References
[1] American Psychiatric Association, 1994. Diagnostic and Statistical Manual of Mental Disorder. American Psychiatric Association,Washington, DC :
[2] American Psychiatric Association, 2013. Diagnostic and Statistical Manual of Mental Disorder. American Psychiatric Association,Washington, DC :
[3] Autism and Developmental Disabilities Monitoring Network Surveillance Year 2008 Principal Investigators, 2012. Prevalence of autism spectrum disorders—autism and developmental disabilities monitoring network, 14 sites, United States, 2008.
MMWR Surveill Summ, 61(3):1-19.
[4] Badner, J.A., Gershon, E.S., 2002. Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.
Mol Psychiatry, 7(1):56-66.
[5] Bailey, A., Le Couteur, A., Gottesman, I., 1995. Autism as a strongly genetic disorder: evidence from a British twin study.
Psychol Med, 25(1):63-77.
[6] Baird, G., Simonoff, E., Pickles, A., 2006. Prevalence of disorders of the autism spectrum in a population cohort of children in south Thames: the special needs and autism project (SNAP).
Lancet, 368(9531):210-215.
[7] Barrett, S., Beck, J.C., Bernier, R., 1999. An autosomal genomic screen for autism. Collaborative linkage study of autism.
Am J Med Genet, 88(6):609-615.
[8] Battye, R., Stevens, A., Perry, R.L., 2001. Repellent signaling by slit requires the leucine-rich repeats.
J Neurosci, 21(12):4290-4298.
[9] Beaty, T.H., Hetmanski, J.B., Fallin, M.D., 2006. Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.
Hum Genet, 120(4):501-518.
[10] Biersmith, B., Liu, Z.C., Bauman, K., 2011. The DOCK protein sponge binds to ELMO and functions in
Drosophila embryonic CNS development.
PLoS ONE, 6(1):e16120
[11] Brugha, T.S., Mcmanus, S., Bankart, J., 2011. Epidemiology of autism spectrum disorders in adults in the community in England.
Arch Gen Psychiatry, 68(5):459-465.
[12] Buxbaum, J.D., Silverman, J.M., Smith, C.J., 2001. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.
Am J Hum Genet, 68(6):1514-1520.
[13] Daz-Anzalda, A., Joober, R., Rivire, J.B., 2004. Association between 7q31 markers and tourette syndrome.
Am J Med Genet A, 127A(1):17-20.
[14] Elsabbagh, M., Divan, G., Koh, Y.J., 2012. Global prevalence of autism and other pervasive developmental disorders.
Autism Res, 5(3):160-179.
[15] Fombonne, E., 2009. Epidemiology of pervasive developmental disorders.
Pediatr Res, 65(6):591-598.
[16] Hallmayer, J., Cleveland, S., Torres, A., 2011. Genetic heritability and shared environmental factors among twin pairs with autism.
Arch Gen Psychiatry, 68(11):1095-1102.
[17] IMGSAC, 1998. A full genome screen for autism with evidence for linkage to a region on chromosome 7q.
Hum Mol Genet, 7(3):571-578.
[18] IMGSAC, 2001. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.
Am J Hum Genet, 69(3):570-581.
[19] Khaniani, M.S., Kalitsis, P., Burgess, T., 2008. An improved diagnostic PCR assay for identification of cryptic heterozygosity for CGG triplet repeat alleles in the Fragile X gene (FMR1).
Mol Cytogenet, 1(1):5
[20] Kim, Y.S., Leventhal, B.L., Koh, Y.J., 2011. Prevalence of autism spectrum disorders in a total population sample.
Am J Psychiatry, 168(9):904-912.
[21] Kleefstra, T., Yntema, H.G., Oudakker, A.R., 2004.
Zinc finger 81 (
ZNF81) mutations associated with X-linked mental retardation.
J Med Genet, 41(5):394-399.
[22] Kogan, M.D., Blumberg, S.J., Schieve, L.A., 2009. Prevalence of parent-reported diagnosis of autism spectrum disorder among children in the US, 2007.
Pediatrics, 124(5):1395-1403.
[23] Krug, D.A., Arick, J., Almond, P., 1980. Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior.
J Child Psychol Psychiatry, 21(3):221-229.
[24] Maestrini, E., Pagnamenta, A.T., Lamb, J.A., 2010. High-density SNP association study and copy number variation analysis of the
AUTS1 and
AUTS5 loci implicate the
IMMP2L-
DOCK4 gene region in autism susceptibility.
Mol Psychiatry, 15(9):954-968.
[25] Miyamoto, Y., Yamauchi, J., 2010. Cellular signaling of Dock family proteins in neural function.
Cell Signal, 22(2):175-182.
[26] Monfort, S., Rosello, M., Orellana, C., 2008. Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of
ZNF533 and duplication of charge syndrome genes.
J Med Genet, 45(7):432-437.
[27] Pagnamenta, A.T., Bacchelli, E., de Jonge, M.V., 2010. Characterization of a family with rare deletions in
CNTNAP5 and
DOCK4 suggests novel risk loci for autism and dyslexia.
Biol Psychiatry, 68(4):320-328.
[28] Petek, E., Windpassinger, C., Vincent, J.B., 2001. Disruption of a novel gene (
IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.
Am J Hum Genet, 68(4):848-858.
[29] Petek, E., Schwarzbraun, T., Noor, A., 2007. Molecular and genomic studies of
IMMP2L and mutation screening in autism and Tourette syndrome.
Mol Genet Genomics, 277(1):71-81.
[30] Schellenberg, G.D., Dawson, G., Sung, Y.J., 2006. Evidence for multiple loci from a genome scan of autism kindreds.
Mol Psychiatry, 11(11):1049-1060.
[31] Schopler, E., Reichler, R.J., Devellis, R.F., 1980. Toward objective classification of childhood autism: childhood autism rating scale (cars).
J Autism Dev Disord, 10(1):91-103.
[32] Shao, Y., Wolpert, C.M., Raiford, K.L., 2002. Genomic screen and follow-up analysis for autistic disorder.
Am J Med Genet, 114(1):99-105.
[33] Shao, Y., Raiford, K.L., Wolpert, C.M., 2002. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.
Am J Hum Genet, 70(4):1058-1061.
[34] Spielman, R.S., Ewens, W.J., 1996. The TDT and other family-based tests for linkage disequilibrium and association.
Am J Hum Genet, 59(5):983-989.
[35] Spielman, R.S., Mcginnis, R.E., Ewens, W.J., 1993. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).
Am J Hum Genet, 52(3):506-516.
[36] Szatmari, P., Paterson, A.D., Zwaigenbaum, L., 2007. Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Nat Genet, 39(3):319-328.
[37] Trikalinos, T.A., Karvouni, A., Zintzaras, E., 2006. A heterogeneity-based genome search meta-analysis for autism-spectrum disorders.
Mol Psychiatry, 11(1):29-36.
[38] Xiao, Y., Peng, Y., Wan, J., 2013. The atypical guanine nucleotide exchange factor Dock4 regulates neurite differentiation through modulation of Rac1 GTPase and actin dynamics.
J Biol Chem, 288(27):20034-20045.
[39] Xu, L.M., Li, J.R., Huang, Y., 2012. AutismKB: an evidence-based knowledgebase of autism genetics.
Nucl Acids Res, 40(D1):D1016-D1022.
[40] Zhou, X., Xu, Y., Wang, J., 2011. Replication of the association of a
MET variant with autism in a Chinese Han population.
PLoS ONE, 6(11):e27428
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