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.
201 to 220 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Vestibulo-ocular reflex dynamics with head-impulses discriminates Usher patients type 1 and 2. | Sci Rep | 2024 | 38355682 | PubTator, text mining | PubMed |
| Spectrum of variants associated with inherited retinal dystrophies in Northeast Mexico. | BMC Ophthalmol | 2024 | 38347443 | PubTator, text mining | PubMed |
| All exons are not created equal-exon vulnerability determines the effect of exonic mutations on splicing. | Nucleic Acids Res | 2024 | 38324470 | PubTator, text mining | PubMed |
| [Genetic characteristic analysis of slight-to-moderate sensorineural hearing loss in children]. | Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi | 2024 | 38297844 | PubTator, text mining | PubMed |
| Identification and validation of a 4-extracellular matrix gene signature associated with prognosis and immune infiltration in lung adenocarcinoma. | Heliyon | 2024 | 38293522 | PubTator, text mining | PubMed |
| Screening copy number variations in 35 unsolved inherited retinal disease families. | Hum Genet | 2024 | 38282009 | PubTator, text mining | PubMed |
| Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids. | Int J Mol Sci | 2024 | 38256087 | PubTator, text mining | PubMed |
| MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population. | BMC Med Genomics | 2024 | 38254107 | PubTator, text mining | PubMed |
| Protein Quality Control Systems and ER Stress as Key Players in SARS-CoV-2-Induced Neurodegeneration. | Cells | 2024 | 38247815 | PubTator, text mining | PubMed |
| Whole genome sequencing enables new genetic diagnosis for inherited retinal diseases by identifying pathogenic variants. | NPJ Genom Med | 2024 | 38245557 | PubTator, text mining | PubMed |
| Genetic diagnosis of childhood sensorineural hearing loss. | Acta Otorrinolaringol Esp (Engl Ed) | 2024 | 38224868 | PubTator, text mining | PubMed |
| Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort. | Ophthalmol Retina | 2024 | 38219857 | PubTator, text mining | PubMed |
| Comprehensive analyses of mitophagy-related genes and mitophagy-related lncRNAs for patients with ovarian cancer. | BMC Womens Health | 2024 | 38218807 | PubTator, text mining | PubMed |
| Highly efficient capture approach for the identification of diverse inherited retinal disorders. | NPJ Genom Med | 2024 | 38195571 | PubTator, text mining | PubMed |
| Genetic profile of syndromic retinitis pigmentosa in Portugal. | Graefes Arch Clin Exp Ophthalmol | 2024 | 38189974 | PubTator, text mining | PubMed |
| How Dedicated Ribosomes Translate a Leaderless mRNA. | J Mol Biol | 2024 | 38185325 | PubTator, text mining | PubMed |
| Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss. | BMC Med Genomics | 2024 | 38167320 | PubTator, text mining | PubMed |
| Carrier frequency estimation of pathogenic variants of autosomal recessive and X-linked recessive mendelian disorders using exome sequencing data in 1,642 Thais. | BMC Med Genomics | 2024 | 38167091 | PubTator, text mining | PubMed |
| Genetics of Retinitis Pigmentosa and Other Hereditary Retinal Disorders in Western Switzerland. | Ophthalmic Res | 2024 | 38160664 | PubTator, text mining | PubMed |
| Functional Vision in Patients With Biallelic USH2A Variants. | Am J Ophthalmol | 2024 | 38135239 | 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=11