Genetic Heterogeneity of Alzheimer’s Disease: Embracing Research Partnerships

por Nacmias, Benedetta, Bagnoli, Silvia, Piaceri, Irene, Sorbi, Sandro
Publicado en J Alzheimers Dis (2018)

Association Study of Genetic Variants in CDKN2A/CDKN2B Genes/Loci with Late-Onset Alzheimer's Disease

por Tedde, Andrea, Piaceri, Irene, Bagnoli, Silvia, Lucenteforte, Ersilia, Ueberham, Uwe, Arendt, Thomas, Sorbi, Sandro, Nacmias, Benedetta
Publicado 2011

Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference

por Sierant, Malgorzata, Paduszynska, Alina, Kazmierczak-Baranska, Julia, Nacmias, Benedetta, Sorbi, Sandro, Bagnoli, Silvia, Sochacka, Elzbieta, Nawrot, Barbara
Publicado 2011

A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer's Disease in Italian Caucasians

por Coppedè, Fabio, Tannorella, Pierpaola, Tognoni, Gloria, Bagnoli, Silvia, Bongioanni, Paolo, Nacmias, Benedetta, Siciliano, Gabriele, Sorbi, Sandro, Bonuccelli, Ubaldo, Migliore, Lucia
Publicado 2014

The Effect of CAG Repeats within the Non-Pathological Range in the HTT Gene on Cognitive Functions in Patients with Subjective Cognitive Decline and Mild Cognitive Impairment

por Bessi, Valentina, Mazzeo, Salvatore, Bagnoli, Silvia, Giacomucci, Giulia, Ingannato, Assunta, Ferrari, Camilla, Padiglioni, Sonia, Franchi, Virginia, Sorbi, Sandro, Nacmias, Benedetta
Publicado en Diagnostics (Basel) (2021)

Fat mass and obesity-associated gene (FTO) is associated to eating disorders susceptibility and moderates the expression of psychopathological traits

por Castellini, Giovanni, Franzago, Marica, Bagnoli, Silvia, Lelli, Lorenzo, Balsamo, Michela, Mancini, Milena, Nacmias, Benedetta, Ricca, Valdo, Sorbi, Sandro, Antonucci, Ivana, Stuppia, Liborio, Stanghellini, Giovanni
Publicado en PLoS One (2017)

Influence of ApoE Genotype and Clock T3111C Interaction with Cardiovascular Risk Factors on the Progression to Alzheimer’s Disease in Subjective Cognitive Decline and Mild Cognitiv...

por Bessi, Valentina, Balestrini, Juri, Bagnoli, Silvia, Mazzeo, Salvatore, Giacomucci, Giulia, Padiglioni, Sonia, Piaceri, Irene, Carraro, Marco, Ferrari, Camilla, Bracco, Laura, Sorbi, Sandro, Nacmias, Benedetta
Publicado en J Pers Med (2020)

Dual Effect of PER2 C111G Polymorphism on Cognitive Functions across Progression from Subjective Cognitive Decline to Mild Cognitive Impairment

por Mazzeo, Salvatore, Bessi, Valentina, Bagnoli, Silvia, Giacomucci, Giulia, Balestrini, Juri, Padiglioni, Sonia, Tomaiuolo, Giulia, Ingannato, Assunta, Ferrari, Camilla, Bracco, Laura, Sorbi, Sandro, Nacmias, Benedetta
Publicado en Diagnostics (Basel) (2021)

Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases

por Gragnani, Laura, Fognani, Elisa, De Re, Valli, Libra, Massimo, Garozzo, Adriana, Caini, Patrizio, Cerretelli, Guia, Giovannelli, Andrea, Lorini, Serena, Monti, Monica, Bagnoli, Silvia, Piaceri, Irene, Zignego, Anna Linda
Publicado en Oncotarget (2017)

Matching Clinical Diagnosis and Amyloid Biomarkers in Alzheimer’s Disease and Frontotemporal Dementia

por Giacomucci, Giulia, Mazzeo, Salvatore, Bagnoli, Silvia, Casini, Matteo, Padiglioni, Sonia, Polito, Cristina, Berti, Valentina, Balestrini, Juri, Ferrari, Camilla, Lombardi, Gemma, Ingannato, Assunta, Sorbi, Sandro, Nacmias, Benedetta, Bessi, Valentina
Publicado en J Pers Med (2021)

