| Mutations in DEPDC5 cause familial focal epilepsy with variable foci LM Dibbens, B De Vries, S Donatello, SE Heron, BL Hodgson, ... Nature genetics 45 (5), 546-551, 2013 | 380 | 2013 |
| Mortality in Dravet syndrome MS Cooper, A Mcintosh, DE Crompton, JM McMahon, A Schneider, ... Epilepsy research 128, 43-47, 2016 | 271 | 2016 |
| Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations IE Scheffer, SE Heron, BM Regan, S Mandelstam, DE Crompton, ... Annals of neurology 75 (5), 782-787, 2014 | 260 | 2014 |
| Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations IE Scheffer, SE Heron, BM Regan, S Mandelstam, DE Crompton, ... Annals of neurology 75 (5), 782-787, 2014 | 260 | 2014 |
| Exome‐based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy RD Bagnall, DE Crompton, S Petrovski, L Lam, C Cutmore, SI Garry, ... Annals of neurology 79 (4), 522-534, 2016 | 246 | 2016 |
| Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation PF Chinnery, DE Crompton, D Birchall, MJ Jackson, A Coulthard, ... Brain 130 (1), 110-119, 2007 | 224 | 2007 |
| Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy MG Ricos, BL Hodgson, T Pippucci, A Saidin, YS Ong, SE Heron, ... Annals of neurology 79 (1), 120-131, 2016 | 209 | 2016 |
| Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 MA Corbett, T Kroes, L Veneziano, MF Bennett, R Florian, AL Schneider, ... Nature communications 10 (1), 4920, 2019 | 122 | 2019 |
| Early onset absence epilepsy: 1 in 10 cases is caused by GLUT1 deficiency T Arsov, SA Mullen, JA Damiano, KM Lawrence, LL Huh, M Nolan, ... Epilepsia 53 (12), e204-e207, 2012 | 121 | 2012 |
| The borderland of epilepsy: clinical and molecular features of phenomena that mimic epileptic seizures DE Crompton, SF Berkovic The Lancet Neurology 8 (4), 370-381, 2009 | 115 | 2009 |
| Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance DE Crompton, IE Scheffer, I Taylor, MJ Cook, PA McKelvie, DF Vears, ... Brain 133 (11), 3221-3231, 2010 | 103 | 2010 |
| Neuroferritinopathy: a window on the role of iron in neurodegeneration DE Crompton, PF Chinnery, C Fey, ARJ Curtis, CM Morris, J Kierstan, ... Blood Cells, Molecules, and Diseases 29 (3), 522-531, 2002 | 98 | 2002 |
| Deconstruction of interhospital transfer workflow in large vessel occlusion: real-world data in the thrombectomy era FC Ng, E Low, E Andrew, K Smith, BCV Campbell, PJ Hand, ... Stroke 48 (7), 1976-1979, 2017 | 97 | 2017 |
| Genetic basis of sudden unexpected death in epilepsy RD Bagnall, DE Crompton, C Semsarian Frontiers in neurology 8, 260615, 2017 | 83 | 2017 |
| Melbourne mobile stroke unit and reperfusion therapy: greater clinical impact of thrombectomy than thrombolysis H Zhao, S Coote, D Easton, F Langenberg, M Stephenson, K Smith, ... Stroke 51 (3), 922-930, 2020 | 78 | 2020 |
| Epileptic spasms are a feature of DEPDC5 mTORopathy GL Carvill, DE Crompton, BM Regan, JM McMahon, J Saykally, M Zemel, ... Neurology: Genetics 1 (2), e17, 2015 | 71 | 2015 |
| Essential and neural transcripts from the Drosophila shaking-B locus are differentially expressed in the embryonic mesoderm and pupal nervous system D Crompton, M Todman, M Wilkin, S Ji, J Davies Developmental biology 170 (1), 142-158, 1995 | 66 | 1995 |
| Neuroferritinopathy in a French family with late onset dominant dystonia PF Chinnery, ARJ Curtis, C Fey, A Coulthard, D Crompton, A Curtis, ... Journal of medical genetics 40 (5), e69-e69, 2003 | 63 | 2003 |
| Spectrum of movement disorders in neuroferritinopathy DE Crompton, PF Chinnery, D Bates, TJ Walls, MJ Jackson, AJ Curtis, ... Movement Disorders: Official Journal of the Movement Disorder Society 20 (1 …, 2005 | 53 | 2005 |
| Risk‐adjusted hospital mortality rates for stroke: evidence from the Australian Stroke Clinical Registry (AuSCR) DA Cadilhac, MF Kilkenny, CR Levi, NA Lannin, AG Thrift, J Kim, ... Medical Journal of Australia 206 (8), 345-350, 2017 | 48 | 2017 |
