Gene · 64072
Papers1,428
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
61 to 80 of 1,428
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Oligogenic analysis across broad phenotypes of 46,XY differences in sex development associated with NR5A1/SF-1 variants: findings from the international SF1next study. | EBioMedicine | 2025 | 40037090 | PubTator, text mining | PubMed |
| Cdh23 Gene Mutation-Induced Vestibular Dysfunction in Mice: Abnormal Stereocilia Bundle and Otolith Development and Activation of p53/FoxO Signaling Pathway. | J Mol Neurosci | 2025 | 39966205 | PubTator, text mining | PubMed |
| Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of >3500 Patients with Inherited Retinal Disease from the United Kingdom. | Ophthalmol Sci | 2025 | 39896422 | PubTator, text mining | PubMed |
| Exploring force-driven stochastic folding dynamics in mechano-responsive proteins and implications in phenotypic variation. | Nat Commun | 2025 | 39863587 | PubTator, text mining | PubMed |
| Identification of novel CDH23 heterozygous variants causing autosomal recessive nonsyndromic hearing loss. | Genes Genomics | 2025 | 39777619 | PubTator, text mining | PubMed |
| Cadherin 23 is a prognostic marker of pancreatic cancer and promotes cell viability in floating culture conditions. | Int J Med Sci | 2025 | 39744166 | PubTator, text mining | PubMed |
| Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali. | HGG Adv | 2025 | 39663698 | PubTator, text mining | PubMed |
| FunCoup 6: advancing functional association networks across species with directed links and improved user experience. | Nucleic Acids Res | 2025 | 39530220 | PubTator, text mining | PubMed |
| Analysis of the genetic etiology of CDH23 gene variation in a child with hearing loss. | QJM | 2025 | 39475434 | PubTator, text mining | PubMed |
| Whole exome-seq and RNA-seq data reveal unique neoantigen profiles in Kenyan breast cancer patients. | Front Oncol | 2024 | 39723380 | PubTator, text mining | PubMed |
| Transcriptomics-informed pharmacology identifies epigenetic and cell cycle regulators that enhance AAV production. | Mol Ther Methods Clin Dev | 2024 | 39687728 | PubTator, text mining | PubMed |
| Heterogeneous Group of Genetically Determined Auditory Neuropathy Spectrum Disorders. | Int J Mol Sci | 2024 | 39684270 | PubTator, text mining | PubMed |
| Segregation of Trans Mutations in the CDH23 Gene in an Emirati Family with Sensorineural Hearing Loss. | Genes (Basel) | 2024 | 39596651 | PubTator, text mining | PubMed |
| Phenotypic and Genetic Spectrum in 309 Consecutive Pediatric Patients with Inherited Retinal Disease. | Int J Mol Sci | 2024 | 39596324 | PubTator, text mining | PubMed |
| Whole-genome sequencing to identify rare variants in East Asian patients with dementia with Lewy bodies. | NPJ Aging | 2024 | 39572598 | PubTator, text mining | PubMed |
| Genetic heterogeneity in autosomal recessive hearing loss: a survey of Brazilian families. | Front Genet | 2024 | 39498320 | PubTator, text mining | PubMed |
| Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients. | J Mol Neurosci | 2024 | 39467922 | PubTator, text mining | PubMed |
| Genotype Characterization and MiRNA Expression Profiling in Usher Syndrome Cell Lines. | Int J Mol Sci | 2024 | 39337481 | PubTator, text mining | PubMed |
| Nanomechanics of wild-type and mutant dimers of the inner-ear tip-link protein protocadherin 15. | Proc Natl Acad Sci U S A | 2024 | 39298473 | PubTator, text mining | PubMed |
| Identification of novel CDH23 variants linked to hearing loss in a Chinese family: A case report. | Medicine (Baltimore) | 2024 | 39287240 | 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
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GET https://conductscience.org/api/genes/v1/64072/papers?page=4