Cite

Diagnostic and Statistical Manual of Mental Disorders, 5th Ed. American Psychiatric Association (APA). American Psychiatric Publications, Arlington, VA, USA, 2013. (http://www.dsm5.org/psychiatrists/practice/dsm.)Diagnostic and Statistical Manual of Mental Disorders5thAmerican Psychiatric Association (APA)American Psychiatric PublicationsArlington, VA, USA2013http://www.dsm5.org/psychiatrists/practice/dsmSearch in Google Scholar

Fombonne E. Epidemiology of pervasive developmental disorders. Pediatr Res. 2009; 65(6): 591-598.FombonneEEpidemiology of pervasive developmental disordersPediatr Res200965659159810.1093/med/9780195371826.003.0007Search in Google Scholar

Kim YS, Leventhal BL, Koh YJ, Fombonne E, Laska E, Lim EC, et al. Prevalence of autism spectrum disorders in a total population sample. Am J Psychiatry. 2011; 168(9): 904-912.KimYSLeventhalBLKohYJFombonneELaskaELimECet alPrevalence of autism spectrum disorders in a total population sampleAm J Psychiatry2011168990491210.1176/appi.ajp.2011.10101532Search in Google Scholar

Fuentes J. Autism spectrum disorders: Ten tips to support me. J Am Acad Child Adolesc Psychiatry. 2014; 53(11): 1145-1146, 1146 e1-3. doi: 10.1016/j. cbpa.2014. 07.017.FuentesJAutism spectrum disorders: Ten tips to support meJ Am Acad Child Adolesc Psychiatry20145311114511461146 e1-3doi: 10.1016/j.cbpa.2014. 07.017Open DOISearch in Google Scholar

Levy SE, Mandell DS, Schultz RT. Autism. Lancet. 2009; 374(9701): 1627-1638.LevySEMandellDSSchultz RTAutism. Lancet200937497011627163810.1016/S0140-6736(09)61376-3Search in Google Scholar

Santangelo SL, Tsatsanis K. What is known about autism: Genes, brain, and behavior. Am J Pharmacogenomics. 2005; 5(2): 71-92.SantangeloSLTsatsanisKWhat is known about autism: Genes, brain, and behaviorAm J Pharmacogenomics200552719210.2165/00129785-200505020-0000115813671Search in Google Scholar

Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, et al. Autism as a strongly genetic disorder: Evidence from a British twin study. Psychol Med. 1995; 25(1): 63-77.BaileyALe CouteurAGottesmanIBoltonPSimonoffEYuzdaEet alAutism as a strongly genetic disorder: Evidence from a British twin studyPsychol Med1995251637710.1017/S00332917000280997792363Search in Google Scholar

Schaefer GB, Mendelsohn NJ, Professional P, Guidelines C. Clinical genetics evaluation in identifying the etiology of autism spectrum disorders. Genet Med. 2008; 10(4): 301-305.SchaeferGBMendelsohnNJProfessionalPGuidelinesCClinical genetics evaluation in identifying the etiology of autism spectrum disordersGenet Med200810430130510.1097/GIM.0b013e31816b5cc9311101218414214Search in Google Scholar

Miles JH, Takahashi TN, Bagby S, Sahota PK, Vaslow DF, Wang CH, et al. Essential versus complex autism: Definition of fundamental prognostic subtypes. Am J Med Genet A. 2005; 135(2): 171-180.MilesJHTakahashiTNBagbySSahotaPKVaslowDFWangCHet alEssential versus complex autism: Definition of fundamental prognostic subtypesAm J Med Genet A2005135217118010.1002/ajmg.a.3059015887228Search in Google Scholar

Miles JH. Autism spectrum disorders – A genetics review. Genet Med. 2011; 13(4): 278-294.MilesJHAutism spectrum disorders – A genetics reviewGenet Med201113427829410.1097/GIM.0b013e3181ff67ba21358411Search in Google Scholar

Banerjee-Basu S, Packer A. SFARI Gene: An evolving database for the autism research community. Dis Model Mech. 2010; 3(3-4): 133-135.Banerjee-BasuSPackerA.SFARI Gene: An evolving database for the autism research communityDis Model Mech201033-413313510.1242/dmm.00543920212079Search in Google Scholar

Reissner C, Klose M, Fairless R, Missler M. Mutational analysis of the neurexin/neuroligin complex reveals essential and regulatory components. Proc Natl Acad Sci USA. 2008; 105(39): 15124-15129.ReissnerCKloseMFairlessRMisslerMMutational analysis of the neurexin/neuroligin complex reveals essential and regulatory componentsProc Natl Acad Sci USA200810539151241512910.1073/pnas.0801639105255162618812509Search in Google Scholar

