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.
921 to 940 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| High-Throughput Sequencing to Identify Mutations Associated with Retinal Dystrophies. | Genes (Basel) | 2021 | 34440443 | PubTator, text mining | PubMed |
| An Overview of the Genetics of ABCA4 Retinopathies, an Evolving Story. | Genes (Basel) | 2021 | 34440414 | PubTator, text mining | PubMed |
| Genetic testing hearing loss: The challenge of non syndromic mimics. | Int J Pediatr Otorhinolaryngol | 2021 | 34433113 | PubTator, text mining | PubMed |
| Genetic alternations and immune characteristics in patients with small cell lung cancer. | Cancer Commun (Lond) | 2021 | 34427988 | PubTator, text mining | PubMed |
| Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variants. | Stem Cell Res | 2021 | 34419747 | PubTator, text mining | PubMed |
| Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. | Transl Psychiatry | 2021 | 34417442 | PubTator, text mining | PubMed |
| The structure-function correlation analysed by OCT and full field ERG in typical and pericentral subtypes of retinitis pigmentosa. | Sci Rep | 2021 | 34413453 | PubTator, text mining | PubMed |
| Patterns of Autofluorescence in Common Genotypes of Retinitis Pigmentosa. | Ophthalmic Surg Lasers Imaging Retina | 2021 | 34410191 | PubTator, text mining | PubMed |
| Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient. | Mol Genet Genomic Med | 2021 | 34405590 | PubTator, text mining | PubMed |
| Fundus Autofluorescence and Clinical Applications. | J Ophthalmic Vis Res | 2021 | 34394872 | PubTator, text mining | PubMed |
| A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report. | BMC Med Genomics | 2021 | 34376197 | PubTator, text mining | PubMed |
| Oncolytic HSV: Underpinnings of Tumor Susceptibility. | Viruses | 2021 | 34372614 | PubTator, text mining | PubMed |
| Comparative analysis of the autism‑related variants between different autistic children in a family pedigree. | Mol Med Rep | 2021 | 34368859 | PubTator, text mining | PubMed |
| Glycolysis Define Two Prognostic Subgroups of Lung Adenocarcinoma With Different Mutation Characteristics and Immune Infiltration Signatures. | Front Cell Dev Biol | 2021 | 34368114 | PubTator, text mining | PubMed |
| Analysis of Interleukin-1 Signaling Alterations of Colon Adenocarcinoma Identified Implications for Immunotherapy. | Front Immunol | 2021 | 34367132 | PubTator, text mining | PubMed |
| Embryology, Malformations, and Rare Diseases of the Cochlea. | Laryngorhinootologie | 2021 | 34352899 | PubTator, text mining | PubMed |
| Complementary Sequential Circulating Tumor Cell (CTC) and Cell-Free Tumor DNA (ctDNA) Profiling Reveals Metastatic Heterogeneity and Genomic Changes in Lung Cancer and Breast Cancer. | Front Oncol | 2021 | 34336686 | PubTator, text mining | PubMed |
| Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children. | Neural Plast | 2021 | 34335733 | PubTator, text mining | PubMed |
Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A). | Am J Med Genet A | 2021 | 34331386 | PubTator, text mining | PubMed |
| Updating the Genetic Landscape of Inherited Retinal Dystrophies. | Front Cell Dev Biol | 2021 | 34327195 | 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=47