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.
21 to 40 of 1,428
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Molecular biology of pituitary neuroendocrine tumors. | J Neurooncol | 2026 | 41639477 | PubTator, text mining | PubMed |
| A Novel Pathogenic Haplotype in CDH23 Causing DFNB12: The Combined Effect of Two Individually Benign Variants | Balkan Med J | 2026 | 41614600 | PubTator, text mining | PubMed |
| A novel germline CDH23 variant as a likely cause of an ultra-giant prolactinoma. | Orphanet J Rare Dis | 2026 | 41612354 | PubTator, text mining | PubMed |
| Free-floating long-term vascularized mesenchymal organoids. | iScience | 2026 | 41568151 | PubTator, text mining | PubMed |
| VASCilia is an open-source, deep learning-based tool for 3D analysis of cochlear hair cell stereocilia bundles. | PLoS Biol | 2026 | 41557732 | PubTator, text mining | PubMed |
| Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal health. | Cell Mol Life Sci | 2026 | 41528484 | PubTator, text mining | PubMed |
| NGS sequencing reveals the cause of hearing loss in a group of Polish patients with an isolated, non-DFNB1 hearing loss. | J Appl Genet | 2026 | 40796707 | PubTator, text mining | PubMed |
| [Identification and functional analysis of a novel variant of CHD23 gene in a Chinese pedigree affected with Non-syndromic autosomal recessive deafness 12]. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2025 | 41811048 | PubTator, text mining | PubMed |
| Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity. | Proc Natl Acad Sci U S A | 2025 | 41359850 | PubTator, text mining | PubMed |
| Multi-Omics Mendelian Randomization Identifies Therapeutic Targets for Sjögren's Disease with Clinical and Bayesian Validation. | J Inflamm Res | 2025 | 41333034 | PubTator, text mining | PubMed |
| From genomic discovery to application in age-related hearing loss: a global bibliometric and cross-ethnic analysis. | Front Aging Neurosci | 2025 | 41255877 | PubTator, text mining | PubMed |
| [Analysis of pathogenic variant carriage for MYO7A, PCDH15, and CDH23 genes among newborns based on high-throughput sequencing technique]. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2025 | 41230578 | PubTator, text mining | PubMed |
| Epidemiological and genetic insights of Usher syndrome in Turkish population: A cross-sectional preliminary study from University of Health Sciences, Turkey. | J Int Med Res | 2025 | 41200749 | PubTator, text mining | PubMed |
| Epigenetic mediation may explain intergenerational associations between maternal obesogenic lifestyle and children's birth weight: findings from the NorthPop prospective birth cohort. | Clin Epigenetics | 2025 | 41163109 | PubTator, text mining | PubMed |
| Identification of a variant in the USH1G gene in a family with Usher syndrome | Biomedica | 2025 | 41060164 | PubTator, text mining | PubMed |
| A multicenter study reveals a novel pathogenic splice-site founder variant in OTOF. | Hum Genomics | 2025 | 41053850 | PubTator, text mining | PubMed |
| Use of the FLEX 28 Dexamethasone-Eluting Cochlear Implant Electrode in Electric-Acoustic Stimulation: A Case Report. | Audiol Res | 2025 | 40981391 | PubTator, text mining | PubMed |
| A Novel 1259 bp Intragenic Deletion in the GJB2 Gene in a Mexican Family with Congenital Profound Hearing Loss. | Audiol Res | 2025 | 40981390 | PubTator, text mining | PubMed |
| Identification of known and novel genetic variants in sensorineural hearing loss: insights from whole exome sequencing in Indian families. | Mol Biol Rep | 2025 | 40928595 | PubTator, text mining | PubMed |
| Pharmacogenetic study of antipsychotic-induced lipid and BMI changes in Chinese schizophrenia patients: A Genome-Wide Association Study. | Transl Psychiatry | 2025 | 40830362 | 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.
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