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 *

211 related articles for article (PubMed ID: 29408620)

  • 21. FADS1-FADS2 and ELOVL2 gene polymorphisms in susceptibility to autism spectrum disorders in Chinese children.
    Sun C; Zou M; Wang X; Xia W; Ma Y; Liang S; Hao Y; Wu L; Fu S
    BMC Psychiatry; 2018 Sep; 18(1):283. PubMed ID: 30180836
    [TBL] [Abstract][Full Text] [Related]  

  • 22. In Silico Elucidation of Deleterious Non-synonymous SNPs in SHANK3, the Autism Spectrum Disorder Gene.
    Owji H; Eslami M; Nezafat N; Ghasemi Y
    J Mol Neurosci; 2020 Oct; 70(10):1649-1667. PubMed ID: 32519210
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evaluating the association between the SHANK3 gene and bipolar disorder.
    Zhang C; Wu Z; Hong W; Peng D; Fang Y
    Psychiatry Res; 2016 Oct; 244():284-8. PubMed ID: 27512916
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Association Study of Polymorphisms in Genes Relevant to Vitamin B12 and Folate Metabolism with Childhood Autism Spectrum Disorder in a Han Chinese Population.
    Zhang Z; Yu L; Li S; Liu J
    Med Sci Monit; 2018 Jan; 24():370-376. PubMed ID: 29348398
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.
    Kuo PH; Chuang LC; Su MH; Chen CH; Chen CH; Wu JY; Yen CJ; Wu YY; Liu SK; Chou MC; Chou WJ; Chiu YN; Tsai WC; Gau SS
    PLoS One; 2015; 10(9):e0138695. PubMed ID: 26398136
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic Evidence for Possible Involvement of the Calcium Channel Gene CACNA1A in Autism Pathogenesis in Chinese Han Population.
    Li J; You Y; Yue W; Jia M; Yu H; Lu T; Wu Z; Ruan Y; Wang L; Zhang D
    PLoS One; 2015; 10(11):e0142887. PubMed ID: 26566276
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.
    Zhou WZ; Zhang J; Li Z; Lin X; Li J; Wang S; Yang C; Wu Q; Ye AY; Wang M; Wang D; Pu TZ; Wu YY; Wei L
    Hum Mutat; 2019 Jun; 40(6):801-815. PubMed ID: 30763456
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Autism-associated Shank3 mutations alter mGluR expression and mGluR-dependent but not NMDA receptor-dependent long-term depression.
    Lee K; Vyas Y; Garner CC; Montgomery JM
    Synapse; 2019 Aug; 73(8):e22097. PubMed ID: 30868621
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study.
    Zheng F; Wang L; Jia M; Yue W; Ruan Y; Lu T; Liu J; Li J; Zhang D
    Behav Brain Funct; 2011 May; 7():14. PubMed ID: 21569632
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Developmental social communication deficits in the Shank3 rat model of phelan-mcdermid syndrome and autism spectrum disorder.
    Berg EL; Copping NA; Rivera JK; Pride MC; Careaga M; Bauman MD; Berman RF; Lein PJ; Harony-Nicolas H; Buxbaum JD; Ellegood J; Lerch JP; Wöhr M; Silverman JL
    Autism Res; 2018 Apr; 11(4):587-601. PubMed ID: 29377611
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association study between genes in Reelin signaling pathway and autism identifies DAB1 as a susceptibility gene in a Chinese Han population.
    Li J; Liu J; Zhao L; Ma Y; Jia M; Lu T; Ruan Y; Li Q; Yue W; Zhang D; Wang L
    Prog Neuropsychopharmacol Biol Psychiatry; 2013 Jul; 44():226-32. PubMed ID: 23333377
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.
    Yu J; He X; Yao D; Li Z; Li H; Zhao Z
    Behav Brain Funct; 2011 May; 7():13. PubMed ID: 21569590
    [TBL] [Abstract][Full Text] [Related]  

  • 34. DIP2C polymorphisms are implicated in susceptibility and clinical phenotypes of autism spectrum disorder.
    Li Y; Sun C; Guo Y; Qiu S; Li Y; Liu Y; Zhong W; Wang H; Cheng Y; Liu Y
    Psychiatry Res; 2022 Oct; 316():114792. PubMed ID: 35987071
    [TBL] [Abstract][Full Text] [Related]  

  • 35. An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function.
    Wang L; Pang K; Han K; Adamski CJ; Wang W; He L; Lai JK; Bondar VV; Duman JG; Richman R; Tolias KF; Barth P; Palzkill T; Liu Z; Holder JL; Zoghbi HY
    Mol Psychiatry; 2020 Oct; 25(10):2534-2555. PubMed ID: 30610205
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Neural Stem Cells from Shank3-ko Mouse Model Autism Spectrum Disorders.
    Grasselli C; Carbone A; Panelli P; Giambra V; Bossi M; Mazzoccoli G; De Filippis L
    Mol Neurobiol; 2020 Mar; 57(3):1502-1515. PubMed ID: 31773410
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comparison of SHANK3 deficiency in animal models: phenotypes, treatment strategies, and translational implications.
    Delling JP; Boeckers TM
    J Neurodev Disord; 2021 Nov; 13(1):55. PubMed ID: 34784886
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Increased rates of cerebral protein synthesis in Shank3 knockout mice: Implications for a link between synaptic protein deficit and dysregulated protein synthesis in autism spectrum disorder/intellectual disability.
    Torossian A; Saré RM; Loutaev I; Smith CB
    Neurobiol Dis; 2021 Jan; 148():105213. PubMed ID: 33276083
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 36(5):865-870. PubMed ID: 33644845
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Unmasking a novel disease gene NEO1 associated with autism spectrum disorders by a hemizygous deletion on chromosome 15 and a functional polymorphism.
    Siu WK; Lam CW; Gao WW; Vincent Tang HM; Jin DY; Mak CM
    Behav Brain Res; 2016 Mar; 300():135-42. PubMed ID: 26518331
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.