Jennifer Crosbie
Jennifer Crosbie
Hospital for Sick Children, Neurosciences &Mental Health
Verified email at - Homepage
Cited by
Cited by
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D Demontis, RK Walters, J Martin, M Mattheisen, TD Als, E Agerbo, ...
Nature genetics 51 (1), 63, 2019
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
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
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
Brain charts for the human lifespan
RAI Bethlehem, J Seidlitz, SR White, JW Vogel, KM Anderson, ...
Nature 604 (7906), 525-533, 2022
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature neuroscience 18 (2), 199-209, 2015
Mostly worse, occasionally better: impact of COVID-19 pandemic on the mental health of Canadian children and adolescents
KT Cost, J Crosbie, E Anagnostou, CS Birken, A Charach, S Monga, ...
European child & adolescent psychiatry, 1-14, 2021
Is the behavior rating inventory of executive function more strongly associated with measures of impairment or executive function?
T McAuley, S Chen, L Goos, R Schachar, J Crosbie
Journal of the International Neuropsychological Society 16 (3), 495-505, 2010
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
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13. 3
NM Williams, B Franke, E Mick, RJL Anney, CM Freitag, M Gill, A Thapar, ...
American Journal of Psychiatry 169 (2), 195-204, 2012
Evidence for an error monitoring deficit in attention deficit hyperactivity disorder
RJ Schachar, S Chen, GD Logan, TJ Ornstein, J Crosbie, A Ickowicz, ...
Journal of abnormal child psychology 32, 285-293, 2004
Response inhibition and ADHD traits: correlates and heritability in a community sample
J Crosbie, P Arnold, A Paterson, J Swanson, A Dupuis, X Li, J Shan, ...
Journal of abnormal child psychology 41, 497-507, 2013
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
A Noor, A Whibley, CR Marshall, PJ Gianakopoulos, A Piton, AR Carson, ...
Science translational medicine 2 (49), 49ra68-49ra68, 2010
Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome‐wide association study of both common and rare variants
L Yang, BM Neale, L Liu, SH Lee, NR Wray, N Ji, H Li, Q Qian, D Wang, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162 …, 2013
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder
R Maier, G Moser, GB Chen, S Ripke, D Absher, I Agartz, H Akil, F Amin, ...
The American Journal of Human Genetics 96 (2), 283-294, 2015
Deficient inhibition as a marker for familial ADHD
J Crosbie, R Schachar
American Journal of Psychiatry 158 (11), 1884-1890, 2001
Validating psychiatric endophenotypes: inhibitory control and attention deficit hyperactivity disorder
J Crosbie, D Pérusse, CL Barr, RJ Schachar
Neuroscience & Biobehavioral Reviews 32 (1), 40-55, 2008
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
D Demontis, GB Walters, G Athanasiadis, R Walters, K Therrien, ...
Nature genetics 55 (2), 198-208, 2023
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder
J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ...
Biological psychiatry 83 (12), 1044-1053, 2018
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
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