| 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 | 2320 | 2010 |
| 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 | 1882 | 2007 |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1654 | 2007 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1374 | 2018 |
| 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 | 1082 | 2014 |
| A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009 | 796 | 2009 |
| 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 | 726 | 2010 |
| Visual social attention in autism spectrum disorder: Insights from eye tracking studies Q Guillon, N Hadjikhani, S Baduel, B Rogé Neuroscience & Biobehavioral Reviews 42, 279-297, 2014 | 560 | 2014 |
| A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium Human Molecular Genetics 7 (3), 571-578, 1998 | 503 | 1998 |
| 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 | 472 | 2017 |
| Microcephaly and macrocephaly in autism E Fombonne, B Rogé, J Claverie, S Courty, J Fremolle Journal of autism and developmental disorders 29, 113-119, 1999 | 454 | 1999 |
| 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 | 451 | 2012 |
| Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24. 32 and a significant overlap with schizophrenia Molecular autism 8, 1-17, 2017 | 344 | 2017 |
| Increased perception of loudness in autism S Khalfa, N Bruneau, B Rogé, N Georgieff, E Veuillet, JL Adrien, ... Hearing research 198 (1-2), 87-92, 2004 | 300 | 2004 |
| Prevention and treatment of post-partum depression: a controlled randomized study on women at risk H Chabrol, F Teissedre, M Saint-Jean, N Teisseyre, B Roge, E Mullet Psychological medicine 32 (6), 1039-1047, 2002 | 272 | 2002 |
| A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ... Human genetics 131, 565-579, 2012 | 229 | 2012 |
| Autisme, comprendre et agir-3e éd.: Santé, éducation, insertion B Rogé Dunod, 2022 | 205 | 2022 |
| Early processing of emotional faces in children with autism: An event-related potential study M Batty, E Meaux, K Wittemeyer, B Rogé, MJ Taylor Journal of experimental child psychology 109 (4), 430-444, 2011 | 157 | 2011 |
| Use of early intervention for young children with autism spectrum disorder across Europe E Salomone, Š Beranová, F Bonnet-Brilhault, M Briciet Lauritsen, ... Autism 20 (2), 233-249, 2016 | 155 | 2016 |
| Screening for autism spectrum disorders: state of the art in Europe P García-Primo, A Hellendoorn, T Charman, H Roeyers, M Dereu, B Roge, ... European child & adolescent psychiatry 23, 1005-1021, 2014 | 151 | 2014 |
