803 related articles for article (PubMed ID: 27602517)
1. 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]
2. 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]
3. 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]
4. Oxytocin ameliorates impaired social behavior in a Chd8 haploinsufficiency mouse model of autism.
Cherepanov SM; Gerasimenko M; Yuhi T; Furuhara K; Tsuji C; Yokoyama S; Nakayama KI; Nishiyama M; Higashida H
BMC Neurosci; 2021 May; 22(1):32. PubMed ID: 33933000
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Chd8 Mutation Leads to Autistic-like Behaviors and Impaired Striatal Circuits.
Platt RJ; Zhou Y; Slaymaker IM; Shetty AS; Weisbach NR; Kim JA; Sharma J; Desai M; Sood S; Kempton HR; Crabtree GR; Feng G; Zhang F
Cell Rep; 2017 Apr; 19(2):335-350. PubMed ID: 28402856
[TBL] [Abstract][Full Text] [Related]
8. Chd8 haploinsufficiency impairs early brain development and protein homeostasis later in life.
Jiménez JA; Ptacek TS; Tuttle AH; Schmid RS; Moy SS; Simon JM; Zylka MJ
Mol Autism; 2020 Oct; 11(1):74. PubMed ID: 33023670
[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 links autism to transient alterations in excitatory and inhibitory trajectories.
Villa CE; Cheroni C; Dotter CP; López-Tóbon A; Oliveira B; Sacco R; Yahya AÇ; Morandell J; Gabriele M; Tavakoli MR; Lyudchik J; Sommer C; Gabitto M; Danzl JG; Testa G; Novarino G
Cell Rep; 2022 Apr; 39(1):110615. PubMed ID: 35385734
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Altered Neocortical Gene Expression, Brain Overgrowth and Functional Over-Connectivity in Chd8 Haploinsufficient Mice.
Suetterlin P; Hurley S; Mohan C; Riegman KLH; Pagani M; Caruso A; Ellegood J; Galbusera A; Crespo-Enriquez I; Michetti C; Yee Y; Ellingford R; Brock O; Delogu A; Francis-West P; Lerch JP; Scattoni ML; Gozzi A; Fernandes C; Basson MA
Cereb Cortex; 2018 Jun; 28(6):2192-2206. PubMed ID: 29668850
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The phenotypic spectrum and genotype-phenotype correlations in 106 patients with variants in major autism gene CHD8.
Dingemans AJM; Truijen KMG; van de Ven S; Bernier R; Bongers EMHF; Bouman A; de Graaff-Herder L; Eichler EE; Gerkes EH; De Geus CM; van Hagen JM; Jansen PR; Kerkhof J; Kievit AJA; Kleefstra T; Maas SM; de Man SA; McConkey H; Patterson WG; Dobson AT; Prijoles EJ; Sadikovic B; Relator R; Stevenson RE; Stumpel CTRM; Heijligers M; Stuurman KE; Löhner K; Zeidler S; Lee JA; Lindy A; Zou F; Tedder ML; Vissers LELM; de Vries BBA
Transl Psychiatry; 2022 Oct; 12(1):421. PubMed ID: 36182950
[TBL] [Abstract][Full Text] [Related]
15. Neurodevelopmental functions of CHD8: new insights and questions.
Basson MA
Biochem Soc Trans; 2024 Feb; 52(1):15-27. PubMed ID: 38288845
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development.
Hurley S; Mohan C; Suetterlin P; Ellingford R; Riegman KLH; Ellegood J; Caruso A; Michetti C; Brock O; Evans R; Rudari F; Delogu A; Scattoni ML; Lerch JP; Fernandes C; Basson MA
Mol Autism; 2021 Feb; 12(1):16. PubMed ID: 33627187
[TBL] [Abstract][Full Text] [Related]
18. Male-Dominant Effects of Chd8 Haploinsufficiency on Synaptic Phenotypes during Development in Mouse Prefrontal Cortex.
Ellingford RA; Tojo M; Basson MA; Andreae LC
ACS Chem Neurosci; 2024 Apr; 15(8):1635-1642. PubMed ID: 38557009
[No Abstract] [Full Text] [Related]
19. 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]
20. Cell-type-specific synaptic imbalance and disrupted homeostatic plasticity in cortical circuits of ASD-associated Chd8 haploinsufficient mice.
Ellingford RA; Panasiuk MJ; de Meritens ER; Shaunak R; Naybour L; Browne L; Basson MA; Andreae LC
Mol Psychiatry; 2021 Jul; 26(7):3614-3624. PubMed ID: 33837267
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
