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.
1 to 20 of 1,771
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Case Report: Rapid loss of endogenous insulin secretion and reversible subcutaneous insulin resistance following exogenous insulin exposure in a patient initially diagnosed with type 2 diabetes. | Front Endocrinol (Lausanne) | 2026 | 42824193 | PubTator, text mining | PubMed |
| Genetic Variants Associated with Response to GLP-1 Receptor Agonists in Diabetes and Obesity. | Life (Basel) | 2026 | 42795351 | PubTator, text mining | PubMed |
| Adult-onset Wolfram syndrome presenting as isolated bilateral optic atrophy. | Can J Ophthalmol | 2026 | 42785371 | PubTator, text mining | PubMed |
| Co-segregation of WFS1 p.Gly494Ser variant with recurrent vasovagal syncope in a multigenerational family: a candidate susceptibility variant needing independent validation. | Front Pediatr | 2026 | 42756402 | PubTator, text mining | PubMed |
| Genetic Heterogeneity in Susceptibility to Familial Thyroid Nodular Disease. | Thyroid | 2026 | 42723469 | PubTator, text mining | PubMed |
| Neuro-ophthalmological manifestations and therapeutic development in Wolfram syndrome. | Best Pract Res Clin Endocrinol Metab | 2026 | 42648929 | PubTator, text mining | PubMed |
| Evaluating the use of GLP-1 receptor agonists in Wolfram syndrome patients. | Front Endocrinol (Lausanne) | 2026 | 42597412 | PubTator, text mining | PubMed |
| Genotype-based severity scoring system in Wolfram Syndrome: correlation with onset of cardinal symptoms and WFS1 gene variant types. | Front Genet | 2026 | 42524523 | PubTator, text mining | PubMed |
Retraction notice to "Proteomic hub proteins CDKN2B, TRAPPC2L, WFS1, and ARPP19 drive biochemical recurrence and metastatic progression in prostate cancer: Protein macromolecule action" [Int. J. Biol. Macromol. 311 (2025) 144059]. | Int J Biol Macromol | 2026 | 42481344 | PubTator, text mining | PubMed |
| Consensus Recommendations for the Clinical Management of Wolfram syndrome Using a Delphi Method. | medRxiv | 2026 | 42428113 | PubTator, text mining | PubMed |
| Revision of diagnosis in a child with type 1 diabetes mellitus due to appropriate genetic testing - Wolfram Syndrome. | BMJ Case Rep | 2026 | 42392675 | PubTator, text mining | PubMed |
| New insights into the complex genetic architecture of age-related hearing loss. | Eur J Med Genet | 2026 | 42379497 | PubTator, text mining | PubMed |
| Integrative genetic and functional analysis of autosomal dominant hearing loss in 108 multigenerational families. | J Mol Med (Berl) | 2026 | 42371110 | PubTator, text mining | PubMed |
| Diagnostic Yield and Clinical Impact of Comprehensive WES/WGS Testing Beyond Common Genetic Causes in Hereditary Optic Atrophy. | Clin Genet | 2026 | 42363686 | PubTator, text mining | PubMed |
| Wolfram syndrome and diabetes mellitus in Aotearoa, New Zealand: Phenotype and response to GLP-1 receptor agonist therapy. | Diabet Med | 2026 | 42324630 | PubTator, text mining | PubMed |
| Pediatric hereditary optic neuropathies in the United Arab Emirates. | Ophthalmic Genet | 2026 | 42299460 | PubTator, text mining | PubMed |
| Targeting WFS1 overcomes KRASG12D dependency and adaptive resistance to KRAS inhibition in pancreatic cancer. | NPJ Precis Oncol | 2026 | 42298062 | PubTator, text mining | PubMed |
| Adiponectin and leptin levels in mothers, fetuses, and neonates with intrauterine growth restriction compared to those with appropriate gestational age. | Front Endocrinol (Lausanne) | 2026 | 42272807 | PubTator, text mining | PubMed |
| Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population-Specific Variants and Clinical Correlations. | Clin Genet | 2026 | 42233699 | PubTator, text mining | PubMed |
| Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families. | Biomolecules | 2026 | 42193970 | 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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