Gene · 7399
Papers2,630
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
101 to 120 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| THE IMPACT OF CYSTOID MACULOPATHY IN USH2A RETINITIS PIGMENTOSA : A Retrospective 5-year Analysis. | Retina | 2025 | 40570190 | PubTator, text mining | PubMed |
| Induced Pluripotent (iPSC) and Mesenchymal (MSC) Stem Cells for In Vitro Disease Modeling and Regenerative Medicine. | Int J Mol Sci | 2025 | 40565081 | PubTator, text mining | PubMed |
| Genetic landscape of inherited retinal dystrophies in a Welsh tertiary referral centre. | Br J Ophthalmol | 2025 | 40541286 | PubTator, text mining | PubMed |
| Outcomes of genetic testing for Usher syndrome in a diverse population cohort from South Florida. | Hum Genomics | 2025 | 40533831 | PubTator, text mining | PubMed |
| ATOH-1 Gene Therapy in Acquired Sensorineural Hearing Loss: A Meta-Analysis and Bioinformatic Analysis of Preclinical Studies. | Hum Gene Ther | 2025 | 40501308 | PubTator, text mining | PubMed |
| Resolving the Diagnostic Odyssey in Inherited Retinal Dystrophies Through Long-Read Genome Sequencing. | Am J Med Genet A | 2025 | 40454438 | PubTator, text mining | PubMed |
| The impact of VUS reclassification on reproductive decision making. | PLoS One | 2025 | 40424322 | PubTator, text mining | PubMed |
| Vestibular Phenotype-Genotype Correlation in a Cohort of 35 European Usher Syndrome Patients. | Am J Audiol | 2025 | 40403698 | 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 |
| 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 |
| First Insights Into the Phenotype and Genotype of Inherited Retinal Disorders in the Democratic Republic of Congo (DRC). | Ann Hum Genet | 2025 | 40377368 | PubTator, text mining | PubMed |
| Ethnic disparities in inherited retinal degenerations. | Can J Ophthalmol | 2025 | 40339601 | PubTator, text mining | PubMed |
| Construction of Two Recombinant Pseudorabies Viruses with Deletion of Virulence Genes and Evaluation of Their Immune Protection in Mice and Piglets. | Vaccines (Basel) | 2025 | 40333253 | PubTator, text mining | PubMed |
| Natural History of Microperimetry and Optical Coherence Tomography in USH2A-Retinopathy: A Structure-Function Association Study. | Am J Ophthalmol | 2025 | 40324556 | PubTator, text mining | PubMed |
| Targeted sequencing identifies 33 novel mutations in 130 ClinGen curated hearing loss genes among 253 pediatric patients: A retrospective case study. | Biomed Rep | 2025 | 40322553 | PubTator, text mining | PubMed |
| Unraveling breast cancer response to neoadjuvant chemotherapy through integrated genomic, transcriptomic, and circulating tumor DNA analysis. | Breast Cancer Res | 2025 | 40312292 | PubTator, text mining | PubMed |
| Clinical Exome-Based Redefinition and Reclassification of Retinitis Pigmentosa. | J Korean Med Sci | 2025 | 40296824 | PubTator, text mining | PubMed |
| A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic Targets. | Am J Med Genet C Semin Med Genet | 2025 | 40248902 | PubTator, text mining | PubMed |
| Single-guide RNA Cas9 and enhanced-deletion Cas9 rescue a recurrent USH2A-related splicing defect. | Mol Ther Nucleic Acids | 2025 | 40235854 | PubTator, text mining | PubMed |
| Optic Nerve Coloboma in a Child With Compound Heterozygous USH2A Variants. | Case Rep Genet | 2025 | 40225234 | 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/v1/7399/papers?page=6