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.
81 to 100 of 1,428
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss. | Sci Rep | 2024 | 39271758 | PubTator, text mining | PubMed |
| Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis. | Clin Genet | 2024 | 39107234 | PubTator, text mining | PubMed |
| Mild retinitis pigmentosa, including sector retinitis pigmentosa associated with 2 pathogenic variants in CDH23. | Ophthalmic Genet | 2024 | 39092760 | PubTator, text mining | PubMed |
| Whole-Exome Sequencing Detecting a Recurrent Pathogenic Mutation, HFE p.His63Asp (H63D) in COVID-19 Patients and Its Effect on Mortality. | Discov Med | 2024 | 39054721 | PubTator, text mining | PubMed |
| A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy. | BMC Ophthalmol | 2024 | 39044131 | PubTator, text mining | PubMed |
| Bioinformatic analysis predicts the regulatory function of noncoding SNPs associated with Long COVID-19 syndrome. | Immunogenetics | 2024 | 39042286 | PubTator, text mining | PubMed |
| Rare Pathogenic Variants Identified in Whole Exome Sequencing of Monozygotic Twins With Autism Spectrum Disorder. | Pediatr Neurol | 2024 | 39038432 | PubTator, text mining | PubMed |
| CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History. | Invest Ophthalmol Vis Sci | 2024 | 39017633 | PubTator, text mining | PubMed |
| Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23. | Stem Cell Res | 2024 | 38878669 | PubTator, text mining | PubMed |
| Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants. | Mol Genet Genomic Med | 2024 | 38860500 | PubTator, text mining | PubMed |
| Germline Variants in Sporadic Pituitary Adenomas. | J Endocr Soc | 2024 | 38745824 | PubTator, text mining | PubMed |
| Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants. | Sci Rep | 2024 | 38720048 | PubTator, text mining | PubMed |
| Novel missense variants in brain morphogenic genes associated with depression and schizophrenia. | Front Psychiatry | 2024 | 38699454 | PubTator, text mining | PubMed |
| Variations in the Cadherin 23 Gene Associated With Noise-Induced Hearing Loss. | J Multidiscip Healthc | 2024 | 38605856 | PubTator, text mining | PubMed |
| Sensory cells in tunicates: insights into mechanoreceptor evolution. | Front Cell Dev Biol | 2024 | 38550380 | PubTator, text mining | PubMed |
| Identification of Coding Variants in 10q22.1 Associated with Vitiligo in the Chinese Han Population. | Genet Test Mol Biomarkers | 2024 | 38546281 | PubTator, text mining | PubMed |
| Autosomal recessive non-syndromic hearing loss genes in Pakistan during the previous three decades. | J Cell Mol Med | 2024 | 38534090 | PubTator, text mining | PubMed |
| Spectrum of genetic variants in bilateral sensorineural hearing loss. | Front Genet | 2024 | 38410152 | PubTator, text mining | PubMed |
| Emergence of slip-ideal-slip behavior in tip-links serve as force filters of sound in hearing. | Nat Commun | 2024 | 38383683 | PubTator, text mining | PubMed |
| A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss. | Iran J Otorhinolaryngol | 2024 | 38259694 | 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/v1/64072/papers?page=5