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Results: 1 to 20 of 260

Cited In for PubMed (Select 19404256)


Association analysis of the Cadherin13 gene with schizophrenia in the Japanese population.

Otsuka I, Watanabe Y, Hishimoto A, Boku S, Mouri K, Shiroiwa K, Okazaki S, Nunokawa A, Shirakawa O, Someya T, Sora I.

Neuropsychiatr Dis Treat. 2015 Jun 2;11:1381-93. doi: 10.2147/NDT.S84736. eCollection 2015.


Investigation of sex differences in the expression of RORA and its transcriptional targets in the brain as a potential contributor to the sex bias in autism.

Hu VW, Sarachana T, Sherrard RM, Kocher KM.

Mol Autism. 2015 May 13;6:7. doi: 10.1186/2040-2392-6-7. eCollection 2015.


Recurrence rates provide evidence for sex-differential, familial genetic liability for autism spectrum disorders in multiplex families and twins.

Werling DM, Geschwind DH.

Mol Autism. 2015 May 13;6:27. doi: 10.1186/s13229-015-0004-5. eCollection 2015.


Autism and Intellectual Disability-Associated KIRREL3 Interacts with Neuronal Proteins MAP1B and MYO16 with Potential Roles in Neurodevelopment.

Liu YF, Sowell SM, Luo Y, Chaubey A, Cameron RS, Kim HG, Srivastava AK.

PLoS One. 2015 Apr 22;10(4):e0123106. doi: 10.1371/journal.pone.0123106. eCollection 2015.


Approaching motor and language deficits in autism from below: a biolinguistic perspective.

Benítez-Burraco A, Boeckx C.

Front Integr Neurosci. 2015 Mar 30;9:25. doi: 10.3389/fnint.2015.00025. eCollection 2015. No abstract available.


High-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disorders.

Butler MG, Rafi SK, Manzardo AM.

Int J Mol Sci. 2015 Mar 20;16(3):6464-95. doi: 10.3390/ijms16036464.


Cadherin-based transsynaptic networks in establishing and modifying neural connectivity.

Friedman LG, Benson DL, Huntley GW.

Curr Top Dev Biol. 2015;112:415-65. doi: 10.1016/bs.ctdb.2014.11.025. Epub 2015 Feb 11.


A Likelihood-Based Framework for Association Analysis of Allele-Specific Copy Numbers.

Hu YJ, Lin DY, Sun W, Zeng D.

J Am Stat Assoc. 2014 Oct;109(508):1533-1545.


No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.

Murdoch JD, Gupta AR, Sanders SJ, Walker MF, Keaney J, Fernandez TV, Murtha MT, Anyanwu S, Ober GT, Raubeson MJ, DiLullo NM, Villa N, Waqar Z, Sullivan C, Gonzalez L, Willsey AJ, Choe SY, Neale BM, Daly MJ, State MW.

PLoS Genet. 2015 Jan 26;11(1):e1004852. doi: 10.1371/journal.pgen.1004852. eCollection 2015 Jan.


Association study between autistic-like traits and polymorphisms in the autism candidate regions RELN, CNTNAP2, SHANK3, and CDH9/10.

Jonsson L, Zettergren A, Pettersson E, Hovey D, Anckarsäter H, Westberg L, Lichtenstein P, Lundström S, Melke J.

Mol Autism. 2014 Dec 16;5(1):55. doi: 10.1186/2040-2392-5-55. eCollection 2014.


Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.

St Pourcain B, Haworth CM, Davis OS, Wang K, Timpson NJ, Evans DM, Kemp JP, Ronald A, Price T, Meaburn E, Ring SM, Golding J, Hakonarson H, Plomin R, Davey Smith G.

Hum Genet. 2015 Jun;134(6):539-51. doi: 10.1007/s00439-014-1514-5. Epub 2014 Dec 17.


Synaptic plasticity, neural circuits, and the emerging role of altered short-term information processing in schizophrenia.

Crabtree GW, Gogos JA.

Front Synaptic Neurosci. 2014 Nov 25;6:28. doi: 10.3389/fnsyn.2014.00028. eCollection 2014. Review.


Developmental regulation of human cortex transcription and its clinical relevance at single base resolution.

Jaffe AE, Shin J, Collado-Torres L, Leek JT, Tao R, Li C, Gao Y, Jia Y, Maher BJ, Hyde TM, Kleinman JE, Weinberger DR.

Nat Neurosci. 2015 Jan;18(1):154-61. doi: 10.1038/nn.3898. Epub 2014 Dec 15.


Genetic epidemiology and insights into interactive genetic and environmental effects in autism spectrum disorders.

Kim YS, Leventhal BL.

Biol Psychiatry. 2015 Jan 1;77(1):66-74. doi: 10.1016/j.biopsych.2014.11.001. Epub 2014 Nov 5.


Social visual engagement in infants and toddlers with autism: early developmental transitions and a model of pathogenesis.

Klin A, Shultz S, Jones W.

Neurosci Biobehav Rev. 2015 Mar;50:189-203. doi: 10.1016/j.neubiorev.2014.10.006. Epub 2014 Oct 16. Review.


Protein interaction networks reveal novel autism risk genes within GWAS statistical noise.

Correia C, Oliveira G, Vicente AM.

PLoS One. 2014 Nov 19;9(11):e112399. doi: 10.1371/journal.pone.0112399. eCollection 2014.


Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant Behavior.

Butler MG, Usrey K, Roberts JL, Schroeder SR, Manzardo AM.

Genet Res Int. 2014;2014:408516. doi: 10.1155/2014/408516. Epub 2014 Oct 20.


Metabolomics as a tool for discovery of biomarkers of autism spectrum disorder in the blood plasma of children.

West PR, Amaral DG, Bais P, Smith AM, Egnash LA, Ross ME, Palmer JA, Fontaine BR, Conard KR, Corbett BA, Cezar GG, Donley EL, Burrier RE.

PLoS One. 2014 Nov 7;9(11):e112445. doi: 10.1371/journal.pone.0112445. eCollection 2014.


MACROD2 gene associated with autistic-like traits in a general population sample.

Jones RM, Cadby G, Blangero J, Abraham LJ, Whitehouse AJ, Moses EK.

Psychiatr Genet. 2014 Dec;24(6):241-8. doi: 10.1097/YPG.0000000000000052.


20q13.2-q13.33 deletion syndrome: A case report.

Butler MG, Usrey KM, Roberts JL, Manzardo AM, Schroeder SR.

J Pediatr Genet. 2013;2(3):157-161.

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