| Theta burst stimulation of the human motor cortex YZ Huang, MJ Edwards, E Rounis, KP Bhatia, JC Rothwell Neuron 45 (2), 201-206, 2005 | 3293 | 2005 |
| The behavioural and motor consequences of focal lesions of the basal ganglia in man KP Bhatia, CD Marsden Brain 117 (4), 859-876, 1994 | 2656* | 1994 |
| Phenomenology and classification of dystonia: a consensus update A Albanese, K Bhatia, SB Bressman, MR DeLong, S Fahn, VSC Fung, ... Movement disorders 28 (7), 863-873, 2013 | 1729 | 2013 |
| Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ... The lancet neurology 7 (7), 583-590, 2008 | 1388 | 2008 |
| Criteria for the diagnosis of corticobasal degeneration MJ Armstrong, I Litvan, AE Lang, TH Bak, KP Bhatia, B Borroni, AL Boxer, ... Neurology 80 (5), 496-503, 2013 | 1231 | 2013 |
| Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria GU Höglinger, G Respondek, M Stamelou, C Kurz, KA Josephs, AE Lang, ... Movement Disorders 32 (6), 853-864, 2017 | 1002 | 2017 |
| Movement Disorders Society Scientific Issues Committee report: SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders. I Litvan, KP Bhatia, DJ Burn, CG Goetz, AE Lang, I McKeith, N Quinn, ... Movement disorders: official journal of the Movement Disorder Society 18 (5 …, 2003 | 907 | 2003 |
| A common LRRK2 mutation in idiopathic Parkinson's disease WP Gilks, PM Abou-Sleiman, S Gandhi, S Jain, A Singleton, AJ Lees, ... The Lancet 365 (9457), 415-416, 2005 | 875 | 2005 |
| A common polymorphism in the brain‐derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS B Cheeran, P Talelli, F Mori, G Koch, A Suppa, M Edwards, H Houlden, ... The Journal of physiology 586 (23), 5717-5725, 2008 | 742 | 2008 |
| Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society KP Bhatia, P Bain, N Bajaj, RJ Elble, M Hallett, ED Louis, J Raethjen, ... Movement Disorders 33 (1), 75-87, 2018 | 580 | 2018 |
| Characterization of PLA2G6 as a locus for dystonia‐parkinsonism C Paisan‐Ruiz, KP Bhatia, A Li, D Hernandez, M Davis, NW Wood, ... Annals of neurology 65 (1), 19-23, 2009 | 499 | 2009 |
| EFNS guidelines on diagnosis and treatment of primary dystonias A Albanese, F Asmus, KP Bhatia, AE Elia, B Elibol, G Filippini, T Gasser, ... European Journal of Neurology 18 (1), 5-18, 2011 | 493 | 2011 |
| Clinical approach to Parkinson's disease: features, diagnosis, and principles of management J Massano, KP Bhatia Cold Spring Harbor perspectives in medicine 2 (6), a008870, 2012 | 464 | 2012 |
| Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype H Houlden, M Baker, HR Morris, N MacDonald, S Pickering–Brown, ... Neurology 56 (12), 1702-1706, 2001 | 451 | 2001 |
| Slater revisited: 6 year follow up study of patients with medically unexplained motor symptoms HL Crimlisk, K Bhatia, H Cope, A David, CD Marsden, MA Ron Bmj 316 (7131), 582-586, 1998 | 426 | 1998 |
| Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder IE Scheffer, SF Berkovic, KP Bhatia, DR Fish, CD Marsden, ... The Lancet 343 (8896), 515-517, 1994 | 405 | 1994 |
| A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS‐ES Task Force A Albanese, MP Barnes, KP Bhatia, E Fernandez‐Alvarez, G Filippini, ... European journal of neurology 13 (5), 433-444, 2006 | 367 | 2006 |
| The syndrome of fixed dystonia: an evaluation of 103 patients A Schrag, M Trimble, N Quinn, K Bhatia Brain 127 (10), 2360-2372, 2004 | 366 | 2004 |
| GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak YG Weber, A Storch, TV Wuttke, K Brockmann, J Kempfle, S Maljevic, ... The Journal of clinical investigation 118 (6), 2157-2168, 2008 | 353 | 2008 |
| Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ... Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014 | 332 | 2014 |
Mark EdwardsProfessor of Neurology, St George's University of LondonVerified email at sgul.ac.uk
