| Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects P Parchi, A Giese, S Capellari, P Brown, W Schulz‐Schaeffer, O Windl, ... Annals of neurology 46 (2), 224-233, 1999 | 1550 | 1999 |
| Molecular basis of phenotypic variability in sporadc creudeldt‐jakob disease P Parchi, R Castellani, S Capellari, B Ghetti, K Young, SG Chen, M Farlow, ... Annals of neurology 39 (6), 767-778, 1996 | 988 | 1996 |
| Quantifying prion disease penetrance using large population control cohorts EV Minikel, SM Vallabh, M Lek, K Estrada, KE Samocha, ... Science translational medicine 8 (322), 322ra9-322ra9, 2016 | 333 | 2016 |
| Genetic influence on the structural variations of the abnormal prion protein P Parchi, W Zou, W Wang, P Brown, S Capellari, B Ghetti, N Kopp, ... Proceedings of the National Academy of Sciences 97 (18), 10168-10172, 2000 | 324 | 2000 |
| Typing prion isoforms P Parchi, S Capellari, SG Chen, RB Petersen, P Gambetti, N Kopp, ... Nature 386 (6622), 232-233, 1997 | 296 | 1997 |
| Skin nerve α-synuclein deposits: a biomarker for idiopathic Parkinson disease V Donadio, A Incensi, V Leta, MP Giannoccaro, C Scaglione, P Martinelli, ... Neurology 82 (15), 1362-1369, 2014 | 270 | 2014 |
| Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification P Parchi, R Strammiello, S Notari, A Giese, JPM Langeveld, A Ladogana, ... Acta neuropathologica 118, 659-671, 2009 | 255 | 2009 |
| Variably protease‐sensitive prionopathy: a new sporadic disease of the prion protein WQ Zou, G Puoti, X Xiao, J Yuan, L Qing, I Cali, M Shimoji, ... Annals of neurology 68 (2), 162-172, 2010 | 245 | 2010 |
| Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study DJH Moss, AF Pardiņas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ... The Lancet Neurology 16 (9), 701-711, 2017 | 242 | 2017 |
| Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann–Sträussler–Scheinker disease P Parchi, SG Chen, P Brown, W Zou, S Capellari, H Budka, J Hainfellner, ... Proceedings of the National Academy of Sciences 95 (14), 8322-8327, 1998 | 225 | 1998 |
| A subtype of sporadic prion disease mimicking fatal familial insomnia P Parchi, S Capellari, S Chin, HB Schwarz, NP Schecter, JD Butts, ... Neurology 52 (9), 1757-1757, 1999 | 205 | 1999 |
| Mixed brain pathologies in dementia: the BrainNet Europe consortium experience GG Kovacs, I Alafuzoff, S Al-Sarraj, T Arzberger, N Bogdanovic, ... Dementia and geriatric cognitive disorders 26 (4), 343-350, 2008 | 188 | 2008 |
| Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease RJ Castellani, M Colucci, Z Xie, W Zou, C Li, P Parchi, S Capellari, ... Neurology 63 (3), 436-442, 2004 | 174 | 2004 |
| Inherited prion diseases Q Kong, WK Surewicz, RB Petersen, W Zou, SG Chen, P Gambetti, ... COLD SPRING HARBOR MONOGRAPH SERIES 41, 673-776, 2004 | 169 | 2004 |
| Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease G Rizzo, P Martinelli, D Manners, C Scaglione, C Tonon, P Cortelli, ... Brain 131 (10), 2690-2700, 2008 | 167 | 2008 |
| Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies M Rossi, N Candelise, S Baiardi, S Capellari, G Giannini, CD Orrų, ... Acta neuropathologica 140, 49-62, 2020 | 163 | 2020 |
| High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions A Franceschini, S Baiardi, AG Hughson, N McKenzie, F Moda, M Rossi, ... Scientific reports 7 (1), 1-8, 2017 | 158 | 2017 |
| Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study I Ferrer, J Armstrong, S Capellari, P Parchi, T Arzberger, J Bell, H Budka, ... Brain Pathology 17 (3), 297-303, 2007 | 157 | 2007 |
| Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease WQ Zou, S Capellari, P Parchi, MS Sy, P Gambetti, SG Chen Journal of Biological Chemistry 278 (42), 40429-40436, 2003 | 153 | 2003 |
| Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis S Capellari, R Strammiello, D Saverioni, H Kretzschmar, P Parchi Acta neuropathologica 121, 21-37, 2011 | 147 | 2011 |
