These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

221 related articles for article (PubMed ID: 26909962)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 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. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Association study of IL-17RC, CHL1, DSCAM and CNTNAP2 genes polymorphisms with adolescent idiopathic scoliosis susceptibility in a Chinese Han population.
    Zhou S; Zhu Z; Qiu X; Wu W; Wang W; Liu Z; Lv F; Qiu Y
    Stud Health Technol Inform; 2012; 176():47-51. PubMed ID: 22744455
    [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. Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort.
    Landini M; Merelli I; Raggi ME; Galluccio N; Ciceri F; Bonfanti A; Camposeo S; Massagli A; Villa L; Salvi E; Cusi D; Molteni M; Milanesi L; Marabotti A; Mezzelani A
    Int J Mol Sci; 2016 Oct; 17(10):. PubMed ID: 27782075
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neurexin gene family variants as risk factors for autism spectrum disorder.
    Wang J; Gong J; Li L; Chen Y; Liu L; Gu H; Luo X; Hou F; Zhang J; Song R
    Autism Res; 2018 Jan; 11(1):37-43. PubMed ID: 29045040
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.