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 | 2525 | 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 | 1749 | 2008 |
Validity and reliability of a rating scale for the primary torsion dystonias RE Burke, S Fahn, CD Marsden, SB Bressman, C Moskowitz, J Friedman Neurology 35 (1), 73-73, 1985 | 1248 | 1985 |
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein LJ Ozelius, JW Hewett, CE Page, SB Bressman, PL Kramer, C Shalish, ... Nature genetics 17 (1), 40-48, 1997 | 1229 | 1997 |
LRRK2 G2019S as a Cause of Parkinson's Disease in Ashkenazi Jews LJ Ozelius, G Senthil, R Saunders-Pullman, E Ohmann, A Deligtisch, ... New England Journal of Medicine 354 (4), 424-425, 2006 | 852 | 2006 |
Analysis of blink rate patterns in normal subjects AR Bentivoglio, SB Bressman, E Cassetta, D Carretta, P Tonali, ... Movement disorders 12 (6), 1028-1034, 1997 | 643 | 1997 |
Mutations in the Na+/K+-ATPase α3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism P de Carvalho Aguiar, KJ Sweadner, JT Penniston, J Zaremba, L Liu, ... Neuron 43 (2), 169-175, 2004 | 596 | 2004 |
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population N Risch, D Leon, L Ozelius, P Kramer, L Almasy, B Singer, S Fahn, ... Nature genetics 9 (2), 152-159, 1995 | 524 | 1995 |
Metabolomic profiling to develop blood biomarkers for Parkinson's disease M Bogdanov, WR Matson, L Wang, T Matson, R Saunders-Pullman, ... Brain 131 (2), 389-396, 2008 | 491 | 2008 |
The Parkinson's progression markers initiative (PPMI)–establishing a PD biomarker cohort K Marek, S Chowdhury, A Siderowf, S Lasch, CS Coffey, ... Annals of clinical and translational neurology 5 (12), 1460-1477, 2018 | 484 | 2018 |
The DYT1 phenotype and guidelines for diagnostic testing SB Bressman, C Sabatti, D Raymond, D De Leon, C Klein, PL Kramer, ... Neurology 54 (9), 1746-1753, 2000 | 438 | 2000 |
Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia T Fuchs, S Gavarini, R Saunders-Pullman, D Raymond, ME Ehrlich, ... Nature genetics 41 (3), 286-288, 2009 | 398 | 2009 |
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease KY Hui, H Fernandez-Hernandez, J Hu, A Schaffner, N Pankratz, NY Hsu, ... Science translational medicine 10 (423), eaai7795, 2018 | 390 | 2018 |
Differential effects of severe vs mild GBA mutations on Parkinson disease Z Gan-Or, I Amshalom, LL Kilarski, A Bar-Shira, M Gana-Weisz, ... Neurology 84 (9), 880-887, 2015 | 376 | 2015 |
Anti–tumor necrosis factor therapy and incidence of Parkinson disease among patients with inflammatory bowel disease I Peter, M Dubinsky, S Bressman, A Park, C Lu, N Chen, A Wang JAMA neurology 75 (8), 939-946, 2018 | 374 | 2018 |
Functional brain networks in DYT1 dystonia D Eidelberg, JR Moeller, A Antonini, K Kazumata, T Nakamura, V Dhawan, ... Annals of neurology 44 (3), 303-312, 1998 | 368 | 1998 |
Cerebellothalamocortical connectivity regulates penetrance in dystonia M Argyelan, M Carbon, M Niethammer, AM Uluğ, HU Voss, SB Bressman, ... Journal of Neuroscience 29 (31), 9740-9747, 2009 | 347 | 2009 |
Occupation and risk of parkinsonism: a multicenter case-control study CM Tanner, GW Ross, SA Jewell, RA Hauser, J Jankovic, SA Factor, ... Archives of neurology 66 (9), 1106-1113, 2009 | 344 | 2009 |
Mutations in GNAL cause primary torsion dystonia T Fuchs, R Saunders-Pullman, I Masuho, MS Luciano, D Raymond, ... Nature genetics 45 (1), 88-92, 2013 | 343 | 2013 |
The diagnosis of dystonia HL Geyer, SB Bressman The Lancet Neurology 5 (9), 780-790, 2006 | 339 | 2006 |