EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia von Sorbi, S., Hort, J., Erkinjuntti, T., Fladby, T., Gainotti, G., Gurvit, H., Nacmias, B., Pasquier, F., Popescu, B. O., Rektorova, I., Religa, D., Rusina, R., Rossor, M., Schmidt, R., Stefanova, E., Warren, J. D., Scheltens, P.

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A proof-of-concept study applying machine learning methods to putative risk factors for eating disorders: results from the multi-centre European project on healthy eating von Krug, I., Linardon, J., Greenwood, C., Youssef, G., Treasure, J., Fernandez-Aranda, F., Karwautz, A., Wagner, G., Collier, D., Anderluh, M., Tchanturia, K., Ricca, V., Sorbi, S., Nacmias, B., Bellodi, L., Fuller-Tyszkiewicz, M.

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Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer’s disease: an 11‐year follow‐up study von Mazzeo, S., Padiglioni, S., Bagnoli, S., Carraro, M., Piaceri, I., Bracco, L., Nacmias, B., Sorbi, S., Bessi, V.

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Long-term use of pharmacological treatment in Alzheimer’s disease: a retrospective cohort study in real-world clinical practice von Lombardi, G, Lombardi, N, Bettiol, A, Crescioli, G, Ferrari, C, Lucidi, G, Polito, C, Berti, V, Bessi, V, Bagnoli, S, Nacmias, B, Vannacci, A, Sorbi, S

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PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment: a 10‐year follow‐up study von Bessi, V., Giacomucci, G., Mazzeo, S., Bagnoli, S., Padiglioni, S., Balestrini, J., Tomaiuolo, G., Piaceri, I., Carraro, M., Bracco, L., Sorbi, S., Nacmias, B.

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MCI conversion to dementia and the APOE genotype: A prediction study with FDG-PET von MOSCONI, L, PERANI, D, BORRONI, B, FRANCESCHI, M, BRACCO, L, PUPI, A, SORBI, S, HERHOLZ, K, NACMIAS, B, HOLTHOFF, V, SALMON, E, BARON, J.-C, DE CRISTOFARO, M. T. R, PADOVANI, A

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Incomplete penetrance in familial Alzheimer’s disease with PSEN1 Ala260Gly mutation von Piaceri, I., Chiari, A., Galli, C., Bagnoli, S., Ferrari, C., Saavedra, S. Trujillo, Molinari, M. A., Vinceti, G., Sorbi, S., Nacmias, B.

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Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene von Rogaev, E. I, Sherrington, R, Rogaeva, E. A, Levesque, G, Ikeda, M, Liang, Y, Chi, H, Lin, C, Holman, K, Tsuda, T, Mar, L, Sorbi, S, Nacmias, B, Piacentini, S, Amaducci, L, Chumakov, I, Cohen, D, Lannfelt, L, Fraser, P. E, Rommens, J. M, George-Hyslop, P. H. St

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The different apoptotic potential of the p53 codon 72 alleles increases with age and modulates in vivo ischaemia-induced cell death von Bonafé, M, Salvioli, S, Barbi, C, Trapassi, C, Tocco, F, Storci, G, Invidia, L, Vannini, I, Rossi, M, Marzi, E, Mishto, M, Capri, M, Olivieri, F, Antonicelli, R, Memo, M, Uberti, D, Nacmias, B, Sorbi, S, Monti, D, Franceschi, C

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Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis von Piaceri, I, Del Mastio, M, Tedde, A, Bagnoli, S, Latorraca, S, Massaro, F, Paganini, M, Corrado, A, Sorbi, S, Nacmias, B

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Early structural changes in individuals at risk of familial Alzheimer’s disease: a volumetry and magnetization transfer MR imaging study von Ginestroni, A., Battaglini, M., Della Nave, R., Moretti, M., Tessa, C., Giannelli, M., Caffarra, P., Nacmias, B., Bessi, V., Sorbi, S., Bracco, L., De Stefano, N., Mascalchi, M.

