| Treatment of pediatric epilepsy: European expert opinion, 2007 JW Wheless, DF Clarke, A Arzimanoglou, D Carpenter Epileptic disorders 9 (4), 353-412, 2007 | 460 | 2007 |
| De novo loss-or gain-of-function mutations in KCNA2 cause epileptic encephalopathy S Syrbe, U Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ... Nature genetics 47 (4), 393-399, 2015 | 284 | 2015 |
| De novo variants in neurodevelopmental disorders with epilepsy HO Heyne, T Singh, H Stamberger, R Abou Jamra, H Caglayan, D Craiu, ... Nature genetics 50 (7), 1048-1053, 2018 | 261 | 2018 |
| GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects K Platzer, H Yuan, H Schütz, A Winschel, W Chen, C Hu, H Kusumoto, ... Journal of medical genetics 54 (7), 460-470, 2017 | 222 | 2017 |
| Ion channels in genetic and acquired forms of epilepsy H Lerche, M Shah, H Beck, J Noebels, D Johnston, A Vincent The Journal of physiology 591 (4), 753-764, 2013 | 195 | 2013 |
| Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy C Mignot, C Von Stülpnagel, C Nava, D Ville, D Sanlaville, G Lesca, ... Journal of medical genetics 53 (8), 511-522, 2016 | 168 | 2016 |
| The distinctive movement disorder of ovarian teratoma‐associated encephalitis TJ Kleinig, PD Thompson, W Matar, A Duggins, TE Kimber, JG Morris, ... Movement Disorders 23 (9), 1256-1261, 2008 | 149 | 2008 |
| Clinical spectrum and genotype–phenotype associations of KCNA2-related encephalopathies S Masnada, UBS Hedrich, E Gardella, J Schubert, C Kaiwar, EW Klee, ... Brain 140 (9), 2337-2354, 2017 | 137 | 2017 |
| Yield of MRI, high-density electric source imaging (HD-ESI), SPECT and PET in epilepsy surgery candidates AM Lascano, T Perneger, S Vulliemoz, L Spinelli, V Garibotto, CM Korff, ... Clinical Neurophysiology 127 (1), 150-155, 2016 | 115 | 2016 |
| Dravet syndrome (severe myoclonic epilepsy in infancy): a retrospective study of 16 patients C Korff, L Laux, K Kelley, J Goldstein, S Koh, D Nordli Jr Journal of child neurology 22 (2), 185-194, 2007 | 108 | 2007 |
| Effectiveness of antiepileptic therapy in patients with PCDH19 mutations J Lotte, T Bast, P Borusiak, A Coppola, JH Cross, P Dimova, A Fogarasi, ... Seizure 35, 106-110, 2016 | 88 | 2016 |
| Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis A Knaus, JT Pantel, M Pendziwiat, N Hajjir, M Zhao, TC Hsieh, ... Genome Medicine 10, 1-13, 2018 | 86 | 2018 |
| Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU C Depienne, C Nava, B Keren, S Heide, A Rastetter, S Passemard, ... Human genetics 136, 463-479, 2017 | 86 | 2017 |
| Food poisoning as a cause of acute liver failure KM Pósfay-Barbe, J Schrenzel, J Frey, R Studer, C Korff, DC Belli, ... The Pediatric infectious disease journal 27 (9), 846-847, 2008 | 86 | 2008 |
| Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers S Weckhuysen, P Holmgren, R Hendrickx, AC Jansen, D Hasaerts, ... Epilepsia 54 (5), e74-e80, 2013 | 83 | 2013 |
| The spectrum of intermediate SCN8A‐related epilepsy KM Johannesen, E Gardella, AC Encinas, AE Lehesjoki, T Linnankivi, ... Epilepsia 60 (5), 830-844, 2019 | 82 | 2019 |
| Severe phenotypic spectrum of biallelic mutations in PRRT2 gene M Delcourt, F Riant, J Mancini, M Milh, V Navarro, E Roze, ... Journal of Neurology, Neurosurgery & Psychiatry 86 (7), 782-785, 2015 | 80 | 2015 |
| Severe childhood encephalopathy with dyskinesia and prolonged cognitive disturbances: evidence for anti‐N‐methyl‐d‐aspartate receptor encephalitis C Poloni, CM Korff, V Ricotti, MD King, ER Perez, C MAYOR‐DUBOIS, ... Developmental Medicine & Child Neurology 52 (5), e78-e82, 2010 | 76 | 2010 |
| A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation F Le Gal, CM Korff, C Monso‐Hinard, MT Mund, M Morris, A Malafosse, ... Epilepsia 51 (9), 1915-1918, 2010 | 73 | 2010 |
| Towards the identification of a genetic basis for L andau‐K leffner s yndrome J Conroy, PA McGettigan, D McCreary, N Shah, K Collins, B Parry‐Fielder, ... Epilepsia 55 (6), 858-865, 2014 | 70 | 2014 |
Joel FLUSSHopitaux universitaires GeneveVerified email at hcuge.ch
