Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease by Rosas, Irene, Martínez, Carmen, Clarimón, Jordi, Lleó, Alberto, Illán-Gala, Ignacio, Dols-Icardo, Oriol, Borroni, Barbara, Almeida, Maria Rosário, van der Zee, Julie, Van Broeckhoven, Christine, Bruni, Amalia C., Anfossi, Maria, Bernardi, Livia, Maletta, Raffaele, Serpente, María, Galimberti, Daniela, Scarpini, Elio, Rossi, Giacomina, Caroppo, Paola, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Nacmias, Benedetta, Sorbi, Sandro, Piaceri, Irene, Bagnoli, Silvia, Antonell, Anna, Sánchez-Valle, Raquel, De la Casa-Fages, Beatriz, Grandas, Francisco, Diez-Fairen, Mónica, Pastor, Pau, Ferrari, Raffaele, Álvarez, Victoria, Menéndez-González, Manuel

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Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation by Galimberti, Daniela, Fenoglio, Chiara, Serpente, Maria, Villa, Chiara, Bonsi, Rossana, Arighi, Andrea, Fumagalli, Giorgio G, Del Bo, Roberto, Bruni, Amalia C, Anfossi, Maria, Clodomiro, Alessandra, Cupidi, Chiara, Nacmias, Benedetta, Sorbi, Sandro, Piaceri, Irene, Bagnoli, Silvia, Bessi, Valentina, Marcone, Alessandra, Cerami, Chiara, Cappa, Stefano F, Filippi, Massimo, Agosta, Federica, Magnani, Giuseppe, Comi, Giancarlo, Franceschi, Massimo, Rainero, Innocenzo, Giordana, Maria Teresa, Rubino, Elisa, Ferrero, Patrizia, Rogaeva, Ekaterina, Xi, Zhengrui, Confaloni, Annamaria, Piscopo, Paola, Bruno, Giuseppe, Talarico, Giuseppina, Cagnin, Annachiara, Clerici, Francesca, Dell’Osso, Bernardo, Comi, Giacomo P, Altamura, A. Carlo, Mariani, Claudio, Scarpini, Elio

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Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood by Ge, Yi-Jun, Zhang, Ya-Ru, Huang, Yu-Yuan, Dong, Qiang, Tan, Lan, Ferrari, Raffaele, Ramasamy, Adaikalavan, Kwok, John B.J., Dobson-Stone, Carol, Schofield, Peter R., Halliday, Glenda M., Piguet, Olivier, Bartley, Lauren, Thompson, Elizabeth, Haan, Eric, Hernández, Isabel, Ruiz, Agustín, Boada, Mercè, Cruchaga, Carlos, Benussi, Luisa, Galimberti, Daniela, Fenoglio, Chiara, Scarpini, Elio, Lleó, Alberto, Nilsson, Karin, Mackenzie, Ian R.A., Hsiung, Ging-Yuek R., Mann, David M.A., Morris, Christopher M., Attems, Johannes, Thomas, Alan J., Pietrini, P., Huey, Edward D., Tierney, Michael C., Pastor, Pau, Razquin, Cristina, Ortega-Cubero, Sara, Perneczky, Robert, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Kurz, Alexander, Rainero, Innocenzo, Rogaeva, Ekaterina, Rossi, Giacomina, Rowe, James B., Schlachetzki, Johannes C.M., Uphill, James, Collinge, John, Mead, Simon, Danek, Adrian, Van Langenhove, Tim, Cappa, Stefano F., Hannequin, Didier, Vercelletto, Martine, Brice, Alexis, Nacmias, Benedetta, Bagnoli, Silvia, Nielsen, Jørgen E., Ibach, Bernd, Gasparoni, Gilles, Gu, Wei, Warren, Jason D., Spillantini, Maria Grazia, Morris, Huw R., Snowden, Julie S., Rollinson, Sara, Richardson, Anna, Gerhard, Alexander, Bruni, Amalia C., Maletta, Raffaele, Cupidi, Chiara, Gallo, Maura, Smirne, Nicoletta, Rademakers, Rosa, Baker, Matt, Dickson, Dennis W., Petersen, Ronald C., Knopman, David, Boeve, Bradley F., Parisi, Joseph E., Seeley, William W., Miller, Bruce L., Karydas, Anna M., van Swieten, John C., Seelaar, Harro, Pijnenburg, Yolande A.L., Logroscino, Giancarlo, Capozzo, Rosa, Puca, Annibale A., Franceschi, Massimo, Postiglione, Alfredo, Sorrentino, Paolo, Kristiansen, Mark, Chiang, Huei-Hsin, Graff, Caroline, Rollin, Adeline, Lebert, Florence, Kapogiannis, Dimitrios, Ferrucci, Luigi, Hardy, John

