john wei
john wei
The Hospital for Sick Children
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Cited by
Cited by
Origins and functional impact of copy number variation in the human genome
DF Conrad, D Pinto, R Redon, L Feuk, O Gokcumen, Y Zhang, J Aerts, ...
Nature 464 (7289), 704-712, 2010
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RKC Yuen, D Merico, M Bookman, JL Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD
AC Lionel, J Crosbie, N Barbosa, T Goodale, B Thiruvahindrapuram, ...
Science translational medicine 3 (95), 95ra75-95ra75, 2011
Towards a comprehensive structural variation map of an individual human genome
AW Pang, JR MacDonald, D Pinto, J Wei, MA Rafiq, DF Conrad, H Park, ...
Genome biology 11 (5), 1-14, 2010
Molecular diagnostic yield of chromosomal microarray analysis and whole-exome sequencing in children with autism spectrum disorder
K Tammimies, CR Marshall, S Walker, G Kaur, B Thiruvahindrapuram, ...
Jama 314 (9), 895-903, 2015
Genome assembly comparison identifies structural variants in the human genome
R Khaja, J Zhang, JR MacDonald, Y He, AM Joseph-George, J Wei, ...
Nature genetics 38 (12), 1413-1418, 2006
Myelination transition zone astrocytes are constitutively phagocytic and have synuclein dependent reactivity in glaucoma
JV Nguyen, I Soto, KY Kim, EA Bushong, E Oglesby, FJ Valiente-Soriano, ...
Proceedings of the National Academy of Sciences 108 (3), 1176-1181, 2011
A discovery resource of rare copy number variations in individuals with autism spectrum disorder
A Prasad, D Merico, B Thiruvahindrapuram, J Wei, AC Lionel, D Sato, ...
G3: Genes| Genomes| Genetics 2 (12), 1665-1685, 2012
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
AC Lionel, K Tammimies, AK Vaags, JA Rosenfeld, JW Ahn, D Merico, ...
Human molecular genetics 23 (10), 2752-2768, 2014
Clinically relevant copy number variations detected in cerebral palsy
M Oskoui, MJ Gazzellone, B Thiruvahindrapuram, M Zarrei, J Andersen, ...
Nature communications 6 (1), 1-7, 2015
Rare genome-wide copy number variation and expression of schizophrenia in 22q11. 2 deletion syndrome
AS Bassett, C Lowther, D Merico, G Costain, EWC Chow, ...
American Journal of Psychiatry 174 (11), 1054-1063, 2017
A high-resolution copy-number variation resource for clinical and population genetics
M Uddin, B Thiruvahindrapuram, S Walker, Z Wang, P Hu, S Lamoureux, ...
Genetics in medicine 17 (9), 747-752, 2015
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes
A Noor, AC Lionel, S Cohen‐Woods, N Moghimi, J Rucker, A Fennell, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 165 …, 2014
Copy number variable microRNAs in schizophrenia and their neurodevelopmental gene targets
W Warnica, D Merico, G Costain, SE Alfred, J Wei, CR Marshall, ...
Biological psychiatry 77 (2), 158-166, 2015
OTUD7A regulates neurodevelopmental phenotypes in the 15q13. 3 microdeletion syndrome
M Uddin, BK Unda, V Kwan, NT Holzapfel, SH White, L Chalil, ...
The American Journal of Human Genetics 102 (2), 278-295, 2018
Copy number variation in Han Chinese individuals with autism spectrum disorder
MJ Gazzellone, X Zhou, AC Lionel, M Uddin, B Thiruvahindrapuram, ...
Journal of neurodevelopmental disorders 6 (1), 1-7, 2014
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants
MS Reuter, S Walker, B Thiruvahindrapuram, J Whitney, I Cohn, ...
Cmaj 190 (5), E126-E136, 2018
A large data resource of genomic copy number variation across neurodevelopmental disorders
M Zarrei, CL Burton, W Engchuan, EJ Young, EJ Higginbotham, ...
NPJ genomic medicine 4 (1), 1-13, 2019
A genotype resource for postmortem brain samples from the Autism Tissue Program
RF Wintle, AC Lionel, P Hu, SD Ginsberg, D Pinto, ...
Autism Research 4 (2), 89-97, 2011
Copy number variation analysis of 100 twin pairs enriched for neurodevelopmental disorders
S Stamouli, BM Anderlid, C Willfors, B Thiruvahindrapuram, J Wei, ...
Twin Research and Human Genetics 21 (1), 1-11, 2018
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