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.
166 related articles for article (PubMed ID: 33308194)
21. A novel missense mutation of the ubiquitin protein ligase E3A gene in a patient with Angelman syndrome. Bai JL; Qu YJ; Zou LP; Yang XY; Liu LJ; Song F Chin Med J (Engl); 2011 Jan; 124(1):84-8. PubMed ID: 21362313 [TBL] [Abstract][Full Text] [Related]
22. Increased gene dosage of Ube3a results in autism traits and decreased glutamate synaptic transmission in mice. Smith SE; Zhou YD; Zhang G; Jin Z; Stoppel DC; Anderson MP Sci Transl Med; 2011 Oct; 3(103):103ra97. PubMed ID: 21974935 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. 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]
27. Sex-biasing influence of autism-associated Montani C; Balasco L; Pagani M; Alvino FG; Barsotti N; de Guzman AE; Galbusera A; de Felice A; Nickl-Jockschat TK; Migliarini S; Casarosa S; Lau P; Mattioni L; Pasqualetti M; Provenzano G; Bozzi Y; Lombardo MV; Gozzi A Sci Adv; 2024 Jul; 10(28):eadg1421. PubMed ID: 38996019 [TBL] [Abstract][Full Text] [Related]
28. A Family-Based Association Study of CYP11A1 and CYP11B1 Gene Polymorphisms With Autism in Chinese Trios. Deng HZ; You C; Xing Y; Chen KY; Zou XB J Child Neurol; 2016 May; 31(6):733-7. PubMed ID: 26690694 [TBL] [Abstract][Full Text] [Related]
29. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder. Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967 [TBL] [Abstract][Full Text] [Related]
30. A pilot study on glutamate receptor and carrier gene variants and risk of childhood autism spectrum. Liu J; Yan J; Qu F; Mo W; Yu H; Hu P; Zhang Z Metab Brain Dis; 2023 Oct; 38(7):2477-2488. PubMed ID: 37578654 [TBL] [Abstract][Full Text] [Related]
31. A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A. Jiang YH; Sahoo T; Michaelis RC; Bercovich D; Bressler J; Kashork CD; Liu Q; Shaffer LG; Schroer RJ; Stockton DW; Spielman RS; Stevenson RE; Beaudet AL Am J Med Genet A; 2004 Nov; 131(1):1-10. PubMed ID: 15389703 [TBL] [Abstract][Full Text] [Related]
32. 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; 350():1-5. PubMed ID: 29753726 [TBL] [Abstract][Full Text] [Related]
33. A novel variant in UBE3A in a family with multigenerational intellectual disability and developmental delay. Zhao X; Zheng Y; Wang L; Wang Y; Mei S; Kong X Mol Genet Genomic Med; 2022 Apr; 10(4):e1883. PubMed ID: 35225435 [TBL] [Abstract][Full Text] [Related]
34. Lack of evidence to support the glyoxalase 1 gene (GLO1) as a risk gene of autism in Han Chinese patients from Taiwan. Wu YY; Chien WH; Huang YS; Gau SS; Chen CH Prog Neuropsychopharmacol Biol Psychiatry; 2008 Oct; 32(7):1740-4. PubMed ID: 18721844 [TBL] [Abstract][Full Text] [Related]
35. Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population. Liu X; Kawamura Y; Shimada T; Otowa T; Koishi S; Sugiyama T; Nishida H; Hashimoto O; Nakagami R; Tochigi M; Umekage T; Kano Y; Miyagawa T; Kato N; Tokunaga K; Sasaki T J Hum Genet; 2010 Mar; 55(3):137-41. PubMed ID: 20094064 [TBL] [Abstract][Full Text] [Related]
36. The Autism Protein Ube3A/E6AP Remodels Neuronal Dendritic Arborization via Caspase-Dependent Microtubule Destabilization. Khatri N; Gilbert JP; Huo Y; Sharaflari R; Nee M; Qiao H; Man HY J Neurosci; 2018 Jan; 38(2):363-378. PubMed ID: 29175955 [No Abstract] [Full Text] [Related]
37. Replication of previous GWAS hits suggests the association between rs4307059 near MSNP1AS and autism in a Chinese Han population. Wang Z; Zhang J; Lu T; Zhang T; Jia M; Ruan Y; Zhang D; Li J; Wang L Prog Neuropsychopharmacol Biol Psychiatry; 2019 Jun; 92():194-198. PubMed ID: 30610940 [TBL] [Abstract][Full Text] [Related]
38. 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]
39. Single Nucleotide Polymorphisms in SLC19A1 and SLC25A9 Are Associated with Childhood Autism Spectrum Disorder in the Chinese Han Population. Liu J; Mo W; Zhang Z; Yu H; Yang A; Qu F; Hu P; Liu Z; Wang S J Mol Neurosci; 2017 Jun; 62(2):262-267. PubMed ID: 28536923 [TBL] [Abstract][Full Text] [Related]
40. Association of oligodendrocytes differentiation regulator gene DUSP15 with autism. Tian Y; Wang L; Jia M; Lu T; Ruan Y; Wu Z; Wang L; Liu J; Zhang D World J Biol Psychiatry; 2017 Mar; 18(2):143-150. PubMed ID: 27223645 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]