| Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes JR Lemke, D Lal, EM Reinthaler, I Steiner, M Nothnagel, M Alber, ... Nature genetics 45 (9), 1067-1072, 2013 | 504 | 2013 |
| Healthcare Access and Quality Index based on mortality from causes amenable to personal health care in 195 countries and territories, 1990–2015: a novel analysis from the … RM Barber, N Fullman, RJD Sorensen, T Bollyky, M McKee, E Nolte, ... The lancet 390 (10091), 231-266, 2017 | 488 | 2017 |
| De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ... The American Journal of Human Genetics 95 (4), 360-370, 2014 | 317 | 2014 |
| The phenotypic spectrum of SCN8A encephalopathy J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ... Neurology 84 (5), 480-489, 2015 | 286 | 2015 |
| 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 | 283 | 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 | 260 | 2018 |
| De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome A Suls, JA Jaehn, A Kecskés, Y Weber, S Weckhuysen, DC Craiu, ... The American Journal of Human Genetics 93 (5), 967-975, 2013 | 247 | 2013 |
| De novo mutations in HCN1 cause early infantile epileptic encephalopathy C Nava, C Dalle, A Rastetter, P Striano, CGF de Kovel, R Nabbout, ... Nature genetics 46 (6), 640-645, 2014 | 245 | 2014 |
| Acutely and retrospectively diagnosed perinatal stroke: a population-based study R Laugesaar, A Kolk, T Tomberg, T Metsvaht, M Lintrop, H Varendi, ... Stroke 38 (8), 2234-2240, 2007 | 203 | 2007 |
| The landscape of epilepsy-related GATOR1 variants S Baldassari, F Picard, NE Verbeek, M van Kempen, EH Brilstra, G Lesca, ... Genetics in Medicine 21 (2), 398-408, 2019 | 188 | 2019 |
| Resuscitation of newborn infants with 21% or 100% oxygen: follow-up at 18 to 24 months OD Saugstad, S Ramji, SF Irani, S El-Meneza, EA Hernandez, M Vento, ... Pediatrics 112 (2), 296-300, 2003 | 180 | 2003 |
| 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 | 167 | 2016 |
| Epilepsy in tuberous sclerosis complex: findings from the TOSCA Study R Nabbout, E Belousova, MP Benedik, T Carter, V Cottin, P Curatolo, ... Epilepsia open 4 (1), 73-84, 2019 | 155 | 2019 |
| Phenotypic spectrum of GABRA1 From generalized epilepsies to severe epileptic encephalopathies K Johannesen, C Marini, S Pfeffer, RS Møller, T Dorn, CE Niturad, ... Neurology 87 (11), 1140-1151, 2016 | 145 | 2016 |
| Shaken baby syndrome and a baby's cry I Talvik, RC Alexander, T Talvik Acta paediatrica 97 (6), 782-785, 2008 | 142 | 2008 |
| Prevalence of childhood epilepsy in Estonia A Beilmann, A Napa, A Sööt, I Talvik, T Talvik Epilepsia 40 (7), 1011-1019, 1999 | 142 | 1999 |
| Gene panel testing in epileptic encephalopathies and familial epilepsies RS Møller, LHG Larsen, KM Johannesen, I Talvik, T Talvik, U Vaher, ... Molecular syndromology 7 (4), 210-219, 2016 | 122 | 2016 |
| Mutations in GABRB3 From febrile seizures to epileptic encephalopathies RS Møller, TV Wuttke, I Helbig, C Marini, KM Johannesen, EH Brilstra, ... Neurology 88 (5), 483-492, 2017 | 113 | 2017 |
| Cerebral blood‐flow velocities in predicting outcome of asphyxiated newborn infants P Ilves, M Lintrop, T Metsvaht, U Vaher, T Talvik Acta paediatrica 93 (4), 523-528, 2004 | 112 | 2004 |
| Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease S Zagaglia, C Selch, JR Nisevic, D Mei, Z Michalak, ... Neurology 91 (22), e2078-e2088, 2018 | 109 | 2018 |
