Gene · 4595
Papers3,741
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
601 to 620 of 3,741
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Unexplained mismatch repair deficiency: Case closed. | HGG Adv | 2023 | 36624813 | PubTator, text mining | PubMed |
| Internet-Based Germline Genetic Testing for Men With Metastatic Prostate Cancer. | JCO Precis Oncol | 2023 | 36623239 | PubTator, text mining | PubMed |
| Clinical application of PARP inhibitors in ovarian cancer: from molecular mechanisms to the current status. | J Ovarian Res | 2023 | 36611214 | PubTator, text mining | PubMed |
| Mutations of TP53 and genes related to homologous recombination repair in breast cancer with germline BRCA1/2 mutations. | Hum Genomics | 2023 | 36604691 | PubTator, text mining | PubMed |
| Clinical utility of Todai OncoPanel in the setting of approved comprehensive cancer genomic profiling tests in Japan. | Cancer Sci | 2023 | 36601953 | PubTator, text mining | PubMed |
| WRN suppresses p53/PUMA-induced apoptosis in colorectal cancer with microsatellite instability/mismatch repair deficiency. | Proc Natl Acad Sci U S A | 2023 | 36598947 | PubTator, text mining | PubMed |
| Expanded genetic testing of GIST patients identifies high proportion of non-syndromic patients with germline alterations. | NPJ Precis Oncol | 2023 | 36593350 | PubTator, text mining | PubMed |
| Brain functional activity-based classification of autism spectrum disorder using an attention-based graph neural network combined with gene expression. | Cereb Cortex | 2023 | 36587290 | PubTator, text mining | PubMed |
| Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease. | J Pediatr Surg | 2023 | 36586783 | PubTator, text mining | PubMed |
| Corded and hyalinized endometrioid endometrial carcinoma with high-grade features: a clinicopathological and TCGA-based molecular analysis. | Virchows Arch | 2023 | 36550216 | PubTator, text mining | PubMed |
| Penetrance of Gastric Adenocarcinoma Susceptibility Genes: A Systematic Review. | Ann Surg Oncol | 2023 | 36528743 | PubTator, text mining | PubMed |
| AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer. | Genes Chromosomes Cancer | 2023 | 36502525 | PubTator, text mining | PubMed |
| Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma. | EBioMedicine | 2023 | 36493725 | PubTator, text mining | PubMed |
| Methylation of CpG island promoters at ZNF625, LONRF2, SDC2 and WDR17 in a patient with numerous non-granular type laterally spreading tumors and colorectal cancer: A case report. | Oncol Lett | 2023 | 36478906 | PubTator, text mining | PubMed |
| Patient uptake of updated genetic testing following uninformative BRCA1 and BRCA2 results. | J Genet Couns | 2023 | 36478495 | PubTator, text mining | PubMed |
| Intra-abdominal desmoid tumors in familial adenomatous polyposis: How much do clinical and surgical variables interfere with their development? | Clinics (Sao Paulo) | 2023 | 36476966 | PubTator, text mining | PubMed |
| Bundles of Auer rods in mature neutrophils in an acute myeloid leukaemia patient with inv(16)(p13.1q22) CBFB-MYH 11. | Br J Haematol | 2023 | 36441114 | PubTator, text mining | PubMed |
| A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genes. | Cancer Med | 2023 | 36426404 | PubTator, text mining | PubMed |
| Return of individual genomic research results within the PRAEGNANT multicenter registry study. | Breast Cancer Res Treat | 2023 | 36409394 | PubTator, text mining | PubMed |
| The genetic alterations of rectal neuroendocrine tumor and indications for therapy and prognosis: a systematic review. | Endocr J | 2023 | 36403965 | 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.
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GET https://conductscience.org/api/genes/v1/4595/papers?page=31