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Items: 1 to 20 of 196

1.

Contact in the genetics of autism and schizophrenia.

Burbach JP, van der Zwaag B.

Trends Neurosci. 2009 Feb;32(2):69-72. doi: 10.1016/j.tins.2008.11.002. Epub 2009 Jan 8.

PMID:
19135727
2.

Disparate diseases due to copycat copy number variations.

Powell CM.

Arch Neurol. 2009 Sep;66(9):1158-9. doi: 10.1001/archneurol.2009.197. No abstract available.

3.

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy.

Friedman JI, Vrijenhoek T, Markx S, Janssen IM, van der Vliet WA, Faas BH, Knoers NV, Cahn W, Kahn RS, Edelmann L, Davis KL, Silverman JM, Brunner HG, van Kessel AG, Wijmenga C, Ophoff RA, Veltman JA.

Mol Psychiatry. 2008 Mar;13(3):261-6. Epub 2007 Jul 24. Erratum in: Mol Psychiatry. 2010 Nov;15(11):1121.

PMID:
17646849
4.

Copy-number variations associated with autism spectrum disorder.

Kakinuma H, Sato H.

Pharmacogenomics. 2008 Aug;9(8):1143-54. doi: 10.2217/14622416.9.8.1143. Review.

PMID:
18681787
5.

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.

Yan J, Oliveira G, Coutinho A, Yang C, Feng J, Katz C, Sram J, Bockholt A, Jones IR, Craddock N, Cook EH Jr, Vicente A, Sommer SS.

Mol Psychiatry. 2005 Apr;10(4):329-32. No abstract available.

PMID:
15622415
6.

Copy-number variations associated with neuropsychiatric conditions.

Cook EH Jr, Scherer SW.

Nature. 2008 Oct 16;455(7215):919-23. doi: 10.1038/nature07458. Review.

PMID:
18923514
7.

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.

Scott-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, Mumford JA, Poldrack RA, Dapretto M, Geschwind DH, Bookheimer SY.

Sci Transl Med. 2010 Nov 3;2(56):56ra80. doi: 10.1126/scitranslmed.3001344.

8.

[Neurodevelopmental disturbance in the pathogenesis of major mental disorders].

Kamiya A, Kitabatake Y, Sawa A.

Brain Nerve. 2008 Apr;60(4):445-52. Review. Japanese.

PMID:
18421986
9.

Genetic causes of syndromic and non-syndromic autism.

Caglayan AO.

Dev Med Child Neurol. 2010 Feb;52(2):130-8. doi: 10.1111/j.1469-8749.2009.03523.x. Epub 2010 Jan 5. Review.

10.

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A.

Am J Hum Genet. 2008 Jan;82(1):160-4. doi: 10.1016/j.ajhg.2007.09.015.

11.

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.

Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T; Paris Autism Research International Sibpair Study.

Nat Genet. 2003 May;34(1):27-9.

12.

Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.

Toma C, Hervás A, Torrico B, Balmaña N, Salgado M, Maristany M, Vilella E, Martínez-Leal R, Planelles MI, Cuscó I, del Campo M, Pérez-Jurado LA, Caballero-Andaluz R, de Diego-Otero Y, Pérez-Costillas L, Ramos-Quiroga JA, Ribasés M, Bayés M, Cormand B.

Psychiatr Genet. 2013 Apr;23(2):82-5. doi: 10.1097/YPG.0b013e32835d6fc6.

PMID:
23277129
13.

Neurexins.

Reissner C, Runkel F, Missler M.

Genome Biol. 2013;14(9):213. Review.

14.

Autism genetics: strategies, challenges, and opportunities.

O'Roak BJ, State MW.

Autism Res. 2008 Feb;1(1):4-17. doi: 10.1002/aur.3. Review.

PMID:
19360646
15.

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW.

Am J Hum Genet. 2008 Jan;82(1):165-73. doi: 10.1016/j.ajhg.2007.09.017.

16.

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.

Whalley HC, O'Connell G, Sussmann JE, Peel A, Stanfield AC, Hayiou-Thomas ME, Johnstone EC, Lawrie SM, McIntosh AM, Hall J.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):941-8. doi: 10.1002/ajmg.b.31241. Epub 2011 Oct 10.

PMID:
21987501
17.

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.

Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005.

18.

Autism spectrum disorders: developmental disconnection syndromes.

Geschwind DH, Levitt P.

Curr Opin Neurobiol. 2007 Feb;17(1):103-11. Epub 2007 Feb 1. Review.

PMID:
17275283
19.

The role of neurexins in schizophrenia and autistic spectrum disorder.

Reichelt AC, Rodgers RJ, Clapcote SJ.

Neuropharmacology. 2012 Mar;62(3):1519-26. doi: 10.1016/j.neuropharm.2011.01.024. Epub 2011 Jan 22. Review.

PMID:
21262241
20.

A genome-wide linkage and association scan reveals novel loci for autism.

Weiss LA, Arking DE; Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly MJ, Chakravarti A.

Nature. 2009 Oct 8;461(7265):802-8. doi: 10.1038/nature08490.

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