| 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 | 1954 | 2007 |
| 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 | 1161 | 2009 |
| 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 | 1138 | 2014 |
| Autism risk factors: genes, environment, and gene-environment interactions P Chaste, M Leboyer Dialogues in clinical neuroscience 14 (3), 281-292, 2012 | 1124 | 2012 |
| 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 | 636 | 2008 |
| 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 | 496 | 2012 |
| Common genetic variants, acting additively, are a major source of risk for autism L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ... Molecular autism 3, 1-13, 2012 | 481 | 2012 |
| 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 | 404 | 2010 |
| Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly JD Buxbaum, G Cai, P Chaste, G Nygren, J Goldsmith, J Reichert, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007 | 335 | 2007 |
| Association between the TPH gene A218C polymorphism and suicidal behavior: A meta‐analysis F Bellivier, P Chaste, A Malafosse American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 124 …, 2004 | 223 | 2004 |
| Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders C Depienne, D Moreno-De-Luca, D Heron, D Bouteiller, A Gennetier, ... Biological psychiatry 66 (4), 349-359, 2009 | 193 | 2009 |
| A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? P Chaste, L Klei, SJ Sanders, V Hus, MT Murtha, JK Lowe, AJ Willsey, ... Biological psychiatry 77 (9), 775-784, 2015 | 161 | 2015 |
| Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders C Pagan, H Goubran-Botros, R Delorme, M Benabou, N Lemière, ... Scientific reports 7 (1), 2096, 2017 | 121 | 2017 |
| Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population P Chaste, N Clement, O Mercati, JL Guillaume, R Delorme, HG Botros, ... PloS one 5 (7), e11495, 2010 | 103 | 2010 |
| The role of causal and intentional judgments in moral reasoning in individuals with high functioning autism M Buon, E Dupoux, P Jacob, P Chaste, M Leboyer, T Zalla Journal of autism and developmental disorders 43, 458-470, 2013 | 102 | 2013 |
| Adjusting head circumference for covariates in autism: clinical correlates of a highly heritable continuous trait P Chaste, L Klei, SJ Sanders, MT Murtha, V Hus, JK Lowe, AJ Willsey, ... Biological Psychiatry 74 (8), 576-584, 2013 | 85 | 2013 |
| Individuals with autism spectrum disorders do not use social stereotypes in irony comprehension T Zalla, F Amsellem, P Chaste, F Ervas, M Leboyer, M Champagne-Lavau PloS one 9 (4), e95568, 2014 | 84 | 2014 |
| Genetic variations of the melatonin pathway in patients with attention‐deficit and hyperactivity disorders P Chaste, N Clement, HG Botros, JL Guillaume, M Konyukh, C Pagan, ... Journal of Pineal Research 51 (4), 394-399, 2011 | 80 | 2011 |
| Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q 11.2, Specifically Breakpoints 1 to 2 P Chaste, SJ Sanders, KN Mohan, L Klei, Y Song, MT Murtha, V Hus, ... Autism Research 7 (3), 355-362, 2014 | 64 | 2014 |
| The Yin and Yang of autism genetics: how rare de novo and common variations affect liability P Chaste, K Roeder, B Devlin Annual review of genomics and human genetics 18 (1), 167-187, 2017 | 62 | 2017 |
