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Gene · 5172

Papers3,149

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

181 to 200 of 3,149

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TitleJournalYearPMIDFound bySource
Mutation spectra and genotype‑phenotype analysis of congenital hypothyroidism in a neonatal population.Biomed Rep202539720292PubTator, text miningPubMed
Newborn screening for deafness genes with cord blood-based multicolour melting curve analysis.Am J Otolaryngol202539700758PubTator, text miningPubMed
Whole-exome sequencing reveals known and candidate genes for hearing impairment in Mali.HGG Adv202539663698PubTator, text miningPubMed
High potency 3-carboxy-2-methylbenzofuran pendrin inhibitors as novel diuretics.Eur J Med Chem202539642691PubTator, text miningPubMed
Establishing the relationship between history of childhood trauma and personality disorder using the ICD-11 classification system.Personal Ment Health202539610219PubTator, text miningPubMed
Clinical Phenotypic Characterization of the SLC26A4 Mutation in Pendred Syndrome/Nonsyndromic Enlarged Vestibular Aqueduct.Laryngoscope202539575919PubTator, text miningPubMed
Correlation between the etiology of severe hearing loss and endolymphatic hydrops.Eur Arch Otorhinolaryngol202539373914PubTator, text miningPubMed
Role of Kir5.1 (Kcnj16) Channels in Regulating Renal Ammonia Metabolism during Metabolic Acidosis in Dahl Salt-Sensitive Rats.Am J Pathol202539341364PubTator, text miningPubMed
Functional Characterization of Thyroid Peroxidase Missense Variants Causing Thyroid Dyshormonogenesis in Asian Indian Population.Horm Res Paediatr202538986456PubTator, text miningPubMed
Correction 2: A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct.J Med Genet202537414549PubTator, text miningPubMed
Exonic Deletions and Deep Intronic Variants of the SLC26A4 Gene Contribute to the Genetic Diagnosis of Unsolved Patients With Enlarged Vestibular Aqueduct.Hum Mutat202440225947PubTator, text miningPubMed
Exploring a novel model for newborn genetic screening in Ningxia, northern China: A retrospective observational study.Medicine (Baltimore)202439969324PubTator, text miningPubMed
Diagnostic Value of Plasma Long Non-coding SLC26A4 Antisense RNA 1 Combined with Magnetic Resonance Imaging in Rectal Cancer.Turk J Gastroenterol202439641247PubTator, text miningPubMed
Spectrum of DNA variants for patients with hearing loss in 4 language families of 15 ethnicities from Southwestern China.Heliyon202439640791PubTator, text miningPubMed
[The analysis of gene screening results for common hereditary hearing loss in 2 102 pregnant women in Dali area].Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi202439534899PubTator, text miningPubMed
Molecular and Clinical Characterization of a Cohort of Autosomal Recessive Sensorineural Hearing Loss in Egyptian Patients.J Mol Neurosci202439467922PubTator, text miningPubMed
A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4.Arch Iran Med202439465527PubTator, text miningPubMed
[Expanded carrier screening for 216 diseases in a cohort of 3 097 healthy Chinese individuals of childbearing age].Zhonghua Fu Chan Ke Za Zhi202439463360PubTator, text miningPubMed
Identifying DNA Variants in a Turkish Cohort with Inner Ear Anomalies.Ear Nose Throat J202439460668PubTator, text miningPubMed
[Auditory characteristics and disease progression trends of patients with common recessive deafness genes GJB2 and SLC26A4].Zhonghua Yi Xue Za Zhi202439414589PubTator, text miningPubMed

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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