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.
81 to 100 of 4,098
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Molecular Profiling of Polish Pediatric Patients with Epilepsy: A Single-Center Diagnostic Experience Using Next-Generation Sequencing. | Genes (Basel) | 2026 | 41751517 | PubTator, text mining | PubMed |
| Novel therapeutics in autism spectrum disorder. | Neurotherapeutics | 2026 | 41748402 | PubTator, text mining | PubMed |
| Beyond Ion Channels: Emerging Roles of FGF12 in Cellular Regulation and Cancer Progression. | Cells | 2026 | 41744813 | PubTator, text mining | PubMed |
| SUDEP update 2026: recent advances in experimental and clinical research. | Curr Opin Neurol | 2026 | 41735792 | PubTator, text mining | PubMed |
| Toward precision medicine in SCN3A variants-associated encephalopathies and epilepsy: optimizing genetic diagnosis and molecular subregional effects. | Front Neurol | 2026 | 41725720 | PubTator, text mining | PubMed |
| Case Report: Prenatal imaging and genetic integrated diagnosis of SCN2A encephalopathy-a case of cryptical cortical dysplasia caused by a loss-of-function frameshift genetic variant. | Front Neurosci | 2026 | 41716663 | PubTator, text mining | PubMed |
| Ancestral intronic splicing regulatory elements in the SCNα gene family. | RNA | 2026 | 41714109 | PubTator, text mining | PubMed |
| Human microglia in brain assembloids display region-specific diversity and respond to hyperexcitable neurons carrying SCN2A mutation. | Sci Adv | 2026 | 41706855 | PubTator, text mining | PubMed |
| Diagnosis of the first seizure-like events in children from third-tier cities in southwestern China: a retrospective cohort study. | BMJ Paediatr Open | 2026 | 41698700 | PubTator, text mining | PubMed |
| Spatial transcriptomics identifies IL-32 as a lipid droplet-associated cytokine linked to tubular injury in human diabetic kidney disease. | Inflamm Res | 2026 | 41653322 | PubTator, text mining | PubMed |
| Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsy. | Epilepsia | 2026 | 41642117 | PubTator, text mining | PubMed |
| Voltage-Gated Sodium Channel NaV1.2: Structural Perspective of the Genetic Variability. | Biochem Genet | 2026 | 41632366 | PubTator, text mining | PubMed |
| Functional Characterization of a De Novo SCN2A Mixed Variant Linked to Early Infantile Developmental and Epileptic Encephalopathy. | Neurol Genet | 2026 | 41630925 | PubTator, text mining | PubMed |
| Adjunctive cannabidiol in intractable pediatric epilepsy: A retrospective study on tolerability, efficacy, and safety across genetic and nongenetic etiologies. | Medicine (Baltimore) | 2026 | 41630268 | PubTator, text mining | PubMed |
| Exploration of Semiconductor Chip-Based Single-Molecule Protein Sequencing for Identification of Hemoglobin Variants. | Anal Chem | 2026 | 41626769 | PubTator, text mining | PubMed |
| Genotypic spectrum in 1215 patients with Dravet syndrome or Dravet syndrome-like phenotype. | Pediatr Res | 2026 | 41617776 | PubTator, text mining | PubMed |
| Exceptionally selective voltage-sensor trapping of NaV1.5 channels by Mg-protoporphyrin impairs cancer cell migration. | Sci Rep | 2026 | 41611918 | PubTator, text mining | PubMed |
| Pseudohypoaldosterism: demystification using network medicine and proposed diagnostic panels. | Hormones (Athens) | 2026 | 41569463 | PubTator, text mining | PubMed |
| Efficacy of Dravet Syndrome Treatments in a Subset of Individuals with 2q24.3 Deletion: A-5 Patient Case Series. | J Child Neurol | 2026 | 41564166 | PubTator, text mining | PubMed |
| Targeted gene panel testing in pediatric epilepsy: Diagnostic outcomes and expanding genetic insights. | Brain Dev | 2026 | 41518736 | 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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GET https://conductscience.org/api/genes/v1/6326/papers?page=5