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.
1,021 to 1,040 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Biomarkers associated with rhythm status after cardioversion in patients with atrial fibrillation. | Sci Rep | 2022 | 35102265 | PubTator, text mining | PubMed |
| Generating 3D human cardiac constructs from pluripotent stem cells. | EBioMedicine | 2022 | 35093634 | PubTator, text mining | PubMed |
| Variant interpretation in molecular autopsy: a useful dilemma. | Int J Legal Med | 2022 | 35091851 | PubTator, text mining | PubMed |
| Exploring the super-relaxed state of myosin in myofibrils from fast-twitch, slow-twitch, and cardiac muscle. | J Biol Chem | 2022 | 35090895 | PubTator, text mining | PubMed |
| An evaluation of pipelines for DNA variant detection can guide a reanalysis protocol to increase the diagnostic ratio of genetic diseases. | NPJ Genom Med | 2022 | 35087072 | PubTator, text mining | PubMed |
| Neonatal-lethal dilated cardiomyopathy due to a homozygous LMOD2 donor splice-site variant. | Eur J Hum Genet | 2022 | 35082396 | PubTator, text mining | PubMed |
| Gene and metabolite expression dependence on body mass index in human myocardium. | Sci Rep | 2022 | 35082386 | PubTator, text mining | PubMed |
| Identification of heart failure with preserved ejection fraction helps risk stratification for hypertrophic cardiomyopathy. | BMC Med | 2022 | 35078475 | PubTator, text mining | PubMed |
| Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy. | CJC Open | 2022 | 35072022 | PubTator, text mining | PubMed |
| Molecular Diagnostic Outcomes from 700 Cases: What Can We Learn from a Retrospective Analysis of Clinical Exome Sequencing? | J Mol Diagn | 2022 | 35065284 | PubTator, text mining | PubMed |
| Genetic predisposition study of heart failure and its association with cardiomyopathy. | Egypt Heart J | 2022 | 35061126 | PubTator, text mining | PubMed |
| The interaction protein of SORBS2 in myocardial tissue to find out the pathogenic mechanism of LVNC disease. | Aging (Albany NY) | 2022 | 35050860 | PubTator, text mining | PubMed |
| Genetic Determinants of Sudden Unexpected Death in Pediatrics. | Genet Med | 2022 | 35027292 | PubTator, text mining | PubMed |
| Advances in understanding the state of titin truncation variants in dilated cardiomyopathy. | Pflugers Arch | 2022 | 35020065 | PubTator, text mining | PubMed |
| Diagnosis of Genetic White Matter Disorders by Singleton Whole-Exome and Genome Sequencing Using Interactome-Driven Prioritization. | Neurology | 2022 | 35012964 | PubTator, text mining | PubMed |
| Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndrome. | iScience | 2022 | 34988410 | PubTator, text mining | PubMed |
| Post-mortem genetic investigation in sudden cardiac death victims: complete exon sequencing of forty genes using next-generation sequencing. | Int J Legal Med | 2022 | 34984526 | PubTator, text mining | PubMed |
Targeted therapies in genetic dilated and hypertrophic cardiomyopathies: from molecular mechanisms to therapeutic targets. A position paper from the Heart Failure Association (HFA) and the Working Group on Myocardial Function of the European Society of Cardiology (ESC). | Eur J Heart Fail | 2022 | 34969177 | PubTator, text mining | PubMed |
| Identification of a novel mutation in the BMPR2 gene in a pulmonary arterial hypertension patient using next-generation sequencing. | J Clin Lab Anal | 2022 | 34953004 | PubTator, text mining | PubMed |
| CRISPR/Cas9 ribonucleoprotein-mediated genome and epigenome editing in mammalian cells. | Adv Drug Deliv Rev | 2022 | 34942274 | 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=52