| 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 | 638 | 2014 |
| The genetic landscapes of autism spectrum disorders G Huguet, E Ey, T Bourgeron Annual review of genomics and human genetics 14 (1), 191-213, 2013 | 531 | 2013 |
| 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 | 481 | 2012 |
| 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 | 394 | 2012 |
| The emerging role of SHANK genes in neuropsychiatric disorders A Guilmatre, G Huguet, R Delorme, T Bourgeron Developmental neurobiology 74 (2), 113-122, 2014 | 294 | 2014 |
| The genetics of autism spectrum disorders G Huguet, M Benabou, T Bourgeron A time for metabolism and hormones, 101-129, 2016 | 227* | 2016 |
| Cntnap4 differentially contributes to GABAergic and dopaminergic synaptic transmission T Karayannis, E Au, JC Patel, I Kruglikov, S Markx, R Delorme, D Héron, ... Nature 511 (7508), 236-240, 2014 | 183 | 2014 |
| Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE C Nava, F Lamari, D Héron, C Mignot, A Rastetter, B Keren, D Cohen, ... Translational psychiatry 2 (10), e179-e179, 2012 | 122 | 2012 |
| Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia A Gialluisi, TFM Andlauer, N Mirza-Schreiber, K Moll, J Becker, ... Molecular psychiatry 26 (7), 3004-3017, 2021 | 119 | 2021 |
| 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 | 115 | 2017 |
| Measuring and estimating the effect sizes of copy number variants on general intelligence in community-based samples G Huguet, C Schramm, E Douard, L Jiang, A Labbe, F Tihy, G Mathonnet, ... JAMA psychiatry 75 (5), 447-457, 2018 | 111 | 2018 |
| Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia A Gialluisi, TFM Andlauer, N Mirza-Schreiber, K Moll, J Becker, ... Translational psychiatry 9 (1), 77, 2019 | 110 | 2019 |
| CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders O Mercati, G Huguet, A Danckaert, G André-Leroux, A Maruani, ... Molecular psychiatry 22 (4), 625-633, 2017 | 88 | 2017 |
| 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 | 78 | 2011 |
| Effect sizes of deletions and duplications on autism risk across the genome E Douard, A Zeribi, C Schramm, P Tamer, MA Loum, S Nowak, Z Saci, ... American Journal of Psychiatry 178 (1), 87-98, 2021 | 74 | 2021 |
| Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway HG Botros, P Legrand, C Pagan, V Bondet, P Weber, M Ben‐Abdallah, ... Journal of pineal research 54 (1), 46-57, 2013 | 71 | 2013 |
| Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders R Waltes, E Duketis, M Knapp, RJL Anney, G Huguet, S Schlitt, ... Human genetics 133, 781-792, 2014 | 69 | 2014 |
| Both rare and common genetic variants contribute to autism in the Faroe Islands CS Leblond, F Cliquet, C Carton, G Huguet, A Mathieu, T Kergrohen, ... NPJ genomic medicine 4 (1), 1, 2019 | 66 | 2019 |
| Genomic architecture of human neuroanatomical diversity R Toro, JB Poline, G Huguet, E Loth, V Frouin, T Banaschewski, ... Molecular Psychiatry 20 (8), 1011-1016, 2015 | 66 | 2015 |
| Zinc deficiency and low enterocyte zinc transporter expression in human patients with autism related mutations in SHANK3 S Pfaender, AK Sauer, S Hagmeyer, K Mangus, L Linta, S Liebau, ... Scientific reports 7 (1), 45190, 2017 | 65 | 2017 |
