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 by 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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EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia by 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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Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer’s disease: an 11‐year follow‐up study by 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 by 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 by 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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Incomplete penetrance in familial Alzheimer’s disease with PSEN1 Ala260Gly mutation by 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 by 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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Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis by 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 by 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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Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease by 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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Metabolic interaction between ApoE genotype and onset age in Alzheimer’s disease: implications for brain reserve by 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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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores by Tesi, Niccolo, Jansen, Iris E, Stringa, Najada, Montrreal, Laura, Antonell, Anna, Franco-Macías, Emilio, Menéndez-González, Manuel, Royo, Jose Luís, Lage, Carmen, Naj, Adam C, Lemstra, Afina W, Benaque, Alba, Benussi, Alberto, Rábano, Alberto, de Mendonça, Alexandre, Arias Pastor, Alfonso, Kok, Almar A L, Espinosa, Ana, Corma-Gómez, Anaïs, Sanabria, Ángela, Haapasalo, Annakaisa, Kinhult Ståhlbom, Anne, Hartmann, Annette M, Spottke, Annika, Borroni, Barbara, Arosio, Beatrice, Nacmias, Benedetta, Nordestgaard, Børge G, Martínez Rodríguez, Carmen, Dufouil, Carole, Holmes, Clive, Aarsland, Dag, Rujescu, Dan, Alcolea, Daniel, Grünblatt, Edna, Dardiotis, Efthimios, Scarpini, Elio, Conti, Elisa, Gelpi, Ellen, Boerwinkle, Eric, Sanchez-Garcia, Florentino, Chêne, Geneviève, Rossi, Giacomina, Spalletta, Gianfranco, Binetti, Giuliano, Bailly, Henri, Zetterberg, Henrik, Appollonio, Ildebrando, Giegling, Ina, Rosas Allende, Irene, Van Dongen, Jasper, Vidal, Jean-Sebastien, Thomassen, Jesper Qvist, Fortea, Juan, Morgan, Kevin, Weinhold, Leonie, Farrer, Lindsay A, Wang, Li-San, Parnetti, Lucilla, Ikram, M Arfan, Tsolaki, Magda, Hulsman, Marc, Pericak-Vance, Margaret A, Esiri, Margaret, Dalmasso, Maria Carolina, Arcaro, Marina, Dichgans, Martin, Ingelsson, Martin, Scherer, Martin, Vyhnalek, Martin, Ewers, Michael, Wagner, Michael, Hiltunen, Mikko, Fornage, Myriam, Seidu, Nazib M, Scarmeas, Nikolaos, Skrobot, Olivia Anna, Lerch, Ondrej, Dionigi Rossi, Paolo, Yang, Qiong, Mayeux, Richard, Vandenberghe, Rik, Kern, Silke, Fostinelli, Silvia, Grimmer, Timo, Jian, Xueqiu, Sánchez-Juan, Pascual, Pastor, Pau, Pérez-Tur, Jordi, Piñol-Ripoll, Gerard, García-Alberca, Jose María, Álvarez, Victoria, Medina, Miguel, Schellenberg, Gerard D, Mather, Karen A, Serrano-Ríos, Manuel, Huisman, Martijn, Clarimón, Jordi, Boada, Mercè, Ramirez, Alfredo

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Alzheimer’s Disease: Role of Size and Location of White Matter Changes in Determining Cognitive Deficits by 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 by 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 by Portaccio, E., Zipoli, V., Goretti, B., Hakiki, B., Nacmias, B., Siracusa, G., Sorbi, S., Amato, M. P.

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Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant by Sherrington, R., Froelich, S., Sorbi, S., Campion, D., Chi, H., Rogaeva, E. A., Levesque, G., Rogaev, E. I., Lin, C., Liang, Y., Ikeda, M., Mar, L., Brice, A., Agid, Y., Percy, M.E., Clerget-Darpoux, F., Piacentini, S., Marcon, G., Nacmias, B., Amaducci, L., Frebourg, T., Lannfelt, L., Rommens, J. M., St George-Hyslop, P. H.

