219 related articles for article (PubMed ID: 35327467)
1. Gene Variants Involved in Nonsense-Mediated mRNA Decay Suggest a Role in Autism Spectrum Disorder.
Marques AR; Santos JX; Martiniano H; Vilela J; Rasga C; Romão L; Vicente AM
Biomedicines; 2022 Mar; 10(3):. PubMed ID: 35327467
[TBL] [Abstract][Full Text] [Related]
2. A Role for Gene-Environment Interactions in Autism Spectrum Disorder Is Supported by Variants in Genes Regulating the Effects of Exposure to Xenobiotics.
Santos JX; Rasga C; Marques AR; Martiniano H; Asif M; Vilela J; Oliveira G; Sousa L; Nunes A; Vicente AM
Front Neurosci; 2022; 16():862315. PubMed ID: 35663546
[TBL] [Abstract][Full Text] [Related]
3. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
Bacchelli E; Cameli C; Viggiano M; Igliozzi R; Mancini A; Tancredi R; Battaglia A; Maestrini E
Sci Rep; 2020 Feb; 10(1):3198. PubMed ID: 32081867
[TBL] [Abstract][Full Text] [Related]
4. Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study.
Abdi M; Aliyev E; Trost B; Kohailan M; Aamer W; Syed N; Shaath R; Gandhi GD; Engchuan W; Howe J; Thiruvahindrapuram B; Geng M; Whitney J; Syed A; Lakshmi J; Hussein S; Albashir N; Hussein A; Poggiolini I; Elhag SF; Palaniswamy S; Kambouris M; de Fatima Janjua M; Tahir MOE; Nazeer A; Shahwar D; Azeem MW; Mokrab Y; Aati NA; Akil A; Scherer SW; Kamal M; Fakhro KA
Genome Med; 2023 Oct; 15(1):81. PubMed ID: 37805537
[TBL] [Abstract][Full Text] [Related]
5. Mapping genetic variants for nonsense-mediated mRNA decay regulation across human tissues.
Sun B; Chen L
Genome Biol; 2023 Jul; 24(1):164. PubMed ID: 37434206
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder.
Du X; Gao X; Liu X; Shen L; Wang K; Fan Y; Sun Y; Luo X; Liu H; Wang L; Wang Y; Gong Z; Wang J; Yu Y; Li F
Front Genet; 2018; 9():594. PubMed ID: 30555518
[TBL] [Abstract][Full Text] [Related]
8. Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
Wang C; Horigane SI; Wakamori M; Ueda S; Kawabata T; Fujii H; Kushima I; Kimura H; Ishizuka K; Nakamura Y; Iwayama Y; Ikeda M; Iwata N; Okada T; Aleksic B; Mori D; Yoshida T; Bito H; Yoshikawa T; Takemoto-Kimura S; Ozaki N
Transl Psychiatry; 2022 Feb; 12(1):84. PubMed ID: 35220405
[TBL] [Abstract][Full Text] [Related]
9. Whole genome analysis of rare deleterious variants adds further evidence to BRSK2 and other risk genes in Autism Spectrum Disorder.
Bacchelli E; Viggiano M; Ceroni F; Visconti P; Posar A; Scaduto M; Sandoni L; Baravelli I; Cameli C; Rochat M; Maresca A; Vaisfeld A; Gentilini D; Calzari L; Carelli V; Zody M; Maestrini E
Res Sq; 2023 Oct; ():. PubMed ID: 37961520
[TBL] [Abstract][Full Text] [Related]
10. Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.
Viggiano M; Ceroni F; Visconti P; Posar A; Scaduto MC; Sandoni L; Baravelli I; Cameli C; Rochat MJ; Maresca A; Vaisfeld A; Gentilini D; Calzari L; Carelli V; Zody MC; Maestrini E; Bacchelli E
NPJ Genom Med; 2024 Mar; 9(1):21. PubMed ID: 38519481
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample.
Jiao J; Zhang M; Yang P; Huang Y; Hu X; Cai J; Yang C; Situ M; Zhang H; Fu L; Guo K; Huang Y
J Mol Neurosci; 2020 Feb; 70(2):219-229. PubMed ID: 31838722
[TBL] [Abstract][Full Text] [Related]
13. Clinical Targeted Panel Sequencing Analysis in Clinical Evaluation of Children with Autism Spectrum Disorder in China.
Hu C; He L; Li H; Ding Y; Zhang K; Li D; Zhu G; Wu B; Xu X; Xu Q
Genes (Basel); 2022 Jun; 13(6):. PubMed ID: 35741772
[TBL] [Abstract][Full Text] [Related]
14. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
[TBL] [Abstract][Full Text] [Related]
15. Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders.
Nguyen LS; Kim HG; Rosenfeld JA; Shen Y; Gusella JF; Lacassie Y; Layman LC; Shaffer LG; Gécz J
Hum Mol Genet; 2013 May; 22(9):1816-25. PubMed ID: 23376982
[TBL] [Abstract][Full Text] [Related]
16. Targeted sequencing and clinical strategies in children with autism spectrum disorder: A cohort study.
Hu C; Wang Y; Li C; Mei L; Zhou B; Li D; Li H; Xu Q; Xu X
Front Genet; 2023; 14():1083779. PubMed ID: 37007974
[No Abstract] [Full Text] [Related]
17. An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder.
Williams SM; An JY; Edson J; Watts M; Murigneux V; Whitehouse AJO; Jackson CJ; Bellgrove MA; Cristino AS; Claudianos C
Mol Psychiatry; 2019 Nov; 24(11):1707-1719. PubMed ID: 29703944
[TBL] [Abstract][Full Text] [Related]
18. Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
Matsunami N; Hadley D; Hensel CH; Christensen GB; Kim C; Frackelton E; Thomas K; da Silva RP; Stevens J; Baird L; Otterud B; Ho K; Varvil T; Leppert T; Lambert CG; Leppert M; Hakonarson H
PLoS One; 2013; 8(1):e52239. PubMed ID: 23341896
[TBL] [Abstract][Full Text] [Related]
19. Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder.
Hashimoto R; Nakazawa T; Tsurusaki Y; Yasuda Y; Nagayasu K; Matsumura K; Kawashima H; Yamamori H; Fujimoto M; Ohi K; Umeda-Yano S; Fukunaga M; Fujino H; Kasai A; Hayata-Takano A; Shintani N; Takeda M; Matsumoto N; Hashimoto H
J Hum Genet; 2016 Mar; 61(3):199-206. PubMed ID: 26582266
[TBL] [Abstract][Full Text] [Related]
20. Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Callaghan DB; Rogic S; Tan PPC; Calli K; Qiao Y; Baldwin R; Jacobson M; Belmadani M; Holmes N; Yu C; Li Y; Li Y; Kurtzke FE; Kuzeljevic B; Yu AY; Hudson M; Mcaughton AJM; Xu Y; Dionne-Laporte A; Girard S; Liang P; Separovic ER; Liu X; Rouleau G; Pavlidis P; Lewis MES
Clin Genet; 2019 Sep; 96(3):199-206. PubMed ID: 31038196
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
