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Items: 1 to 20 of 117

1.

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.

Toma C, Pierce KD, Shaw AD, Heath A, Mitchell PB, Schofield PR, Fullerton JM.

PLoS Genet. 2018 Dec 26;14(12):e1007535. doi: 10.1371/journal.pgen.1007535. eCollection 2018 Dec.

2.

Genetic variants in the CNTNAP2 gene are associated with gender differences among dyslexic children in China.

Gu H, Hou F, Liu L, Luo X, Nkomola PD, Xie X, Li X, Song R.

EBioMedicine. 2018 Aug;34:165-170. doi: 10.1016/j.ebiom.2018.07.007. Epub 2018 Jul 13.

3.

Evaluation of CNTNAP2 gene rs2107856 polymorphism in Turkish population with pseudoexfoliation syndrome.

Karaca I, Yilmaz SG, Palamar M, Onay H, Akgun B, Aytacoglu B, Aykut A, Ozkinay FF.

Int Ophthalmol. 2019 Jan;39(1):167-173. doi: 10.1007/s10792-017-0800-3. Epub 2017 Dec 19.

PMID:
29260496
4.

CNTNAP2 mutations and autosomal dominant epilepsy with auditory features.

Leonardi E, Dazzo E, Aspromonte MC, Tabaro F, Pascarelli S, Tosatto SCE, Michelucci R, Murgia A, Nobile C.

Epilepsy Res. 2018 Jan;139:51-53. doi: 10.1016/j.eplepsyres.2017.11.006. Epub 2017 Nov 21.

PMID:
29179159
5.

Mouse Cntnap2 and Human CNTNAP2 ASD Alleles Cell Autonomously Regulate PV+ Cortical Interneurons.

Vogt D, Cho KKA, Shelton SM, Paul A, Huang ZJ, Sohal VS, Rubenstein JLR.

Cereb Cortex. 2018 Nov 1;28(11):3868-3879. doi: 10.1093/cercor/bhx248.

6.

Persistent microglial activation and synaptic loss with behavioral abnormalities in mouse offspring exposed to CASPR2-antibodies in utero.

Coutinho E, Menassa DA, Jacobson L, West SJ, Domingos J, Moloney TC, Lang B, Harrison PJ, Bennett DLH, Bannerman D, Vincent A.

Acta Neuropathol. 2017 Oct;134(4):567-583. doi: 10.1007/s00401-017-1751-5. Epub 2017 Jul 28.

7.

From CNTNAP2 to Early Expressive Language in Infancy: The Mediation Role of Rapid Auditory Processing.

Riva V, Cantiani C, Benasich AA, Molteni M, Piazza C, Giorda R, Dionne G, Marino C.

Cereb Cortex. 2018 Jun 1;28(6):2100-2108. doi: 10.1093/cercor/bhx115.

PMID:
28498932
8.

The association of CNTNAP2 rs7794745 gene polymorphism and autism in Iranian population.

Zare S, Mashayekhi F, Bidabadi E.

J Clin Neurosci. 2017 May;39:189-192. doi: 10.1016/j.jocn.2017.01.008. Epub 2017 Mar 9.

PMID:
28284582
9.

Associations between the CNTNAP2 gene, dorsolateral prefrontal cortex, and cognitive performance on the Stroop task.

Zhu B, Chen C, Xue G, Lei X, Wang Y, Li J, Moyzis RK, Li J, Dong Q, Lin C.

Neuroscience. 2017 Feb 20;343:21-29. doi: 10.1016/j.neuroscience.2016.11.021. Epub 2016 Dec 1.

PMID:
27916731
10.

Family-based genetic association study of CNTNAP2 polymorphisms and sociality endophenotypes in Korean patients with autism spectrum disorders.

Yoo HJ, Kim BN, Kim JW, Shin MS, Park TW, Son JW, Chung US, Park M, Kim SA.

Psychiatr Genet. 2017 Feb;27(1):38-39. doi: 10.1097/YPG.0000000000000150. No abstract available.

PMID:
27574960
11.

Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum.

Smogavec M, Cleall A, Hoyer J, Lederer D, Nassogne MC, Palmer EE, Deprez M, Benoit V, Maystadt I, Noakes C, Leal A, Shaw M, Gecz J, Raymond L, Reis A, Shears D, Brockmann K, Zweier C.

J Med Genet. 2016 Dec;53(12):820-827. doi: 10.1136/jmedgenet-2016-103880. Epub 2016 Jul 20.

PMID:
27439707
12.

The clinical spectrum of Caspr2 antibody-associated disease.

van Sonderen A, Ariño H, Petit-Pedrol M, Leypoldt F, Körtvélyessy P, Wandinger KP, Lancaster E, Wirtz PW, Schreurs MW, Sillevis Smitt PA, Graus F, Dalmau J, Titulaer MJ.

Neurology. 2016 Aug 2;87(5):521-8. doi: 10.1212/WNL.0000000000002917. Epub 2016 Jul 1.

13.

A common variant of the CNTNAP2 gene is associated with structural variation in the left superior occipital gyrus.

Uddén J, Snijders TM, Fisher SE, Hagoort P.

Brain Lang. 2017 Sep;172:16-21. doi: 10.1016/j.bandl.2016.02.003. Epub 2016 Apr 5.

PMID:
27059522
14.

Single nucleotide polymorphisms in the CNTNAP2 gene in Brazilian patients with autistic spectrum disorder.

Nascimento PP, Bossolani-Martins AL, Rosan DB, Mattos LC, Brandão-Mattos C, Fett-Conte AC.

Genet Mol Res. 2016 Feb 5;15(1). doi: 10.4238/gmr.15017422.

15.

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
16.

The role of candidate-gene CNTNAP2 in childhood apraxia of speech and specific language impairment.

Centanni TM, Sanmann JN, Green JR, Iuzzini-Seigel J, Bartlett C, Sanger WG, Hogan TP.

Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):536-43. doi: 10.1002/ajmg.b.32325. Epub 2015 Jun 19.

PMID:
26097074
17.

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.

18.

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
19.

A common copy number variation polymorphism in the CNTNAP2 gene: sexual dimorphism in association with healthy aging and disease.

Iakoubov L, Mossakowska M, Szwed M, Puzianowska-Kuznicka M.

Gerontology. 2015;61(1):24-31. doi: 10.1159/000363320. Epub 2014 Aug 18.

PMID:
25139204
20.

Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome.

Watson CM, Crinnion LA, Tzika A, Mills A, Coates A, Pendlebury M, Hewitt S, Harrison SM, Daly C, Roberts P, Carr IM, Sheridan EG, Bonthron DT.

Am J Med Genet A. 2014 Oct;164A(10):2649-55. doi: 10.1002/ajmg.a.36679. Epub 2014 Jul 16.

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