Communication, interventions, and scientific advances in autism: A commentary

2007, Prevalence of autism spectrum disorders, MMWR, 56, SS

Fombonne, 2004, Validation of the diagnosis of autism in general practitioner records, BMC Public Health, 3, 4

Deykin, 1979, The incidence of seizures among children with autism, Am J Psychiatry, 136, 1310, 10.1176/ajp.136.10.1310

Kanner, 1971, Eleven autistic children regionally reported in 1943, Autism Child Schizophr, 1, 119, 10.1007/BF01537953

Stokstad, 2001, Development: new hints into the biological basis of autism, Science, 294, 34, 10.1126/science.294.5540.34

Folstein, 2001, Genetics of autism: complex aetiology for a heterogeneous disorder, Nat Rev Genet, 2, 943, 10.1038/35103559

Kanner, 1943, Autistic disturbances of affective contact, Nervous Child, 2, 217

Lord, 2000, The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism, J Autism Dev Disord, 30, 205, 10.1023/A:1005592401947

Paul, R. Promoting social communication in high functioning individuals with autistic spectrum disorders. Child Adolesc Psychiatr Clin N Am. 2003, 12:87–106, vi–vii.

Piven, 1997, Broader autism phenotype: evidence form a family history study of multiple-incidence autism families, Am J Psychiatry, 154, 185, 10.1176/ajp.154.2.185

Baron-Cohen, 2006, The hyper-systemizing, assortative mating theory of autism, Prog Neuropsychopharmacol Biol Psychiatry, 30, 865, 10.1016/j.pnpbp.2006.01.010

Amaral, 2008, Neuroanatomy of autism, Trends Neurosci, 31, 137, 10.1016/j.tins.2007.12.005

Gabriels, 2005, Repetitive behaviors in autism: relationships with associate clinical features, Res Dev Disabil, 26, 169, 10.1016/j.ridd.2004.05.003

Noens, 2006, The ComFor: an instrument for the indication of augmentative communication in people with autism and intellectual disability, J Intellect Disabil Res, 50, 621, 10.1111/j.1365-2788.2006.00807.x

Williams, 2006, Neuropsychological functioning in children with autism: further evidence for disordered complex information processing, Child Neuropsychol, 12, 279, 10.1080/09297040600681190

Mazefsky, 2007, Emotion perception in Asperger's syndrome and high-functioning autism: the importance of diagnostic criteria and cue intensity, J Autism Dev Disord, 37, 1086, 10.1007/s10803-006-0251-6

Koyama, 2007, Cognitive and symptom profiles in Asperger's syndrome and high-functioning autism, Psychiatry Clin Neurosci, 61, 99, 10.1111/j.1440-1819.2007.01617.x

Barbaro, 2007, A comparative study of the use and understanding of self-presentational display rules in children with high functioning autism and Asperger's disorder, J Autism Dev Disord, 37, 1235, 10.1007/s10803-006-0267-y

Macintosh, 2004, Annotation: the similarities and differences between autistic disorder and Asperger's disorder: a review of the empirical evidence, J Child Psychol Psychiatry, 45, 421, 10.1111/j.1469-7610.2004.00234.x

Hobson, 2005, Foundations for self and other: a study in autism, Dev Sci, 8, 481, 10.1111/j.1467-7687.2005.00439.x

Villalobos, 2005, Reduced functional connectivity between V1 and inferior frontal cortex associated with visuomotor performance in autism, NeuroImage, 25, 916, 10.1016/j.neuroimage.2004.12.022

Williams, 2005, Verbal and spatial working memory in Autism, J Autism Dev Disord, 35, 747, 10.1007/s10803-005-0021-x

Frith, 2001, Mind blindness and the brain in autism, Neuron, 32, 969, 10.1016/S0896-6273(01)00552-9

Peterson, 2005, Mind and body: concepts of human cognition, physiology and false belief in children with autism or typical development, J Autism Dev Disord, 35, 487, 10.1007/s10803-005-5039-6

Williams, 2008, Self–other relations in social development and autism: multiple roles for mirror neurons and other brain bases, Autism Res, 1, 73, 10.1002/aur.15

Schippers, 2009, Playing charades in the fMRI: are mirror and/or mentalizing areas involved in gestural communication?, PLoS One, 4, e6801, 10.1371/journal.pone.0006801

Wood JJ, Drahota A, Sze K, Van Dyke M, Decker K, Fujii C, Bahng C, Renno P, Hwang WC, Spiker M. Brief report: effects of cognitive behavioral therapy on parent-reported autism symptoms in school-age children with high-functioning autism. J Autism Dev Disord 2009;39:1608–12.