The Brain-Derived Neurotrophic Factor Val66Met Polymorphism Can Protect Against Cognitive Impairment in Multiple Sclerosis

por Portaccio, Emilio, Bellinvia, Angelo, Prestipino, Elio, Nacmias, Benedetta, Bagnoli, Silvia, Razzolini, Lorenzo, Pastò, Luisa, Niccolai, Claudia, Goretti, Benedetta, Fonderico, Mattia, Zimatore, Giovanni Bosco, Losignore, Nunzia Alessandra, Sorbi, Sandro, Amato, Maria Pia
Publicado en Front Neurol (2021)

Monomeric ß-amyloid interacts with type-1 insulin-like growth factor receptors to provide energy supply to neurons

por Giuffrida, Maria L., Tomasello, Marianna F., Pandini, Giuseppe, Caraci, Filippo, Battaglia, Giuseppe, Busceti, Carla, Di Pietro, Paola, Pappalardo, Giuseppe, Attanasio, Francesco, Chiechio, Santina, Bagnoli, Silvia, Nacmias, Benedetta, Sorbi, Sandro, Vigneri, Riccardo, Rizzarelli, Enrico, Nicoletti, Ferdinando, Copani, Agata
Publicado en Front Cell Neurosci (2015)

Human iPSC-Derived Hippocampal Spheroids: An Innovative Tool for Stratifying Alzheimer Disease Patient-Specific Cellular Phenotypes and Developing Therapies

por Pomeshchik, Yuriy, Klementieva, Oxana, Gil, Jeovanis, Martinsson, Isak, Hansen, Marita Grønning, de Vries, Tessa, Sancho-Balsells, Anna, Russ, Kaspar, Savchenko, Ekaterina, Collin, Anna, Vaz, Ana Rita, Bagnoli, Silvia, Nacmias, Benedetta, Rampon, Claire, Sorbi, Sandro, Brites, Dora, Marko-Varga, György, Kokaia, Zaal, Rezeli, Melinda, Gouras, Gunnar K., Roybon, Laurent
Publicado en Stem Cell Reports (2020)

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia

por Ferrari, Raffaele, Grassi, Mario, Graziano, Francesca, Palluzzi, Fernando, Archetti, Silvana, Bonomi, Elisa, Bruni, Amalia C., Maletta, Raffaele G., Bernardi, Livia, Cupidi, Chiara, Colao, Rosanna, Rainero, Innocenzo, Rubino, Elisa, Pinessi, Lorenzo, Galimberti, Daniela, Scarpini, Elio, Serpente, Maria, Nacmias, Benedetta, Piaceri, Irene, Bagnoli, Silvia, Rossi, Giacomina, Giaccone, Giorgio, Tagliavini, Fabrizio, Benussi, Luisa, Binetti, Giuliano, Ghidoni, Roberta, Singleton, Andrew, Hardy, John, Momeni, Parastoo, Padovani, Alessandro, Borroni, Barbara
Publicado en J Alzheimers Dis (2017)

Predictors of Function, Activity, and Participation of Stroke Patients Undergoing Intensive Rehabilitation: A Multicenter Prospective Observational Study Protocol

por Hakiki, Bahia, Paperini, Anita, Castagnoli, Chiara, Hochleitner, Ines, Verdesca, Sonia, Grippo, Antonello, Scarpino, Maenia, Maiorelli, Antonio, Mosca, Irene Eleonora, Gemignani, Paola, Borsotti, Marco, Gabrielli, Maria Assunta, Salvadori, Emilia, Poggesi, Anna, Lucidi, Giulia, Falsini, Catiuscia, Gentilini, Monica, Martini, Monica, Luisi, Maria Luisa Eliana, Biffi, Barbara, Mainardi, Paolo, Barretta, Teresa, Pancani, Silvia, Mannini, Andrea, Campagnini, Silvia, Bagnoli, Silvia, Ingannato, Assunta, Nacmias, Benedetta, Macchi, Claudio, Carrozza, Maria Chiara, Cecchi, Francesca
Publicado en Front Neurol (2021)

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

por Ferrari, Raffaele, Grassi, Mario, Salvi, Erika, Borroni, Barbara, Palluzzi, Fernando, Pepe, Daniele, D'Avila, Francesca, Padovani, Alessandro, Archetti, Silvana, Rainero, Innocenzo, Rubino, Elisa, Pinessi, Lorenzo, Benussi, Luisa, Binetti, Giuliano, Ghidoni, Roberta, Galimberti, Daniela, Scarpini, Elio, Serpente, Maria, Rossi, Giacomina, Giaccone, Giorgio, Tagliavini, Fabrizio, Nacmias, Benedetta, Piaceri, Irene, Bagnoli, Silvia, Bruni, Amalia C., Maletta, Raffaele G., Bernardi, Livia, Postiglione, Alfredo, Milan, Graziella, Franceschi, Massimo, Puca, Annibale A., Novelli, Valeria, Barlassina, Cristina, Glorioso, Nicola, Manunta, Paolo, Singleton, Andrew, Cusi, Daniele, Hardy, John, Momeni, Parastoo
Publicado en Neurobiol Aging (2015)

