adolescent Medicine
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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
BA Fernandez, W Roberts, B Chung, R Weksberg, S Meyn, P Szatmari, ...
Journal of medical genetics 47 (3), 195-203, 2010
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
Pediatric stroke among hong kong chinese subjects
B Chung, V Wong
Pediatrics 114 (2), e206-e212, 2004
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
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
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
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
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
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
NSD1 mutations generate a genome-wide DNA methylation signature
S Choufani, C Cytrynbaum, BHY Chung, AL Turinsky, D Grafodatskaya, ...
Nature communications 6 (1), 1-7, 2015
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
Down syndrome in diverse populations
P Kruszka, AR Porras, AK Sobering, FA Ikolo, S La Qua, V Shotelersuk, ...
American Journal of Medical Genetics Part A 173 (1), 42-53, 2017
Febrile seizures in southern Chinese children: incidence and recurrence
B Chung, LCY Wat, V Wong
Pediatric neurology 34 (2), 121-126, 2006
The evaluation of Wallerian degeneration in chronic paediatric middle cerebral artery infarction using diffusion tensor MR imaging
PL Khong, LJ Zhou, GC Ooi, BHY Chung, RTF Cheung, VCN Wong
Cerebrovascular Diseases 18 (3), 240-247, 2004
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins
P Szafranski, T Gambin, AV Dharmadhikari, KC Akdemir, SN Jhangiani, ...
Human genetics 135 (5), 569-586, 2016
Noonan syndrome in diverse populations
P Kruszka, AR Porras, YA Addissie, A Moresco, S Medrano, GTK Mok, ...
American Journal of Medical Genetics Part A 173 (9), 2323-2334, 2017
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