Gene · 6833
Papers4,205
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 4,205
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Optimizing treatment of cardiovascular risk factors in cerebral small vessel disease using genetics. | Brain | 2025 | 39661645 | PubTator, text mining | PubMed |
| The p.(Gly111Arg) ABCC8 Variant: A Founder Mutation Causing Congenital Hyperinsulinism in the Indian Agarwal Community. | Clin Genet | 2025 | 39601258 | PubTator, text mining | PubMed |
| Identification of heterozygous mutations of ABCC8 gene responsible for maturity-onset diabetes of the young with exome sequencing. | Acta Diabetol | 2025 | 39556225 | PubTator, text mining | PubMed |
| A Comprehensive Target Panel Allows to Extend the Genetic Spectrum of Neuroendocrine Tumors. | Neuroendocrinology | 2025 | 39536727 | PubTator, text mining | PubMed |
| Congenital hyperinsulinemia and diabetes caused by ABCC8 variant in a family: a case report. | QJM | 2025 | 39514111 | 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 |
| The association of SUR1 polymorphisms with acute infarct size: The MRI-GENIE study. | J Stroke Cerebrovasc Dis | 2025 | 39489406 | PubTator, text mining | PubMed |
| Unraveling the genetic basis of MODY: insights from next-generation sequencing. | J Appl Genet | 2025 | 39361122 | PubTator, text mining | PubMed |
| [Striking manifestation and unexpected therapeutic course of diabetes mellitus in a 22-year-old male patient]. | Inn Med (Heidelb) | 2025 | 39342034 | PubTator, text mining | PubMed |
| RELATIONSHIP BETWEEN TRPM4 RS8104571 GENOTYPE, CIRCULATING TRPM4 AND SUR1, AND CLINICAL OUTCOME FOLLOWING TRAUMATIC BRAIN INJURY. | Shock | 2025 | 39227352 | PubTator, text mining | PubMed |
| The obesity-related mutation gene on nonalcoholic fatty liver disease. | Hum Genet | 2025 | 38985322 | PubTator, text mining | PubMed |
| Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study. | J Clin Endocrinol Metab | 2025 | 38963811 | PubTator, text mining | PubMed |
| Congenital Hyperinsulinism of a Large Italian Cohort: A Retrospective Study. | Horm Res Paediatr | 2025 | 38806014 | PubTator, text mining | PubMed |
| Diazoxide-unresponsive Hyperinsulinemic Hypoglycaemia in a Preterm Infant with Heterozygous Insulin Receptor Gene Mutation | J Clin Res Pediatr Endocrinol | 2025 | 37074094 | PubTator, text mining | PubMed |
| Non-surgical Treatment May be Appropriate for Most Chinese Children With Monogenic Congenital Hyperinsulinism Based on a Retrospective Study of 121 Patients. | Pediatr Diabetes | 2024 | 40302972 | PubTator, text mining | PubMed |
| Incidence, Phenotypes, and Genotypes of Neonatal Diabetes: A 16-Year Experience. The Rare Genetic Etiologies of Neonatal Diabetes Are Common in Sudan. | Pediatr Diabetes | 2024 | 40302952 | PubTator, text mining | PubMed |
| Case Report: The importance of genetic counseling for families with hyperinsulinism. | Front Pediatr | 2024 | 39895985 | PubTator, text mining | PubMed |
| Congenital hyperinsulinism in the Ukraine: a 10-year national study. | Front Endocrinol (Lausanne) | 2024 | 39741883 | PubTator, text mining | PubMed |
| Precision therapy for Developmental delay, Epilepsy and Neonatal Diabetes syndrome in the era of genomics. | Med J Armed Forces India | 2024 | 39734857 | PubTator, text mining | PubMed |
| ABCC8 polymorphisms rs757110 and rs1801261 association with sulfonylurea therapy of Iraqi type 2 diabetics. | Wiad Lek | 2024 | 39715135 | 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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