Area of research
Psychiatry and Mental health · Pediatrics, Perinatology and Child Health
Research interest
Research focused on Epilepsy and Neuroscience, with related work in Genome-wide association study, Hippocampal formation, Temporal lobe. Notable publications include 'Identification of common variants associated with human hippocampal and intracranial volumes', 'Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study', and 'Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies'.
Genome-wide association meta-analyses of drug-resistant epilepsy
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Novel risk loci in LGI1-antibody encephalitis: genome-wide association study discovery and validation cohorts
The impact of <scp>COVID</scp>‐19 on people with epilepsy: Global results from the coronavirus and epilepsy study
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
Taking action on climate change: Testimonials and position statement from the International League Against Epilepsy Climate Change Commission
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression
Event‐based modeling in temporal lobe epilepsy demonstrates progressive atrophy from cross‐sectional data
A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies
Postictal Psychosis in Epilepsy: A Clinicogenetic Study
Exploring the prevalence and profile of epilepsy across Europe using a standard retrospective chart review: Challenges and opportunities
Impact of the COVID-19 pandemic on people with epilepsy: Findings from the Brazilian arm of the COV-E study
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study
Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study
Could the 2017 ILAE and the four-dimensional epilepsy classifications be merged to a new “Integrated Epilepsy Classification”?
Elevation of plasma tRNA fragments precedes seizures in human epilepsy
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition
Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
Mapping cortical brain asymmetry in 17,141 healthy individuals worldwide via the ENIGMA Consortium
Dual-center, dual-platform microRNA profiling identifies potential plasma biomarkers of adult temporal lobe epilepsy
Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia
MicroRNA-22 Controls Aberrant Neurogenesis and Changes in Neuronal Morphology After Status Epilepticus
The phenotype of bilateral hippocampal sclerosis and its management in “real life” clinical settings
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study
A microRNA‐129‐5p/Rbfox crosstalk coordinates homeostatic downscaling of excitatory synapses
Mapping Cortical Brain Asymmetry in 17,141 Healthy Individuals Worldwide via the ENIGMA Consortium
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A
Identification of common variants associated with human hippocampal and intracranial volumes