655 related articles for article (PubMed ID: 28831199)
1. Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.
Li J; Wang L; Guo H; Shi L; Zhang K; Tang M; Hu S; Dong S; Liu Y; Wang T; Yu P; He X; Hu Z; Zhao J; Liu C; Sun ZS; Xia K
Mol Psychiatry; 2017 Sep; 22(9):1282-1290. PubMed ID: 28831199
[TBL] [Abstract][Full Text] [Related]
2. Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.
Wu H; Li H; Bai T; Han L; Ou J; Xun G; Zhang Y; Wang Y; Duan G; Zhao N; Chen B; Du X; Yao M; Zou X; Zhao J; Hu Z; Eichler EE; Guo H; Xia K
Clin Genet; 2020 Feb; 97(2):338-346. PubMed ID: 31674007
[TBL] [Abstract][Full Text] [Related]
3. CHD8 haploinsufficiency results in autistic-like phenotypes in mice.
Katayama Y; Nishiyama M; Shoji H; Ohkawa Y; Kawamura A; Sato T; Suyama M; Takumi T; Miyakawa T; Nakayama KI
Nature; 2016 Sep; 537(7622):675-679. PubMed ID: 27602517
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
O'Roak BJ; Vives L; Fu W; Egertson JD; Stanaway IB; Phelps IG; Carvill G; Kumar A; Lee C; Ankenman K; Munson J; Hiatt JB; Turner EH; Levy R; O'Day DR; Krumm N; Coe BP; Martin BK; Borenstein E; Nickerson DA; Mefford HC; Doherty D; Akey JM; Bernier R; Eichler EE; Shendure J
Science; 2012 Dec; 338(6114):1619-22. PubMed ID: 23160955
[TBL] [Abstract][Full Text] [Related]
9. Targeted sequencing and integrative analysis of 3,195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genes.
Wang T; Zhang Y; Liu L; Wang Y; Chen H; Fan T; Li J; Xia K; Sun Z
J Genet Genomics; 2021 Apr; 48(4):312-323. PubMed ID: 33994118
[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. 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]
12. 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]
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. Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.
Li J; Cai T; Jiang Y; Chen H; He X; Chen C; Li X; Shao Q; Ran X; Li Z; Xia K; Liu C; Sun ZS; Wu J
Mol Psychiatry; 2016 Feb; 21(2):290-7. PubMed ID: 25849321
[TBL] [Abstract][Full Text] [Related]
15. Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum Disorder.
Reis VN; Kitajima JP; Tahira AC; Feio-Dos-Santos AC; Fock RA; Lisboa BC; Simões SN; Krepischi AC; Rosenberg C; Lourenço NC; Passos-Bueno MR; Brentani H
PLoS One; 2017; 12(1):e0170386. PubMed ID: 28118382
[TBL] [Abstract][Full Text] [Related]
16. Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.
Li J; Wang L; Yu P; Shi L; Zhang K; Sun ZS; Xia K
Am J Med Genet B Neuropsychiatr Genet; 2017 Jul; 174(5):568-577. PubMed ID: 28407358
[TBL] [Abstract][Full Text] [Related]
17. Non-coding de novo mutations in chromatin interactions are implicated in autism spectrum disorder.
Kim IB; Lee T; Lee J; Kim J; Lee S; Koh IG; Kim JH; An JY; Lee H; Kim WK; Ju YS; Cho Y; Yu SJ; Kim SA; Oh M; Han DW; Kim E; Choi JK; Yoo HJ; Lee JH
Mol Psychiatry; 2022 Nov; 27(11):4680-4694. PubMed ID: 35840799
[TBL] [Abstract][Full Text] [Related]
18. CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
Sugathan A; Biagioli M; Golzio C; Erdin S; Blumenthal I; Manavalan P; Ragavendran A; Brand H; Lucente D; Miles J; Sheridan SD; Stortchevoi A; Kellis M; Haggarty SJ; Katsanis N; Gusella JF; Talkowski ME
Proc Natl Acad Sci U S A; 2014 Oct; 111(42):E4468-77. PubMed ID: 25294932
[TBL] [Abstract][Full Text] [Related]
19. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.
Cotney J; Muhle RA; Sanders SJ; Liu L; Willsey AJ; Niu W; Liu W; Klei L; Lei J; Yin J; Reilly SK; Tebbenkamp AT; Bichsel C; Pletikos M; Sestan N; Roeder K; State MW; Devlin B; Noonan JP
Nat Commun; 2015 Mar; 6():6404. PubMed ID: 25752243
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]