Gene · 6326
Papers4,098
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
181 to 200 of 4,098
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Generation and characterization of human-induced pluripotent stem cell lines from patients with autism spectrum disorder and SCN2A variants. | Hum Cell | 2025 | 40111547 | PubTator, text mining | PubMed |
| In silico screening to search for selective sodium channel blockers: When size matters. | Brain Res | 2025 | 40096941 | PubTator, text mining | PubMed |
| Rapid and Visual Molecular Detection of High Hb F Determinants; HPFH6, Asian Indian inv-del (Aγδβ)0-Thalassemia, and Thai del-inv-ins (Aγδβ)0-Thalassemia Using LAMP Colorimetric Phenol Red Assays. | Hemoglobin | 2025 | 40091622 | PubTator, text mining | PubMed |
| Landscape of small nucleic acid therapeutics: moving from the bench to the clinic as next-generation medicines. | Signal Transduct Target Ther | 2025 | 40059188 | PubTator, text mining | PubMed |
| Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility. | Nat Commun | 2025 | 40050271 | PubTator, text mining | PubMed |
| [Hematological Characteristics of Neonates with Abnormal Hemoglobin and Their Parents in Guangzhou Area]. | Zhongguo Shi Yan Xue Ye Xue Za Zhi | 2025 | 40017204 | PubTator, text mining | PubMed |
| A De Novo SCN2A Variant in a Patient with Adult-Onset Dystonia Parkinsonism and Nigrostriatal Denervation. | Mov Disord Clin Pract | 2025 | 39985302 | PubTator, text mining | PubMed |
| Infantile Epileptic Spasms Syndrome: Unveiling clinical and genetic variability in a case series from Argentina. | Seizure | 2025 | 39933386 | PubTator, text mining | PubMed |
| Vineland-3 Growth Scale Values: Psychometric Properties for Clinical Trial Readiness in SCN2A. | J Child Adolesc Psychopharmacol | 2025 | 39887012 | PubTator, text mining | PubMed |
| Fetal hematological phenotypes of various hemoglobinopathies and demonstration of embryonic hemoglobins on capillary electrophoresis: a large cohort data from prenatal screening program. | Diagnosis (Berl) | 2025 | 39876800 | PubTator, text mining | PubMed |
| Design, synthesis and structure-activity relationship of novel 1,2,4-triazolopyrimidin-5-one derivatives targeting GABAA1 and Nav1.2 with antiepileptic activity. | Eur J Med Chem | 2025 | 39874632 | PubTator, text mining | PubMed |
| Exploring the molecular characterization of PANoptosis-related genes with features of immune dysregulation in Alzheimer's disease based on bulk and single-nuclei RNA sequencing. | Metab Brain Dis | 2025 | 39841296 | PubTator, text mining | PubMed |
| Nociceptor sodium channels shape subthreshold phase, upstroke, and shoulder of action potentials. | J Gen Physiol | 2025 | 39836077 | PubTator, text mining | PubMed |
| In silico toxicology investigation of μ-conotoxin KIIIA on human Na+ channel Nav1.2. | Int J Biol Macromol | 2025 | 39832599 | PubTator, text mining | PubMed |
| Neonatal Encephalopathy: Novel Phenotypes and Genotypes Identified by Genome Sequencing. | Neurol Genet | 2025 | 39810752 | PubTator, text mining | PubMed |
| The Feasibility of Personalized Endpoints in Assessing Treatment Outcomes for Rare Diseases: A Pilot Study of Goal Attainment Scaling in SCN2A-Associated Developmental Epileptic Encephalopathy. | Value Health | 2025 | 39733836 | PubTator, text mining | PubMed |
| Rare dysfunctional SCN2A variants are associated with malformation of cortical development. | Epilepsia | 2025 | 39707911 | PubTator, text mining | PubMed |
| In vitro human ion channel assays predictive of drug-induced seizure. | Toxicol Sci | 2025 | 39661496 | PubTator, text mining | PubMed |
| Genetic neonatal seizures in the neonatal intensive care unit: Diagnostic and prognostic implications for three families. | Epileptic Disord | 2025 | 39570101 | PubTator, text mining | PubMed |
| Human IPSC-Derived Microglia Sense and Dampen Hyperexcitability of Cortical Neurons Carrying the Epilepsy-Associated SCN2A-L1342P Mutation. | J Neurosci | 2025 | 39557580 | 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
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