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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers by Zhang, Ming, Ferrari, Raffaele, Tartaglia, Maria Carmela, Keith, Julia, Surace, Ezequiel I, Wolf, Uri, Sato, Christine, Grinberg, Mark, Liang, Yan, Xi, Zhengrui, Dupont, Kyle, McGoldrick, Philip, Weichert, Anna, McKeever, Paul M, Schneider, Raphael, McCorkindale, Michael D, Manzoni, Claudia, Rademakers, Rosa, Graff-Radford, Neill R, Dickson, Dennis W, Parisi, Joseph E, Boeve, Bradley F, Petersen, Ronald C, Miller, Bruce L, Seeley, William W, van Swieten, John C, van Rooij, Jeroen, Pijnenburg, Yolande, van der Zee, Julie, Van Broeckhoven, Christine, Le Ber, Isabelle, Van Deerlin, Vivianna, Suh, EunRan, Rohrer, Jonathan D, Mead, Simon, Graff, Caroline, Öijerstedt, Linn, Pickering-Brown, Stuart, Rollinson, Sara, Rossi, Giacomina, Tagliavini, Fabrizio, Brooks, William S, Dobson-Stone, Carol, Halliday, Glenda M, Hodges, John R, Piguet, Olivier, Binetti, Giuliano, Benussi, Luisa, Ghidoni, Roberta, Nacmias, Benedetta, Sorbi, Sandro, Bruni, Amalia C, Galimberti, Daniela, Scarpini, Elio, Rainero, Innocenzo, Rubino, Elisa, Clarimon, Jordi, Lleó, Alberto, Ruiz, Agustin, Hernández, Isabel, Pastor, Pau, Diez-Fairen, Monica, Borroni, Barbara, Pasquier, Florence, Deramecourt, Vincent, Lebouvier, Thibaud, Perneczky, Robert, Diehl-Schmid, Janine, Grafman, Jordan, Huey, Edward D, Mayeux, Richard, Nalls, Michael A, Hernandez, Dena, Singleton, Andrew, Momeni, Parastoo, Zeng, Zhen, Hardy, John, Robertson, Janice, Zinman, Lorne, Rogaeva, Ekaterina

