Gene · 7466
Papers1,771
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
21 to 40 of 1,771
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| In silico Genotype-Phenotype Correlation Analysis of Inherited Variations in Autism Spectrum Disorder Families Identify an Interplay between Sensory Function and Repetitive-behaviour Genes. | J Mol Neurosci | 2026 | 42184043 | PubTator, text mining | PubMed |
| Human biliary atresia extrahepatic cholangiocyte organoids express increased ER and oxidative stress, altered drug metabolism and cell polarity changes. | Front Bioeng Biotechnol | 2026 | 42183052 | PubTator, text mining | PubMed |
| Unilateral Retinitis Pigmentosa, Glial Tissue Abnormality, and Microphthalmia in a Young Female Patient: A Case Report. | Cureus | 2026 | 42181425 | PubTator, text mining | PubMed |
| Expanding the phenotype of Wolfram syndrome: adult presentation with a novel WFS1 variant. | JCEM Case Rep | 2026 | 42093864 | PubTator, text mining | PubMed |
| rs10010131A in WFS1 is Associated with Elevated Serum Urea in Type 2 Diabetes Patients Treated with SGLT2 Inhibitors. | Ther Clin Risk Manag | 2026 | 42078124 | PubTator, text mining | PubMed |
| Bilateral diabetic Charcot neuroarthropathy of the knee in a young woman with diabetes suspected of Wolfram-like syndrome. | Diabetol Int | 2026 | 42040055 | PubTator, text mining | PubMed |
| Natural history of 15 patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy. | Orphanet J Rare Dis | 2026 | 42001184 | PubTator, text mining | PubMed |
| Hereditary cataract associated with a novel variant in WFS1. | Ophthalmic Genet | 2026 | 41987496 | PubTator, text mining | PubMed |
| Evaluating the Use of GLP-1 Receptor Agonists in Wolfram syndrome Patients. | medRxiv | 2026 | 41959758 | PubTator, text mining | PubMed |
| Type 2 Diabetes Mellitus or Maturity Onset Diabetes in the Young Due to Wolfram Syndrome Gene-1 Mutation-A Perplexing Case. | AACE Endocrinol Diabetes | 2026 | 41938311 | PubTator, text mining | PubMed |
| Neurofilament light chain but not glial fibrillary acidic protein serum levels are elevated in Wolfram syndrome. | Front Neurosci | 2026 | 41929703 | PubTator, text mining | PubMed |
| Genotype-Based Severity Scoring System in Wolfram Syndrome: Correlation with Onset of Cardinal Symptoms and WFS1 Gene Variant Types. | medRxiv | 2026 | 41929334 | PubTator, text mining | PubMed |
| Abstracts from The XXV Brazilian Diabetes Society Meeting. | Diabetol Metab Syndr | 2026 | 41913261 | PubTator, text mining | PubMed |
| Regulated transformation system (RTS): sddi-mediated programmable shut-off and mode switching of base editors. | Nucleic Acids Res | 2026 | 41909950 | PubTator, text mining | PubMed |
| WFS1-related isolated diabetes induced by a WFS1 missense mutation: focus on the isolated diabetes phenotype. | Orphanet J Rare Dis | 2026 | 41896889 | PubTator, text mining | PubMed |
| Optic Atrophy in Wolfram Syndrome Type 1: A Retrospective Analysis of Visual Outcomes and Biomarker Correlates. | J Neuroophthalmol | 2026 | 41870390 | PubTator, text mining | PubMed |
| Ophthalmic, Systemic and Genetic Features in Wolfram Syndrome. | Neuroophthalmology | 2026 | 41847277 | PubTator, text mining | PubMed |
| Entorhinal Cortex Wolframin-1-expressing neurons propagate tau to CA1 neurons and impair hippocampal memory. | bioRxiv | 2026 | 41757076 | PubTator, text mining | PubMed |
| Review Article: Overview of Clinical Genetics of Diabetes Mellitus. | Genes (Basel) | 2026 | 41751598 | PubTator, text mining | PubMed |
| The Intersection of m6A Methylation and Immune Response in PCOS: A Bioinformatics Perspective. | Immun Inflamm Dis | 2026 | 41725222 | 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.
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