Gene · 4607
Papers3,985
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
81 to 100 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Quantitative Histological Insights Into Sudden Arrhythmic Death Syndrome: Findings From a Forensic Autopsy Cohort. | APMIS | 2026 | 41747709 | PubTator, text mining | PubMed |
| Single-Cell Multi-Omics Profiling of Human Septal Myectomy Tissue: Toward Precision Medicine in Obstructive Hypertrophic Cardiomyopathy. | J Pers Med | 2026 | 41745380 | PubTator, text mining | PubMed |
| Biomarker Profiling of Cardiac Causes for Chest Pain in Non-acute Coronary Syndrome Patients in West Virginia. | Cureus | 2026 | 41743145 | PubTator, text mining | PubMed |
| From polygenic risk to digital twins: the future of personalised cardiovascular medicine. | Front Cardiovasc Med | 2026 | 41736831 | PubTator, text mining | PubMed |
| Digenic sarcomeric variants in paediatric dilated cardiomyopathy and maternal peripartum cardiomyopathy: a familial case report. | Eur Heart J Case Rep | 2026 | 41728227 | PubTator, text mining | PubMed |
| Right coronary artery originated from left coronary sinus associated with children hypertrophic cardiomyopathy: report of two cases and literature review. | Open Med (Wars) | 2026 | 41726140 | PubTator, text mining | PubMed |
| Novel biomarkers distinguish heart failure with preserved vs reduced ejection fraction. | ESC Heart Fail | 2026 | 41711204 | PubTator, text mining | PubMed |
| Cardiovascular diseases and risk factors associated with sudden cardiac death in amateur athletes: a scoping review. | Front Public Health | 2026 | 41710313 | PubTator, text mining | PubMed |
| MYBPC3 (c.194 C > T) mutation-mediated RyR2 dysfunction contributes to pathogenic phenotypes of DCM revealed by HiPSC modeling. | Cell Mol Life Sci | 2026 | 41703309 | PubTator, text mining | PubMed |
| Hypertrophic cardiomyopathy: comprehensive insights into pathogenic genes and genotype-phenotype associations. | Front Cell Dev Biol | 2026 | 41695390 | PubTator, text mining | PubMed |
| Comments on: "Genotype-phenotype associations in sarcomeric hypertrophic cardiomyopathy associated with mutations in the MYBPC3 gene: Systematic review and meta-analysis". | J Cardiol | 2026 | 41651343 | PubTator, text mining | PubMed |
| Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies. | Res Sq | 2026 | 41646289 | PubTator, text mining | PubMed |
| Gene Therapy for Heart Failure. | J Cardiovasc Transl Res | 2026 | 41642391 | PubTator, text mining | PubMed |
| Cross-dataset transcriptomic analyses identify a conserved ENPP2+ macrophage-fibroblast activation axis in hypertrophic cardiomyopathy. | Brief Bioinform | 2026 | 41642196 | PubTator, text mining | PubMed |
| Phenotypic, Epidemiologic, and Imaging Features of Hypertrophic Cardiomyopathy: A Single-Center Experience. | Anatol J Cardiol | 2026 | 41636064 | PubTator, text mining | PubMed |
| Heart Failure With Mildly Reduced Ejection Fraction: A Call for a Precision Medicine Approach. | JACC Adv | 2026 | 41609287 | PubTator, text mining | PubMed |
| Heterogeneity and optimal study design between cell lines in induced pluripotent stem cell-based cardiac disease modeling. | Stem Cells Transl Med | 2026 | 41604239 | PubTator, text mining | PubMed |
| Cardiomyopathy in Northwestern Mexico: Clinical Spectrum, Morphological Variants, and Sarcomere Gene Mutations. | Arch Med Res | 2026 | 41581477 | PubTator, text mining | PubMed |
| A Novel A-Kinase-Anchoring Protein 9 Variant in Premature Coronary Artery Disease: A Case Series. | Mol Genet Genomic Med | 2026 | 41574642 | PubTator, text mining | PubMed |
| Early Onset Heart Failure due to RBM20 Variant: A Case Report Emphasizing Genetic Diagnosis and Arrhythmic Risk Stratification. | Clin Case Rep | 2026 | 41567528 | 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/v1/4607/papers?page=5