SORBI, SANDRO
SORBI, SANDRO
Neuroscienze, Psicologia, Area del Farmaco e Salute del Bambino (NEUROFARBA)
"Alpha2 macroglobulin and Alzheimer's disease"
1999 ROGAEVA E.; S. SORBI; ST GEORGE-HYSLOP P.H.; FARRR L.A; PERICAK-VANCE M.A
"Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity"
1998 ROGAEVA E; PREMKUMAR S.; SONG Y.S.; S. SORBI; BRINDLE N
"stato dell'arte" della ricerca
2012 Sorbi S; Bagnoli S; Piaceri I; Ferrari C; Lombardi G; Nacmias B
5-HT2A promoter polymorphism in anorexia nervosa.
1998 S. Sorbi; B. Nacmias; A. Tedde; V. Ricca; B. Mezzani; C. M. Rotella
5-HT2A receptor gene polymorphism and eating disorders.
2002 Ricca V; Nacmias B; Cellini E; Di Bernardo M; Rotella CM; Sorbi S.
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa
1999 Nacmias B; Ricca V; Tedde A; Mezzani B; Rotella CM; Sorbi S.
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers
2018 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
A case of limbic encephalitis evolving into a frontotemporal dementia-like picture
2019 Lombardi G.; Mata S.; Berti V.; Padiglioni S.; Ginestroni A.; Piaceri I.; Bagnoli S.; Nacmias B.; De Cristofaro M.T.; Pupi A.; Sorbi S.
A comparison of unawareness in frontotemporal dementia and Alzheimer's disease.
2008 E. Salmon; D. Perani; F. Collette; D. Feyers; E. Kalbe; V. Holthoff; S. Sorbi; K. Herholz
A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia
2022 van der Ende, Emma L; Bron, Esther E; Poos, Jackie M; Jiskoot, Lize C; Panman, Jessica L; Papma, Janne M; Meeter, Lieke H; Dopper, Elise G P; Wilke, Carlo; Synofzik, Matthis; Heller, Carolin; Swift, Imogen J; Sogorb-Esteve, Aitana; Bouzigues, Arabella; Borroni, Barbara; Sanchez-Valle, Raquel; Moreno, Fermin; Graff, Caroline; Laforce, Robert; Galimberti, Daniela; Masellis, Mario; Tartaglia, Maria Carmela; Finger, Elizabeth; Vandenberghe, Rik; Rowe, James B; de Mendonça, Alexandre; Tagliavini, Fabrizio; Santana, Isabel; Ducharme, Simon; Butler, Christopher R; Gerhard, Alexander; Levin, Johannes; Danek, Adrian; Otto, Markus; Pijnenburg, Yolande A L; Sorbi, Sandro; Zetterberg, Henrik; Niessen, Wiro J; Rohrer, Jonathan D; Klein, Stefan; van Swieten, John C; Venkatraghavan, Vikram; Seelaar, Harro; Afonso, Sónia; Almeida, Maria Rosario; Anderl-Straub, Sarah; Andersson, Christin; Antonell, Anna; Archetti, Silvana; Arighi, Andrea; Balasa, Mircea; Barandiaran, Myriam; Bargalló, Nuria; Bartha, Robart; Bender, Benjamin; Benussi, Alberto; Benussi, Luisa; Bessi, Valentina; Binetti, Giuliano; Black, Sandra; Bocchetta, Martina; Borrego-Ecija, Sergi; Bras, Jose; Bruffaerts, Rose; Cañada, Marta; Cantoni, Valentina; Caroppo, Paola; Cash, David; Castelo-Branco, Miguel; Convery, Rhian; Cope, Thomas; Di Fede, Giuseppe; Díez, Alina; Duro, Diana; Fenoglio, Chiara; Ferrari, Camilla; Ferreira, Catarina B; Fox, Nick; Freedman, Morris; Fumagalli, Giorgio; Gabilondo, Alazne; Gasparotti, Roberto; Gauthier, Serge; Gazzina, Stefano; Giaccone, Giorgio; Gorostidi, Ana; Greaves, Caroline; Guerreiro, Rita; Hoegen, Tobias; Indakoetxea, Begoña; Jelic, Vesna; Karnath, Hans-Otto; Keren, Ron; Langheinrich, Tobias; Leitão, Maria João; Lladó, Albert; Lombardi, Gemma; Loosli, Sandra; Maruta, Carolina; Mead, Simon; Miltenberger, Gabriel; van