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.
1,001 to 1,020 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Left Ventricular Noncompaction Is Associated with Valvular Regurgitation and a Variety of Arrhythmias. | J Cardiovasc Dev Dis | 2022 | 35200702 | PubTator, text mining | PubMed |
| It Is Not Carved in Stone-The Need for a Genetic Reevaluation of Variants in Pediatric Cardiomyopathies. | J Cardiovasc Dev Dis | 2022 | 35200695 | PubTator, text mining | PubMed |
| Familial Hypertrophic Cardiomyopathy With Fasciculoventricular Accessory Pathway. | JACC Case Rep | 2022 | 35199016 | PubTator, text mining | PubMed |
| Genetic associations of protein-coding variants in human disease. | Nature | 2022 | 35197637 | PubTator, text mining | PubMed |
| Proteomic profiling of sporadic late-onset nemaline myopathy. | Ann Clin Transl Neurol | 2022 | 35187860 | PubTator, text mining | PubMed |
| Implications of structural right ventricular involvement in patients with hypertrophic cardiomyopathy. | Eur Heart J Qual Care Clin Outcomes | 2022 | 35179204 | PubTator, text mining | PubMed |
| Pediatric Hypertrophic Cardiomyopathy: Exploring the Genotype-Phenotype Association. | J Am Heart Assoc | 2022 | 35179047 | PubTator, text mining | PubMed |
| Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank. | Nat Genet | 2022 | 35177841 | PubTator, text mining | PubMed |
| Heart Failure Subtypes and Cardiomyopathies in Women. | Circ Res | 2022 | 35175847 | PubTator, text mining | PubMed |
| A novel Troponin I mutation associated with severe restrictive cardiomyopathy-a case report of a 27-year-old woman with fatigue. | Eur Heart J Case Rep | 2022 | 35174310 | PubTator, text mining | PubMed |
| Hypertrophic Cardiomyopathy and Atrial Fibrillation: A Review. | Cureus | 2022 | 35165560 | PubTator, text mining | PubMed |
| A 0/1h-algorithm using cardiac myosin-binding protein C for early diagnosis of myocardial infarction. | Eur Heart J Acute Cardiovasc Care | 2022 | 35149868 | PubTator, text mining | PubMed |
| Investigating Genetic and Other Determinants of First-Onset Myocardial Infarction in Malaysia: Protocol for the Malaysian Acute Vascular Events Risk Study. | JMIR Res Protoc | 2022 | 35142634 | PubTator, text mining | PubMed |
Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry. | Eur Heart J Qual Care Clin Outcomes | 2022 | 35138368 | PubTator, text mining | PubMed |
| Creatine kinase-(MB) and hepcidin as candidate biomarkers for early diagnosis of pulmonary tuberculosis: a proof-of-concept study in Lambaréné, Gabon. | Infection | 2022 | 35133607 | PubTator, text mining | PubMed |
| Causative Variants for Inherited Cardiac Conditions in a Southeast Asian Population Cohort. | Circ Genom Precis Med | 2022 | 35130036 | PubTator, text mining | PubMed |
| Translation of New and Emerging Therapies for Genetic Cardiomyopathies. | JACC Basic Transl Sci | 2022 | 35128211 | PubTator, text mining | PubMed |
| Role of genetic testing in cardiomyopathies: Α primer for cardiologists. | World J Cardiol | 2022 | 35126870 | PubTator, text mining | PubMed |
| Ambulatory electrocardiography, heart rate variability, and pharmacologic stress testing in cats with subclinical hypertrophic cardiomyopathy. | Sci Rep | 2022 | 35121794 | PubTator, text mining | PubMed |
| Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning. | JMIR Med Inform | 2022 | 35107432 | 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=51