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Author Details
Full Name
Chantal Depondt
Affiliation
Hopital Universitaire de Bruxelles - Hopital Erasme
ORCID
Career Start Year
2002
Papers
93
H Index
38
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37754551
Prognostic value of early electrographic biomarkers of epileptogenesis in high-risk ischaemic stroke patients.
Eur J Neurol
2024
36869701
Diagnostic and therapeutic approaches in refractory insular epilepsy.
Epilepsia
2023
34388852
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies.
Neuropathol Appl Neurobiol
2022
36534060
Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy.
Ann Neurol
2022
35896547
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression.
Nat Commun
2022
35333312
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.
Brain
2022
35298028
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam.
Epilepsia
2022
34569149
Genomic analysis of "microphenotypes" in epilepsy.
Am J Med Genet A
2022
33341393
Evaluating risk to people with epilepsy during the COVID-19 pandemic: Preliminary findings from the COV-E study.
Epilepsy Behav
2021
34490891
Accurate detection of typical absence seizures in adults and children using a two-channel electroencephalographic wearable behind the ears.
Epilepsia
2021
34481281
Impact of the COVID-19 pandemic on people with epilepsy: Findings from the Brazilian arm of the COV-E study.
Epilepsy Behav
2021
34562685
Duration of nonconvulsive seizures in critically ill patients.
Epilepsy Behav
2021
34018700
Assessing the role of rare genetic variants in drug-resistant, non-lesional focal epilepsy.
Ann Clin Transl Neurol
2021
34177598
Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications.
Front Pharmacol
2021
34060026
Brivaracetam Retention Rate and Seizure Outcomes in Patients with Drug-Resistant Focal Epilepsy Included in the Medical Need Program in Belgium: A Real-World, Multicenter, Chart Review.
Drugs Real World Outcomes
2021
34049028
Assessment of a standardized EEG reactivity protocol after cardiac arrest.
Clin Neurophysiol
2021
32141622
Testing association of rare genetic variants with resistance to three common antiseizure medications.
Epilepsia
2020
33208365
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study.
Sci Adv
2020
32759205
Development and validation of a predictive model of drug-resistant genetic generalized epilepsy.
Neurology
2020
32308125
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
Pharmacogenomics
2020
30941098
Role of Epileptic Activity in Older Adults With Delirium, a Prospective Continuous EEG Study.
Front Neurol
2019
31819912
Genomic and clinical predictors of lacosamide response in refractory epilepsies.
Epilepsia Open
2019
31440723
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy.
Epilepsia Open
2019
31594733
Epileptic activity in neurological deterioration after ischemic stroke, a continuous EEG study.
Clin Neurophysiol
2019
31247119
The Epilepsy Surgery Grading Scale: Validation in an independent population with drug-resistant focal epilepsy.
Epilepsia
2019
30868120
A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine.
Epilepsia Open
2019
29288229
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
Neurology
2018
29930110
Analysis of shared heritability in common disorders of the brain.
Science
2018
29901232
The phenotype of bilateral hippocampal sclerosis and its management in "real life" clinical settings.
Epilepsia
2018
30033060
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control study.
Lancet Neurol
2018
30308426
Long-term seizure outcomes in patients with drug resistant epilepsy.
Seizure
2018
29365066
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study.
Brain
2018
27771198
Yield of repeated intermittent EEG for seizure detection in critically ill adults.
Neurophysiol Clin
2017
28098162
Novel genetic loci associated with hippocampal volume.
Nat Commun
2017
28857179
Comparative effectiveness of antiepileptic drugs in patients with mesial temporal lobe epilepsy with hippocampal sclerosis.
Epilepsia
2017
27977874
Reply.
Ann Neurol
2017
26054379
Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6.
Cerebellum
2016
26567031
The Prognostic Value of 48-h Continuous EEG During Therapeutic Hypothermia After Cardiac Arrest.
Neurocrit Care
2016
27583304
MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43).
Neurol Genet
2016
27694991
Novel genetic loci underlying human intracranial volume identified through genome-wide association.
Nat Neurosci
2016
27123485
Copy number variants in absence epilepsy: Further complications of the picture.
Neurol Genet
2016
26914931
Midazolam and thiopental for the treatment of refractory status epilepticus: a retrospective comparison of efficacy and safety.
J Neurol
2016
25607358
Common genetic variants influence human subcortical brain structures.
Nature
2015
25566998
Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.
Lancet Neurol
2015
23896816
Intravenous lacosamide in refractory seizure clusters and status epilepticus: comparison of 200 and 400 mg loading doses.
Neurocrit Care
2014
24836528
EEG patterns compatible with nonconvulsive status epilepticus are common in elderly patients with delirium: a prospective study with continuous EEG monitoring.
Epilepsy Behav
2014
24719489
Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations.
Neurology
2014
24399358
The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.
Brain Imaging Behav
2014
23452606
[Epilepsy pharmacogenetics : science or fiction?].
Med Sci (Paris)
2013
24014518
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.
Brain
2013
1 - 50 of 93
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