Palmen, 2008, Improving question asking in high-functioning adolescents with autism spectrum disorders: effectiveness of small-group training, Autism, 12, 83, 10.1177/1362361307085265

Bryan, 2000, Teaching on-task and on-schedule behaviors to high-functioning children with autism via picture activity schedules, J Autism Dev Disord, 30, 553, 10.1023/A:1005687310346

Lopata, 2008, Effectiveness of a manualized summer social treatment program for high-functioning children with autism spectrum disorders, J Autism Dev Disord, 38, 890, 10.1007/s10803-007-0460-7

Bolte, 2002, The development and evaluation of a computer-based program to test and to teach the recognition of facial affect, Int J Circumpolar Health, 2, 61

Preston D, Carter M. A review of the efficacy of the picture exchange communication system intervention. J Autism Dev Disord 2009;39:1471–86.

Berkowitz, 1990, comparison of two methods of prompting in training discrimination of communication book pictures by autistic students, J Autism Dev Disord, 20, 255, 10.1007/BF02284722

Betz, 2008, Using joint activity schedules to promote peer engagement in preschoolers with autism, J Appl Behav Anal, 41, 237, 10.1901/jaba.2008.41-237

Carr, 1987, Acquisition of sign language by autistic children. III: generalized descriptive phrases, J Autism Dev Disord, 17, 217, 10.1007/BF01495057

Jamain, 2003, Paris Autism Research International Sibpair Study. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism, Nat Genet, 34, 27, 10.1038/ng1136

Muhle, 2004, The genetics of autism, Pediatrics, 113, 472, 10.1542/peds.113.5.e472

Polleux, 2004, Toward a developmental neurobiology of autism, Ment Retard Dev Disabil Res Rev, 10, 303, 10.1002/mrdd.20044

Shastry, 2003, Molecular genetics of autism spectrum disorders, J Hum Genet, 48, 495, 10.1007/s10038-003-0064-9

Wassink, 2000, The molecular genetics of autism, Curr Psychiatry Rep, 2, 170, 10.1007/s11920-000-0063-x

Yang, 2007, A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence, Int J Dev Neurosci, 25, 69, 10.1016/j.ijdevneu.2006.12.002

Yonan, 2003, Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction, Genes Brain Behav, 2, 303, 10.1034/j.1601-183X.2003.00041.x

Fombonne, 2004, Validation of the diagnosis of autism in general practitioner records, BMC Public Health, 3, 4

Newschaffer, 2007, The epidemiology of autism spectrum disorders, Annu Rev Public Health, 28, 235, 10.1146/annurev.publhealth.28.021406.144007

Le Couteur, 1996, A broader phenotype of autism: the clinical spectrum in twins, J Clin Psychol Psychiatry, 37, 785, 10.1111/j.1469-7610.1996.tb01475.x

Bespalova, 2003, Disease susceptibility genes for autism, Ann Med, 35, 274, 10.1080/07853890310005966

Hill, 2003, Understanding autism: insights from mind and brain, Philos Trans R Soc Lond B Biol Sci, 358, 281, 10.1098/rstb.2002.1209

Bhasin, 2007, Sociodemographic risk factors for autism in a US metropolitan area, J Autism Dev Disord, 37, 667, 10.1007/s10803-006-0194-y

Larsson, 2005, Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status, Am J Epidemiol, 161, 916, 10.1093/aje/kwi123

Glasson, 2004, Perinatal factors and the development of autism: a population study, Arch Gen Psychiatry, 61, 618, 10.1001/archpsyc.61.6.618

