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Journal Abstract Search

465 related items for PubMed ID: 30629339

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

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  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Behavioral phenotypes and neurobiological mechanisms in the Shank1 mouse model for autism spectrum disorder: A translational perspective.
    Sungur AÖ, Schwarting RKW, Wöhr M.
    Behav Brain Res; 2018 Oct 15; 352():46-61. PubMed ID: 28963042
    [Abstract] [Full Text] [Related]

  • 7. SHANK1 Deletions in Males with Autism Spectrum Disorder.
    Sato D, Lionel AC, Leblond CS, Prasad A, Pinto D, Walker S, O'Connor I, Russell C, Drmic IE, Hamdan FF, Michaud JL, Endris V, Roeth R, Delorme R, Huguet G, Leboyer M, Rastam M, Gillberg C, Lathrop M, Stavropoulos DJ, Anagnostou E, Weksberg R, Fombonne E, Zwaigenbaum L, Fernandez BA, Roberts W, Rappold GA, Marshall CR, Bourgeron T, Szatmari P, Scherer SW.
    Am J Hum Genet; 2012 May 04; 90(5):879-87. PubMed ID: 22503632
    [Abstract] [Full Text] [Related]

  • 8. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
    Leblond CS, Nava C, Polge A, Gauthier J, Huguet G, Lumbroso S, Giuliano F, Stordeur C, Depienne C, Mouzat K, Pinto D, Howe J, Lemière N, Durand CM, Guibert J, Ey E, Toro R, Peyre H, Mathieu A, Amsellem F, Rastam M, Gillberg IC, Rappold GA, Holt R, Monaco AP, Maestrini E, Galan P, Heron D, Jacquette A, Afenjar A, Rastetter A, Brice A, Devillard F, Assouline B, Laffargue F, Lespinasse J, Chiesa J, Rivier F, Bonneau D, Regnault B, Zelenika D, Delepine M, Lathrop M, Sanlaville D, Schluth-Bolard C, Edery P, Perrin L, Tabet AC, Schmeisser MJ, Boeckers TM, Coleman M, Sato D, Szatmari P, Scherer SW, Rouleau GA, Betancur C, Leboyer M, Gillberg C, Delorme R, Bourgeron T.
    PLoS Genet; 2014 Sep 04; 10(9):e1004580. PubMed ID: 25188300
    [Abstract] [Full Text] [Related]

  • 9. Early communication deficits in the Shank1 knockout mouse model for autism spectrum disorder: Developmental aspects and effects of social context.
    Sungur AÖ, Schwarting RK, Wöhr M.
    Autism Res; 2016 Jun 04; 9(6):696-709. PubMed ID: 26419918
    [Abstract] [Full Text] [Related]

  • 10. Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.
    Liu Y, Du Y, Liu W, Yang C, Liu Y, Wang H, Gong X.
    PLoS One; 2013 Jun 04; 8(2):e56639. PubMed ID: 23468870
    [Abstract] [Full Text] [Related]

  • 11. Repetitive behaviors in the Shank1 knockout mouse model for autism spectrum disorder: developmental aspects and effects of social context.
    Sungur AÖ, Vörckel KJ, Schwarting RK, Wöhr M.
    J Neurosci Methods; 2014 Aug 30; 234():92-100. PubMed ID: 24820912
    [Abstract] [Full Text] [Related]

  • 12. SHANK1 and autism spectrum disorders.
    Gong X, Wang H.
    Sci China Life Sci; 2015 Oct 30; 58(10):985-90. PubMed ID: 26335738
    [Abstract] [Full Text] [Related]

  • 13. A study of single nucleotide polymorphisms in CD157, AIM2 and JARID2 genes in Han Chinese children with autism spectrum disorder.
    Mo W, Liu J, Zhang Z, Yu H, Yang A, Qu F, Hu P, Liu Z, Hu F.
    Nord J Psychiatry; 2018 Apr 30; 72(3):179-183. PubMed ID: 29216786
    [Abstract] [Full Text] [Related]

  • 14. Modeling autism by SHANK gene mutations in mice.
    Jiang YH, Ehlers MD.
    Neuron; 2013 Apr 10; 78(1):8-27. PubMed ID: 23583105
    [Abstract] [Full Text] [Related]

  • 15. Two single-nucleotide polymorphisms of the RELN gene and symptom-based and developmental deficits among children and adolescents with autistic spectrum disorders in the Tianjin, China.
    Wang GF, Ye S, Gao L, Han Y, Guo X, Dong XP, Su YY, Zhang X.
    Behav Brain Res; 2018 Sep 17; 350():1-5. PubMed ID: 29753726
    [Abstract] [Full Text] [Related]

  • 16. In vitro zinc supplementation alters synaptic deficits caused by autism spectrum disorder-associated Shank2 point mutations in hippocampal neurons.
    Vyas Y, Jung Y, Lee K, Garner CC, Montgomery JM.
    Mol Brain; 2021 Jun 24; 14(1):95. PubMed ID: 34167580
    [Abstract] [Full Text] [Related]

  • 17. Genome-wide association analysis of autism identified multiple loci that have been reported as strong signals for neuropsychiatric disorders.
    Xia L, Ou J, Li K, Guo H, Hu Z, Bai T, Zhao J, Xia K, Zhang F.
    Autism Res; 2020 Mar 24; 13(3):382-396. PubMed ID: 31647196
    [Abstract] [Full Text] [Related]

  • 18. 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 24; 34(5):1410-1423. PubMed ID: 33950402
    [Abstract] [Full Text] [Related]

  • 19. The association of SHANK3 gene polymorphism and autism.
    Mashayekhi F, Mizban N, Bidabadi E, Salehi Z.
    Minerva Pediatr (Torino); 2021 Jun 24; 73(3):251-255. PubMed ID: 27271042
    [Abstract] [Full Text] [Related]

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