Íscia Lopes‐Cendes

Research interests

Publications

• The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commission

  Epilepsia · 2022 · https://doi.org/10.1111/epi.17301

• The genetic architecture of the human cerebral cortex

  Science · 2020 · https://doi.org/10.1126/science.aay6690

• Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

  Nature Communications · 2018 · https://doi.org/10.1038/s41467-018-07524-z

• Genetic testing in the epilepsies—Report of the ILAE Genetics Commission

  Epilepsia · 2010 · 10.1111/j.1528-1167.2009.02429.x

• Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24

  The American Journal of Human Genetics · 1998 · 10.1086/302047

• Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

  Nature Genetics · 1998 · https://doi.org/10.1038/2470

• Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2

  Nature Genetics · 1996 · https://doi.org/10.1038/ng1196-269

• Autosomal dominant nocturnal frontal lobe epilepsy

  Brain · 1995 · https://doi.org/10.1093/brain/118.1.61

• Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy

  Brain · 1994 · 10.1093/brain/117.4.739

• Atrophy of mesial structures in patients with temporal lobe epilepsy: Cause or consequence of repeated seizures?

  Annals of Neurology · 1993 · 10.1002/ana.410340607

• MRI volumetric measurement of amygdala and hippocampus in temporal lobe epilepsy

  Neurology · 1993 · 10.1212/wnl.43.4.719

• Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy

  Neurology · 1993 · 10.1212/wnl.43.6.1083

Current projects

No projects listed.