Gene · 2202
Papers1,739
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
121 to 140 of 1,739
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Sex Distributions in Non-ABCA4 Autosomal Macular Dystrophies. | Invest Ophthalmol Vis Sci | 2024 | 38700873 | PubTator, text mining | PubMed |
| Small peptide CSF fingerprint of amyotrophic lateral sclerosis. | PLoS One | 2024 | 38687737 | PubTator, text mining | PubMed |
| Replication study identified EFEMP1 association with varicose vein predisposition among Indians. | Eur J Med Res | 2024 | 38609985 | PubTator, text mining | PubMed |
| Identification of prospective aging drug targets via Mendelian randomization analysis. | Aging Cell | 2024 | 38572516 | PubTator, text mining | PubMed |
| Stop codon variant in EFEMP1 is associated with primary open-angle glaucoma due to impaired regulation of aqueous humor outflow. | Exp Eye Res | 2024 | 38467175 | PubTator, text mining | PubMed |
| EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder. | Am J Med Genet A | 2024 | 38348595 | PubTator, text mining | PubMed |
| Proteomic Associations of NT-proBNP (N-Terminal Pro-B-Type Natriuretic Peptide) in Heart Failure With Preserved Ejection Fraction. | Circ Heart Fail | 2024 | 38299345 | PubTator, text mining | PubMed |
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes. | Prog Retin Eye Res | 2024 | 38278208 | PubTator, text mining | PubMed |
| Development of a stemness-related prognostic index to provide therapeutic strategies for bladder cancer. | NPJ Precis Oncol | 2024 | 38245587 | PubTator, text mining | PubMed |
| Next-generation sequencing-based gene panel tests for the detection of rare variants and hypomorphic alleles associated with primary open-angle glaucoma. | PLoS One | 2024 | 38241218 | PubTator, text mining | PubMed |
| Enterocolic granulomatous phlebitis associated with epidermal growth factor-containing fibulin-like extracellular matrix protein 1 deposition and focal amyloid properties: A case report. | Pathol Int | 2024 | 38240415 | PubTator, text mining | PubMed |
| Secretomics reveals hormone-therapy of breast cancer may induce survival by facilitating hypercoagulation and immunomodulation in vitro. | Sci Rep | 2024 | 38233507 | PubTator, text mining | PubMed |
| Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom Cohort. | Ophthalmol Retina | 2024 | 38219857 | PubTator, text mining | PubMed |
| The intricate cellular ecosystem of human peripheral veins as revealed by single-cell transcriptomic analysis. | PLoS One | 2024 | 38206912 | PubTator, text mining | PubMed |
| Identification of aging-related genes in diagnosing osteoarthritis via integrating bioinformatics analysis and machine learning. | Aging (Albany NY) | 2024 | 38175691 | PubTator, text mining | PubMed |
| Circulating cell-free DNA methylation patterns as non-invasive biomarkers to monitor colorectal cancer treatment efficacy without referencing primary site mutation profiles. | Mol Cancer | 2024 | 38172877 | PubTator, text mining | PubMed |
| Early parental deprivation during primate infancy has a lifelong impact on gene expression in the male marmoset brain. | Sci Rep | 2024 | 38172165 | PubTator, text mining | PubMed |
| Feeder-free generation and characterization of endocardial and cardiac valve cells from human pluripotent stem cells. | iScience | 2024 | 38170020 | PubTator, text mining | PubMed |
| Gene Therapy for Inherited Retinal Diseases: From Laboratory Bench to Patient Bedside and Beyond. | Ophthalmol Ther | 2024 | 38113023 | PubTator, text mining | PubMed |
| Human cord plasma proteomic analysis reveals sexually dimorphic proteins associated with intrauterine growth restriction. | Proteomics | 2024 | 38059784 | 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/v1/2202/papers?page=7