275 related articles for article (PubMed ID: 33950402)
1. 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]
2. 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]
3. Association between Genetic Variants in
Fang F; Ge M; Liu J; Zhang Z; Yu H; Zhu S; Xu L; Shao L
Behav Neurol; 2021; 2021():4150926. PubMed ID: 34257739
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Comprehensive systematic review and meta-analysis of the association between common genetic variants and autism spectrum disorder.
Fang Y; Cui Y; Yin Z; Hou M; Guo P; Wang H; Liu N; Cai C; Wang M
Gene; 2023 Dec; 887():147723. PubMed ID: 37598788
[TBL] [Abstract][Full Text] [Related]
7. Novel and known minor alleles of CNTNAP2 gene variants are associated with comorbidity of intellectual disability and epilepsy phenotypes: a case-control association study reveals potential biomarkers.
Ul Mudassir B; Agha Z
Mol Biol Rep; 2024 Feb; 51(1):276. PubMed ID: 38315301
[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. 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]
10. Common variants of the autism-associated CNTNAP2 gene contribute to the modulatory effect of social function mediated by temporal cortex.
Li D; Zhang L; Bai T; Huang W; Ji GJ; Yang T; Zhang Y; Tian Y; Qiu B; Wang K
Behav Brain Res; 2021 Jul; 409():113319. PubMed ID: 33901431
[TBL] [Abstract][Full Text] [Related]
11. Effect of CNTNAP2 polymorphism on receptive language in children with autism spectrum disorder without language developmental delay.
Shiota Y; Hirosawa T; Yoshimura Y; Tanaka S; Hasegawa C; Iwasaki S; Sano M; An KM; Yokoyama S; Kikuchi M
Neuropsychopharmacol Rep; 2022 Sep; 42(3):352-355. PubMed ID: 35733350
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Genetics of autism spectrum disorder: an umbrella review of systematic reviews and meta-analyses.
Qiu S; Qiu Y; Li Y; Cong X
Transl Psychiatry; 2022 Jun; 12(1):249. PubMed ID: 35705542
[TBL] [Abstract][Full Text] [Related]
14. SHANK1 polymorphisms and SNP-SNP interactions among SHANK family: A possible cue for recognition to autism spectrum disorder in infant age.
Qiu S; Li Y; Bai Y; Shi J; Cui H; Gu Y; Ren Y; Zhao Q; Zhang K; Lu M; Wang Y; Li Y; Zhong W; Zhu X; Liu Y; Cheng Y; Qiao Y; Liu Y
Autism Res; 2019 Mar; 12(3):375-383. PubMed ID: 30629339
[TBL] [Abstract][Full Text] [Related]
15. 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; 8(10):e77906. PubMed ID: 24147096
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Learning delays in a mouse model of Autism Spectrum Disorder.
Rendall AR; Truong DT; Fitch RH
Behav Brain Res; 2016 Apr; 303():201-7. PubMed ID: 26873041
[TBL] [Abstract][Full Text] [Related]
18. Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder.
Chien YL; Chen YC; Gau SS
Neuroimage Clin; 2021; 31():102729. PubMed ID: 34271514
[TBL] [Abstract][Full Text] [Related]
19. Genetic association between SHANK2 polymorphisms and susceptibility to autism spectrum disorder.
Bai Y; Qiu S; Li Y; Li Y; Zhong W; Shi M; Zhu X; Jiang H; Yu Y; Cheng Y; Liu Y
IUBMB Life; 2018 Aug; 70(8):763-776. PubMed ID: 29934968
[TBL] [Abstract][Full Text] [Related]
20. Language deficits in specific language impairment, attention deficit/hyperactivity disorder, and autism spectrum disorder: An analysis of polygenic risk.
Nudel R; Christiani CAJ; Ohland J; Uddin MJ; Hemager N; Ellersgaard DV; Spang KS; Burton BK; Greve AN; Gantriis DL; Bybjerg-Grauholm J; Jepsen JRM; Thorup AAE; Mors O; Nordentoft M; Werge T
Autism Res; 2020 Mar; 13(3):369-381. PubMed ID: 31577390
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
