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.
41 to 60 of 1,441
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Genetic Variants Associated with Breast Cancer Are Detected by Whole-Exome Sequencing in Vietnamese Patients. | Diagnostics (Basel) | 2025 | 40941673 | PubTator, text mining | PubMed |
| CHD8-related neurodevelopmental disorder with non-epileptic myoclonus in an adult. | Epileptic Disord | 2025 | 40932683 | PubTator, text mining | PubMed |
| Genetic Investigation of Fetuses With Isolated Unilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience. | Prenat Diagn | 2025 | 40848233 | PubTator, text mining | PubMed |
| Unraveling the Role of Topoisomerase 3β (TOP3B) in mRNA Translation and Human Disease. | Wiley Interdiscip Rev RNA | 2025 | 40754336 | PubTator, text mining | PubMed |
| Multi-proteomic profiling of the varicella-zoster virus-host interface reveals host susceptibilities to severe infection. | Nat Microbiol | 2025 | 40739040 | PubTator, text mining | PubMed |
| Applications and techniques of single-cell RNA sequencing across diverse species. | Brief Bioinform | 2025 | 40698863 | PubTator, text mining | PubMed |
| Unveiling Hidden Genetic Architectures: Molecular Diagnostic Yield of Whole Exome Sequencing in 50 Children With Autism Spectrum Disorder Negative for Copy Number Variations. | Genet Res (Camb) | 2025 | 40642607 | PubTator, text mining | PubMed |
| Induced Pluripotent (iPSC) and Mesenchymal (MSC) Stem Cells for In Vitro Disease Modeling and Regenerative Medicine. | Int J Mol Sci | 2025 | 40565081 | PubTator, text mining | PubMed |
| Identification of Therapeutic Targets in Autism Spectrum Disorder through CHD8-Notch Pathway Interaction Analysis. | PLoS One | 2025 | 40526590 | PubTator, text mining | PubMed |
| CHD8 Variant and Rett Syndrome: Overlapping Phenotypes, Molecular Convergence, and Expanding the Genetic Spectrum. | Hum Mutat | 2025 | 40496977 | PubTator, text mining | PubMed |
| Multimodal analyses reveal genes driving electrophysiological maturation of neurons in the primate prefrontal cortex. | Neuron | 2025 | 40398411 | PubTator, text mining | PubMed |
| CHD8 interacts with BCL11A to induce oncogenic transcription in triple negative breast cancer. | EMBO J | 2025 | 40328966 | PubTator, text mining | PubMed |
| Neural connections and molecular mechanisms underlying motor skill deficits in genetic models of autism spectrum disorders. | Prog Neurobiol | 2025 | 40254176 | PubTator, text mining | PubMed |
| Small SNPs, Big Effects: A Review of Single Nucleotide Variations and Polymorphisms in Key Genes Associated With Autism Spectrum Disorder. | Int J Dev Neurosci | 2025 | 40223535 | PubTator, text mining | PubMed |
| A CHD8-TRRAP axis facilitates MYC and E2F target gene regulation in human neural stem cells. | iScience | 2025 | 40104050 | PubTator, text mining | PubMed |
| Offspring genetic diversity regulates rearing experiences that predict differential susceptibility to Chd8 haploinsufficiency. | Res Sq | 2025 | 40092436 | PubTator, text mining | PubMed |
| Single-cell analyses reveal increased gene expression variability in human neurodevelopmental conditions. | Am J Hum Genet | 2025 | 40056913 | PubTator, text mining | PubMed |
| Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility. | Nat Commun | 2025 | 40050271 | PubTator, text mining | PubMed |
| Genetic variants and phenotypic data curated for the CAGI6 intellectual disability panel challenge. | Hum Genet | 2025 | 40019509 | PubTator, text mining | PubMed |
| Single-cell delineation of the microbiota-gut-brain axis: Probiotic intervention in Chd8 haploinsufficient mice. | Cell Genom | 2025 | 39914389 | PubTator, text mining | PubMed |
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.
For software
Read this list from software.
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GET https://conductscience.org/api/genes/v1/57680/papers?page=3