| 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 | 1607 | 1999 |
| Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity GC Telling, P Parchi, SJ DeArmond, P Cortelli, P Montagna, R Gabizon, ... Science 274 (5295), 2079-2082, 1996 | 1044 | 1996 |
| 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 | 1018 | 1996 |
| Sporadic and familial CJD: classification and characterisation P Gambetti, Q Kong, W Zou, P Parchi, SG Chen British medical bulletin 66 (1), 213-239, 2003 | 675 | 2003 |
| Truncated forms of the human prion protein in normal brain and in prion diseases SG Chen, DB Teplow, P Parchi, JK Teller, P Gambetti, L Autilio-Gambetti Journal of Biological Chemistry 270 (32), 19173-19180, 1995 | 597 | 1995 |
| Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium I Alafuzoff, T Arzberger, S Al‐Sarraj, I Bodi, N Bogdanovic, H Braak, ... Brain pathology 18 (4), 484-496, 2008 | 467 | 2008 |
| CSF biomarker variability in the Alzheimer's Association quality control program N Mattsson, U Andreasson, S Persson, MC Carrillo, S Collins, S Chalbot, ... Alzheimer's & Dementia 9 (3), 251-261, 2013 | 397 | 2013 |
| Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. L Monari, SG Chen, P Brown, P Parchi, RB Petersen, J Mikol, F Gray, ... Proceedings of the National Academy of Sciences 91 (7), 2839-2842, 1994 | 395 | 1994 |
| 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 | 360 | 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 | 340 | 2000 |
| Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium I Alafuzoff, PG Ince, T Arzberger, S Al-Sarraj, J Bell, I Bodi, N Bogdanovic, ... Acta neuropathologica 117, 635-652, 2009 | 319 | 2009 |
| Typing prion isoforms. P Parchi, S Capellari, SG Chen, RB Petersen, P Gambetti, N Kopp, ... | 310 | 1997 |
| 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 | 271 | 2009 |
| Fatal familial insomnia and familial Creutzfeldt‐Jakob disease: clinical, pathological and molecular features P Gambetti, P Parchi, RB Petersen, SG Chen, E Lugaresi Brain pathology 5 (1), 43-51, 1995 | 266 | 1995 |
| 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 | 264 | 2010 |
| 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 Orrù, ... Acta neuropathologica 140, 49-62, 2020 | 254 | 2020 |
| Tau gene mutation in familial progressive subcortical gliosis M Goedert, MG Spillantini, RA Crowther, SG Chen, P Parchi, M Tabaton, ... Nature Medicine 5 (4), 454-457, 1999 | 245 | 1999 |
| 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 | 236 | 1998 |
| Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA P Parchi, L De Boni, D Saverioni, ML Cohen, I Ferrer, P Gambetti, E Gelpi, ... Acta neuropathologica 124, 517-529, 2012 | 220 | 2012 |
| 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 | 212 | 1999 |
Sabina CapellariDipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna e IRCCS ISNB, BolognaAdresse e-mail validée de unibo.it
