| Analysis of shared heritability in common disorders of the brain Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ... Science 360 (6395), eaap8757, 2018 | 1196 | 2018 |
| Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ... The Lancet Neurology 18 (12), 1091-1102, 2019 | 1098 | 2019 |
| Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ... Cell 179 (7), 1469-1482. e11, 2019 | 843 | 2019 |
| New insights into the genetic etiology of Alzheimer’s disease and related dementias C Bellenguez, F Küçükali, IE Jansen, L Kleineidam, S Moreno-Grau, ... Nature genetics 54 (4), 412-436, 2022 | 331 | 2022 |
| International study on the psychometric attributes of the non-motor symptoms scale in Parkinson disease P Martinez-Martin, C Rodriguez-Blazquez, K Abe, KB Bhattacharyya, ... Neurology 73 (19), 1584-1591, 2009 | 299 | 2009 |
| Patients with adult‐onset dystonic tremor resembling parkinsonian tremor have scans without evidence of dopaminergic deficit (SWEDDs) SA Schneider, MJ Edwards, P Mir, C Cordivari, J Hooker, J Dickson, ... Movement disorders: official journal of the Movement Disorder Society 22 (15 …, 2007 | 282 | 2007 |
| Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: a clinical and electrophysiological study P Schwingenschuh, D Ruge, MJ Edwards, C Terranova, P Katschnig, ... Movement disorders 25 (5), 560-569, 2010 | 256 | 2010 |
| Efficacy of long‐term continuous subcutaneous apomorphine infusion in advanced Parkinson's disease with motor fluctuations: a multicenter study PJ Garcia Ruiz, Á Sesar Ignacio, B Ares Pensado, A Castro Garcia, ... Movement disorders: official journal of the Movement Disorder Society 23 (8 …, 2008 | 251 | 2008 |
| Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study DJH Moss, AF Pardiñas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ... The Lancet Neurology 16 (9), 701-711, 2017 | 247 | 2017 |
| Cerebellar magnetic stimulation decreases levodopa-induced dyskinesias in Parkinson disease G Koch, L Brusa, F Carrillo, EL Gerfo, S Torriero, M Oliveri, P Mir, ... Neurology 73 (2), 113-119, 2009 | 211 | 2009 |
| Changes in intracortical circuits of the human motor cortex following theta burst stimulation of the lateral cerebellum G Koch, F Mori, B Marconi, C Codecà, C Pecchioli, S Salerno, S Torriero, ... Clinical Neurophysiology 119 (11), 2559-2569, 2008 | 191 | 2008 |
| Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients I Trender-Gerhard, MG Sweeney, P Schwingenschuh, P Mir, MJ Edwards, ... Journal of Neurology, Neurosurgery & Psychiatry 80 (8), 839-845, 2009 | 183 | 2009 |
| Abnormalities in motor cortical plasticity differentiate manifesting and nonmanifesting DYT1 carriers MJ Edwards, YZ Huang, P Mir, JC Rothwell, KP Bhatia Movement disorders: official journal of the Movement Disorder Society 21 (12 …, 2006 | 156 | 2006 |
| De novo coding variants are strongly associated with Tourette disorder AJ Willsey, TV Fernandez, D Yu, RA King, A Dietrich, J Xing, SJ Sanders, ... Neuron 94 (3), 486-499. e9, 2017 | 140 | 2017 |
| Effects of two weeks of cerebellar theta burst stimulation in cervical dystonia patients G Koch, P Porcacchia, V Ponzo, F Carrillo, MT Cáceres-Redondo, ... Brain stimulation 7 (4), 564-572, 2014 | 132 | 2014 |
| In vivo cholinergic basal forebrain atrophy predicts cognitive decline in de novo Parkinson’s disease NJ Ray, S Bradburn, C Murgatroyd, U Toseeb, P Mir, GK Kountouriotis, ... Brain 141 (1), 165-176, 2018 | 131 | 2018 |
| Secondary and primary dystonia: pathophysiological differences M Kojovic, I Pareés, P Kassavetis, FJ Palomar, P Mir, JT Teo, C Cordivari, ... Brain 136 (7), 2038-2049, 2013 | 117 | 2013 |
| Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families I Karagiannidis, S Dehning, P Sandor, Z Tarnok, R Rizzo, T Wolanczyk, ... Journal of medical genetics 50 (11), 760-764, 2013 | 113 | 2013 |
| Carotid body autotransplantation in Parkinson disease: a clinical and positron emission tomography study A Minguez-Castellanos, F Escamilla-Sevilla, GR Hotton, JJ Toledo-Aral, ... Journal of Neurology, Neurosurgery & Psychiatry 78 (8), 825-831, 2007 | 112 | 2007 |
| Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores I De Rojas, S Moreno-Grau, N Tesi, B Grenier-Boley, V Andrade, ... Nature communications 12 (1), 3417, 2021 | 111 | 2021 |
Kailash BhatiaProfessor of Clinical Neurology, Institute of Neurology, UCL, Queen Square, London WC1N 3BG,E-mail megerősítve itt: ucl.ac.uk
