Investigating Epigenetic and Neuroimaging Profiles in Bipolar Disorder and Behavioral Variant Frontotemporal Dementia: An integrated epigenetic-neuroimaging approach von 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

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Inflammatory molecules in Frontotemporal Dementia: Cerebrospinal fluid signature of progranulin mutation carriers von 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

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Late‐onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation von 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.

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Plasma microglial-derived extracellular vesicles are increased in frail patients with Mild Cognitive Impairment and exert a neurotoxic effect von 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.

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Inflammatory expression profile in peripheral blood mononuclear cells from patients with Nasu-Hakola Disease von 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.

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DCUN1D1 is a risk factor for frontotemporal lobar degeneration von 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.

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Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort von 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.

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Inflammatory plasma profile in genetic symptomatic and presymptomatic Frontotemporal Dementia − A GENFI study von 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

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Late-onset presentation and phenotypic heterogeneity of the rareR377W PSEN1mutation von 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.

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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 von 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

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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia von Mishra, Aniket, Ferrari, Raffaele, Heutink, Peter, Hardy, John, Pijnenburg, Yolande, Posthuma, Danielle

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CXCR4 involvement in neurodegenerative diseases von 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.

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Long Non-Coding RNA Profile in Genetic Symptomatic and Presymptomatic Frontotemporal Dementia: A GENFI Study von Serpente, M, Fenoglio, C, Arcaro, M, Carandini, T, Sacchi, L, Pintus, M, Rotondo, E, Borracci, V, Ghezzi, L, Bouzigues, A, Russell, LL, Foster, PH, Ferry-Bolder, E, van Swieten, JC, Jiskoot, LC, Seelaar, H, Sánchez Valle, R, Laforce, R, Graff, C, Vandenberghe, R, de Mendonça, A, Tiraboschi, P, Santana, I, Gerhard, A, Levin, J, Sorbi, S, Otto, M, Pasquier, F, Ducharme, S, Butler, CR, Le Ber, I, Finger, E, Tartaglia, MC, Masellis, M, Rowe, JB, Synofzik, M, Moreno, F, Borroni, B, Rohrer, JD, Arighi, A, Galimberti, D

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Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS von Taskesen, E., Mishra, A., van der Sluis, S., Ferrari, R., Veldink, J. H., van Es, M. A., Smit, A. B., Posthuma, D., Pijnenburg, Y.

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Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia von 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.

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Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of lon... von van der Lee, Sven J., Conway, Olivia J., Jansen, Iris, Carrasquillo, Minerva M., Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R., Stringa, Najada, Chen, Jason A., Zettergren, Anna, Andlauer, Till F. M., Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E., Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J., Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A., Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M., Indakoetxea, Begoña, Collij, Lyduine E., Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W., van Berckel, Bart N. M., Wiendl, Heinz, Strickland, Samantha L., Pastor, Pau, Rodríguez Rodríguez, Eloy, Boeve, Bradley F., Petersen, Ronald C., Ferman, Tanis J., van Gerpen, Jay A., Reinders, Marcel J. T., Uitti, Ryan J., Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K., van Schoor, Natasja M., Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K., Ross, Owen A., Dickson, Dennis W., Graff-Radford, Neill R., Knopman, David, Rademakers, Rosa, Lemstra, Afina W., Pijnenburg, Yolande A. L., Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A., Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A., Sørensen, Thorkild I. A., Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, Clarimón, Jordi, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W., Ramirez, Alfredo, Ruiz, Agustín, Slagboom, Eline, van der Flier, Wiesje M., Holstege, Henne

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Author Correction: Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation... von Taskesen, E., Mishra, A., van der Sluis, S., Ferrari, R., Veldink, J. H., van Es, M. A., Smit, A. B., Posthuma, D., Pijnenburg, Y.

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Protein network analysis reveals selectively vulnerable regions and biological processes in FTD von 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

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Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease von Jakobsdottir, J., Raybould, R., Vronskaya, M., White, C.C., Herms, S., Smith, A.V., Funk, C.C., Sánchez-Juan, P., Wolters, F.J., Zhao, Y., Malamon, J., Dombroski, B., Whitehead, P., Cantwell, L.B., Burgess, J.D., Adams, H.H., Chakrabarty, P., Beiser, A.S., Lannfelt, L., Mecocci, P., Eiriksdottir, G., Henández, I., Tarraga, L., Albert, M.S., Emilsson, V., Doody, R.S., Spalletta, G., Frosch, M.P., Kamboh, M.I., Marshall, R., Fairén, M.D., Uphill, J., Hughes, J.T., Orfei, M.D., Ciaramella, A., Mayhaus, M., Brookes, K., Cupidi, C., Gill, M., Apostolova, L.G., Asthana, S., Boeve, B.F., Burke, J.R., Buxbaum, J.D., Cairns, N.J., Chui, H.C., Gearing, M., Harrell, L.E., Jarvik, G.P., Leverenz, J.B., Li, G., Lieberman, A.P., McCormick, W.C., Miller, C.A., Pankratz, V.S., Raskind, M., Tanzi, R.E., Troncoso, J.C., Wingo, T.S., Garzia, F., Vandenberghe, R., Fernadez, C.M., Lilius, L., Koivisto, A.M., Dermecourt, V., Fievet, N., Brice, A., Ritchie, K., Dubois, B., Himali, J.J., Tschanz, J., Fitzpatrick, A.L., Kukull, W.A., Larson, E.B., Rotter, J.I., Coto, E., Gallo, M., Galimberti, D., Tsuang, D.W., Daniele, A., Nacmias, B., Rubinsztein, D.C., Bras, J., Collinge, J., Tsolaki, M., Uitterlinden, A.G., Powell, J., Golde, T.E., De Jager, P.L., Ertekin-Taner, N., Passmore, P., Younkin, S.G., Ortega-Cubero, S., Jones, L., Mayeux, R., Amin, N., Holmans, P.A., Pericak-Vance, M.A., Lambert, J.C., Destefano, Anita L.

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DCUN1D1 is a risk factor for frontotemporal lobar degeneration: DCUN1D1 is a risk factor for FTLD von 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.

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