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.
61 to 80 of 1,771
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Diabetes Insipidus as an Early Clinical Indicator of Wolfram Syndrome Type 1: Evidence From a Symptom-Based Screening Approach. | Pediatr Diabetes | 2025 | 41080637 | PubTator, text mining | PubMed |
| Wolfram-like Syndrome: Shedding Light on a Variant of Wolfram Syndrome. | AACE Endocrinol Diabetes | 2025 | 41048689 | PubTator, text mining | PubMed |
| Meta-evolutionary exome analysis identifies novel type 2 diabetes mellitus genes in the UK Biobank and all of us. | PLoS Genet | 2025 | 41026804 | PubTator, text mining | PubMed |
| Circadian Rhythm and Psychiatric Features in Wolfram Syndrome: Toward Chrono Diagnosis and Chronotherapy. | Diagnostics (Basel) | 2025 | 41008710 | PubTator, text mining | PubMed |
| Case Report: Rapid cataract development preceding diabetes mellitus in WFS1 spectrum disorder. | Front Ophthalmol (Lausanne) | 2025 | 40995355 | PubTator, text mining | PubMed |
| Diabetes mellitus and pregnancy in Wolfram syndrome type 1: a case report with review of clinical and pathophysiological aspects. | Front Med (Lausanne) | 2025 | 40988749 | PubTator, text mining | PubMed |
| Role of necroptosis-related genes in immune activity and prognosis of colorectal cancer. | Front Immunol | 2025 | 40959081 | PubTator, text mining | PubMed |
| Could R-Ketamine and Wolfram Syndrome Inform Understanding of Depression and Suicidality? A Sigma-1 Receptor-Based Perspective. | Hum Psychopharmacol | 2025 | 40955171 | PubTator, text mining | PubMed |
| WFS1 gene mutation associated with pediatric diabetes mellitus and congenital deafness: A case report. | World J Diabetes | 2025 | 40837343 | PubTator, text mining | PubMed |
| Maturity onset diabetes of the young and beyond: the changing face of single-gene diabetes. | Eur J Endocrinol | 2025 | 40819284 | PubTator, text mining | PubMed |
| Rare Variants in NEUROD1 and PDX1 Are Low-Penetrance Causes of MODY, Whereas Those in APPL1 and WFS1 Are Not Associated With MODY. | Diabetes | 2025 | 40779032 | PubTator, text mining | PubMed |
| Topology of WFS1 Variants Linked With Islet Function and Higher Risk of Urological Symptoms in WFS1-Associated Disease. | Pediatr Diabetes | 2025 | 40777921 | PubTator, text mining | PubMed |
| Erratum. Liraglutide Treatment Reverses Unconventional Cellular Defects in Induced Pluripotent Stem Cell-Derived β-Cells Harboring a Partially Functional WFS1 Variant. Diabetes 2025;74:1273-1288. | Diabetes | 2025 | 40763279 | PubTator, text mining | PubMed |
| Clinical and Genetic Characteristics of Patients with Early-Onset Diabetes Involving at Least Two Consecutive Generations: Whole-Exome Sequencing in Probands from 25 Pedigrees. | Curr Med Sci | 2025 | 40694255 | PubTator, text mining | PubMed |
| Characterization of Novel WFS1 Variants in Three Diabetes Pedigrees. | J Diabetes | 2025 | 40641032 | PubTator, text mining | PubMed |
| Non-syndromic WFS1 mutations are not a rare cause of diabetes in Pakistan. | Diabetes Res Clin Pract | 2025 | 40617298 | PubTator, text mining | PubMed |
| The significance of ophthalmological evaluation in the correct diagnosis of pediatric insulin-dependent diabetes mellitus: lessons from novel WFS1 variants. | Diabetes Metab | 2025 | 40527387 | PubTator, text mining | PubMed |
| Gene expression inference based on graph neural networks using L1000 data. | Brief Bioinform | 2025 | 40505083 | PubTator, text mining | PubMed |
| A Hidden Diagnosis: Neurogenic Bladder Leading to Acute Kidney Failure in Wolfram Syndrome. | Cureus | 2025 | 40486361 | PubTator, text mining | PubMed |
| [Molecular genetics in pediatric endocrinology: 35 years of research]. | Probl Endokrinol (Mosk) | 2025 | 40411325 | 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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