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.
41 to 60 of 1,428
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Role of Pcdh15 in the development of intrinsic polarity of inner ear hair cells. | PLoS Genet | 2025 | 40802839 | PubTator, text mining | PubMed |
| Case report of paroxysmal dystonia in a child with KBG syndrome: Expansion of the phenotype and utility of whole exome sequencing. | Medicine (Baltimore) | 2025 | 40760574 | PubTator, text mining | PubMed |
| [Genetic and clinical phenotypic analysis of Usher syndrome-associated gene variants]. | Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi | 2025 | 40744884 | PubTator, text mining | PubMed |
| Aryl hydrocarbon receptor interacting protein and syndromic gene variants detected in Turkish isolated pituitary adenoma families by whole exome sequencing. | Sci Rep | 2025 | 40624119 | PubTator, text mining | PubMed |
| Cyclic Cushing syndrome associated with cadherin-23 and multiple endocrine neoplasia type 1 gene mutations accompanied by bilateral primary papillary thyroid carcinoma. | Pol Arch Intern Med | 2025 | 40613740 | PubTator, text mining | PubMed |
| Enhanced identification of novel pathogenic variants in hereditary hearing loss through physical phasing with integrated short and long-read sequencing data. | Mol Genet Genomics | 2025 | 40549196 | PubTator, text mining | PubMed |
| Trends and mechanisms of Alzheimer's disease and hearing impairment: A 20-year perspective. | Ageing Res Rev | 2025 | 40499729 | PubTator, text mining | PubMed |
| Outcomes of cochlear implants in patients with PCDH15 mutations: a clinical study. | Front Genet | 2025 | 40486680 | PubTator, text mining | PubMed |
| Genomic and clinical insights into ovarian cancer: subtype-specific alterations and predictors of metastasis and relapse. | Discov Oncol | 2025 | 40411628 | PubTator, text mining | PubMed |
| Clinical application of preimplantation genetic testing based on low-coverage next-generation sequencing with linkage analyses in hereditary hearing loss families. | J Assist Reprod Genet | 2025 | 40389765 | PubTator, text mining | PubMed |
| TCR-Based Therapy Directed against Kallikrein-Related Peptidase 4 Is Safe and Effective against Prostate Cancer. | Cancer Immunol Res | 2025 | 40387827 | PubTator, text mining | PubMed |
| The Diverse Genetic Landscape of Hearing Impairment in South African Families. | Clin Genet | 2025 | 40371963 | PubTator, text mining | PubMed |
| Germline genetic variants in young-onset sporadic pituitary macroadenomas: A multigene panel analysis. | J Clin Transl Endocrinol | 2025 | 40248171 | PubTator, text mining | PubMed |
| From bench to bedside in the sella: translational developments in pituitary tumour genetics. | Endocr Relat Cancer | 2025 | 40197437 | PubTator, text mining | PubMed |
| Generation of two induced pluripotent stem cell lines carrying the CDH23 c.1515-12G > A variant. | Stem Cell Res | 2025 | 40184886 | PubTator, text mining | PubMed |
| Systematic genetic assessment of hearing loss using whole-genome sequencing identifies pathogenic variants. | Exp Mol Med | 2025 | 40164689 | PubTator, text mining | PubMed |
| Genetic Characterization of Turkish Patients with Pituitary Neuroendocrine Tumors. | Turk Neurosurg | 2025 | 40129208 | PubTator, text mining | PubMed |
| Novel genetic determinants contribute to hearing loss in a central European cohort with enlarged vestibular aqueduct. | Mol Med | 2025 | 40121402 | PubTator, text mining | PubMed |
| Clinical Exome Sequencing Identifies, Two Homozygous LOXHD1 Variants in Two Inbred Families With Pre-Lingual Hearing Loss From South India. | Ann Hum Genet | 2025 | 40070250 | PubTator, text mining | PubMed |
| Discovering the pathogenesis of a VUS variant in CDH23 associated with sensorineural hearing loss in an Iranian family. | Mol Biol Rep | 2025 | 40047980 | 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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