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P02-64 Glucocorticoid receptor gene polymorphisms in Italian patients with anorexia and bulimia nervosa by Nacmias, B, Cellini, E, Ricca, V, Castellini, G, Tedde, A, Bagnoli, S, Sorbi, S

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Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa by Gabrovsek, M., Brecelj-Anderluh, M., Bellodi, L., Cellini, E., Di Bella, D., Estivill, X., Fernandez-Aranda, F., Freeman, B., Geller, F., Gratacos, M., Haigh, R., Hebebrand, J., Hinney, A., Holliday, J., Hu, X., Karwautz, A., Nacmias, B., Ribases, M., Remschmidt, H., Komel, R., Sorbi, S., Tomori, M., Treasure, J., Wagner, G., Zhao, J., Collier, D.A.

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Immunoproteasome and LMP2 polymorphism in aged and Alzheimer's disease brains by Mishto, Michele, Bellavista, Elena, Santoro, Aurelia, Stolzing, Alexandra, Ligorio, Claudia, Nacmias, Benedetta, Spazzafumo, Liana, Chiappelli, Martina, Licastro, Federico, Sorbi, Sandro, Pession, Annalisa, Ohm, Thomas, Grune, Tilman, Franceschi, Claudio

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Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies by Baker, Jessica H., Gordon, Scott, Mattheisen, Manuel, Ripke, Stephan, Yao, Shuyang, Adan, Roger A.H., Boraska Perica, Vesna, Cichon, Sven, Cone, Roger D., DeSocio, Janiece E., Docampo, Elisa, Escaramís, Geòrgia, Esko, Tõnu, Favaro, Angela, Fischer, Krista, Föcker, Manuel, Gonidakis, Fragiskos, Guillaume, Sébastien, Guo, Yiran, Hakonarson, Hakon, Hebebrand, Johannes, Helder, Sietske G., Herms, Stefan, Herzog, Wolfgang, Huckins, Laura M., Hudson, James I., Karhunen, Leila, Karwautz, Andreas, Kennedy, James L., Klump, Kelly L., Le Hellard, Stephanie, Lin, Bochao Danae, Meulenbelt, Ingrid, Mitchell, Karen, Monteleone, Alessio Maria, Nacmias, Benedetta, Ophoff, Roel A., Padyukov, Leonid, Palotie, Aarno, Pinto, Dalila, Ricca, Valdo, Ritschel, Franziska, Santonastaso, Paolo, Scherag, André, Seitz, Jochen, Slachtova, Lenka, Slof‐Op't Landt, Margarita C.T., Slopien, Agnieszka, Szatkiewicz, Jin P., Wagner, Gudrun, Walton, Esther, Widen, Elisabeth, Crawford, Steven, Johnson, Craig, Mitchell, James, Whiteman, David C., Birgegård, Andreas, Norring, Claes, Polimanti, Renato, Clarke, Toni‐Kim, Degenhardt, Franziska, Docherty, Anna R., Foo, Jerome C., Fox, Louis, Frank, Josef, Hack, Laura M., Lahti, Jari, Lahti‐Pulkkinen, Marius, Loukola, Anu, Palviainen, Teemu, Saccone, Nancy L., Salvatore, Jessica E., Strohmaier, Jana, Wang, Jen‐Chyong, Wills, Amanda G., Boardman, Jason D., Choi, Doo‐Sup, Culverhouse, Robert C., Dahmen, Norbert, Domingue, Benjamin W., Gäebel, Wolfgang, Ising, Marcus, Keyes, Margaret, Lucae, Susanne, Nurnberger, John I., Preuss, Ulrich, Bierut, Laura J., Brown, Sandra A., Costello, E. Jane, Eriksson, Johan G., Foroud, Tatiana M., Hesselbrock, Victor, Johnson, Eric O., Stallings, Michael C., Vrieze, Scott, Wade, Tracey D., Heath, Andrew C., Martin, Nicholas G., Breen, Gerome, Bulik, Cynthia M.

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