Diagnostic and Statistical Manual of Mental Disorders, 4th Ed. (Text Revision) (DSM-IV-TR). American Psychiatric Association, Washington, DC, USA, 2000.Diagnostic and Statistical Manual of Mental Disorders4th(Text Revision) (DSM-IV-TR)American Psychiatric AssociationWashington, DC, USA2000Search in Google Scholar

Schopler E, Reichler RJ, DeVellis RF, Daly K. Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS). J Autism Dev Disord. 1980; 10(1): 91-103.SchoplerEReichlerRJDeVellisRFDalyKToward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)J Autism Dev Disord19801019110310.1007/BF024084366927682Search in Google Scholar

Sucuoglu B, Oktem F, Akkok F, Gokler B. A study of the scales for the assessment of the children with autism. (Turkish) J Psychiatry Psychopharmacol Psychol. 1996; 4(2): 116-121.SucuogluBOktemFAkkokFGoklerBA study of the scales for the assessment of the children with autism(Turkish) J Psychiatry Psychopharmacol Psychol199642116121Search in Google Scholar

World Health Organization. ICD-10: International Statistical Classification of Diseases and Related Health Problems, 10th revision, 2nd Ed. WHO, Geneva, Switzerland, 2002. (http://www.who.int/iris/handle/10665/42980).World Health OrganizationICD-10: International Statistical Classification of Diseases and Related Health Problems, 10th revision, 2nd Ed. WHO, Geneva, Switzerland2002http://www.who.int/iris/handle/10665/42980Search in Google Scholar

Feng J, Schroer R, Yan J, Song W, Yang C, Bockholt A, et al. High frequency of neurexin 1β signal peptide structural variants in patients with autism. Neurosci Lett. 2006; 409(1): 10-13.FengJSchroerRYanJSongWYangCBockholtAet alHigh frequency of neurexin 1β signal peptide structural variants in patients with autismNeurosci Lett20064091101310.1016/j.neulet.2006.08.01717034946Search in Google Scholar

Kim H-G, Kishikawa S, Higgins AW, Seong I-S, Donovan DJ, Shen Y, et al. Disruption of neurexin 1 associated with autism spectrum disorder. Am J Hum Genet. 2008; 82(1): 199-207.KimH-GKishikawaSHigginsAWSeongI-SDonovanDJShenYet alDisruption of neurexin 1 associated with autism spectrum disorderAm J Hum Genet200882119920710.1016/j.ajhg.2007.09.011225396118179900Search in Google Scholar

Baron-Cohen S, Wheelwright S, Skinner R, Martin J, Clubley E. The autism-spectrum quotient (AQ): Evidence from Asperger syndrome/high-functioning autism, males and females, scientists and mathematicians. J Autism Dev Disord. 2001; 31(1): 5-17.Baron-CohenSWheelwrightSSkinnerRMartinJClubleyEThe autism-spectrum quotient (AQ): Evidence from Asperger syndrome/high-functioning autism, males and females, scientists and mathematiciansJ Autism Dev Disord200131151710.1023/A:1005653411471Search in Google Scholar

Köse S, Bora E, Erermis S, Aydin C. Psychometric features of Turkish version of autism-spectrum quotient. (Turkish) Anadolu Psikiyatri Derg. 2010; 11: 253-260.KöseSBoraEErermisSAydinCPsychometric features of Turkish version of autism-spectrum quotient(Turkish) Anadolu Psikiyatri Derg201011253260Search in Google Scholar

Duong L, Klitten LL, Møller RS, Ingason A, Jakobsen KD, Skjødt C, et al. Mutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disorders. Am J Med Genet B Neuropsychiatr Genet. 2012; 159B(3): 354-358.DuongLKlittenLLMøllerRSIngasonAJakobsenKDSkjødtCet alMutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disordersAm J Med Genet B Neuropsychiatr Genet2012159B335435810.1002/ajmg.b.3203622337556Search in Google Scholar

Sasson NJ, Faso DJ, Parlier M, Daniels JL, Piven J. When father doesn’t know best: Selective disagreement between self-report and informant report of the broad autism phenotype in parents of a child with autism. Autism Res. 2014; 7(6): 731-739.SassonNJFasoDJParlierMDanielsJLPivenJWhen father doesn’t know best: Selective disagreement between self-report and informant report of the broad autism phenotype in parents of a child with autismAutism Res20147673173910.1002/aur.142525339495Search in Google Scholar

eISSN:
1311-0160
Language:
English
Publication timeframe:
2 times per year
Journal Subjects:
Medicine, Basic Medical Science, other