Croen, 2002, Descriptive epidemiology of autism in a California population: who is at risk?, J Autism Dev Disord, 32, 217, 10.1023/A:1015405914950

Reichenberg, 2006, Advancing paternal age and autism, Arch Gen Psychiatry, 63, 1026, 10.1001/archpsyc.63.9.1026

Eaton, 2001, Obstetric complications and risk for severe psychopathology in childhood, J Autism Dev Disord, 31, 279, 10.1023/A:1010743203048

Hultman, 2002, Perinatal risk factors for infantile autism, Epidemiology, 13, 417, 10.1097/00001648-200207000-00009

King MD, Fountain C, Dakhlallah D, Bearman PS. Estimated autism risk and older reproductive age. Am J Public Health 2009;99:1673–9.

Abrahams, 2008, Advances in autism genetics: on the threshold of a new neurobiology, Nat Rev Genet, 9, 341, 10.1038/nrg2346

Freitag, 2007, The genetics of autistic disorders and its clinical relevance: a review of the literature, Mol Psychiatry, 12, 2, 10.1038/sj.mp.4001896

Hoekstra, 2007, Heritability of autistic traits in the general population, Arch Pediatr Adolesc Med, 161, 372, 10.1001/archpedi.161.4.372

Persico, 2006, Searching for ways out of the autism maze: genetic, epigenetic and environmental clues, Trends Neurosci, 29, 349, 10.1016/j.tins.2006.05.010

Yang, 2007, A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence, Int J Dev Neurosci, 25, 69, 10.1016/j.ijdevneu.2006.12.002

Cook, 2008, Copy-number variations associated with neuropsychiatric conditions, Nature, 455, 919, 10.1038/nature07458

Sebat, 2007, Strong association of de novo copy number mutations with autism, Science, 316, 445, 10.1126/science.1138659

Szatmari, 2007, Mapping autism risk loci using genetic linkage and chromosomal rearrangements, Nat Genet, 39, 319, 10.1038/ng1985

Liu, 2007, Genome-wide linkage analyses of quantitative and categorical autism subphenotypes, Biol Psychiatry, 64, 561, 10.1016/j.biopsych.2008.05.023

Trottier, 1999, Etiology of infantile autism: a review of recent advances in genetic and neurobiological research, J Psychiatry Neurosci, 24, 103

Arndt, 2005, The teratology of autism, Int J Dev Neurosci, 23, 189, 10.1016/j.ijdevneu.2004.11.001

Rutter, 2005, Incidence of autism spectrum disorders: changes over time and their meaning, Acta Paediatr, 94, 2, 10.1080/08035250410023124

Szpir, 2006, Tracing the origins of autism: a spectrum of new studies, Environ Health Perspect, 114, A412, 10.1289/ehp.114-a412

Baron-Cohen, 2005, Sex differences in the brain: implications for explaining autism, Science, 310, 819, 10.1126/science.1115455

Manning, 2001, The 2nd to 4th digit ratio and autism, Dev Med Child Neurol, 43, 160, 10.1017/S0012162201000317

Auyeung, 2009, Fetal testosterone predicts sexually differentiated childhood behavior in girls and in boys, Psychol Sci, 20, 144, 10.1111/j.1467-9280.2009.02279.x

Moss J, Howlin P. Autism spectrum disorders in genetic syndromes: implications for diagnosis, intervention and understanding the wider autism spectrum disorder population. J Intellect Disabil Res 2009;53:852–73.

Cohen, 2005, Specific genetic disorders and autism: clinical contribution towards their identification, J Autism Dev Disord, 35, 103, 10.1007/s10803-004-1038-2

Berger-Sweeney, 2003, Using mice to model cognitive deficits in neurologic disorders: narrowing in on Rett syndrome, Curr Neurol Neurosci Rep, 3, 185, 10.1007/s11910-003-0075-0

Kohtz, 2004, Developmental regulation of EVF-1, a novel non-coding RNA transcribed upstream of the mouse Dlx6 gene, Gene Expr Patterns, 4, 407, 10.1016/j.modgep.2004.01.007

Artigas-Pallerés, 2005, Syndromic autism: II. Genetic syndromes associated with autism, Rev Neurol, 1, S151

