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.
901 to 920 of 3,741
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Germline predisposition to pediatric Ewing sarcoma is characterized by inherited pathogenic variants in DNA damage repair genes. | Am J Hum Genet | 2022 | 35512711 | PubTator, text mining | PubMed |
| Transcriptome analysis provides critical answers to the "variants of uncertain significance" conundrum. | Hum Mutat | 2022 | 35510381 | PubTator, text mining | PubMed |
| Late-Breaking Abstracts for ECO2022. | Obes Facts | 2022 | 35500565 | PubTator, text mining | PubMed |
| Unraveling the Genetic Architecture of Hepatoblastoma Risk: Birth Defects and Increased Burden of Germline Damaging Variants in Gastrointestinal/Renal Cancer Predisposition and DNA Repair Genes. | Front Genet | 2022 | 35495172 | PubTator, text mining | PubMed |
| Whole-genome and transcriptome analysis of advanced adrenocortical cancer highlights multiple alterations affecting epigenome and DNA repair pathways. | Cold Spring Harb Mol Case Stud | 2022 | 35483882 | PubTator, text mining | PubMed |
| Environmental and genetic risk factors for gastric cancer. | J Surg Oncol | 2022 | 35481919 | PubTator, text mining | PubMed |
| Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome. | Int J Mol Med | 2022 | 35475445 | PubTator, text mining | PubMed |
| A Rare Case of Juvenile Polyposis Syndrome Mimicking Ménétrier's Disease. | Cureus | 2022 | 35475041 | PubTator, text mining | PubMed |
| Germline mutations in penetrant cancer predisposition genes are rare in men with prostate cancer selecting active surveillance. | Cancer Med | 2022 | 35467778 | PubTator, text mining | PubMed |
| Molecular studies in familial dilated cardiomyopathy - A pilot study. | Int J Cardiol Heart Vasc | 2022 | 35463915 | PubTator, text mining | PubMed |
| A Novel Missense Variant in Actin Binding Domain of MYH7 Is Associated With Left Ventricular Noncompaction. | Front Cardiovasc Med | 2022 | 35463789 | PubTator, text mining | PubMed |
| Germline MBD4 deficiency causes a multi-tumor predisposition syndrome. | Am J Hum Genet | 2022 | 35460607 | PubTator, text mining | PubMed |
| Impact of DNA damage response defects in cancer cells on response to immunotherapy and radiotherapy. | J Med Imaging Radiat Oncol | 2022 | 35460184 | PubTator, text mining | PubMed |
| Genome Integrity and Neurological Disease. | Int J Mol Sci | 2022 | 35456958 | PubTator, text mining | PubMed |
| Identification and Somatic Characterization of the Germline PTEN Promoter Variant rs34149102 in a Family with Gastrointestinal and Breast Tumors. | Genes (Basel) | 2022 | 35456450 | PubTator, text mining | PubMed |
| Identification of a Cancer-Predisposing Germline POT1 p.Ile49Metfs*7 Variant by Targeted Sequencing of a Splenic Marginal Zone Lymphoma. | Genes (Basel) | 2022 | 35456397 | PubTator, text mining | PubMed |
| Live-Cell Imaging of the Contractile Velocity and Transient Intracellular Ca2+ Fluctuations in Human Stem Cell-Derived Cardiomyocytes. | Cells | 2022 | 35455960 | PubTator, text mining | PubMed |
| Advances in the Diagnosis and Therapeutic Management of Gastroenteropancreatic Neuroendocrine Neoplasms (GEP-NENs). | Cancers (Basel) | 2022 | 35454934 | PubTator, text mining | PubMed |
| Perspectives on Ovarian Cancer 1809 to 2022 and Beyond. | Diagnostics (Basel) | 2022 | 35453839 | PubTator, text mining | PubMed |
| Germline testing and genetic counselling in prostate cancer. | Nat Rev Urol | 2022 | 35449224 | 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=46