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Gene · 57680

Papers1,441

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

TitleJournalYearPMIDFound bySource
Discovery of a DNA methylation profile in individuals with Sifrim-Hitz-Weiss syndrome.Am J Hum Genet202539824190PubTator, text miningPubMed
Oligogenic risk score for Gilles de la Tourette syndrome reveals a genetic continuum of tic disorders.J Appl Genet202539792217PubTator, text miningPubMed
SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systems.Mol Ther202539741407PubTator, text miningPubMed
Unravelling lipidomic disruptions across multiple tissues in Chd8-mutant ASD mice through integration of lipidomics and single-cell transcriptomics.Gut202539358004PubTator, text miningPubMed
Identification of novel genetic variants associated with oral squamous cell carcinoma (OSCC) in South-West coast of India using targeted exome sequencing.Gene202539278377PubTator, text miningPubMed
Association of CHD8 Gene Polymorphic Variants with the Clinical Phenotype of Autism Spectrum Disorder.J Clin Med202439685474PubTator, text miningPubMed
Chromatin accessibility: biological functions, molecular mechanisms and therapeutic application.Signal Transduct Target Ther202439627201PubTator, text miningPubMed
Expansion of phenotypic and genotypic data in autism spectrum disorders due to variants in the CHD8 gene.Neurogenetics202439576488PubTator, text miningPubMed
The Deficiency of the ASD-Related Gene CHD8 Disrupts Behavioral Patterns and Inhibits Hippocampal Neurogenesis in Mice.J Mol Neurosci202439480606PubTator, text miningPubMed
Key Synaptic Pathology in Autism Spectrum Disorder: Genetic Mechanisms and Recent Advances.J Integr Neurosci202439473158PubTator, text miningPubMed
Resolving complex duplication variants in autism spectrum disorder using long-read genome sequencing.Genome Res202439472019PubTator, text miningPubMed
Association of genetic variants with autism spectrum disorder in Japanese children revealed by targeted sequencing.Front Genet202439280100PubTator, text miningPubMed
Genetic modifiers and ascertainment drive variable expressivity of complex disorders.medRxiv202439252907PubTator, text miningPubMed
Cell type-specific dysregulation of gene expression due to Chd8 haploinsufficiency during mouse cortical development.bioRxiv202439185167PubTator, text miningPubMed
Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes.Cell Rep202439154337PubTator, text miningPubMed
Molecular and network disruptions in neurodevelopment uncovered by single cell transcriptomics analysis of CHD8 heterozygous cerebral organoids.Heliyon202439149047PubTator, text miningPubMed
Whole-genome sequencing identifies novel genes for autism in Chinese trios.Sci China Life Sci202439126614PubTator, text miningPubMed
Revealing the clinical impact of MTOR and ARID2 gene mutations on MALT lymphoma of the alimentary canal using targeted sequencing.Diagn Pathol202439054516PubTator, text miningPubMed
Comprehensive Analysis of the Expression, Prognosis, and Immune Infiltrates for Chromodomain-Helicase-DNA-Binding Proteins in Breast Tumor.Asian Pac J Cancer Prev202438809626PubTator, text miningPubMed
The choreography of chromatin in RNA polymerase III regulation.Biochem Soc Trans202438666598PubTator, text miningPubMed

gene-search-2026-11-11-0.2.0

Sources 12

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
  • GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
  • HGNCCC0
  • NCBI GenePublic domain (US government)
  • NIH's project files and grant-paper linksPublic domain
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
  • GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
  • HGNCCC0: https://www.genenames.org/about/license/
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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