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.
1,201 to 1,220 of 2,630
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Phenotypic Subtyping and Re-Analysis of Existing Methylation Data from Autistic Probands in Simplex Families Reveal ASD Subtype-Associated Differentially Methylated Genes and Biological Functions. | Int J Mol Sci | 2020 | 32961747 | PubTator, text mining | PubMed |
| Helper virus-free gutless adenovirus (HF-GLAd): a new platform for gene therapy. | BMB Rep | 2020 | 32958121 | PubTator, text mining | PubMed |
| Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA. | Mol Med Rep | 2020 | 32945453 | PubTator, text mining | PubMed |
| Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations. | Sci Rep | 2020 | 32938956 | PubTator, text mining | PubMed |
| The Importance of Early Genetic Diagnostics of Hearing Loss in Children. | Medicina (Kaunas) | 2020 | 32937936 | PubTator, text mining | PubMed |
| An algorithm to quantify intratumor heterogeneity based on alterations of gene expression profiles. | Commun Biol | 2020 | 32917965 | PubTator, text mining | PubMed |
| Wavelength of light and photophobia in inherited retinal dystrophy. | Sci Rep | 2020 | 32908200 | PubTator, text mining | PubMed |
| Genetic testing for inherited eye conditions in over 6,000 individuals through the eyeGENE network. | Am J Med Genet C Semin Med Genet | 2020 | 32893963 | PubTator, text mining | PubMed |
| Multimodal imaging and genetic characteristics of Chinese patients with USH2A-associated nonsyndromic retinitis pigmentosa. | Mol Genet Genomic Med | 2020 | 32893482 | PubTator, text mining | PubMed |
| Paving the Road for RNA Therapeutics. | Trends Pharmacol Sci | 2020 | 32893005 | PubTator, text mining | PubMed |
| Functional, Morphological, and Evolutionary Characterization of Hearing in Subterranean, Eusocial African Mole-Rats. | Curr Biol | 2020 | 32888484 | PubTator, text mining | PubMed |
| Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization. | Invest Ophthalmol Vis Sci | 2020 | 32881472 | PubTator, text mining | PubMed |
| CRISPR-Cas9 DNA Base-Editing and Prime-Editing. | Int J Mol Sci | 2020 | 32872311 | PubTator, text mining | PubMed |
| Exome sequencing reveals novel candidate gene variants associated with clinical characteristics in alopecia areata patients. | J Dermatol Sci | 2020 | 32868181 | PubTator, text mining | PubMed |
| A very early diagnosis of Alstrӧm syndrome by next generation sequencing. | BMC Med Genet | 2020 | 32867697 | PubTator, text mining | PubMed |
| Immunogenomic Profiling and Classification of Prostate Cancer Based on HIF-1 Signaling Pathway. | Front Oncol | 2020 | 32850440 | PubTator, text mining | PubMed |
| A novel tumor mutational burden estimation model as a predictive and prognostic biomarker in NSCLC patients. | BMC Med | 2020 | 32843031 | PubTator, text mining | PubMed |
| Mutational Landscape and Environmental Effects in Bladder Cancer. | Int J Mol Sci | 2020 | 32842545 | PubTator, text mining | PubMed |
| Photoreceptor-Specific Loss of Perifoveal Temporal Contrast Sensitivity in Retinitis Pigmentosa. | Transl Vis Sci Technol | 2020 | 32821524 | PubTator, text mining | PubMed |
| Direct Delivery of Antisense Oligonucleotides to the Middle and Inner Ear Improves Hearing and Balance in Usher Mice. | Mol Ther | 2020 | 32818431 | 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=61