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.
101 to 120 of 1,771
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Good cochlear implantation outcomes in subjects with mono-allelic WFS1-associated sensorineural hearing loss - a case series. | Int J Audiol | 2025 | 39422244 | PubTator, text mining | PubMed |
| Unraveling the genetic basis of MODY: insights from next-generation sequencing. | J Appl Genet | 2025 | 39361122 | PubTator, text mining | PubMed |
| Genetic Heterogeneity in Four Probands Reveals HGSNAT, KDM6B, LMNA and WFS1 Related Neurodevelopmental Disorders. | Biomedicines | 2024 | 39767643 | PubTator, text mining | PubMed |
| Patients with a Wide Range of Disorders Related to WFS1 Gene Variants: Novel Mutations and Genotype-Phenotype Correlations. | Genes (Basel) | 2024 | 39766859 | PubTator, text mining | PubMed |
| Genetic analysis of patients with low-frequency non-syndromic hearing loss. | Mol Genet Genomics | 2024 | 39720982 | PubTator, text mining | PubMed |
| Integration of multi-omics transcriptome-wide analysis for the identification of novel therapeutic drug targets in diabetic retinopathy. | J Transl Med | 2024 | 39719581 | PubTator, text mining | PubMed |
| A NOVEL DE NOVO LIKELY PATHOGENIC VARIANT OF WFS-1 GENE IN A PAKISTANI CHILD WITH NON-CLASSIC WFS-1 SPECTRUM DISORDER. | J Ayub Med Coll Abbottabad | 2024 | 39609996 | PubTator, text mining | PubMed |
| Beyond Wolfram Syndrome 1: The WFS1 Gene's Role in Alzheimer's Disease and Sleep Disorders. | Biomolecules | 2024 | 39595565 | PubTator, text mining | PubMed |
| Defects of WFS1-mediated peptide hormones secretion contribute to the manifestations of Wolfram syndrome. | Life Sci | 2024 | 39510168 | PubTator, text mining | PubMed |
| The immunological and prognostic significance of the diabetes mellitus-related gene WFS1 in endometrial cancer. | Front Immunol | 2024 | 39478865 | PubTator, text mining | PubMed |
| Insights from a Wolfram syndrome cohort: clinical and molecular findings from a specialized diabetes reference center. | Arch Endocrinol Metab | 2024 | 39420940 | PubTator, text mining | PubMed |
| OBSESSIVE COMPULSIVE DISORDER AND CONSTITUTIONAL DELAY OF GROWTH AND PUBERTY IN WOLFRAM SYNDROME: NEW ASPECTS AND A NOVEL WFS1 MUTATION. | Acta Endocrinol (Buchar) | 2024 | 39372310 | PubTator, text mining | PubMed |
| Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy. | Sci Rep | 2024 | 39363032 | PubTator, text mining | PubMed |
| The WFS1-ZnT3-Zn2+ Axis Regulates the Vicious Cycle of Obesity and Depression. | Adv Sci (Weinh) | 2024 | 39258564 | PubTator, text mining | PubMed |
| Novel WFS1 variants are associated with different diabetes phenotypes. | Front Genet | 2024 | 39221226 | PubTator, text mining | PubMed |
| Wolfram Syndrome 1: A Neuropsychiatric Perspective on a Rare Disease. | Genes (Basel) | 2024 | 39202345 | PubTator, text mining | PubMed |
| MODY Only Monogenic? A Narrative Review of the Novel Rare and Low-Penetrant Variants. | Int J Mol Sci | 2024 | 39201476 | PubTator, text mining | PubMed |
| A deep phenotyping study in mouse and iPSC models to understand the role of oligodendroglia in optic neuropathy in Wolfram syndrome. | Acta Neuropathol Commun | 2024 | 39198924 | PubTator, text mining | PubMed |
| Wolfram Syndrome Type I Case Report and Review-Focus on Early Diagnosis and Genetic Variants. | Medicina (Kaunas) | 2024 | 39064493 | PubTator, text mining | PubMed |
| ER calcium depletion as a key driver for impaired ER-to-mitochondria calcium transfer and mitochondrial dysfunction in Wolfram syndrome. | Nat Commun | 2024 | 39034309 | 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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/7466/papers?page=6