547 related articles for article (PubMed ID: 25752243)
1. 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]
2. The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes.
Wilkinson B; Grepo N; Thompson BL; Kim J; Wang K; Evgrafov OV; Lu W; Knowles JA; Campbell DB
Transl Psychiatry; 2015 May; 5(5):e568. PubMed ID: 25989142
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in cerebral organoids derived from iPS cells.
Wang P; Mokhtari R; Pedrosa E; Kirschenbaum M; Bayrak C; Zheng D; Lachman HM
Mol Autism; 2017; 8():11. PubMed ID: 28321286
[TBL] [Abstract][Full Text] [Related]
5. Heterozygous deletion of the autism-associated gene CHD8 impairs synaptic function through widespread changes in gene expression and chromatin compaction.
Shi X; Lu C; Corman A; Nikish A; Zhou Y; Platt RJ; Iossifov I; Zhang F; Pan JQ; Sanjana NE
Am J Hum Genet; 2023 Oct; 110(10):1750-1768. PubMed ID: 37802044
[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. CHD8 dosage regulates transcription in pluripotency and early murine neural differentiation.
Sood S; Weber CM; Hodges HC; Krokhotin A; Shalizi A; Crabtree GR
Proc Natl Acad Sci U S A; 2020 Sep; 117(36):22331-22340. PubMed ID: 32839322
[TBL] [Abstract][Full Text] [Related]
8. Autism-associated CHD8 keeps proliferation of human neural progenitors in check by lengthening the G1 phase of the cell cycle.
Coakley-Youngs E; Ranatunga M; Richardson S; Getti G; Shorter S; Fivaz M
Biol Open; 2022 Sep; 11(9):. PubMed ID: 36222238
[TBL] [Abstract][Full Text] [Related]
9. CHD8 intragenic deletion associated with autism spectrum disorder.
Stolerman ES; Smith B; Chaubey A; Jones JR
Eur J Med Genet; 2016 Apr; 59(4):189-94. PubMed ID: 26921529
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
Shibutani M; Horii T; Shoji H; Morita S; Kimura M; Terawaki N; Miyakawa T; Hatada I
Int J Mol Sci; 2017 Aug; 18(9):. PubMed ID: 28867767
[TBL] [Abstract][Full Text] [Related]
12. Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology.
Barnard RA; Pomaville MB; O'Roak BJ
Front Neurosci; 2015; 9():477. PubMed ID: 26733790
[TBL] [Abstract][Full Text] [Related]
13. Oligodendrocyte dysfunction due to Chd8 mutation gives rise to behavioral deficits in mice.
Kawamura A; Katayama Y; Nishiyama M; Shoji H; Tokuoka K; Ueta Y; Miyata M; Isa T; Miyakawa T; Hayashi-Takagi A; Nakayama KI
Hum Mol Genet; 2020 May; 29(8):1274-1291. PubMed ID: 32142125
[TBL] [Abstract][Full Text] [Related]
14. The autism-associated protein CHD8 is required for cerebellar development and motor function.
Kawamura A; Katayama Y; Kakegawa W; Ino D; Nishiyama M; Yuzaki M; Nakayama KI
Cell Rep; 2021 Apr; 35(1):108932. PubMed ID: 33826902
[TBL] [Abstract][Full Text] [Related]
15. Germline Chd8 haploinsufficiency alters brain development in mouse.
Gompers AL; Su-Feher L; Ellegood J; Copping NA; Riyadh MA; Stradleigh TW; Pride MC; Schaffler MD; Wade AA; Catta-Preta R; Zdilar I; Louis S; Kaushik G; Mannion BJ; Plajzer-Frick I; Afzal V; Visel A; Pennacchio LA; Dickel DE; Lerch JP; Crawley JN; Zarbalis KS; Silverman JL; Nord AS
Nat Neurosci; 2017 Aug; 20(8):1062-1073. PubMed ID: 28671691
[TBL] [Abstract][Full Text] [Related]
16. Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children.
Wang J; Liu J; Gao Y; Wang K; Jiang K
BMC Pediatr; 2018 Oct; 18(1):338. PubMed ID: 30376831
[TBL] [Abstract][Full Text] [Related]
17. Deletion of the autism-related gene Chd8 alters activity-dependent transcriptional responses in mouse postmitotic neurons.
Kawamura A; Nishiyama M
Commun Biol; 2023 Jun; 6(1):593. PubMed ID: 37268684
[TBL] [Abstract][Full Text] [Related]
18. The autism risk factor CHD8 is a chromatin activator in human neurons and functionally dependent on the ERK-MAPK pathway effector ELK1.
Haddad Derafshi B; Danko T; Chanda S; Batista PJ; Litzenburger U; Lee QY; Ng YH; Sebin A; Chang HY; Südhof TC; Wernig M
Sci Rep; 2022 Dec; 12(1):22425. PubMed ID: 36575212
[TBL] [Abstract][Full Text] [Related]
19. Gene-Environment Interactions in Developmental Neurotoxicity: a Case Study of Synergy between Chlorpyrifos and CHD8 Knockout in Human BrainSpheres.
Modafferi S; Zhong X; Kleensang A; Murata Y; Fagiani F; Pamies D; Hogberg HT; Calabrese V; Lachman H; Hartung T; Smirnova L
Environ Health Perspect; 2021 Jul; 129(7):77001. PubMed ID: 34259569
[TBL] [Abstract][Full Text] [Related]
20. A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.
Merner N; Forgeot d'Arc B; Bell SC; Maussion G; Peng H; Gauthier J; Crapper L; Hamdan FF; Michaud JL; Mottron L; Rouleau GA; Ernst C
Am J Med Genet A; 2016 May; 170A(5):1225-35. PubMed ID: 26789910
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
