Gene · 3785
Papers2,279
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
201 to 220 of 2,279
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Familial KCNQ2 mutation: a psychiatric perspective. | Psychiatr Genet | 2024 | 38108335 | PubTator, text mining | PubMed |
| Biallelic pathogenic variants of PARS2 cause developmental and epileptic encephalopathy with spike-and-wave activation in sleep. | Mol Genet Genomic Med | 2024 | 38087948 | PubTator, text mining | PubMed |
| Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy. | Epilepsia | 2024 | 38073125 | PubTator, text mining | PubMed |
| Impacted spike frequency adaptation associated with reduction of KCNQ2/3 exacerbates seizure activity in temporal lobe epilepsy. | Hippocampus | 2024 | 38049972 | PubTator, text mining | PubMed |
| Neurodevelopmental Outcomes Prediction in Newborns with Seizures Caused by KCNQ2 Gene Defects. | Neonatology | 2024 | 38043515 | PubTator, text mining | PubMed |
| Genetic analysis and literature review of a Poirier-Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2B. | Mol Genet Genomic Med | 2024 | 38037515 | PubTator, text mining | PubMed |
| Distinctive Amplitude-Integrated EEG Ictal Pattern and Targeted Therapy with Carbamazepine in KCNQ2 and KCNQ3 Neonatal Epilepsy: A Case Series. | Neuropediatrics | 2024 | 37827512 | PubTator, text mining | PubMed |
| Crosstalk between cholesterol and PIP2 in the regulation of Kv7.2/Kv7.3 channels. | Biol Chem | 2024 | 37552610 | PubTator, text mining | PubMed |
| Health care concerns in parents of children with different genetic developmental and epileptic encephalopathies: A qualitative study. | Dev Med Child Neurol | 2024 | 37482918 | PubTator, text mining | PubMed |
| Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes. | Seizure | 2024 | 37353388 | PubTator, text mining | PubMed |
| The 2022 European postgraduate (residency) programme in neurology in a historical and international perspective. | Eur J Neurol | 2024 | 37294693 | PubTator, text mining | PubMed |
| Biallelic variants of KCNQ2 in early infantile developmental and epileptic encephalopathy. | Seizure | 2024 | 36934001 | PubTator, text mining | PubMed |
| "Fifth-day fits" revisited: A literature review of benign idiopathic neonatal seizures and comparison with KCNQ2- and KCNQ3-associated benign familial epilepsy syndromes. | Ann Child Neurol Soc | 2023 | 42563870 | PubTator, text mining | PubMed |
| Pyridoxine-dependent epilepsy: Current perspectives and questions for future research. | Ann Child Neurol Soc | 2023 | 40832147 | PubTator, text mining | PubMed |
Validation of targeted next-generation sequencing panels in a cohort of Polish patients with epilepsy: assessing variable performance across clinical endophenotypes and uncovering novel genetic variants. | Front Neurol | 2023 | 38328757 | PubTator, text mining | PubMed |
| Intellectual Disability and Epilepsy: The High Incidence and the Risks of Status Epilepticus and Sudden Death Require Improved Therapies. | Epilepsy Curr | 2023 | 38269346 | PubTator, text mining | PubMed |
| Prospective evaluation of NGS-based sequencing in epilepsy patients: results of seven NASGE-associated diagnostic laboratories. | Front Neurol | 2023 | 38125836 | PubTator, text mining | PubMed |
| Pathophysiology of ion channels in amyotrophic lateral sclerosis. | Mol Brain | 2023 | 38102715 | PubTator, text mining | PubMed |
| Comprehensive assessment of the genetic characteristics of small for gestational age newborns in NICU: from diagnosis of genetic disorders to prediction of prognosis. | Genome Med | 2023 | 38093364 | PubTator, text mining | PubMed |
| Prognostic Analysis of KCNQ2 Patients via Combining EEG Deep Features and Machine Learning Classifiers. | Annu Int Conf IEEE Eng Med Biol Soc | 2023 | 38083766 | 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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