John Vincent
John Vincent
Centre for Addiction & Mental Health, Toronto, Canada
Verified email at camh.ca
Title
Cited by
Cited by
Year
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
20112010
Structural variation of chromosomes in autism spectrum disorder
CR Marshall, A Noor, JB Vincent, AC Lionel, L Feuk, J Skaug, M Shago, ...
The American Journal of Human Genetics 82 (2), 477-488, 2008
18622008
A reference panel of 64,976 haplotypes for genotype imputation
S McCarthy, S Das, W Kretzschmar, O Delaneau, AR Wood, A Teumer, ...
Nature genetics 48 (10), 1279, 2016
16512016
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
P Szatmari, A Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ...
Nature genetics 39 (3), 319, 2007
14932007
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984-995, 2013
13372013
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4
P Sklar, S Ripke, LJ Scott, OA Andreassen, S Cichon, N Craddock, ...
Nature genetics 43 (10), 977, 2011
13132011
Genome-wide association study identifies 30 loci associated with bipolar disorder
EA Stahl, G Breen, AJ Forstner, A McQuillin, S Ripke, V Trubetskoy, ...
Nature genetics 51 (5), 793-803, 2019
6972019
Contribution of SHANK3 mutations to autism spectrum disorder
R Moessner, CR Marshall, JS Sutcliffe, J Skaug, D Pinto, J Vincent, ...
The American Journal of Human Genetics 81 (6), 1289-1297, 2007
6522007
Meta-analysis and imputation refines the association of 15q25 with smoking quantity
JZ Liu, F Tozzi, DM Waterworth, SG Pillai, P Muglia, L Middleton, ...
Nature genetics 42 (5), 436-440, 2010
6402010
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
6162010
Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways
L Sang, JJ Miller, KC Corbit, RH Giles, MJ Brauer, EA Otto, LM Baye, ...
Cell 145 (4), 513-528, 2011
5232011
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
GN Mnatzakanian, H Lohi, I Munteanu, SE Alfred, T Yamada, ...
Nature genetics 36 (4), 339-341, 2004
3752004
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
3742012
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
3392019
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry
LJ Scott, P Muglia, XQ Kong, W Guan, M Flickinger, R Upmanyu, F Tozzi, ...
Proceedings of the National Academy of Sciences 106 (18), 7501-7506, 2009
3192009
The genetic basis of non-syndromic intellectual disability: a review
L Kaufman, M Ayub, JB Vincent
Journal of neurodevelopmental disorders 2 (4), 182-209, 2010
3142010
A role for common fragile site induction in amplification of human oncogenes
A Hellman, E Zlotorynski, SW Scherer, J Cheung, JB Vincent, DI Smith, ...
Cancer cell 1 (1), 89-97, 2002
3052002
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
T Network, ...
Nature neuroscience 18 (2), 199, 2015
2972015
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
2712018
Human chromosome 7: DNA sequence and biology
SW Scherer, J Cheung, JR MacDonald, LR Osborne, K Nakabayashi, ...
Science 300 (5620), 767-772, 2003
2452003
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Articles 1–20