| The clinicopathologic spectrum of focal cortical dysplasias: A consensus classification proposed by an ad hoc task force of the ILAE Diagnostic Methods Commission 1 I Blümcke, M Thom, E Aronica, DD Armstrong, HV Vinters, A Palmini, ... Epilepsia 52 (1), 158-174, 2011 | 2014 | 2011 |
| A developmental and genetic classification for malformations of cortical development: update 2012 AJ Barkovich, R Guerrini, RI Kuzniecky, GD Jackson, WB Dobyns Brain 135 (5), 1348-1369, 2012 | 1989 | 2012 |
| Terminology and classification of the cortical dysplasias A Palmini, I Najm, G Avanzini, T Babb, R Guerrini, N Foldvary-Schaefer, ... Neurology 62 (6_suppl_3), S2-S8, 2004 | 1231 | 2004 |
| Histopathological findings in brain tissue obtained during epilepsy surgery I Blumcke, R Spreafico, G Haaker, R Coras, K Kobow, CG Bien, M Pfäfflin, ... New England Journal of Medicine 377 (17), 1648-1656, 2017 | 876 | 2017 |
| Classification system for malformations of cortical development: update 2001 AJ Barkovich, RI Kuzniecky, GD Jackson, R Guerrini, WB Dobyns Neurology 57 (12), 2168-2178, 2001 | 706 | 2001 |
| Epilepsy in children R Guerrini The Lancet 367 (9509), 499-524, 2006 | 685 | 2006 |
| Lamotrigine and seizure aggravation in severe myoclonic epilepsy R Guerrini, C Dravet, P Genton, A Belmonte, A Kaminska, O Dulac Epilepsia 39 (5), 508-512, 1998 | 583 | 1998 |
| Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology A Arzimanoglou, J French, WT Blume, JH Cross, JP Ernst, M Feucht, ... The Lancet Neurology 8 (1), 82-93, 2009 | 579 | 2009 |
| Malformations of cortical development: clinical features and genetic causes R Guerrini, WB Dobyns The Lancet Neurology 13 (7), 710-726, 2014 | 519 | 2014 |
| Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly K Poirier, N Lebrun, L Broix, G Tian, Y Saillour, C Boscheron, E Parrini, ... Nature genetics 45 (6), 639-647, 2013 | 519 | 2013 |
| Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study CD Whelan, A Altmann, JA Botía, N Jahanshad, DP Hibar, J Absil, ... Brain 141 (2), 391-408, 2018 | 478 | 2018 |
| 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 | 468 | 2014 |
| Proposed criteria for referral and evaluation of children for epilepsy surgery: recommendations of the Subcommission for Pediatric Epilepsy Surgery JH Cross, P Jayakar, D Nordli, O Delalande, M Duchowny, HG Wieser, ... Epilepsia 47 (6), 952-959, 2006 | 442 | 2006 |
| Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex VL Sheen, VS Ganesh, M Topcu, G Sebire, A Bodell, RS Hill, PE Grant, ... Nature genetics 36 (1), 69-76, 2004 | 417 | 2004 |
| Somatic mutations in cerebral cortical malformations SS Jamuar, ATN Lam, M Kircher, AM D’Gama, J Wang, BJ Barry, X Zhang, ... New England Journal of Medicine 371 (8), 733-743, 2014 | 389 | 2014 |
| Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations E Parrini, A Ramazzotti, WB Dobyns, D Mei, F Moro, P Veggiotti, C Marini, ... Brain 129 (7), 1892-1906, 2006 | 384 | 2006 |
| Benign familial neonatal‐infantile seizures: characterization of a new sodium channelopathy SF Berkovic, SE Heron, L Giordano, C Marini, R Guerrini, RE Kaplan, ... Annals of neurology 55 (4), 550-557, 2004 | 376 | 2004 |
| Mutations of ARX are associated with striking pleiotropy and consistent genotype–phenotype correlation M Kato, S Das, K Petras, K Kitamura, K Morohashi, DN Abuelo, M Barr, ... Human mutation 23 (2), 147-159, 2004 | 362 | 2004 |
| Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial L Lagae, J Sullivan, K Knupp, L Laux, T Polster, M Nikanorova, ... The Lancet 394 (10216), 2243-2254, 2019 | 342 | 2019 |
| Congenital bilateral perisylvian syndrome: study of 31 patients R Kuzniecky, F Andermann, R Guerrini, TCMC Study The Lancet 341 (8845), 608-612, 1993 | 342 | 1993 |