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Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa von Hübel, Christopher, Bryois, Julien, Hinney, Anke, Leppä, Virpi M., Mattheisen, Manuel, Medland, Sarah E., Giusti-Rodríguez, Paola, Alfredsson, Lars, Berrettini, Wade H., Boni, Claudette, Burghardt, Roland, Cichon, Sven, Cone, Roger D., Courtet, Philippe, Crowley, James J., Davis, Oliver S. P., de Zwaan, Martina, Dikeos, Dimitris, Dina, Christian, Duncan, Laramie E., Egberts, Karin, Estivill, Xavier, Favaro, Angela, Fernández-Aranda, Fernando, Fichter, Manfred M., Forstner, Andreas J., Forzan, Monica, Franklin, Christopher S., Giegling, Ina, Guillaume, Sébastien, Hakonarson, Hakon, Hatzikotoulas, Konstantinos, Hauser, Joanna, Helder, Sietske G., Herpertz-Dahlmann, Beate, Herzog, Wolfgang, Huckins, Laura M., Hudson, James I., Inoko, Hidetoshi, Janout, Vladimir, Julià, Antonio, Kalsi, Gursharan, Kaminská, Deborah, Karhunen, Leila, Keski-Rahkonen, Anna, Kim, Youl-Ri, Knudsen, Gun Peggy S., La Via, Maria C., Levitan, Robert D., Lin, Bochao Danae, Luykx, Jurjen, Marsal, Sara, Marshall, Christian R., McDevitt, Sara, McGuffin, Peter, Metspalu, Andres, Monteleone, Alessio Maria, Monteleone, Palmiero, Munn-Chernoff, Melissa A., Navratilova, Marie, O’Toole, Julie K., Palotie, Aarno, Raevuori, Anu, Ramoz, Nicolas, Reichborn-Kjennerud, Ted, Ritschel, Franziska, Roberts, Marion, Rotondo, Alessandro, Rujescu, Dan, Rybakowski, Filip, Santonastaso, Paolo, Scherer, Stephen W., Schmidt, Ulrike, Schosser, Alexandra, Slagboom, P. Eline, Sorbi, Sandro, Szatkiewicz, Jin P., Tenconi, Elena, Tortorella, Alfonso, Treasure, Janet, Tziouvas, Konstantinos, van Elburg, Annemarie A., van Furth, Eric F., Zipfel, Stephan, Bergen, Andrew W., Boden, Joseph M., Johnson, Craig, Kaye, Walter H., Mitchell, James E., Olsen, Catherine M., Woodside, D. Blake, Stuber, Garret D., Gordon, Scott, Henders, Anjali K., Juréus, Anders, Petersen, Liselotte, Wade, Tracey D., Landén, Mikael, Sullivan, Patrick F., Breen, Gerome

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Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease von Bryois, Julien, Skene, Nathan G., Hansen, Thomas Folkmann, Kogelman, Lisette J. A., Watson, Hunna J., Liu, Zijing, Brueggeman, Leo, Breen, Gerome, Bulik, Cynthia M., Arenas, Ernest, Hjerling-Leffler, Jens, Sullivan, Patrick F.

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Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease von CARRIERI, Giuseppina, BONAFE, Massimiliano, FERACO, Emidio, ANDREEV, Kirill F, YASHIN, Anatoli I, FRANCESCHI, Claudio, DE BENEDICTIS, Giovanna, DE LUCA, Maria, ROSE, Giuseppina, VARCASIA, Ottavia, BRUNI, Amalia, MALETTA, Raffaele, NACMIAS, Benedetta, SORBI, Sandro, CORSONELLO, Francesco

