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.
1,761 to 1,780 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Pathogenic and Uncertain Genetic Variants Have Clinical Cardiac Correlates in Diverse Biobank Participants. | J Am Heart Assoc | 2020 | 32009526 | PubTator, text mining | PubMed |
| Systematic Comparison of High-throughput Single-Cell and Single-Nucleus Transcriptomes during Cardiomyocyte Differentiation. | Sci Rep | 2020 | 32001747 | PubTator, text mining | PubMed |
| Exercise and myocardial injury in hypertrophic cardiomyopathy. | Heart | 2020 | 32001622 | PubTator, text mining | PubMed |
| Genes frequently associated with sudden death in primary hypertrophic cardiomyopathy. | Arch Cardiol Mex | 2020 | 31996869 | PubTator, text mining | PubMed |
| Quality of whole genome sequencing from blood versus saliva derived DNA in cardiac patients. | BMC Med Genomics | 2020 | 31996208 | PubTator, text mining | PubMed |
| Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patients. | J Cachexia Sarcopenia Muscle | 2020 | 31991054 | PubTator, text mining | PubMed |
| B4GALNT1 induces angiogenesis, anchorage independence growth and motility, and promotes tumorigenesis in melanoma by induction of ganglioside GM2/GD2. | Sci Rep | 2020 | 31988291 | PubTator, text mining | PubMed |
| Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction. | Mol Genet Genomic Med | 2020 | 31985165 | PubTator, text mining | PubMed |
| Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic Cardiomyopathy. | Circulation | 2020 | 31983222 | PubTator, text mining | PubMed |
| Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging. | Proc Natl Acad Sci U S A | 2020 | 31980526 | PubTator, text mining | PubMed |
| Genome Editing for the Understanding and Treatment of Inherited Cardiomyopathies. | Int J Mol Sci | 2020 | 31979133 | PubTator, text mining | PubMed |
| The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly. | Nat Commun | 2020 | 31974348 | PubTator, text mining | PubMed |
| The Emergence of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes (hiPSC-CMs) as a Platform to Model Arrhythmogenic Diseases. | Int J Mol Sci | 2020 | 31963859 | PubTator, text mining | PubMed |
| Potential digenic inheritance of familial hypertrophic cardiomyopathy identified by whole-exome sequencing. | Mol Genet Genomic Med | 2020 | 31960626 | PubTator, text mining | PubMed |
| MyBP-C: one protein to govern them all. | J Muscle Res Cell Motil | 2020 | 31960266 | PubTator, text mining | PubMed |
| A comparison of gene expression and DNA methylation patterns across tissues and species. | Genome Res | 2020 | 31953346 | PubTator, text mining | PubMed |
| Functional characterization of human myosin-binding protein C3 variants associated with hypertrophic cardiomyopathy reveals exon-specific cardiac phenotypes in zebrafish model. | J Cell Physiol | 2020 | 31943169 | PubTator, text mining | PubMed |
| Retrospective analysis of clinical phenotype and prognosis of hypertrophic cardiomyopathy complicated with hypertension. | Sci Rep | 2020 | 31941943 | PubTator, text mining | PubMed |
| Aberrant DNA methylation profile exacerbates inflammation and neurodegeneration in multiple sclerosis patients. | J Neuroinflammation | 2020 | 31937331 | PubTator, text mining | PubMed |
| Utility of genetic testing in athletes. | Clin Cardiol | 2020 | 31925963 | 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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/4607/papers?page=89