244 related articles for article (PubMed ID: 23277129)
1. 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. PubMed ID: 23277129
[TBL] [Abstract][Full Text] [Related]
2. Cntnap2 expression in the cerebellum of Foxp2(R552H) mice, with a mutation related to speech-language disorder.
Fujita E; Tanabe Y; Momoi MY; Momoi T
Neurosci Lett; 2012 Jan; 506(2):277-80. PubMed ID: 22133810
[TBL] [Abstract][Full Text] [Related]
3. The WNT2 gene polymorphism associated with speech delay inherent to autism.
Lin PI; Chien YL; Wu YY; Chen CH; Gau SS; Huang YS; Liu SK; Tsai WC; Chiu YN
Res Dev Disabil; 2012; 33(5):1533-40. PubMed ID: 22522212
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 26559825
[TBL] [Abstract][Full Text] [Related]
5. 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; 14(12):e1007535. PubMed ID: 30586385
[TBL] [Abstract][Full Text] [Related]
6. 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; 15(1):. PubMed ID: 26909962
[TBL] [Abstract][Full Text] [Related]
7. Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean population.
Park Y; Won S; Nam M; Chung JH; Kwack K
J Child Neurol; 2014 Dec; 29(12):NP207-11. PubMed ID: 24356376
[TBL] [Abstract][Full Text] [Related]
8. 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; 69(9):825-31. PubMed ID: 21193173
[TBL] [Abstract][Full Text] [Related]
9. 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. PubMed ID: 28284582
[TBL] [Abstract][Full Text] [Related]
10. CNTNAP2 gene polymorphisms in autism spectrum disorder and language impairment among Bangladeshi children: a case-control study combined with a meta-analysis.
Uddin MS; Azima A; Aziz MA; Aka TD; Jafrin S; Millat MS; Siddiqui SA; Uddin MG; Hussain MS; Islam MS
Hum Cell; 2021 Sep; 34(5):1410-1423. PubMed ID: 33950402
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 21310003
[TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 21987501
[TBL] [Abstract][Full Text] [Related]
13. Evaluation of FOXP2 as an autism susceptibility gene.
Wassink TH; Piven J; Vieland VJ; Pietila J; Goedken RJ; Folstein SE; Sheffield VC
Am J Med Genet; 2002 Jul; 114(5):566-9. PubMed ID: 12116195
[TBL] [Abstract][Full Text] [Related]
14. A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.
Han TU; Park J; Domingues CF; Moretti-Ferreira D; Paris E; Sainz E; Gutierrez J; Drayna D
Neurobiol Dis; 2014 Sep; 69():23-31. PubMed ID: 24807205
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 18179893
[TBL] [Abstract][Full Text] [Related]
16. A functional genetic link between distinct developmental language disorders.
Vernes SC; Newbury DF; Abrahams BS; Winchester L; Nicod J; Groszer M; Alarcón M; Oliver PL; Davies KE; Geschwind DH; Monaco AP; Fisher SE
N Engl J Med; 2008 Nov; 359(22):2337-45. PubMed ID: 18987363
[TBL] [Abstract][Full Text] [Related]
17. Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.
Li H; Yamagata T; Mori M; Momoi MY
Brain Dev; 2005 Apr; 27(3):207-10. PubMed ID: 15737702
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 20414140
[TBL] [Abstract][Full Text] [Related]
19. 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; 11(1):e1004852. PubMed ID: 25621974
[TBL] [Abstract][Full Text] [Related]
20. Association between CNTNAP2 polymorphisms and autism: A family-based study in the chinese han population and a meta-analysis combined with GWAS data of psychiatric genomics consortium.
Zhang T; Zhang J; Wang Z; Jia M; Lu T; Wang H; Yue W; Zhang D; Li J; Wang L
Autism Res; 2019 Apr; 12(4):553-561. PubMed ID: 30681286
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]