Gene · 4647
Papers1,877
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 1,877
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Molecular genetic analysis of pulmonary benign metastasizing leiomyoma and intravenous leiomyomatosis: a comparative study using whole exome sequencing. | Discov Oncol | 2025 | 40434516 | PubTator, text mining | PubMed |
| Syndromic forms of inherited retinal dystrophies: a comprehensive molecular diagnosis of consanguineous Pakistani families using capture panel sequencing. | Mol Vis | 2025 | 40384762 | PubTator, text mining | PubMed |
| The Diverse Genetic Landscape of Hearing Impairment in South African Families. | Clin Genet | 2025 | 40371963 | PubTator, text mining | PubMed |
| Clinical manifestations of dual-gene variants involving ABCA4 in retinal dystrophies. | BMC Ophthalmol | 2025 | 40269797 | PubTator, text mining | PubMed |
| Genetic Risk Factors in Normal Pressure Hydrocephalus: What We Know and What Is Next. | Mov Disord | 2025 | 40266017 | PubTator, text mining | PubMed |
| Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome. | Invest Ophthalmol Vis Sci | 2025 | 40257781 | PubTator, text mining | PubMed |
| Bilateral Vasoproliferative Tumors in Usher Syndrome. | Case Rep Ophthalmol | 2025 | 40241930 | PubTator, text mining | PubMed |
| A Tonotopic Regulatory Axis Governing Isoform-Specific MYO7A Expression in Cochlear Hair Cells. | bioRxiv | 2025 | 40236169 | PubTator, text mining | PubMed |
| Systematic identification of disease-causing promoter and untranslated region variants in 8040 undiagnosed individuals with rare disease. | Genome Med | 2025 | 40229884 | PubTator, text mining | PubMed |
| Testicular stage- and cell-specific expression of F-actin-binding proteins†. | Biol Reprod | 2025 | 40207874 | PubTator, text mining | PubMed |
| Usher Syndrome: New Insights into Classification, Genotype-Phenotype Correlation, and Management. | Genes (Basel) | 2025 | 40149483 | PubTator, text mining | PubMed |
| Select autosomal dominant DFNA11 deafness variants activate Myo7A targeting in epithelial cells. | J Cell Sci | 2025 | 40110717 | PubTator, text mining | PubMed |
| The filopodial myosin DdMyo7 is a slow, calcium-regulated motor. | J Biol Chem | 2025 | 40043952 | PubTator, text mining | PubMed |
| 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 |
| Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran. | Mol Genet Genomic Med | 2025 | 39967327 | 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 |
| Extent of genetic and epigenetic factor reprogramming via a single viral vector construct in deaf adult mice. | Hear Res | 2025 | 39848037 | PubTator, text mining | PubMed |
| Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity search. | Hum Genet | 2025 | 39755840 | PubTator, text mining | PubMed |
| MYO7A is required for the functional integrity of the mechanoelectrical transduction complex in hair cells of the adult cochlea. | Proc Natl Acad Sci U S A | 2025 | 39746042 | 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 |
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/v1/4647/papers?page=4