These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 33837267)

  • 21. Postnatal Tshz3 Deletion Drives Altered Corticostriatal Function and Autism Spectrum Disorder-like Behavior.
    Chabbert D; Caubit X; Roubertoux PL; Carlier M; Habermann B; Jacq B; Salin P; Metwaly M; Frahm C; Fatmi A; Garratt AN; Severac D; Dubois E; Kerkerian-Le Goff L; Fasano L; Gubellini P
    Biol Psychiatry; 2019 Aug; 86(4):274-285. PubMed ID: 31060802
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The complex etiology of autism spectrum disorder due to missense mutations of CHD8.
    Shiraishi T; Katayama Y; Nishiyama M; Shoji H; Miyakawa T; Mizoo T; Matsumoto A; Hijikata A; Shirai T; Mayanagi K; Nakayama KI
    Mol Psychiatry; 2024 Jul; 29(7):2145-2160. PubMed ID: 38438524
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. Clinical Phenotypes of Carriers of Mutations in CHD8 or Its Conserved Target Genes.
    Beighley JS; Hudac CM; Arnett AB; Peterson JL; Gerdts J; Wallace AS; Mefford HC; Hoekzema K; Turner TN; O'Roak BJ; Eichler EE; Bernier RA
    Biol Psychiatry; 2020 Jan; 87(2):123-131. PubMed ID: 31526516
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Common CHD8 Genomic Targets Contrast With Model-Specific Transcriptional Impacts of
    Wade AA; Lim K; Catta-Preta R; Nord AS
    Front Mol Neurosci; 2018; 11():481. PubMed ID: 30692911
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Chromatin Remodeler CHD8 in Autism and Brain Development.
    Hoffmann A; Spengler D
    J Clin Med; 2021 Jan; 10(2):. PubMed ID: 33477995
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. The Autism-Associated Gene Scn2a Contributes to Dendritic Excitability and Synaptic Function in the Prefrontal Cortex.
    Spratt PWE; Ben-Shalom R; Keeshen CM; Burke KJ; Clarkson RL; Sanders SJ; Bender KJ
    Neuron; 2019 Aug; 103(4):673-685.e5. PubMed ID: 31230762
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Chd8 haploinsufficiency impacts rearing experience in C57BL/6 mice.
    Tabbaa M; Levitt P
    Genes Brain Behav; 2024 Apr; 23(2):e12892. PubMed ID: 38560770
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Non-synaptic function of the autism spectrum disorder-associated gene SYNGAP1 in cortical neurogenesis.
    Birtele M; Del Dosso A; Xu T; Nguyen T; Wilkinson B; Hosseini N; Nguyen S; Urenda JP; Knight G; Rojas C; Flores I; Atamian A; Moore R; Sharma R; Pirrotte P; Ashton RS; Huang EJ; Rumbaugh G; Coba MP; Quadrato G
    Nat Neurosci; 2023 Dec; 26(12):2090-2103. PubMed ID: 37946050
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The Mechanisms of CHD8 in Neurodevelopment and Autism Spectrum Disorders.
    Weissberg O; Elliott E
    Genes (Basel); 2021 Jul; 12(8):. PubMed ID: 34440307
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Chd8 mutation in oligodendrocytes alters microstructure and functional connectivity in the mouse brain.
    Kawamura A; Abe Y; Seki F; Katayama Y; Nishiyama M; Takata N; Tanaka KF; Okano H; Nakayama KI
    Mol Brain; 2020 Nov; 13(1):160. PubMed ID: 33228730
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Setd5 haploinsufficiency alters neuronal network connectivity and leads to autistic-like behaviors in mice.
    Moore SM; Seidman JS; Ellegood J; Gao R; Savchenko A; Troutman TD; Abe Y; Stender J; Lee D; Wang S; Voytek B; Lerch JP; Suh H; Glass CK; Muotri AR
    Transl Psychiatry; 2019 Jan; 9(1):24. PubMed ID: 30655503
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.