406 related articles for article (PubMed ID: 29703944)
1. 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]
2. 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]
3. Outgroup Machine Learning Approach Identifies Single Nucleotide Variants in Noncoding DNA Associated with Autism Spectrum Disorder.
Varma M; Paskov KM; Jung JY; Sierra Chrisman B; Stockham NT; Washington PY; Wall DP
Pac Symp Biocomput; 2019; 24():260-271. PubMed ID: 30864328
[TBL] [Abstract][Full Text] [Related]
4. Paternally inherited cis-regulatory structural variants are associated with autism.
Brandler WM; Antaki D; Gujral M; Kleiber ML; Whitney J; Maile MS; Hong O; Chapman TR; Tan S; Tandon P; Pang T; Tang SC; Vaux KK; Yang Y; Harrington E; Juul S; Turner DJ; Thiruvahindrapuram B; Kaur G; Wang Z; Kingsmore SF; Gleeson JG; Bisson D; Kakaradov B; Telenti A; Venter JC; Corominas R; Toma C; Cormand B; Rueda I; Guijarro S; Messer KS; Nievergelt CM; Arranz MJ; Courchesne E; Pierce K; Muotri AR; Iakoucheva LM; Hervas A; Scherer SW; Corsello C; Sebat J
Science; 2018 Apr; 360(6386):327-331. PubMed ID: 29674594
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Genome-wide association study and identification of chromosomal enhancer maps in multiple brain regions related to autism spectrum disorder.
Zhang L; Liu L; Wen Y; Ma M; Cheng S; Yang J; Li P; Cheng B; Du Y; Liang X; Zhao Y; Ding M; Guo X; Zhang F
Autism Res; 2019 Jan; 12(1):26-32. PubMed ID: 30157312
[TBL] [Abstract][Full Text] [Related]
7. Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder.
Krishnan A; Zhang R; Yao V; Theesfeld CL; Wong AK; Tadych A; Volfovsky N; Packer A; Lash A; Troyanskaya OG
Nat Neurosci; 2016 Nov; 19(11):1454-1462. PubMed ID: 27479844
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.
Cameli C; Viggiano M; Rochat MJ; Maresca A; Caporali L; Fiorini C; Palombo F; Magini P; Duardo RC; Ceroni F; Scaduto MC; Posar A; Seri M; Carelli V; Visconti P; Bacchelli E; Maestrini E
J Cell Mol Med; 2021 Mar; 25(5):2459-2470. PubMed ID: 33476483
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.
Devanna P; Chen XS; Ho J; Gajewski D; Smith SD; Gialluisi A; Francks C; Fisher SE; Newbury DF; Vernes SC
Mol Psychiatry; 2018 May; 23(5):1375-1384. PubMed ID: 28289279
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder.
Griswold AJ; Van Booven D; Cuccaro ML; Haines JL; Gilbert JR; Pericak-Vance MA
Neurogenetics; 2018 Jan; 19(1):17-26. PubMed ID: 29151244
[TBL] [Abstract][Full Text] [Related]
14. Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
Forsyth JK; Nachun D; Gandal MJ; Geschwind DH; Anderson AE; Coppola G; Bearden CE
Biol Psychiatry; 2020 Jan; 87(2):150-163. PubMed ID: 31500805
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide, integrative analysis implicates microRNA dysregulation in autism spectrum disorder.
Wu YE; Parikshak NN; Belgard TG; Geschwind DH
Nat Neurosci; 2016 Nov; 19(11):1463-1476. PubMed ID: 27571009
[TBL] [Abstract][Full Text] [Related]
16. Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
Wang L; Zhang Y; Li K; Wang Z; Wang X; Li B; Zhao G; Fang Z; Ling Z; Luo T; Xia L; Li Y; Guo H; Hu Z; Li J; Sun Z; Xia K
Mol Autism; 2020 Oct; 11(1):75. PubMed ID: 33023636
[TBL] [Abstract][Full Text] [Related]
17. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
C Yuen RK; Merico D; Bookman M; L Howe J; Thiruvahindrapuram B; Patel RV; Whitney J; Deflaux N; Bingham J; Wang Z; Pellecchia G; Buchanan JA; Walker S; Marshall CR; Uddin M; Zarrei M; Deneault E; D'Abate L; Chan AJ; Koyanagi S; Paton T; Pereira SL; Hoang N; Engchuan W; Higginbotham EJ; Ho K; Lamoureux S; Li W; MacDonald JR; Nalpathamkalam T; Sung WW; Tsoi FJ; Wei J; Xu L; Tasse AM; Kirby E; Van Etten W; Twigger S; Roberts W; Drmic I; Jilderda S; Modi BM; Kellam B; Szego M; Cytrynbaum C; Weksberg R; Zwaigenbaum L; Woodbury-Smith M; Brian J; Senman L; Iaboni A; Doyle-Thomas K; Thompson A; Chrysler C; Leef J; Savion-Lemieux T; Smith IM; Liu X; Nicolson R; Seifer V; Fedele A; Cook EH; Dager S; Estes A; Gallagher L; Malow BA; Parr JR; Spence SJ; Vorstman J; Frey BJ; Robinson JT; Strug LJ; Fernandez BA; Elsabbagh M; Carter MT; Hallmayer J; Knoppers BM; Anagnostou E; Szatmari P; Ring RH; Glazer D; Pletcher MT; Scherer SW
Nat Neurosci; 2017 Apr; 20(4):602-611. PubMed ID: 28263302
[TBL] [Abstract][Full Text] [Related]
18. Understanding the impact of SNPs associated with autism spectrum disorder on biological pathways in the human fetal and adult cortex.
Golovina E; Fadason T; Lints TJ; Walker C; Vickers MH; O'Sullivan JM
Sci Rep; 2021 Aug; 11(1):15867. PubMed ID: 34354167
[TBL] [Abstract][Full Text] [Related]
19. The landscape of copy number variations in Finnish families with autism spectrum disorders.
Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I
Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927
[TBL] [Abstract][Full Text] [Related]
20. Genetic architecture of autism spectrum disorder: Lessons from large-scale genomic studies.
Choi L; An JY
Neurosci Biobehav Rev; 2021 Sep; 128():244-257. PubMed ID: 34166716
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
