| [Alterations in synapsis formation and function in autism disorders] CM Durand, P Chaste, F Fauchereau, C Betancur, M Leboyer, ... Médecine Sciences 24 (1), 25-28, 2008 | 9* | 2008 |
| A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint D Tentler, G Brandberg, C Betancur, C Gillberg, G Annerén, C Orsmark, ... American Journal of Medical Genetics 105 (8), 729-736, 2001 | 27 | 2001 |
| A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism PBS Celestino-Soper, S Violante, EL Crawford, R Luo, AC Lionel, ... Proceedings of the National Academy of Sciences 109 (21), 7974-7981, 2012 | 153 | 2012 |
| A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3 AT Pagnamenta, R Holt, M Yusuf, D Pinto, K Wing, C Betancur, ... Journal of Neurodevelopmental Disorders 3 (2), 124-131, 2011 | 46 | 2011 |
| A framework for an evidence-based gene list relevant to autism spectrum disorder CP Schaaf, C Betancur, RKC Yuen, JR Parr, DH Skuse, L Gallagher, ... Nature Reviews Genetics 21 (6), 367-376, 2020 | 102 | 2020 |
| 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 |
| A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region LA McInnes, A Nakamine, M Pilorge, T Brandt, P Jiménez González, ... Molecular Autism 1 (1), 5, 2010 | 58 | 2010 |
| 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 (4), 565-579, 2012 | 229 | 2012 |
| Abnormal melatonin synthesis in autism spectrum disorders J Melke, HG Botros, P Chaste, C Betancur, G Nygren, H Anckarsäter, ... Molecular Psychiatry 13 (1), 90-98, 2008 | 602 | 2008 |
| Absence of association between a polymorphic GGC repeat in the 5'untranslated region of the reelin gene and autism MO Krebs, C Betancur, S Leroy, MC Bourdel, C Gillberg, M Leboyer Molecular Psychiatry 7 (7), 801, 2002 | 106 | 2002 |
| Activity of the hypothalamic-pituitary-adrenal axis in mice selected for left-or right-handedness C Betancur, C Sandi, S Vitiello, J Borrell, C Guaza, PJ Neveu Brain Research 589 (2), 302-306, 1992 | 20 | 1992 |
| Acute and chronic effects of methamphetamine on tele-methylhistamine levels in mouse brain: selective involvement of the D2 and not D3 receptor S Morisset, C Pilon, J Tardivel-Lacombe, D Weinstein, W Rostene, ... Journal of Pharmacology and Experimental Therapeutics 300 (2), 621-628, 2002 | 60 | 2002 |
| Altered expression of vesicular glutamate transporters VGLUT1 and VGLUT2 in Parkinson disease A Kashani, C Betancur, B Giros, E Hirsch, S El Mestikawy Neurobiology of Aging 28 (4), 568-578, 2007 | 142 | 2007 |
| Altered neurotensin mRNA expression in mice lacking the dopamine transporter C Roubert, C Spielewoy, P Soubrié, M Hamon, B Giros, C Betancur Neuroscience 123 (2), 537-546, 2004 | 11 | 2004 |
| An investigation of ribosomal protein L10 gene in autism spectrum disorders X Gong, R Delorme, F Fauchereau, CM Durand, P Chaste, C Betancur, ... BMC Medical Genetics 10 (1), 7, 2009 | 29 | 2009 |
| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1375 | 2018 |
| Analysis of transmission of novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene in patients with autism MB Lauritsen, M Nyegaard, C Betancur, C Colineaux, TL Josiassen, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 121 …, 2003 | 10 | 2003 |
| Analysis of X chromosome inactivation in autism spectrum disorders X Gong, E Bacchelli, F Blasi, C Toma, C Betancur, P Chaste, R Delorme, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008 | 61 | 2008 |
| Association between left-handedness and allergy: A reappraisal C Betancur, A Vélez, G Cabanieu, M Le Moal, PJ Neveu Neuropsychologia 28 (2), 223-227, 1990 | 63 | 1990 |
