155 related articles for article (PubMed ID: 32243819)
1. Co-localization between Sequence Constraint and Epigenomic Information Improves Interpretation of Whole-Genome Sequencing Data.
Xu D; Wang C; Kiryluk K; Buxbaum JD; Ionita-Laza I
Am J Hum Genet; 2020 Apr; 106(4):513-524. PubMed ID: 32243819
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A genome-wide scan statistic framework for whole-genome sequence data analysis.
He Z; Xu B; Buxbaum J; Ionita-Laza I
Nat Commun; 2019 Jul; 10(1):3018. PubMed ID: 31289270
[TBL] [Abstract][Full Text] [Related]
4. Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.
Zhou J; Park CY; Theesfeld CL; Wong AK; Yuan Y; Scheckel C; Fak JJ; Funk J; Yao K; Tajima Y; Packer A; Darnell RB; Troyanskaya OG
Nat Genet; 2019 Jun; 51(6):973-980. PubMed ID: 31133750
[TBL] [Abstract][Full Text] [Related]
5. Identification of de novo Mutations in the Chinese Autism Spectrum Disorder Cohort via Whole-Exome Sequencing Unveils Brain Regions Implicated in Autism.
Yuan B; Wang M; Wu X; Cheng P; Zhang R; Zhang R; Yu S; Zhang J; Du Y; Wang X; Qiu Z
Neurosci Bull; 2023 Oct; 39(10):1469-1480. PubMed ID: 36881370
[TBL] [Abstract][Full Text] [Related]
6. Topologically associating domains define the impact of de novo promoter variants on autism spectrum disorder risk.
Nakamura T; Ueda J; Mizuno S; Honda K; Kazuno AA; Yamamoto H; Hara T; Takata A
Cell Genom; 2024 Feb; 4(2):100488. PubMed ID: 38280381
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
9. Patterns of de novo tandem repeat mutations and their role in autism.
Mitra I; Huang B; Mousavi N; Ma N; Lamkin M; Yanicky R; Shleizer-Burko S; Lohmueller KE; Gymrek M
Nature; 2021 Jan; 589(7841):246-250. PubMed ID: 33442040
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Increased burden of deleterious variants in essential genes in autism spectrum disorder.
Ji X; Kember RL; Brown CD; Bućan M
Proc Natl Acad Sci U S A; 2016 Dec; 113(52):15054-15059. PubMed ID: 27956632
[TBL] [Abstract][Full Text] [Related]
12. Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.
Marco EJ; Aitken AB; Nair VP; da Gente G; Gerdes MR; Bologlu L; Thomas S; Sherr EH
BMC Med Genomics; 2018 May; 11(1):50. PubMed ID: 29801487
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The Contribution of Mosaic Variants to Autism Spectrum Disorder.
Freed D; Pevsner J
PLoS Genet; 2016 Sep; 12(9):e1006245. PubMed ID: 27632392
[TBL] [Abstract][Full Text] [Related]
15. Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
Leppa VM; Kravitz SN; Martin CL; Andrieux J; Le Caignec C; Martin-Coignard D; DyBuncio C; Sanders SJ; Lowe JK; Cantor RM; Geschwind DH
Am J Hum Genet; 2016 Sep; 99(3):540-554. PubMed ID: 27569545
[TBL] [Abstract][Full Text] [Related]
16. Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder.
Schmitz-Abe K; Sanchez-Schmitz G; Doan RN; Hill RS; Chahrour MH; Mehta BK; Servattalab S; Ataman B; Lam AN; Morrow EM; Greenberg ME; Yu TW; Walsh CA; Markianos K
Sci Rep; 2020 Aug; 10(1):14045. PubMed ID: 32820185
[TBL] [Abstract][Full Text] [Related]
17. Noncoding de novo mutations in
Zhang Y; Ahsan MU; Wang K
medRxiv; 2024 May; ():. PubMed ID: 38766206
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders.
D'Abate L; Walker S; Yuen RKC; Tammimies K; Buchanan JA; Davies RW; Thiruvahindrapuram B; Wei J; Brian J; Bryson SE; Dobkins K; Howe J; Landa R; Leef J; Messinger D; Ozonoff S; Smith IM; Stone WL; Warren ZE; Young G; Zwaigenbaum L; Scherer SW
Nat Commun; 2019 Dec; 10(1):5519. PubMed ID: 31801954
[TBL] [Abstract][Full Text] [Related]
20. Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.
Nemirovsky SI; Córdoba M; Zaiat JJ; Completa SP; Vega PA; González-Morón D; Medina NM; Fabbro M; Romero S; Brun B; Revale S; Ogara MF; Pecci A; Marti M; Vazquez M; Turjanski A; Kauffman MA
PLoS One; 2015; 10(2):e0116358. PubMed ID: 25646853
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]