Investigating Epigenetic and Neuroimaging Profiles in Bipolar Disorder and Behavioral Variant Frontotemporal Dementia: An integrated epigenetic-neuroimaging approach
Delvecchio, G, Serpente, M, L Di Consoli, Rotondo, E, Borraci, V, Scola, E, Triuzi, F M, Castellani, M, Arighi, A, Scarpini, E, Galimberti, D, Brambilla, P
Published in European psychiatry (01.08.2024)
Published in European psychiatry (01.08.2024)
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Inflammatory molecules in Frontotemporal Dementia: Cerebrospinal fluid signature of progranulin mutation carriers
Galimberti, D, Bonsi, R, Fenoglio, C, Serpente, M, Cioffi, S.M.G, Fumagalli, G, Arighi, A, Ghezzi, L, Arcaro, M, Mercurio, M, Rotondo, E, Scarpini, E
Published in Brain, behavior, and immunity (01.10.2015)
Published in Brain, behavior, and immunity (01.10.2015)
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Late‐onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation
Scarioni, M., Arighi, A., Fenoglio, C., Sorrentino, F., Serpente, M., Rotondo, E., Mercurio, M., Marotta, G., Dijkstra, A. A., Pijnenburg, Y. A. L., Scarpini, E., Galimberti, D.
Published in European journal of neurology (01.12.2020)
Published in European journal of neurology (01.12.2020)
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Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu-Hakola Disease
Galimberti, D., Fenoglio, C., Ghezzi, L., Serpente, M., Arcaro, M., D'Anca, M., De Riz, M., Arighi, A., Fumagalli, G.G., Pietroboni, A.M., Piccio, L., Scarpini, E.
Published in Cytokine (Philadelphia, Pa.) (01.04.2019)
Published in Cytokine (Philadelphia, Pa.) (01.04.2019)
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Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect
Visconte, C., Golia, M.T., Fenoglio, C., Serpente, M., Gabrielli, M., Arcaro, M., Sorrentino, F., Busnelli, M., Arighi, A., Fumagalli, G., Rotondo, E., Rossi, P., Arosio, B., Scarpini, E., Verderio, C., Galimberti, D.
Published in GeroScience (01.06.2023)
Published in GeroScience (01.06.2023)
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DCUN1D1 is a risk factor for frontotemporal lobar degeneration
Villa, C., Venturelli, E., Fenoglio, C., Clerici, F., Marcone, A., Benussi, L., Gallone, S., Scalabrini, D., Cortini, F., Serpente, M., Martinelli Boneschi, F., Cappa, S., Binetti, G., Mariani, C., Rainero, I., Giordana, M. T., Bresolin, N., Scarpini, E., Galimberti, D.
Published in European journal of neurology (01.07.2009)
Published in European journal of neurology (01.07.2009)
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Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort
Martinelli-Boneschi, F., Esposito, F., Scalabrini, D., Fenoglio, C., Rodegher, M. E., Brambilla, P., Colombo, B., Ghezzi, A., Capra, R., Collimedaglia, L., Coniglio, G., De Riz, M., Serpente, M., Cantoni, C., Scarpini, E., Martinelli, V., Galimberti, D., Comi, G.
Published in European journal of neurology (01.05.2010)
Published in European journal of neurology (01.05.2010)
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Journal Article
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
Ferrari, Raffaele, Wang, Yunpeng, Vandrovcova, Jana, Guelfi, Sebastian, Witeolar, Aree, Karch, Celeste M, Schork, Andrew J, Fan, Chun C, Brewer, James B, Momeni, Parastoo, Schellenberg, Gerard D, Dillon, William P, Sugrue, Leo P, Hess, Christopher P, Yokoyama, Jennifer S, Bonham, Luke W, Rabinovici, Gil D, Miller, Bruce L, Andreassen, Ole A, Dale, Anders M, Hardy, John, Desikan, Rahul S
Published in Journal of neurology, neurosurgery and psychiatry (01.02.2017)
Published in Journal of neurology, neurosurgery and psychiatry (01.02.2017)
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Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study
Galimberti, Daniela, Fumagalli, Giorgio G., Fenoglio, Chiara, Cioffi, Sara M.G., Arighi, Andrea, Serpente, Maria, Borroni, Barbara, Padovani, Alessandro, Tagliavini, Fabrizio, Masellis, Mario, Tartaglia, Maria Carmela, van Swieten, John, Meeter, Lieke, Graff, Caroline, de Mendonça, Alexandre, Bocchetta, Martina, Rohrer, Jonathan D., Scarpini, Elio, Andersson, Christin, Archetti, Silvana, Arighi, Andrea, Benussi, Luisa, Binetti, Giuliano, Black, Sandra, Cash, David, Cosseddu, Maura, Dick, Katrina M., Fallström, Marie, Ferreira, Carlos, Finger, Elizabeth, Fox, Nick, Freedman, Morris, Frisoni, Giovanni, Gazzina, Stefano, Ghidoni, Roberta, Grisoli, Marina, Jelic, Vesna, Jiskoot, Lize, Keren, Ron, Laforce, Robert, Lombardi, Gemma, Maruta, Carolina, Mead, Simon, Meeter, Lieke, van Minkelen, Rick, Nacmias, Benedetta, Öijerstedt, Linn, Ourselin, Sebastien, Panman, Jessica, Pievani, Michela, Polito, Cristina, Prioni, Sara, Rademakers, Rosa, Redaelli, Veronica, Rogaeva, Ekaterina, Rossi, Giacomina, Besta, Carlo, Rossor, Martin, Rowe, James, Sorbi, Sandro, Tang-Wai, David, Thomas, David L., Thonberg, Hakan, Tiraboschi, Pietro, Verdelho, Ana, Warren, Jason
