| 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 | 2318 | 2010 |
| Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007 | 1654 | 2007 |
| Common genetic variants on 5p14. 1 associate with autism spectrum disorders K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ... Nature 459 (7246), 528-533, 2009 | 1131 | 2009 |
| A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009 | 793 | 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 | 723 | 2010 |
| Genomic and epigenetic evidence for oxytocin receptor deficiency in autism SG Gregory, JJ Connelly, AJ Towers, J Johnson, D Biscocho, ... BMC medicine 7, 1-13, 2009 | 668 | 2009 |
| Autism and maternally derived aberrations of chromosome 15q RJ Schroer, MC Phelan, RC Michaelis, EC Crawford, SA Skinner, ... American journal of medical genetics 76 (4), 327-336, 1998 | 497 | 1998 |
| Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes Y Shao, ML Cuccaro, ER Hauser, KL Raiford, MM Menold, CM Wolpert, ... The American Journal of Human Genetics 72 (3), 539-548, 2003 | 461 | 2003 |
| Repetitive behaviors in autism: Relationships with associated clinical features RL Gabriels, ML Cuccaro, DE Hill, BJ Ivers, E Goldson Research in developmental disabilities 26 (2), 169-181, 2005 | 460 | 2005 |
| 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 | 449 | 2012 |
| Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism DQ Ma, PL Whitehead, MM Menold, ER Martin, AE Ashley-Koch, H Mei, ... The American Journal of Human Genetics 77 (3), 377-388, 2005 | 426 | 2005 |
| Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R ML Cuccaro, Y Shao, J Grubber, M Slifer, CM Wolpert, SL Donnelly, ... Child psychiatry and human development 34, 3-17, 2003 | 390 | 2003 |
| Identification of MeCP2 mutations in a series of females with autistic disorder RM Carney, CM Wolpert, SA Ravan, M Shahbazian, A Ashley-Koch, ... Pediatric neurology 28 (3), 205-211, 2003 | 308 | 2003 |
| Genomic screen and follow‐up analysis for autistic disorder Y Shao, CM Wolpert, KL Raiford, MM Menold, SL Donnelly, SA Ravan, ... American journal of medical genetics 114 (1), 99-105, 2002 | 308 | 2002 |
| Race and gender differences in the treatment of psychiatric disorders in young adolescents SP Cuffe, JL Waller, ML Cuccaro, AJ Pumariega, CZ Garrison Journal of the American Academy of Child & Adolescent Psychiatry 34 (11 …, 1995 | 300 | 1995 |
| A genome‐wide association study of autism reveals a common novel risk locus at 5p14. 1 D Ma, D Salyakina, JM Jaworski, I Konidari, PL Whitehead, AN Andersen, ... Annals of human genetics 73 (3), 263-273, 2009 | 277 | 2009 |
| Genetic studies of autistic disorder and chromosome 7 A Ashley-Koch, CM Wolpert, MM Menold, L Zaeem, S Basu, SL Donnelly, ... Genomics 61 (3), 227-236, 1999 | 257 | 1999 |
| Accelerated head growth in early development of individuals with autism YA Dementieva, DD Vance, SL Donnelly, LA Elston, CM Wolpert, ... Pediatric neurology 32 (2), 102-108, 2005 | 241 | 2005 |
| Analysis of the RELN gene as a genetic risk factor for autism DA Skaar, Y Shao, JL Haines, JE Stenger, J Jaworski, ER Martin, ... Molecular psychiatry 10 (6), 563-571, 2005 | 239 | 2005 |
| 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 |