Hutcheson, 2004, Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes, BMC Med Genet, 5, 12, 10.1186/1471-2350-5-12

2001, A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p, Am J Hum Genet, 69, 570, 10.1086/323264

2001, Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q, Hum Mol Genet, 10, 973, 10.1093/hmg/10.9.973

Alarcon, 2002, Autism genetic research exchanges consortium. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families, Am J Hum Genet, 70, 60, 10.1086/338241

Bacchelli, 2003, International Molecular Genetics Study of Autism Consortium (IMGSAC). Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene, Mol Psychiatry, 8, 916, 10.1038/sj.mp.4001340

Bradford, 2001, Incorporating language phenotypes strengthens evidence of linkage to autism, Am J Med Genet, 105, 539, 10.1002/ajmg.1497

Keller, 2003, The neurobiological context of autism, Mol Neurobiol, 28, 1, 10.1385/MN:28:1:1

Liu, 2001, Autism Genetic Resource Exchange Consortium. A genomewide screen for autism susceptibility loci, Am J Hum Genet, 69, 327, 10.1086/321980

Risch, 1999, A genomic screen of autism: evidence for a multilocus etiology, Am J Hum Genet, 65, 493, 10.1086/302497

Shao, 2002, Genomic screen and followup analysis for autism disorders, Am J Med Genet (Neuropsych), 114, 99, 10.1002/ajmg.10153

Wassink, 2000, The molecular genetics of autism, Curr Psychiatry Rep, 2, 170, 10.1007/s11920-000-0063-x

Ylisaukko-oja, 2004, Genome-wide scan for loci of Asperger's syndrome, Mol Psychiatry, 9, 161, 10.1038/sj.mp.4001385

Bayou, 2008, Autism: an overview of genetic aetiology, Tunis Med, 86, 573

Yoo, 2009, Microsatellite marker in gamma-aminobutyric acid- a receptor beta 3 subunit gene and autism spectrum disorders in Korean trios, Yonsei Med J, 50, 304, 10.3349/ymj.2009.50.2.304

Raznahan, 2009, Serotonin transporter genotype and neuroanatomy in autism spectrum disorders, Psychiatr Genet, 19, 147, 10.1097/YPG.0b013e32832a505a

Campbell, 2008, Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder, Autism Res, 1, 159, 10.1002/aur.27

Varga, 2009, The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly, Genet Med, 11, 111, 10.1097/GIM.0b013e31818fd762

Yang, 2008, Association of the homeobox transcription factor gene ENGRAILED 2 with autistic disorder in Chinese children, Neurospychobiology, 57, 3, 10.1159/000123115

Buxbaum, 2009, Multiple rare variants in the etiology of autism spectrum disorders, Dialogues Clin Neurosci, 11, 35, 10.31887/DCNS.2009.11.1/jdbuxbaum

Bucan, 2009, Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes, PLoS Genet, 5, e1000536, 10.1371/journal.pgen.1000536

Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguem E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C. Screening for genomic rearrangements and methylation abnormalities of the 15q11-113 region in autism spectrum disorders. Biol Psychiatry 2009;66:349–59.

Glessner, 2009, Autism genome-wide copy number variation reveals ubiquitin and neuronal genes, Nature, 459, 569, 10.1038/nature07953

Wang, 2009, Common genetic variants on 5p14.1 associate with autism spectrum disorders, Nature, 459, 528, 10.1038/nature07999

Yan, 2008, Analysis of the neuroligin 4Y gene in patients with autism, Psychiatr Genet, 18, 204, 10.1097/YPG.0b013e3282fb7fe6

Lawson-Yuen, 2008, Familial deletion within NLGN 4 associated with autism and Tourette syndrome, Eur J Hum Genet, 16, 614, 10.1038/sj.ejhg.5202006

Jamain, 2008, Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism, Proc Natl Acad Sci U S A, 105, 1710, 10.1073/pnas.0711555105

Tabuchi, 2007, A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice, Science, 318, 71, 10.1126/science.1146221

Chadman, 2008, Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin mice, Autism Res, 1, 147, 10.1002/aur.22

