Publikace
- A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy2019 | 2. lékařská fakulta
- Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals2019 | 2. lékařská fakulta
- Genetické příčiny epilepsií2018 | 2. lékařská fakulta
- HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign genera lized epilepsy and beyond2018 | 2. lékařská fakulta
- Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data2017 | 2. lékařská fakulta
- Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects2017 | 2. lékařská fakulta
- Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes2017 | 2. lékařská fakulta
- De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy2015 | 2. lékařská fakulta
- The phenotypic spectrum of SCN8A encephalopathy2015 | 2. lékařská fakulta
- De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies2014 | 2. lékařská fakulta
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