| Frontotemporal dementia and its subtypes: a genome-wide association study R Ferrari, DG Hernandez, MA Nalls, JD Rohrer, A Ramasamy, JBJ Kwok, ... The Lancet Neurology 13 (7), 686-699, 2014 | 372 | 2014 |
| Circulating levels of soluble receptor for advanced glycation end products in Alzheimer disease and vascular dementia E Emanuele, A D’Angelo, C Tomaino, G Binetti, R Ghidoni, P Politi, ... Archives of neurology 62 (11), 1734-1736, 2005 | 257 | 2005 |
| Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases R Ferrari, Y Wang, J Vandrovcova, S Guelfi, A Witeolar, CM Karch, ... Journal of Neurology, Neurosurgery & Psychiatry 88 (2), 152-164, 2017 | 124 | 2017 |
| Heterogeneity within a large kindred with frontotemporal dementia: a novel progranulin mutation AC Bruni, P Momeni, L Bernardi, C Tomaino, F Frangipane, J Elder, ... Neurology 69 (2), 140-147, 2007 | 87 | 2007 |
| The effects of APOE and tau gene variability on risk of frontotemporal dementia L Bernardi, RG Maletta, C Tomaino, N Smirne, M Di Natale, M Perri, ... Neurobiology of aging 27 (5), 702-709, 2006 | 82 | 2006 |
| A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia R Ferrari, M Grassi, E Salvi, B Borroni, F Palluzzi, D Pepe, F D'Avila, ... Neurobiology of aging 36 (10), 2904. e13-2904. e26, 2015 | 68 | 2015 |
| Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy L Bernardi, F Frangipane, N Smirne, R Colao, G Puccio, SAM Curcio, ... Neurobiology of aging 33 (12), 2948. e1-2948. e10, 2012 | 57 | 2012 |
| Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia L Bernardi, C Tomaino, M Anfossi, M Gallo, S Geracitano, A Costanzo, ... Neurobiology of aging 30 (11), 1825-1833, 2009 | 56 | 2009 |
| Worldwide distribution of PSEN1 Met146Leu mutation: A large variability for a founder mutation AC Bruni, L Bernardi, R Colao, E Rubino, N Smirne, F Frangipane, ... Neurology 74 (10), 798-806, 2010 | 48 | 2010 |
| A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers M Zhang, R Ferrari, MC Tartaglia, J Keith, EI Surace, U Wolf, C Sato, ... Brain 141 (10), 2895-2907, 2018 | 42 | 2018 |
| g-Linolenic Acid Supplementation Can Affect Cancer Cell Proliferation via Modification of Fatty Acid Composition AP Silvana Hrelia,1 Alessandra Bordoni, PierLuigi Biagi, Carlo A. Rossi ... BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 225 (2), 441-447, 1996 | 41* | 1996 |
| Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family ME Conidi, L Bernardi, G Puccio, N Smirne, MG Muraca, SAM Curcio, ... Neurology 84 (22), 2266-2273, 2015 | 38 | 2015 |
| Clinical manifestations of highly prevalent corticosteroid-binding globulin mutations in a village in southern Italy G Cizza, L Bernardi, N Smirne, R Maletta, C Tomaino, A Costanzo, ... The Journal of Clinical Endocrinology & Metabolism 96 (10), E1684-E1693, 2011 | 37 | 2011 |
| Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease I Rosas, C Martínez, J Clarimón, A Lleó, I Illán-Gala, O Dols-Icardo, ... Neurobiology of Aging 87, 139. e1-139. e7, 2020 | 35 | 2020 |
| Relation of apolipoprotein (a) size to Alzheimer’s disease and vascular dementia E Emanuele, E Peros, C Tomaino, E Feudatari, L Bernardi, G Binetti, ... Dementia and geriatric cognitive disorders 18 (2), 189-196, 2004 | 35 | 2004 |
| From beta amyloid to altered proteostasis in Alzheimer’s disease AC Bruni, L Bernardi, C Gabelli Ageing research reviews 64, 101126, 2020 | 34 | 2020 |
| Role of Niemann-Pick type C disease mutations in dementia C Cupidi, F Frangipane, M Gallo, A Clodomiro, R Colao, L Bernardi, ... Journal of Alzheimer's Disease 55 (3), 1249-1259, 2017 | 33 | 2017 |
| AβPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions L Bernardi, S Geracitano, R Colao, G Puccio, M Gallo, M Anfossi, ... Journal of Alzheimer's Disease 17 (2), 383-389, 2009 | 32 | 2009 |
| Mutations in prion protein gene: pathogenic mechanisms in C-terminal vs. N-terminal domain, a review L Bernardi, AC Bruni International Journal of Molecular Sciences 20 (14), 3606, 2019 | 26 | 2019 |
| The first deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL S Bianchi, MT Dotti, GN Gallus, C D'Eramo, I Di Donato, L Bernardi, ... Neurobiology of aging 34 (9), 2234. e9-2234. e12, 2013 | 26 | 2013 |
