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For: Nisar S, Hashem S, Bhat AA, Syed N, Yadav S, Azeem MW, Uddin S, Bagga P, Reddy R, Haris M. Association of genes with phenotype in autism spectrum disorder. Aging (Albany NY) 2019;11:10742-70. [PMID: 31744938 DOI: 10.18632/aging.102473] [Cited by in Crossref: 6] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Tayanloo-beik A, Hamidpour SK, Abedi M, Shojaei H, Tavirani MR, Namazi N, Larijani B, Arjmand B. Zebrafish Modeling of Autism Spectrum Disorders, Current Status and Future Prospective. Front Psychiatry 2022;13:911770. [DOI: 10.3389/fpsyt.2022.911770] [Reference Citation Analysis]
2 Iyshwarya B, Vajagathali M, Ramakrishnan V. Investigation of Genetic Polymorphism in Autism Spectrum Disorder: a Pathogenesis of the Neurodevelopmental Disorder. Adv Neurodev Disord. [DOI: 10.1007/s41252-022-00251-z] [Reference Citation Analysis]
3 Polikowsky HG, Shaw DM, Petty LE, Chen HH, Pruett DG, Linklater JP, Viljoen KZ, Beilby JM, Highland HM, Levitt B, Avery CL, Mullan Harris K, Jones RM, Below JE, Kraft SJ. Population-based genetic effects for developmental stuttering. HGG Adv 2022;3:100073. [PMID: 35047858 DOI: 10.1016/j.xhgg.2021.100073] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Dean DD, Agarwal S, Muthuswamy S, Asim A. Brain exosomes as minuscule information hub for Autism Spectrum Disorder. Expert Rev Mol Diagn 2021;:1-9. [PMID: 34720032 DOI: 10.1080/14737159.2021.2000395] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
5 Li S, Guo Z, Ioffe JB, Hu Y, Zhen Y, Zhou X. Text mining of gene-phenotype associations reveals new phenotypic profiles of autism-associated genes. Sci Rep 2021;11:15269. [PMID: 34315992 DOI: 10.1038/s41598-021-94742-z] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Fernandes CAE, Cardoso AFH, Lopes CR, Henriques MMV, Pereira EPMN. Etiological investigation of genetic cause in autism spectrum disorder. Sci Med 2021;31:e39581. [DOI: 10.15448/1980-6108.2021.1.39581] [Reference Citation Analysis]
7 Wang Y, Zhang J, Song W, Tian X, Liu Y, Wang Y, Ma J, Wang C, Yan G. A proteomic analysis of urine biomarkers in autism spectrum disorder. J Proteomics 2021;242:104259. [PMID: 33957315 DOI: 10.1016/j.jprot.2021.104259] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
8 Uddin MG, Siddiqui SA, Uddin MS, Aziz MA, Hussain MS, Furhatun-noor, Millat MS, Sen N, Muhuri B, Islam MS. Genetic variants of ZNF385B and COMT are associated with autism spectrum disorder in the Bangladeshi children. Meta Gene 2020;26:100820. [DOI: 10.1016/j.mgene.2020.100820] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
9 Xie Q, Li Z, Wang Y, Zaidi S, Baranova A, Zhang F, Cao H. Preeclampsia Drives Molecular Networks to Shift Toward Greater Vulnerability to the Development of Autism Spectrum Disorder. Front Neurol 2020;11:590. [PMID: 32760337 DOI: 10.3389/fneur.2020.00590] [Cited by in F6Publishing: 2] [Reference Citation Analysis]