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richard delorme
richard delorme
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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
23662010
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
CM Durand, C Betancur, TM Boeckers, J Bockmann, P Chaste, ...
Nature genetics 39 (1), 25-27, 2007
19382007
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
14572018
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
11572019
Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders
B Hofvander, R Delorme, P Chaste, A Nydén, E Wentz, O Ståhlberg, ...
BMC psychiatry 9, 1-9, 2009
11532009
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...
The American Journal of Human Genetics 94 (5), 677-694, 2014
11242014
Brain charts for the human lifespan
RAI Bethlehem, J Seidlitz, SR White, JW Vogel, KM Anderson, ...
Nature 604 (7906), 525-533, 2022
9962022
Melatonin: pharmacology, functions and therapeutic benefits
S Tordjman, S Chokron, R Delorme, A Charrier, E Bellissant, N Jaafari, ...
Current neuropharmacology 15 (3), 434-443, 2017
9402017
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
7382010
Updated European Consensus Statement on diagnosis and treatment of adult ADHD
JJS Kooij, D Bijlenga, L Salerno, R Jaeschke, I Bitter, J Balazs, J Thome, ...
European psychiatry 56 (1), 14-34, 2019
7012019
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
CS Leblond, C Nava, A Polge, J Gauthier, G Huguet, S Lumbroso, ...
PLoS genetics 10 (9), e1004580, 2014
6612014
Abnormal melatonin synthesis in autism spectrum disorders
J Melke, H Goubran Botros, P Chaste, C Betancur, G Nygren, ...
Molecular psychiatry 13 (1), 90-98, 2008
6292008
Enhancing studies of the connectome in autism using the autism brain imaging data exchange II
A Di Martino, D O’connor, B Chen, K Alaerts, JS Anderson, M Assaf, ...
Scientific data 4 (1), 1-15, 2017
5932017
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders
DJ Weiner, EM Wigdor, S Ripke, RK Walters, JA Kosmicki, J Grove, ...
Nature genetics 49 (7), 978-985, 2017
4972017
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
CS Leblond, J Heinrich, R Delorme, C Proepper, C Betancur, G Huguet, ...
PLoS genetics 8 (2), e1002521, 2012
4942012
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
4572012
Genome-wide association study of obsessive-compulsive disorder
SE Stewart, D Yu, JM Scharf, BM Neale, JA Fagerness, CA Mathews, ...
Molecular psychiatry 18 (7), 788-798, 2013
4132013
Revealing the complex genetic architecture of obsessive-compulsive disorder using meta-analysis
D Posthuma
Molecular psychiatry 23 (5), 1181-1188, 2018
4032018
Key role for gene dosage and synaptic homeostasis in autism spectrum disorders
R Toro, M Konyukh, R Delorme, C Leblond, P Chaste, F Fauchereau, ...
Trends in genetics 26 (8), 363-372, 2010
4022010
SHANK1 deletions in males with autism spectrum disorder
D Sato, AC Lionel, CS Leblond, A Prasad, D Pinto, S Walker, I O'Connor, ...
The American Journal of Human Genetics 90 (5), 879-887, 2012
4012012
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