Kwon, 2006, Pten regulates neuronal arborization and social interaction in mice, Neuron, 50, 377, 10.1016/j.neuron.2006.03.023

Crino, 1999, New developments in the neurobiology of the tuberous sclerosis complex, Neurology, 53, 1384, 10.1212/WNL.53.7.1384

Holmes, 2007, Tuberous Sclerosis Study Group. Tuberous sclerosis complex and epilepsy: recent developments and future challenges, Epilepsia, 48, 617, 10.1111/j.1528-1167.2007.01035.x

Ess, 2006, The neurobiology of tuberous sclerosis complex, Semin Pediatr Neurol, 13, 37, 10.1016/j.spen.2006.01.009

Ehninger, 2008, Reversal of learning deficits in a Tsc2+/− mouse model of tuberous sclerosis, Nat Med, 14, 843, 10.1038/nm1788

Liu, 2005, Oxytocin receptors in brain cortical regions are reduced in haploinsufficient (+/−) reeler mice, Neurol Res, 27, 339, 10.1179/016164105X35602

Carter, 2007, Sex differences in oxytocin and vasopressin: implications for autism spectrum disorders?, Behav Brain Res, 176, 170, 10.1016/j.bbr.2006.08.025

Crawley, 2007, Social approach behaviors in oxytocin knockout mice: comparison to two independent lines tested in different laboratory environments, Neuropeptides, 41, 145, 10.1016/j.npep.2007.02.002

McFarlane, 2008, Autism-like behavioral phenotypes in BTBR T+tf/J mice, Genes Brain Behav, 7, 152, 10.1111/j.1601-183X.2007.00330.x

Moy, 2004, Sociability and preference for social novelty in five inbred strains: an approach to assess autistic-like behaviors in mice, Genes Brain Behav, 3, 287, 10.1111/j.1601-1848.2004.00076.x

Moy, 2007, Mouse behavioral tasks relevant to autism: phenotypes of ten inbred strains, Behav Brain Res, 176, 4, 10.1016/j.bbr.2006.07.030

Yang, 2007, Social approach behaviors are similar on conventional versus reverse lighting cycles, and in replications across cohorts, in BTBR T+tf/J, C57BL/6J, and vasopressin receptor 1B mutant mice, Frontiers Behav Neurosci, 1, 1, 10.3389/neuro.08.001.2007

Yang, 2007, Social deficits in BTBR T+tf/J mice are unchanged by cross-fostering with C57BL/6J mothers, Int J Dev Neurosci, 25, 515, 10.1016/j.ijdevneu.2007.09.008

Yang, 2009, Postnatal lesion evidence against a primary role for the corpus callosum in mouse sociability, Eur J Neurosci, 29, 1663, 10.1111/j.1460-9568.2009.06714.x

Happé, 1996, Theory of mind in the brain. Evidence from a PET scan study of Asperger syndrome, Neuroreport, 8, 197, 10.1097/00001756-199612200-00040

Rejón Altable, 2009, Concept of representation and mental symptoms. The case of theory of mind, Psychopathology, 42, 219, 10.1159/000218519

Lind SE, Bowler DM. Recognition memory, self–other source memory, and theory-of-mind in children with autism spectrum disorder. J Autism Dev Disord 2009;39:1231–9.

Crawley, 2007, Mouse behavioral assays relevant to the symptoms of autism, Brain Pathol, 17, 448, 10.1111/j.1750-3639.2007.00096.x

MacPherson, 2008, Impaired fear memory, altered object memory and modified hippocampal synaptic plasticity in split-brain mice, Brain Res, 1210, 179, 10.1016/j.brainres.2008.03.008

Kusek, 2007, Localization of two new X-linked quantitative trait loci controlling corpus callosum size in the mouse, Genes Brain Behav, 6, 359, 10.1111/j.1601-183X.2006.00264.x

Scattoni, 2008, Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism, PLoS One, 3, e3067, 10.1371/journal.pone.0003067

Picker, 2006, An altered neonatal behavioral phenotype in Mecp2 mutant mice, Neuroreport, 17, 541, 10.1097/01.wnr.0000208995.38695.2f