Gene · 6792
Papers1,482
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
101 to 120 of 1,482
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study. | Epilepsy Res | 2024 | 39003968 | PubTator, text mining | PubMed |
| A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism. | Int J Mol Sci | 2024 | 39000022 | PubTator, text mining | PubMed |
| The impact of developmental and epileptic encephalopathies on families: a qualitative study. | Eur J Pediatr | 2024 | 38965081 | PubTator, text mining | PubMed |
| CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy. | J Neurol | 2024 | 38874638 | PubTator, text mining | PubMed |
| Population-based study of rare epilepsy incidence in a US urban population. | Epilepsia | 2024 | 38795333 | PubTator, text mining | PubMed |
| Early Developmental Intervention and Enriched Environment in CDKL5 Developmental and Epileptic Encephalopathy: A Case Report. | Neurol Clin Pract | 2024 | 38660576 | PubTator, text mining | PubMed |
| Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder. | Sci Rep | 2024 | 38649688 | PubTator, text mining | PubMed |
| X-Linked Epilepsies: A Narrative Review. | Int J Mol Sci | 2024 | 38612920 | PubTator, text mining | PubMed |
| Prevalence of Endocrinopathies in a Cohort of Patients with Rett Syndrome: A Two-Center Observational Study. | Genes (Basel) | 2024 | 38540345 | PubTator, text mining | PubMed |
| Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision Medicine. | Genes (Basel) | 2024 | 38540325 | PubTator, text mining | PubMed |
| Genetic determinants of global developmental delay and intellectual disability in Ukrainian children. | J Neurodev Disord | 2024 | 38539105 | PubTator, text mining | PubMed |
| Epileptic spasms in clusters without hypsarrhythmia in infancy and childhood: A single age-dependent type of epilepsy or well-defined epileptic syndrome? | Epilepsy Res | 2024 | 38518433 | PubTator, text mining | PubMed |
| Communication of individuals with CDKL5 deficiency disorder as observed by caregivers: A descriptive qualitative study. | Am J Med Genet A | 2024 | 38425131 | PubTator, text mining | PubMed |
| CDKL5 Deficiency Disorder: Some Lessons Learned 20 Years After the First Description. | Am J Intellect Dev Disabil | 2024 | 38411242 | PubTator, text mining | PubMed |
| Variable expression of MECP2, CDKL5, and FMR1 in the human brain: Implications for gene restorative therapies. | Proc Natl Acad Sci U S A | 2024 | 38386709 | PubTator, text mining | PubMed |
| Exonuclease-enhanced prime editors. | Nat Methods | 2024 | 38302659 | PubTator, text mining | PubMed |
| Rett syndrome in Ireland: a demographic study. | Orphanet J Rare Dis | 2024 | 38291497 | PubTator, text mining | PubMed |
| Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. | Int J Mol Sci | 2024 | 38279250 | PubTator, text mining | PubMed |
| Current Overview of CDKL-5 Deficiency Disorder Treatment. | Pediatr Rep | 2024 | 38251311 | PubTator, text mining | PubMed |
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements. | Nat Commun | 2024 | 38233393 | 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/v1/6792/papers?page=6