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PEREZ PALMA, EDUARDO ESTEBAN
Dataset - Conserved patterns across ion channels correlate with variant pathogenicity and clinical phenotypes
Genomic analysis of AlphaFold2-predicted structures identifies maps of 3D essential sites in 243 neurodevelopmental disorder-associated proteins
Dataset - Gene variant effects across sodium channelopathies predict function and guide precision therapy
Molecular dynamics simulations reveal molecular mechanisms for the gain and loss of function effects of four SCN2A variants
Structural mapping of GABRB3 variants reveals genotype–phenotype correlations
Gain-of-function SCN1A variants cause spectrum of early onset epileptic encephalopathies that respond to sodium channel blocking therapies
Genomic analysis in Chilean pediatric patients with drug-resistant epilepsy
Comparison of variant effects in SCN-gene paralogs predict function across sodium channelopathies
Dataset - Identification and quantification of oligogenic loss-of-function disorders
Copy Number Variation Analysis from SNP Genotyping Microarrays in Large Cohorts of Neurological Disorders