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Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores von de Rojas, Itziar, Tesi, Niccolo, Zettergren, Anna, Montrreal, Laura, Antonell, Anna, Bis, Joshua C., González-Perez, Antonio, Calero, Miguel, Blesa, Rafael, Sotolongo-Grau, Oscar, Benaque, Alba, Benussi, Alberto, de Mendonça, Alexandre, Arias Pastor, Alfonso, Espinosa, Ana, Sanabria, Ángela, DeStefano, Anita L., Schneider, Anja, Haapasalo, Annakaisa, Tybjærg-Hansen, Anne, Hartmann, Annette M., Spottke, Annika, Corbatón-Anchuelo, Arturo, Arosio, Beatrice, Nacmias, Benedetta, Kunkle, Brian W., Charbonnier, Camille, Martínez Rodríguez, Carmen, Reynolds, Chandra A., Fenoglio, Chiara, Van Broeckhoven, Christine, Clark, Christopher, Buiza-Rueda, Dolores, Alcolea, Daniel, Grünblatt, Edna, Dardiotis, Efthimios, Conti, Elisa, Boerwinkle, Eric, Ferri, Evelyn, Pasquier, Florence, Mangialasche, Francesca, Hadjigeorgiou, Georgios, Spalletta, Gianfranco, Soininen, Hilkka, Rainero, Innocenzo, Hort, Jakub, Kornhuber, Johannes, Pineda, Juan A., Fortea, Juan, Popp, Julius, Buerger, Katharina, Molina-Porcel, Laura, Wang, Li-San, Farotti, Lucia, Tsolaki, Magda, Rosende-Roca, Maitée, Hulsman, Marc, Spallazzi, Marco, Bernal Sánchez-Arjona, María, Dalmasso, Maria Carolina, Fernández-Fuertes, Marta, Herrmann, Martin J., Vyhnalek, Martin, Yannakoulia, Mary, Schmid, Matthias, Armstrong, Nicola J., Skrobot, Olivia Anna, Quenez, Olivier, Bossù, Paola, Caffarra, Paolo, Dionigi Rossi, Paolo, Sakka, Paraskevi, Riederer, Peter, Kalaria, Rajesh N., Mayeux, Richard, Vandenberghe, Rik, Sorbi, Sandro, Hägg, Sara, Engelborghs, Sebastiaan, Helisalmi, Seppo, Kern, Silke, Boschi, Silvia, Fostinelli, Silvia, Gil, Silvia, Ciccone, Simona, Djurovic, Srdjan, Riedel-Heller, Steffi, Kuulasmaa, Teemu, del Ser, Teodoro, Ngandu, Tiia, García-Alberca, Jose María, Lleó, Alberto, Real, Luis M., Mir, Pablo, Scheltens, Philip, Holstege, Henne, Amouyel, Philippe, Blennow, Kaj, Andreassen, Ole A., Posthuma, Danielle

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Metabolic interaction between ApoE genotype and onset age in Alzheimer’s disease: implications for brain reserve von Mosconi, L, Herholz, K, Prohovnik, I, Nacmias, B, De Cristofaro, M T R, Fayyaz, M, Bracco, L, Sorbi, S, Pupi, A

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Alzheimer’s Disease: Role of Size and Location of White Matter Changes in Determining Cognitive Deficits von Bracco, L., Piccini, C., Moretti, M., Mascalchi, M., Sforza, A., Nacmias, B., Cellini, E., Bagnoli, S., Sorbi, S.

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Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease von Poleggi, A., Bizzarro, A., Acciarri, A., Antuono, P., Bagnoli, S., Cellini, E., Forno, G. Dal, Giannattasio, C., Lauria, A., Matera, M. G., Nacmias, B., Puopolo, M., Seripa, D., Sorbi, S., Wekstein, D. R., Pocchiari, M., Masullo, C.

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ApolipoproteinE epsilon 4 allele is not associated with disease course and severity in multiple sclerosis von Portaccio, E., Zipoli, V., Goretti, B., Hakiki, B., Nacmias, B., Siracusa, G., Sorbi, S., Amato, M. P.

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APOE and Alzheimer disease: a major gene with semi-dominant inheritance von Genin, E, Hannequin, D, Wallon, D, Sleegers, K, Hiltunen, M, Combarros, O, Bullido, M J, Engelborghs, S, De Deyn, P, Berr, C, Pasquier, F, Dubois, B, Tognoni, G, Fiévet, N, Brouwers, N, Bettens, K, Arosio, B, Coto, E, Del Zompo, M, Mateo, I, Epelbaum, J, Frank-Garcia, A, Helisalmi, S, Porcellini, E, Pilotto, A, Forti, P, Ferri, R, Scarpini, E, Siciliano, G, Solfrizzi, V, Sorbi, S, Spalletta, G, Valdivieso, F, Vepsäläinen, S, Alvarez, V, Bosco, P, Mancuso, M, Panza, F, Nacmias, B, Bossù, P, Hanon, O, Piccardi, P, Annoni, G, Seripa, D, Galimberti, D, Licastro, F, Soininen, H, Dartigues, J-F, Kamboh, M I, Van Broeckhoven, C, Lambert, J C, Amouyel, P, Campion, D

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