A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

por van der Zee, Julie, Gijselinck, Ilse, Dillen, Lubina, Van Langenhove, Tim, Theuns, Jessie, Engelborghs, Sebastiaan, Philtjens, Stéphanie, Vandenbulcke, Mathieu, Sleegers, Kristel, Sieben, Anne, Bäumer, Veerle, Maes, Githa, Corsmit, Ellen, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl-Schmid, Janine, de Mendonça, Alexandre, Miltenberger-Miltenyi, Gabriel, Pereira, Sónia, Pimentel, José, Nacmias, Benedetta, Bagnoli, Silvia, Sorbi, Sandro, Graff, Caroline, Chiang, Huei-Hsin, Westerlund, Marie, Sanchez-Valle, Raquel, Llado, Albert, Gelpi, Ellen, Santana, Isabel, Almeida, Maria Rosário, Santiago, Beatriz, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, Synofzik, Matthis, Maetzler, Walter, vom Hagen, Jennifer Müller, Schöls, Ludger, Heneka, Michael T, Jessen, Frank, Matej, Radoslav, Parobkova, Eva, Kovacs, Gabor G, Ströbel, Thomas, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Danek, Adrian, Arzberger, Thomas, Fabrizi, Gian Maria, Testi, Silvia, Salmon, Eric, Santens, Patrick, Martin, Jean-Jacques, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Van Broeckhoven, Christine
Publicado 2013

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

por van der Zee, Julie, Van Langenhove, Tim, Kovacs, Gabor G., Dillen, Lubina, Deschamps, William, Engelborghs, Sebastiaan, Matěj, Radoslav, Vandenbulcke, Mathieu, Sieben, Anne, Dermaut, Bart, Smets, Katrien, Van Damme, Philip, Merlin, Céline, Laureys, Annelies, Van Den Broeck, Marleen, Mattheijssens, Maria, Peeters, Karin, Benussi, Luisa, Binetti, Giuliano, Ghidoni, Roberta, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Pastor, Pau, Razquin, Cristina, Ortega-Cubero, Sara, Hernández, Isabel, Boada, Mercè, Ruiz, Agustín, de Mendonça, Alexandre, Miltenberger-Miltényi, Gabriel, do Couto, Frederico Simões, Sorbi, Sandro, Nacmias, Benedetta, Bagnoli, Silvia, Graff, Caroline, Chiang, Huei-Hsin, Thonberg, Håkan, Perneczky, Robert, Diehl-Schmid, Janine, Alexopoulos, Panagiotis, Frisoni, Giovanni B., Bonvicini, Christian, Synofzik, Matthis, Maetzler, Walter, vom Hagen, Jennifer Müller, Schöls, Ludger, Haack, Tobias B., Strom, Tim M., Prokisch, Holger, Dols-Icardo, Oriol, Clarimón, Jordi, Lleó, Alberto, Santana, Isabel, Almeida, Maria Rosário, Santiago, Beatriz, Heneka, Michael T., Jessen, Frank, Ramirez, Alfredo, Sanchez-Valle, Raquel, Llado, Albert, Gelpi, Ellen, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Parobkova, Eva, Fabrizi, Gian Maria, Testi, Silvia, Salmon, Eric, Ströbel, Thomas, Santens, Patrick, Robberecht, Wim, De Jonghe, Peter, Martin, Jean-Jacques, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Sleegers, Kristel, Van Broeckhoven, Christine
Publicado 2014

