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.
81 to 100 of 1,771
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Clinical application of preimplantation genetic testing based on low-coverage next-generation sequencing with linkage analyses in hereditary hearing loss families. | J Assist Reprod Genet | 2025 | 40389765 | PubTator, text mining | PubMed |
| The Diverse Genetic Landscape of Hearing Impairment in South African Families. | Clin Genet | 2025 | 40371963 | PubTator, text mining | PubMed |
| Proteomic hub proteins CDKN2B, TRAPPC2L, WFS1, and ARPP19 drive biochemical recurrence and metastatic progression in prostate cancer: Protein macromolecule action. | Int J Biol Macromol | 2025 | 40345286 | PubTator, text mining | PubMed |
| Coexposure to extreme heat, wildfire burn zones, and wildfire smoke in the Western US from 2006 to 2020. | Sci Adv | 2025 | 40305597 | PubTator, text mining | PubMed |
| Improving mitochondria-associated endoplasmic reticulum membranes integrity as converging therapeutic strategy for rare neurodegenerative diseases and cancer. | Biochim Biophys Acta Mol Cell Res | 2025 | 40216201 | PubTator, text mining | PubMed |
| Liraglutide Treatment Reverses Unconventional Cellular Defects in Induced Pluripotent Stem Cell-Derived β-Cells Harboring a Partially Functional WFS1 Variant. | Diabetes | 2025 | 40202504 | PubTator, text mining | PubMed |
| Reciprocal rescue of Wolfram syndrome by two causative genes. | EMBO Rep | 2025 | 40181095 | PubTator, text mining | PubMed |
| MyoD1 localization at the nuclear periphery is mediated by association of WFS1 with active enhancers. | Nat Commun | 2025 | 40097443 | PubTator, text mining | PubMed |
| Interpretation of de novo mutations (DNM) and genetic counseling for sporadic hearing loss based on family trio-based sequencing. | Yi Chuan | 2025 | 40068948 | PubTator, text mining | PubMed |
| Natural history of patients with autosomal dominant WFS1 pathogenic variants associated with sensorineural hearing loss and optic atrophy. | medRxiv | 2025 | 40061310 | PubTator, text mining | PubMed |
| Sodium valproate, a potential repurposed treatment for the neurodegeneration in Wolfram syndrome (TREATWOLFRAM): trial protocol for a pivotal multicentre, randomised double-blind controlled trial. | BMJ Open | 2025 | 40010822 | PubTator, text mining | PubMed |
| β cell dedifferentiation, the underlying mechanism of diabetes in Wolfram syndrome. | Sci Transl Med | 2025 | 39970233 | PubTator, text mining | PubMed |
| Identification of a pathogenic founder variant in the WFS1 gene that causes Wolfram syndrome in the Druze population. | Front Pediatr | 2025 | 39944315 | PubTator, text mining | PubMed |
| Genetic Structure of Hereditary Forms of Diabetes Mellitus in Russia. | Int J Mol Sci | 2025 | 39859454 | PubTator, text mining | PubMed |
| The Heterozygous p.A684V Variant in the WFS1 Gene Is a Mutational Hotspot Causing a Severe Hearing Loss Phenotype. | Genes (Basel) | 2025 | 39858604 | PubTator, text mining | PubMed |
| Early trigeminal and sensory impairment and lysosomal dysfunction in accurate models of Wolfram syndrome. | Exp Neurol | 2025 | 39662795 | PubTator, text mining | PubMed |
| The phenotypic spectrum of syndromic optic atrophy associated with variants in WFS1: with reclassification of p.Val606Gly as a likely benign variant. | Ophthalmic Genet | 2025 | 39552476 | PubTator, text mining | PubMed |
| A WFS1 variant disrupting acceptor splice site uncovers the impact of alternative splicing on beta cell apoptosis in a patient with Wolfram syndrome. | Diabetologia | 2025 | 39520565 | PubTator, text mining | PubMed |
| Molecular and Clinical Profiles of Pediatric Monogenic Diabetes Subtypes: Comprehensive Genetic Analysis of 138 Patients. | J Clin Endocrinol Metab | 2025 | 39504571 | PubTator, text mining | PubMed |
| Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genes. | Brain | 2025 | 39423307 | 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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