263 related articles for article (PubMed ID: 28867767)
21. The role of ARID1B, a BAF chromatin remodeling complex subunit, in neural development and behavior.
Moffat JJ; Jung EM; Ka M; Smith AL; Jeon BT; Santen GWE; Kim WY
Prog Neuropsychopharmacol Biol Psychiatry; 2019 Mar; 89():30-38. PubMed ID: 30149092
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency.
Sim JC; White SM; Fitzpatrick E; Wilson GR; Gillies G; Pope K; Mountford HS; Torring PM; McKee S; Vulto-van Silfhout AT; Jhangiani SN; Muzny DM; Leventer RJ; Delatycki MB; Amor DJ; Lockhart PJ
Orphanet J Rare Dis; 2014 Mar; 9():43. PubMed ID: 24674232
[TBL] [Abstract][Full Text] [Related]
25. Clinical phenotype of ASD-associated
Earl RK; Turner TN; Mefford HC; Hudac CM; Gerdts J; Eichler EE; Bernier RA
Mol Autism; 2017; 8():54. PubMed ID: 29034068
[TBL] [Abstract][Full Text] [Related]
26. NEXMIF/KIDLIA Knock-out Mouse Demonstrates Autism-Like Behaviors, Memory Deficits, and Impairments in Synapse Formation and Function.
Gilbert J; O'Connor M; Templet S; Moghaddam M; Di Via Ioschpe A; Sinclair A; Zhu LQ; Xu W; Man HY
J Neurosci; 2020 Jan; 40(1):237-254. PubMed ID: 31704787
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Identification of a molecular network regulated by multiple ASD high risk genes.
Wan L; Yang G; Yan Z
Hum Mol Genet; 2024 Jun; 33(13):1176-1185. PubMed ID: 38588587
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. 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]
31. 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]
32. ASH1L haploinsufficiency results in autistic-like phenotypes in mice and links Eph receptor gene to autism spectrum disorder.
Yan Y; Tian M; Li M; Zhou G; Chen Q; Xu M; Hu Y; Luo W; Guo X; Zhang C; Xie H; Wu QF; Xiong W; Liu S; Guan JS
Neuron; 2022 Apr; 110(7):1156-1172.e9. PubMed ID: 35081333
[TBL] [Abstract][Full Text] [Related]
33. De novo variants in the Helicase-C domain of CHD8 are associated with severe phenotypes including autism, language disability and overgrowth.
An Y; Zhang L; Liu W; Jiang Y; Chen X; Lan X; Li G; Hang Q; Wang J; Gusella JF; Du Y; Shen Y
Hum Genet; 2020 Apr; 139(4):499-512. PubMed ID: 31980904
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. KMT2E Haploinsufficiency Manifests Autism-Like Behaviors and Amygdala Neuronal Development Dysfunction in Mice.
Li YJ; Li CY; Li CY; Hu DX; Xv ZB; Zhang SH; Li Q; Zhang P; Tian B; Lan XL; Chen XQ
Mol Neurobiol; 2023 Mar; 60(3):1609-1625. PubMed ID: 36534336
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Juvenile Shank3b deficient mice present with behavioral phenotype relevant to autism spectrum disorder.
Balaan C; Corley MJ; Eulalio T; Leite-Ahyo K; Pang APS; Fang R; Khadka VS; Maunakea AK; Ward MA
Behav Brain Res; 2019 Jan; 356():137-147. PubMed ID: 30134148
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Early communication deficits in the Shank1 knockout mouse model for autism spectrum disorder: Developmental aspects and effects of social context.
Sungur AÖ; Schwarting RK; Wöhr M
Autism Res; 2016 Jun; 9(6):696-709. PubMed ID: 26419918
[TBL] [Abstract][Full Text] [Related]
40. Haploinsufficiency of autism causative gene
Huang TN; Yen TL; Qiu LR; Chuang HC; Lerch JP; Hsueh YP
Mol Autism; 2019; 10():5. PubMed ID: 30792833
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