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

por van der Zee, Julie, Gijselinck, Ilse, Van Mossevelde, Sara, Perrone, Federica, Dillen, Lubina, Heeman, Bavo, Bäumer, Veerle, Engelborghs, Sebastiaan, De Bleecker, Jan, Baets, Jonathan, Gelpi, Ellen, Rojas‐García, Ricardo, Clarimón, Jordi, Lleó, Alberto, Diehl‐Schmid, Janine, Alexopoulos, Panagiotis, Perneczky, Robert, Synofzik, Matthis, Just, Jennifer, Schöls, Ludger, Graff, Caroline, Thonberg, Håkan, Borroni, Barbara, Padovani, Alessandro, Jordanova, Albena, Sarafov, Stayko, Tournev, Ivailo, de Mendonça, Alexandre, Miltenberger‐Miltényi, Gabriel, Simões do Couto, Frederico, Ramirez, Alfredo, Jessen, Frank, Heneka, Michael T., Gómez‐Tortosa, Estrella, Danek, Adrian, Cras, Patrick, Vandenberghe, Rik, De Jonghe, Peter, De Deyn, Peter P., Sleegers, Kristel, Cruts, Marc, Van Broeckhoven, Christine, Goeman, Johan, Nuytten, Dirk, Smets, Katrien, Robberecht, Wim, Damme, Philip Van, Bleecker, Jan De, Santens, Patrick, Dermaut, Bart, Versijpt, Jan, Michotte, Alex, Ivanoiu, Adrian, Deryck, Olivier, Bergmans, Bruno, Delbeck, Jean, Bruyland, Marc, Willems, Christiana, Salmon, Eric, Pastor, Pau, Ortega‐Cubero, Sara, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Hernández, Isabel, Boada, Mercè, Ruiz, Agustín, Sorbi, Sandro, Nacmias, Benedetta, Bagnoli, Silvia, Sorbi, Sandro, Sanchez‐Valle, Raquel, Llado, Albert, Santana, Isabel, Rosário Almeida, Maria, Frisoni, Giovanni B, Maetzler, Walter, Matej, Radoslav, Fraidakis, Matthew J., Kovacs, Gabor G., Fabrizi, Gian Maria, Testi, Silvia
Publicado en Hum Mutat (2017)

C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

por Costa, Beatrice, Manzoni, Claudia, Bernal-Quiros, Manuel, Kia, Demis A., Aguilar, Miquel, Alvarez, Ignacio, Alvarez, Victoria, Andreassen, Ole, Anfossi, Maria, Bagnoli, Silvia, Benussi, Luisa, Bernardi, Livia, Binetti, Giuliano, Blackburn, Daniel, Boada, Mercè, Borroni, Barbara, Bowns, Lucy, Bråthen, Geir, Bruni, Amalia C., Chiang, Huei-Hsin, Clarimon, Jordi, Colville, Shuna, Conidi, Maria E., Cope, Tom E., Cruchaga, Carlos, Cupidi, Chiara, Di Battista, Maria Elena, Diehl-Schmid, Janine, Diez-Fairen, Monica, Dols-Icardo, Oriol, Durante, Elisabetta, Flisar, Dušan, Frangipane, Francesca, Galimberti, Daniela, Gallo, Maura, Gallucci, Maurizio, Ghidoni, Roberta, Graff, Caroline, Grafman, Jordan H., Grossman, Murray, Hardy, John, Hernández, Isabel, Holloway, Guy J.T., Huey, Edward D., Illán-Gala, Ignacio, Karydas, Anna, Khoshnood, Behzad, Kramberger, Milica G., Kristiansen, Mark, Lewis, Patrick A., Lleó, Alberto, Madhan, Gaganjit K., Maletta, Raffaele, Maver, Aleš, Menendez-Gonzalez, Manuel, Milan, Graziella, Miller, Bruce, Mol, Merel O., Momeni, Parastoo, Moreno-Grau, Sonia, Morris, Chris M., Nacmias, Benedetta, Nilsson, Christer, Novelli, Valeria, Öijerstedt, Linn, Padovani, Alessandro, Pal, Suvankar, Panchbhaya, Yasmin, Pastor, Pau, Peterlin, Borut, Piaceri, Irene, Pickering-Brown, Stuart, Pijnenburg, Yolande A.L., Puca, Annibale A., Rainero, Innocenzo, Rendina, Antonella, Richardson, Anna M.T., Rogaeva, Ekaterina, Rogelj, Boris, Rollinson, Sara, Rossi, Giacomina, Rossmeier, Carola, Rowe, James B., Rubino, Elisa, Ruiz, Agustín, Sanchez-Valle, Raquel, Sando, Sigrid B., Santillo, Alexander F., Saxon, Jennifer, Scarpini, Elio, Serpente, Maria, Smirne, Nicoletta, Sorbi, Sandro, Suh, EunRan, Tagliavini, Fabrizio, Thompson, Jennifer C., Trojanowski, John Q., Van Deerlin, Vivianna M., Van der Zee, Julie, Van Broeckhoven, Christine, van Rooij, Jeroen, Van Swieten, John C., Veronesi, Arianna, Vitale, Emilia, Waldö, Maria L., Woodward, Cathy, Yokoyama, Jennifer, Escott-Price, Valentina, Polke, James M., Ferrari, Raffaele
Publicado en Neurology (2020)