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Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes by Reus, Lianne M., Pasaniuc, Bogdan, Posthuma, Danielle, Boltz, Toni, Ferrari, Raffaele, Hernandez, Dena G., Nalls, Michael A., Rohrer, Jonathan D., Ramasamy, Adaikalavan, Brooks, William S., Halliday, Glenda M., Piguet, Olivier, Bartley, Lauren, Hernández, Isabel, Ruiz, Agustín, Boada, Mercè, Borroni, Barbara, Padovani, Alessandro, Cruchaga, Carlos, Cairns, Nigel J., Benussi, Luisa, Ghidoni, Roberta, Forloni, Gianluigi, Galimberti, Daniela, Fenoglio, Chiara, Scarpini, Elio, Blesa, Rafael, Mackenzie, Ian R.A., Hsiung, Ging-Yuek R., Mann, David M.A., Attems, Johannes, Thomas, Alan J., Huey, Edward D., Tierney, Michael C., Razquin, Cristina, Ortega-Cubero, Sara, Alonso, Elena, Perneczky, Robert, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Rubino, Elisa, Rogaeva, Ekaterina, St. George-Hyslop, Peter, Rossi, Giacomina, Rowe, James B., Schlachetzki, Johannes C.M., Uphill, James, Collinge, John, Danek, Adrian, Van Deerlin, Vivianna M., Trojanowski, John Q., van der Zee, Julie, Cappa, Stefano F., Hannequin, Didier, Brice, Alexis, Nacmias, Benedetta, Sorbi, Sandro, Bagnoli, Silvia, Piaceri, Irene, Nielsen, Jørgen E., Hjermind, Lena E., Riemenschneider, Matthias, Ibach, Bernd, Gasparoni, Gilles, Pichler, Sabrina, Warren, Jason D., Morris, Huw R., Heutink, Peter, Snowden, Julie S., Rollinson, Sara, Gerhard, Alexander, Bruni, Amalia C., Frangipane, Francesca, Cupidi, Chiara, Anfossi, Maria, Gallo, Maura, Smirne, Nicoletta, Rademakers, Rosa, Dickson, Dennis W., Graff-Radford, Neill R., Petersen, Ronald C., Josephs, Keith A., Boeve, Bradley F., Parisi, Joseph E., Seeley, William W., Pijnenburg, Yolande A.L., Scheltens, Philip, Puca, Annibale A., Postiglione, Alfredo, Milan, Graziella, Sorrentino, Paolo, Kristiansen, Mark, Chiang, Huei-Hsin, Graff, Caroline, Kapogiannis, Dimitrios, Ferrucci, Luigi, Pickering-Brown, Stuart, Singleton, Andrew B., Pijnenburg, Yolande A.L., Ophoff, Roel A.

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The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family by Gallo, Maura, Frangipane, Francesca, Cupidi, Chiara, De Bartolo, Matteo, Turone, Sabina, Ferrari, Camilla, Nacmias, Benedetta, Grimaldi, Giuliana, Laganà, Valentina, Colao, Rosanna, Bernardi, Livia, Anfossi, Maria, Conidi, Maria Elena, Vasso, Franca, Curcio, Sabrina Anna Maria, Mirabelli, Maria, Smirne, Nicoletta, Torchia, Giusi, Muraca, Maria Gabriella, Puccio, Gianfranco, Di Lorenzo, Raffaele, Piccininni, Maristella, Tedde, Andrea, Maletta, Raffaele Giovanni, Sorbi, Sandro, Bruni, Amalia Cecilia

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Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia by Rosas, Irene, Martínez, Carmen, Coto, Eliecer, Clarimón, Jordi, Lleó, Alberto, Illán-Gala, Ignacio, Dols-Icardo, Oriol, Borroni, Barbara, Almeida, Maria Rosário, van der Zee, Julie, Van Broeckhoven, Christine, Bruni, Amalia C., Anfossi, Maria, Bernardi, Livia, Maletta, Raffaele, Serpente, María, Galimberti, Daniela, Scarpini, Elio, Rossi, Giacomina, Caroppo, Paola, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Nacmias, Benedetta, Sorbi, Sandro, Piaceri, Irene, Bagnoli, Silvia, Antonell, Anna, Sánchez-Valle, Raquel, De la Casa-Fages, Beatriz, Grandas, Francisco, Diez-Fairen, Mónica, Pastor, Pau, Ferrari, Raffaele, Queimaliños-Perez, Daniel, Pérez-Oliveira, Sergio, Álvarez, Victoria, Menéndez-González, Manuel

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Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis by Gao, Yixin, Wang, Ting, Yu, Xinghao, Zhao, Huashuo, Zeng, Ping

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Angela R.: a familial Alzheimer’s disease case in the days of Auguste D by Borrello, Laura, Cupidi, Chiara, Laganà, Valentina, Anfossi, Maria, Conidi, Maria Elena, Smirne, Nicoletta, Taverniti, Maria, Guarasci, Roberto, Bruni, Amalia Cecilia