Published in Neurobiology of aging (01.02.2018)
Published in Neurobiology of aging (01.02.2018)
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Inflammatory plasma profile in genetic symptomatic and presymptomatic Frontotemporal Dementia − A GENFI study
Fenoglio, Chiara, Serpente, Maria, Arcaro, Marina, Carandini, Tiziana, Sacchi, Luca, Pintus, Manuela, Rotondo, Emanuela, Borracci, Vittoria, Ghezzi, Laura, Bouzigues, Arabella, Russell, Lucy L., Foster, Phoebe H., Ferry-Bolder, Eve, van Swieten, John C., Jiskoot, Lize C., Seelaar, Harro, Sánchez Valle, Raquel, Laforce, Robert, Graff, Caroline, Vandenberghe, Rik, de Mendonça, Alexandre, Tiraboschi, Pietro, Santana, Isabel, Gerhard, Alexander, Levin, Johannes, Sorbi, Sandro, Otto, Markus, Pasquier, Florence, Ducharme, Simon, Butler, Chris R., Ber, Isabelle Le, Finger, Elizabeth, Carmela Tartaglia, Maria, Masellis, Mario, Rowe, James B., Synofzik, Matthis, Moreno, Fermin, Borroni, Barbara, Rohrer, Jonathan D., Arighi, Andrea, Galimberti, Daniela
Published in Brain, behavior, and immunity (01.11.2024)
Published in Brain, behavior, and immunity (01.11.2024)
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CXCR4 involvement in neurodegenerative diseases
Bonham, Luke W, Karch, Celeste M, Fan, Chun C, Tan, Chin, Geier, Ethan G, Wang, Yunpeng, Wen, Natalie, Broce, Iris J, Li, Yi, Barkovich, Matthew J, Ferrari, Raffaele, Hardy, John, Momeni, Parastoo, Höglinger, Günter, Müller, Ulrich, Hess, Christopher P, Sugrue, Leo P, Dillon, William P, Schellenberg, Gerard D, Miller, Bruce L, Andreassen, Ole A, Dale, Anders M, Barkovich, A James, Yokoyama, Jennifer S, Desikan, Rahul S
Published in Translational psychiatry (11.04.2018)
Published in Translational psychiatry (11.04.2018)
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Journal Article
Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
Taskesen, E, Mishra, A, van der Sluis, S, Ferrari, R, Veldink, J H, van Es, M A, Smit, A B, Posthuma, D, Pijnenburg, Y
Published in Scientific reports (21.08.2017)
Published in Scientific reports (21.08.2017)
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Journal Article
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
Bonham, Luke W, Steele, Natasha Z R, Karch, Celeste M, Broce, Iris, Geier, Ethan G, Wen, Natalie L, Momeni, Parastoo, Hardy, John, Miller, Zachary A, Gorno-Tempini, Maria Luisa, Hess, Christopher P, Lewis, Patrick, Miller, Bruce L, Seeley, William W, Manzoni, Claudia, Desikan, Rahul S, Baranzini, Sergio E, Ferrari, Raffaele, Yokoyama, Jennifer S
Published in Scientific reports (26.07.2019)
Published in Scientific reports (26.07.2019)
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Journal Article
Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS
Taskesen, E, Mishra, A, van der Sluis, S, Ferrari, R, Veldink, J H, van Es, M A, Smit, A B, Posthuma, D, Pijnenburg, Y
Published in Scientific reports (14.05.2018)
Published in Scientific reports (14.05.2018)
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Journal Article
Protein network analysis reveals selectively vulnerable regions and biological processes in FTD
Bonham, Luke W, Steele, Natasha Z R, Karch, Celeste M, Manzoni, Claudia, Geier, Ethan G, Wen, Natalie, Ofori-Kuragu, Aaron, Momeni, Parastoo, Hardy, John, Miller, Zachary A, Hess, Christopher P, Lewis, Patrick, Miller, Bruce L, Seeley, William W, Baranzini, Sergio E, Desikan, Rahul S, Ferrari, Raffaele, Yokoyama, Jennifer S
Published in Neurology. Genetics (01.10.2018)
Published in Neurology. Genetics (01.10.2018)
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Journal Article
DCUN1D1 is a risk factor for frontotemporal lobar degeneration: DCUN1D1 is a risk factor for FTLD
Villa, C., Venturelli, E., Fenoglio, C., Clerici, F., Marcone, A., Benussi, L., Gallone, S., Scalabrini, D., Cortini, F., Serpente, M., Martinelli Boneschi, F., Cappa, S., Binetti, G., Mariani, C., Rainero, I., Giordana, M. T., Bresolin, N., Scarpini, E., Galimberti, D.
Published in European journal of neurology (01.07.2009)
Published in European journal of neurology (01.07.2009)
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