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Journal Abstract Search

201 related items for PubMed ID: 28536923

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  • 2. Association between genetic variants in SLC25A12 and risk of autism spectrum disorders: An integrated meta-analysis.
    Liu J, Yang A, Zhang Q, Yang G, Yang W, Lei H, Quan J, Qu F, Wang M, Zhang Z, Yu K.
    Am J Med Genet B Neuropsychiatr Genet; 2015 Jun; 168B(4):236-46. PubMed ID: 25921325
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  • 3. A Study of Single Nucleotide Polymorphisms of the SLC19A1/RFC1 Gene in Subjects with Autism Spectrum Disorder.
    Mahmuda NA, Yokoyama S, Huang JJ, Liu L, Munesue T, Nakatani H, Hayashi K, Yagi K, Yamagishi M, Higashida H.
    Int J Mol Sci; 2016 May 19; 17(5):. PubMed ID: 27213354
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  • 5. Polymorphisms in Vitamin D Receptor Genes in Association with Childhood Autism Spectrum Disorder.
    Zhang Z, Li S, Yu L, Liu J.
    Dis Markers; 2018 May 19; 2018():7862892. PubMed ID: 29581796
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  • 7. Association between autism spectrum disorder and polymorphisms in genes encoding serotine and dopamine receptors.
    Liu J, Fu H, Kong J, Yu H, Zhang Z.
    Metab Brain Dis; 2021 Jun 19; 36(5):865-870. PubMed ID: 33644845
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  • 14. Analysis of association between components of the folate metabolic pathway and autism spectrum disorder in eastern Indian subjects.
    Saha S, Saha T, Rajamma U, Sinha S, Mukhopadhyay K.
    Mol Biol Rep; 2022 Feb 19; 49(2):1281-1293. PubMed ID: 34792727
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  • 15. 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 19; 11(1):37-43. PubMed ID: 29045040
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  • 16. Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder.
    Fang F, Ge M, Liu J, Zhang Z, Yu H, Zhu S, Xu L, Shao L.
    Behav Neurol; 2021 Jan 19; 2021():4150926. PubMed ID: 34257739
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  • 17. Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.
    Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD.
    Am J Psychiatry; 2004 Apr 19; 161(4):662-9. PubMed ID: 15056512
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  • 19. 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
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