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Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy by Bernardi, Livia, Frangipane, Francesca, Smirne, Nicoletta, Colao, Rosanna, Puccio, Gianfranco, Curcio, Sabrina A.M, Mirabelli, Maria, Maletta, Raffaele, Anfossi, Maria, Gallo, Maura, Geracitano, Silvana, Conidi, Maria Elena, Di Lorenzo, Raffale, Clodomiro, Alessandra, Cupidi, Chiara, Marzano, Sandra, Comito, Francesco, Valenti, Vincenzo, Zirilli, Maria Angela, Ghani, Mahdi, Xi, Zhengrui, Sato, Christine, Moreno, Danielle, Borelli, Annelisa, Leone, Rosa Anna, St. George-Hyslop, Peter, Rogaeva, Ekaterina, Bruni, Amalia C

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The novel PSEN1 M84V mutation associated to frontal disexecutive syndrome, spastic paraparesis and cerebellar atrophy in a dominant Alzheimer’s disease family by Gallo, Maura, Frangipane, Francesca, Cupidi, Chiara, De Bartolo, Matteo, Turone, Sabina, Ferrari, Camilla, Nacmias, Benedetta, Grimaldi, Giuliana, Laganà, Valentina, Colao, Rosanna, Bernardi, Livia, Anfossi, Maria, Conidi, Maria Elena, Vasso, Franca, Curcio, Sabrina Anna Maria, Mirabelli, Maria, Smirne, Nicoletta, Torchia, Giusi, Muraca, Maria Gabriella, Puccio, Gianfranco, Di Lorenzo, Raffaele, Piccininni, Maristella, Tedde, Andrea, Maletta, Raffaele Giovanni, Sorbi, Sandro, Bruni, Amalia Cecilia

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Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome by Bernardi, Livia, Cupidi, Chiara, Frangipane, Francesca, Anfossi, Maria, Gallo, Maura, Conidi, Maria Elena, Vasso, Franca, Colao, Rosanna, Puccio, Gianfranco, Curcio, Sabrina A.M, Mirabelli, Maria, Clodomiro, Alessandra, Di Lorenzo, Raffaele, Smirne, Nicoletta, Maletta, Raffaele, Bruni, Amalia C

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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal dementia and GRN mutations: a genome-wide association study by Pottier, Cyril, Zhou, Xiaolai, Perkerson, Ralph B., Baker, Matt, Jenkins, Gregory D., Serie, Daniel J., Ghidoni, Roberta, Benussi, Luisa, Binetti, Giuliano, de Munain, Adolfo López, Zulaica, Miren, Moreno, Fermin, Le Ber, Isabelle, Pasquier, Florence, Hannequin, Didier, Sánchez-Valle, Raquel, Antonell, Anna, Lladó, Albert, Parsons, Tammee M., Finch, NiCole A., Finger, Elizabeth C., Lippa, Carol F., Huey, Edward D., Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Rissman, Robert A., Slawek, Jaroslaw, Sitek, Emilia, Johannsen, Peter, Nielsen, Jørgen E., Ren, Yingxue, van Blitterswijk, Marka, DeJesus-Hernandez, Mariely, Christopher, Elizabeth, Murray, Melissa E., Bieniek, Kevin F., Evers, Bret M., Ferrari, Camilla, Rollinson, Sara, Richardson, Anna, Scarpini, Elio, Fumagalli, Giorgio G., Padovani, Alessandro, Hardy, John, Momeni, Parastoo, Ferrari, Raffaele, Frangipane, Francesca, Maletta, Raffaele, Anfossi, Maria, Gallo, Maura, Petrucelli, Leonard, Suh, EunRan, Lopez, Oscar L., Wong, Tsz H., van Rooij, Jeroen G. J., Seelaar, Harro, Mead, Simon, Caselli, Richard J., Reiman, Eric M., Sabbagh, Marwan Noel, Kjolby, Mads, Nykjaer, Anders, Karydas, Anna M., Boxer, Adam L., Grinberg, Lea T., Grafman, Jordan, Spina, Salvatore, Oblak, Adrian, Mesulam, M-Marsel, Weintraub, Sandra, Geula, Changiz, Hodges, John R., Piguet, Olivier, Brooks, William S., Irwin, David J., Trojanowski, John Q., Lee, Edward B., Josephs, Keith A., Parisi, Joseph E., Ertekin-Taner, Nilüfer, Knopman, David S., Nacmias, Benedetta, Piaceri, Irene, Bagnoli, Silvia, Sorbi, Sandro, Gearing, Marla, Glass, Jonathan, Beach, Thomas G., Black, Sandra E., Masellis, Mario, Rogaeva, Ekaterina, Vonsattel, Jean-Paul, Honig, Lawrence S., Kofler, Julia, Bruni, Amalia C., Snowden, Julie, Mann, David, Pickering-Brown, Stuart