Minkelen, Rick; Mitchell, Sara; Moore, Katrina; Nacmias, Benedetta; Nicholas, Jennifer; Öijerstedt, Linn; Olives, Jaume; Ourselin, Sebastien; Padovani, Alessandro; Peakman, Georgia; Pievani, Michela; Pijnenburg, Yolande; Polito, Cristina; Premi, Enrico; Prioni, Sara; Prix, Catharina; Rademakers, Rosa; Redaelli, Veronica; Rittman, Tim; Rogaeva, Ekaterina; Rosa-Neto, Pedro; Rossi, Giacomina; Rosser, Martin; Santiago, Beatriz; Scarpini, Elio; Schönecker, Sonja; Semler, Elisa; Shafei, Rachelle; Shoesmith, Christen; Tábuas-Pereira, Miguel; Tainta, Mikel; Taipa, Ricardo; Tang-Wai, David; Thomas, David L; Thompson, Paul; Thonberg, Hakan; Timberlake, Carolyn; Tiraboschi, Pietro; Todd, Emily; Van Damme, Philip; Vandenbulcke, Mathieu; Veldsman, Michele; Verdelho, Ana; Villanua, Jorge; Warren, Jason; Woollacott, Ione; Wlasich, Elisabeth; Zulaica, Miren
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.
2002 Elena Cellini; Silvia Piacentini; Benedetta Nacmias; Paolo Forleo; Andrea Tedde; Silvia Bagnoli; Monica Ciantelli; Sandro Sorbi
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.
2014 Fogh, I; Ratti, A; Gelleram, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, L; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, FL; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, AM; Signorini, S; Shatunov, A; Jones, A; Shaw, PJ; Morrison, KE; Farmer, AE; Van Damme, P; Robberecht, W; Chiò, A; Traynor, BJ; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, PM; Leigh, NP; Glass, JD; Overste, D; Diekstra, FP; Veldink, JH; van Es, MA; Shaw, CE; Weale, ME; Lewis, CM; Williams, J; Brown, RH; Landers, JE; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, GP; D'Alfonso, S; van den Berg, LH; Taroni, F; Al-Chalabi, A; Powell, J; Silani, V; the SLAGEN Consortium and Collaborators
A new paraplegin mutation in a patient with primary progressive multiple sclerosis
2020 Bellinvia A.; Pasto L.; Niccolai C.; Tessa A.; Carrai R.; Martinelli C.; Moretti M.; Amato M.P.; Santorelli F.M.; Sorbi S.; Mata S.
A new social-family model for eating disorders: A European multicentre project using a case-control design
2015 Krug, Isabel; Fuller-Tyszkiewicz, Matthew; Anderluh, Marija; Bellodi, Laura; Bagnoli, Silvia; Collier, David; Fernandez-Aranda, Fernando; Karwautz, Andreas; Mitchell, Sarah; Nacmias, Benedetta; Ricca, Valdo; Sorbi, Sandro; Tchanuria, Kate; Wagner, Gudrun; Treasure, Janet; Micali, Nadia
A novel Alzheimer disease locus located near the gene encoding tau protein
2016 Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M; Lambert, J-C; Chung, J; Naj, A C; Kunkle, B W; Wang, L-S; Bis, J C; Bellenguez, C; Harold, D; Lunetta, K L; Destefano, A L; Grenier-Boley, B; Sims, R; Beecham, G W; Smith, A V; Chouraki, V; Hamilton-Nelson, K L; Ikram, M A; Fievet, N; Denning, N; Martin, E R; Schmidt, H; Kamatani, Y; Dunstan, M L; Valladares, O; Laza, A R; Zelenika, D; Ramirez, A; Foroud, T M; Choi, S-H; Boland, A; Becker, T; Kukull, W A; van der Lee, S J; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, A L; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, D A; Amin, N; Berr, C; Tsolaki, Magda; Buxbaum, J D; Lopez, O L; Deramecourt, V; Fox, N C; Cantwell, L B; Tárraga, L; Dufouil, C; Hardy, J; Crane, P K; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, T H; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, J-F; Hampel, H; Kamboh, M I; de Bruijn, R F A G; Tzourio, C; Pastor, P; Larson, E B; Rotter, J I; O'Donovan, M C; Montine, T J; Nalls, M A; Mead, S; Reiman, E M; