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Gene · 773

Papers4,421

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 4,421

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TitleJournalYearPMIDFound bySource
GAA-FGF14 Expansions and CACNA1A Variants: Phenotypic Overlap and Diagnostic Implications.Mov Disord202540879304PubTator, text miningPubMed
Genetic Insights into Hemiplegic Migraine: Whole Exome Sequencing Highlights Vascular Pathway Involvement via Association Analysis.Genes (Basel)202540869943PubTator, text miningPubMed
CACNA1A Genetic Variants and Their Potential Involvement in Migraine Pathogenesis.Int J Mol Sci202540869402PubTator, text miningPubMed
Spatial perspective taking is impaired in spinocerebellar ataxias and Friedreich ataxia.Sci Rep202540850980PubTator, text miningPubMed
Autonomous multi-robot synthesis and optimization of metal halide perovskite nanocrystals.Nat Commun202540846706PubTator, text miningPubMed
A diagnostic challenge: spinocerebellar ataxia type 6 presenting with dystonia and parkinsonism.BMJ Case Rep202540846501PubTator, text miningPubMed
Familial hemiplegic migraine due to CACNA1A and PNKD mutations in epilepsy with forced normalization: A case report.Medicine (Baltimore)202540826761PubTator, text miningPubMed
Unveiling migraine subtype heterogeneity and risk loci: integrated genome-wide association study and single-cell transcriptomics discovery.J Headache Pain202540826382PubTator, text miningPubMed
Metabolism-Mediated FGF5 Association with Stroke: Based on Mendelian Randomization and Bioinformatics Analysis.J Multidiscip Healthc202540765733PubTator, text miningPubMed
Neuro-Ophthalmological Manifestations of Episodic Ataxia Type 2 Due to a Novel CACNA1A Mutation.Mov Disord Clin Pract202540765518PubTator, text miningPubMed
Comprehensive identification of pathogenic tandem repeat expansions in sporadic amyotrophic lateral sclerosis: advantages of long-read vs. short-read sequencing.Exp Biol Med (Maywood)202540746751PubTator, text miningPubMed
Magnetic resonance imaging for spinocerebellar ataxia: a bibliometric analysis based on web of science.Front Neurol202540734822PubTator, text miningPubMed
Gene-Based Burden Testing of Rare Variants in Hemiplegic Migraine: A Computational Approach to Uncover the Genetic Architecture of a Rare Brain Disorder.Genes (Basel)202540725463PubTator, text miningPubMed
Polymorphisms in CACNA1A, CACNA1C, and CACNA1H Genes in Korean Pediatric Patients with Developmental Delay and Intellectual Disability: A Focus on Epilepsy Comorbidity.Genes (Basel)202540725423PubTator, text miningPubMed
Prolonged apnea in a boy with epilepsy and a novel gain-of-function missense CACNA1A variant indicating SUDEP risk.Front Neurol202540703772PubTator, text miningPubMed
Anacyphrethines A and B as potent analgesics: Multiple ion channel inhibitors with an unprecedented chemical architecture.Acta Pharm Sin B202540698126PubTator, text miningPubMed
Involuntary Eye Movements as a Clue to Diagnosis.Mov Disord Clin Pract202540654295PubTator, text miningPubMed
Sexual identity inequalities in the co-occurrence of poor mental health and health risk behaviours-a national cross-sectional study.BMC Med202540629367PubTator, text miningPubMed
Teaching NeuroImage: Cortical DWI Hyperintensity, Cerebellar Atrophy, and Presentation With Prolonged Postictal Hemiparesis Suggest CACNA1A-Related Disorder.Neurology202540549992PubTator, text miningPubMed
CACNA1A loss-of-function affects neurogenesis in human iPSC-derived neural models.Cell Mol Life Sci202540514452PubTator, text miningPubMed

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.

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