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Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia by Bernardi, Livia, Tomaino, Carmine, Anfossi, Maria, Gallo, Maura, Geracitano, Silvana, Costanzo, Angela, Colao, Rosanna, Puccio, Gianfranco, Frangipane, Francesca, Curcio, Sabrina A.M, Mirabelli, Maria, Smirne, Nicoletta, Iapaolo, David, Maletta, Raffaele Giovanni, Bruni, Amalia C

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Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia by Anfossi, Maria, Vuono, Romina, Maletta, Raffaele, Virdee, Kanwar, Mirabelli, Maria, Colao, Rosanna, Puccio, Gianfranco, Bernardi, Livia, Frangipane, Francesca, Gallo, Maura, Geracitano, Silvana, Tomaino, Carmine, Curcio, Sabrina Anna Maria, Zannino, Giuseppa, Lamenza, Francesco, Duyckaerts, Charles, Spillantini, Maria Grazia, Losso, Maria Adele, Bruni, Amalia C

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Epidemiology and genetics of FTD: a door-to-door survey in Southern Italy by Bernardi, Livia, Frangipane, Francesca, Smirne, Nicoletta, Colao, Rosanna, Puccio, Gianfranco, Curcio, Sabrina AM, Mirabelli, Maria, Maletta, Raffaele, Anfossi, Maria, Gallo, Maura, Geracitano, Silvana, Conidi, Maria Elena, Di Lorenzo, Raffale, Clodomiro, Alessandra, Cupidi, Chiara, Marzano, Sandra, Comito, Francesco, Valenti, Vincenzo, Zirilli, Maria Angela, Ghani, Mahdi, Xi, Zhengrui, Sato, Christine, Moreno, Danielle, Borelli, Annelisa, Leone, Rosa Anna, St George-Hyslop, Peter, Rogaeva, Ekaterina, Bruni, Amalia C.

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Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism by Bernardi, L., Tomaino, C., Anfossi, M., Gallo, M., Geracitano, S., Puccio, G., Colao, R., Frangipane, F., Mirabelli, M., Smirne, N., Giovanni Maletta, R., Bruni, A. C.

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Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia by Gallo, Maura, Tomaino, Carmine, Puccio, Gianfranco, Frangipane, Francesca, Curcio, Sabrina A. M., Bernardi, Livia, Geracitano, Silvana, Anfossi, Maria, Mirabelli, Maria, Colao, Rosanna, Vasso, Franca, Smirne, Nicoletta, Maletta, Raffaele G., Bruni, Amalia Cecilia

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Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease by Tomaino, Carmine, Bernardi, Livia, Anfossi, Maria, Costanzo, Angela, Ferrise, Francesca, Gallo, Maura, Geracitano, Silvana, Maletta, Raffaele, Curcio, Sabrina A M, Mirabelli, Maria, Colao, Rosanna, Frangipane, Francesca, Puccio, Gianfranco, Calignano, Cinzia, Muraca, Maria Gabriella, Paonessa, Annamaria, Smirne, Nicoletta, Leotta, Attilio, Bruni, Amalia C

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Epidemiology of Frontotemporal dementia in southern Italy by Bruni, Amalia C, Frangipane, Francesca, Colao, Rosanna, Puccio, Gianfranco, Curcio, Sabrina A.M, Mirabelli, Maria, Maletta, Raffaele, Anfossi, Maria, Bernardi, Livia, Gallo, Maura, Geracitano, Silvana, Tomaino, Carmine, Muraca, Maria G, Clodomiro, Alessandra, Di Lorenzo, Raffaele, Comito, Francesco, Valenti, Vincenzo, Marzano, Sandra, Smirne, Nicoletta

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