163 related articles for article (PubMed ID: 26518331)
1. 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]
2. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.
Yin CL; Chen HI; Li LH; Chien YL; Liao HM; Chou MC; Chou WJ; Tsai WC; Chiu YN; Wu YY; Lo CZ; Wu JY; Chen YT; Gau SS
Mol Autism; 2016; 7():23. PubMed ID: 27042285
[TBL] [Abstract][Full Text] [Related]
3. Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients.
Yang Z; Matsumoto A; Nakayama K; Jimbo EF; Kojima K; Nagata K; Iwamoto S; Yamagata T
Brain Dev; 2016 Jan; 38(1):91-9. PubMed ID: 25957987
[TBL] [Abstract][Full Text] [Related]
4. Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.
Wu J; Yu P; Jin X; Xu X; Li J; Li Z; Wang M; Wang T; Wu X; Jiang Y; Cai W; Mei J; Min Q; Xu Q; Zhou B; Guo H; Wang P; Zhou W; Hu Z; Li Y; Cai T; Wang Y; Xia K; Jiang YH; Sun ZS
J Genet Genomics; 2018 Oct; 45(10):527-538. PubMed ID: 30392784
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.
Zhang L; Qin Y; Gong X; Peng R; Cai C; Zheng Y; Du Y; Wang H
Transl Psychiatry; 2019 Jan; 9(1):31. PubMed ID: 30670685
[TBL] [Abstract][Full Text] [Related]
7. PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder.
Pijuan J; Ortigoza-Escobar JD; Ortiz J; Alcalá A; Calvo MJ; Cubells M; Hernando-Davalillo C; Palau F; Hoenicka J
Autism Res; 2021 Jun; 14(6):1088-1100. PubMed ID: 33749153
[TBL] [Abstract][Full Text] [Related]
8. Refining critical regions in 15q24 microdeletion syndrome pertaining to autism.
Liu Y; Zhang Y; Zarrei M; Dong R; Yang X; Zhao D; Scherer SW; Gai Z
Am J Med Genet B Neuropsychiatr Genet; 2020 Jun; 183(4):217-226. PubMed ID: 31953991
[TBL] [Abstract][Full Text] [Related]
9. 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; 8(2):e56639. PubMed ID: 23468870
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Copy number and sequence variants implicate APBA2 as an autism candidate gene.
Babatz TD; Kumar RA; Sudi J; Dobyns WB; Christian SL
Autism Res; 2009 Dec; 2(6):359-64. PubMed ID: 20029827
[TBL] [Abstract][Full Text] [Related]
13. The Netrin-4/ Neogenin-1 axis promotes neuroblastoma cell survival and migration.
Villanueva AA; Falcón P; Espinoza N; R LS; Milla LA; Hernandez-SanMiguel E; Torres VA; Sanchez-Gomez P; Palma V
Oncotarget; 2017 Feb; 8(6):9767-9782. PubMed ID: 28038459
[TBL] [Abstract][Full Text] [Related]
14. Association between SHANK3 polymorphisms and susceptibility to autism spectrum disorder.
Qiu S; Li Y; Li Y; Zhong W; Shi M; Zhao Q; Zhang K; Wang Y; Lu M; Zhu X; Jiang H; Yu Y; Cheng Y; Liu Y
Gene; 2018 Apr; 651():100-105. PubMed ID: 29408620
[TBL] [Abstract][Full Text] [Related]
15. GABA
Yang S; Guo X; Dong X; Han Y; Gao L; Su Y; Dai W; Zhang X
Sci Rep; 2017 Jun; 7(1):3290. PubMed ID: 28607477
[TBL] [Abstract][Full Text] [Related]
16. Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.
Chiocchetti AG; Kopp M; Waltes R; Haslinger D; Duketis E; Jarczok TA; Poustka F; Voran A; Graab U; Meyer J; Klauck SM; Fulda S; Freitag CM
Mol Psychiatry; 2015 Jul; 20(7):839-49. PubMed ID: 25224256
[TBL] [Abstract][Full Text] [Related]
17. Whole-exome sequencing identifies a novel heterozygous missense variant of the EN2 gene in two unrelated patients with autism spectrum disorder.
Hnoonual A; Sripo T; Limprasert P
Psychiatr Genet; 2016 Dec; 26(6):297-301. PubMed ID: 27755371
[TBL] [Abstract][Full Text] [Related]
18. Mutation screening of the UBE3A gene in Chinese Han population with autism.
Zhao X; Zhang R; Yu S
BMC Psychiatry; 2020 Dec; 20(1):589. PubMed ID: 33308194
[TBL] [Abstract][Full Text] [Related]
19. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
da Silva Montenegro EM; Costa CS; Campos G; Scliar M; de Almeida TF; Zachi EC; Silva IMW; Chan AJS; Zarrei M; Lourenço NCV; Yamamoto GL; Scherer S; Passos-Bueno MR
Autism Res; 2020 Feb; 13(2):199-206. PubMed ID: 31696658
[TBL] [Abstract][Full Text] [Related]
20. Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.
Ishizuka K; Kimura H; Wang C; Xing J; Kushima I; Arioka Y; Oya-Ito T; Uno Y; Okada T; Mori D; Aleksic B; Ozaki N
PLoS One; 2016; 11(4):e0153224. PubMed ID: 27058588
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]