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Items: 1 to 20 of 103

1.

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.

2.

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
3.

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.

4.

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.

5.

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2.

Tan GC, Doke TF, Ashburner J, Wood NW, Frackowiak RS.

Neuroimage. 2010 Nov 15;53(3):1030-42. doi: 10.1016/j.neuroimage.2010.02.018. Epub 2010 Feb 20.

6.

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.

7.

Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.

Chiocchetti AG, Kopp M, Waltes R, Haslinger D, Duketis E, Jarczok TA, Poustka F, Voran A, Graab U, Meyer J, Klauck SM, Fulda S, Freitag CM.

Mol Psychiatry. 2015 Jul;20(7):839-49. doi: 10.1038/mp.2014.103. Epub 2014 Sep 16.

PMID:
25224256
8.

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
9.

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.

10.

CNTNAP2 gene in high functioning autism: no association according to family and meta-analysis approaches.

Werling AM, Bobrowski E, Taurines R, Gundelfinger R, Romanos M, Grünblatt E, Walitza S.

J Neural Transm (Vienna). 2016 Mar;123(3):353-63. doi: 10.1007/s00702-015-1458-5. Epub 2015 Nov 11.

PMID:
26559825
11.

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
12.

CNTNAP2 variants affect early language development in the general population.

Whitehouse AJ, Bishop DV, Ang QW, Pennell CE, Fisher SE.

Genes Brain Behav. 2011 Jun;10(4):451-6. doi: 10.1111/j.1601-183X.2011.00684.x. Epub 2011 Mar 1. Erratum in: Genes Brain Behav. 2012 Jun;11(4):501.

13.

Selective Dysregulation of Hippocampal Inhibition in the Mouse Lacking Autism Candidate Gene CNTNAP2.

Jurgensen S, Castillo PE.

J Neurosci. 2015 Oct 28;35(43):14681-7. doi: 10.1523/JNEUROSCI.1666-15.2015.

14.

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.

Li X, Hu Z, He Y, Xiong Z, Long Z, Peng Y, Bu F, Ling J, Xun G, Mo X, Pan Q, Zhao J, Xia K.

Psychiatr Genet. 2010 Jun;20(3):113-7. doi: 10.1097/YPG.0b013e32833a216f.

PMID:
20414140
15.

Altered structural brain connectivity in healthy carriers of the autism risk gene, CNTNAP2.

Dennis EL, Jahanshad N, Rudie JD, Brown JA, Johnson K, McMahon KL, de Zubicaray GI, Montgomery G, Martin NG, Wright MJ, Bookheimer SY, Dapretto M, Toga AW, Thompson PM.

Brain Connect. 2011;1(6):447-59. doi: 10.1089/brain.2011.0064. Erratum in: Brain Connect. 2012;2(6):356.

16.

Learning delays in a mouse model of Autism Spectrum Disorder.

Rendall AR, Truong DT, Fitch RH.

Behav Brain Res. 2016 Apr 15;303:201-7. doi: 10.1016/j.bbr.2016.02.006. Epub 2016 Feb 9.

17.

Defining the contribution of CNTNAP2 to autism susceptibility.

Sampath S, Bhat S, Gupta S, O'Connor A, West AB, Arking DE, Chakravarti A.

PLoS One. 2013 Oct 17;8(10):e77906. doi: 10.1371/journal.pone.0077906. eCollection 2013.

18.

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.

Peñagarikano O, Abrahams BS, Herman EI, Winden KD, Gdalyahu A, Dong H, Sonnenblick LI, Gruver R, Almajano J, Bragin A, Golshani P, Trachtenberg JT, Peles E, Geschwind DH.

Cell. 2011 Sep 30;147(1):235-46. doi: 10.1016/j.cell.2011.08.040.

19.

A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits.

Stein MB, Yang BZ, Chavira DA, Hitchcock CA, Sung SC, Shipon-Blum E, Gelernter J.

Biol Psychiatry. 2011 May 1;69(9):825-31. doi: 10.1016/j.biopsych.2010.11.008. Epub 2010 Dec 30.

20.

Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.

Wassink TH, Hazlett HC, Epping EA, Arndt S, Dager SR, Schellenberg GD, Dawson G, Piven J.

Arch Gen Psychiatry. 2007 Jun;64(6):709-17.

PMID:
17548752

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