| De novo mutations in epileptic encephalopathies Nature 501 (7466), 217-221, 2013 | 1501 | 2013 |
| HLA-A* 3101 and carbamazepine-induced hypersensitivity reactions in Europeans M McCormack, A Alfirevic, S Bourgeois, JJ Farrell, D Kasperavičiūtė, ... New England Journal of Medicine 364 (12), 1134-1143, 2011 | 1104 | 2011 |
| Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis SR Irani, AW Michell, B Lang, P Pettingill, P Waters, MR Johnson, ... Annals of neurology 69 (5), 892-900, 2011 | 972 | 2011 |
| Improved heritability estimation from genome-wide SNPs D Speed, G Hemani, MR Johnson, DJ Balding The American Journal of Human Genetics 91 (6), 1011-1021, 2012 | 729 | 2012 |
| Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis SE Baranzini, J Wang, RA Gibson, N Galwey, Y Naegelin, F Barkhof, ... Human molecular genetics 18 (4), 767-778, 2009 | 579 | 2009 |
| Faciobrachial dystonic seizures: the influence of immunotherapy on seizure control and prevention of cognitive impairment in a broadening phenotype SR Irani, CJ Stagg, JM Schott, CR Rosenthal, SA Schneider, P Pettingill, ... Brain 136 (10), 3151-3162, 2013 | 470 | 2013 |
| Reevaluation of SNP heritability in complex human traits D Speed, N Cai, Ucleb Consortium, MR Johnson, S Nejentsev, ... Nature genetics 49 (7), 986-992, 2017 | 450 | 2017 |
| ABCB1 genotype and PGP expression, function and therapeutic drug response: a critical review and recommendations for future research GD Leschziner, T Andrew, M Pirmohamed, MR Johnson The pharmacogenomics journal 7 (3), 154-179, 2007 | 370 | 2007 |
| 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 | 322 | 2014 |
| Facial expression processing after amygdalotomy AW Young, DJ Hellawell, C Van de Wal, M Johnson Neuropsychologia 34 (1), 31-39, 1996 | 322 | 1996 |
| Rare deletions at 16p13. 11 predispose to a diverse spectrum of sporadic epilepsy syndromes EL Heinzen, RA Radtke, TJ Urban, GL Cavalleri, C Depondt, AC Need, ... The American Journal of Human Genetics 86 (5), 707-718, 2010 | 279 | 2010 |
| De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies CT Myers, JM McMahon, AL Schneider, S Petrovski, AS Allen, GL Carvill, ... The American Journal of Human Genetics 99 (2), 287-298, 2016 | 257 | 2016 |
| Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ... The American Journal of Human Genetics 105 (2), 267-282, 2019 | 248 | 2019 |
| The role of [18F]fluoro-2-deoxyglucose-PET scanning in the diagnosis of paraneoplastic neurological disorders JH Rees, SF Hain, MR Johnson, RAC Hughes, DC Costa, PJ Ell, G Keir, ... Brain 124 (11), 2223-2231, 2001 | 186 | 2001 |
| Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study D Kasperavičiūtė, CB Catarino, EL Heinzen, C Depondt, GL Cavalleri, ... Brain 133 (7), 2136-2147, 2010 | 183 | 2010 |
| Intrinsic severity as a determinant of antiepileptic drug refractoriness MA Rogawski, MR Johnson Epilepsy currents 8 (5), 127-130, 2008 | 179 | 2008 |
| Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies RJL Anney, A Avbersek, D Balding, L Baum, F Becker, SF Berkovic, ... The Lancet Neurology, 2014 | 171 | 2014 |
| Ultra-rare genetic variation in common epilepsies: a case-control sequencing study AS Allen, ST Bellows, SF Berkovic, J Bridgers, R Burgess, G Cavalleri, ... The Lancet Neurology 16 (2), 135-143, 2017 | 170 | 2017 |
| Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus MR Johnson, J Behmoaras, L Bottolo, ML Krishnan, K Pernhorst, ... Nature communications 6 (1), 6031, 2015 | 158 | 2015 |
| Immunotherapy-responsive seizure-like episodes with potassium channel antibodies SR Irani, C Buckley, A Vincent, OC Cockerell, P Rudge, MR Johnson, ... Neurology 71 (20), 1647-1648, 2008 | 154 | 2008 |
