john wei
john wei
The Hospital for Sick Children
Verified email at sickkids.ca
Title
Cited by
Cited by
Year
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
19712010
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
4682017
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
3292011
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
3152010
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
2882015
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
2012006
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
1722011
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
1692012
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
1182014
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
1122015
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
642017
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
642015
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
642014
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
502015
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
472018
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
452014
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
442018
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
402019
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
282011
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
212018
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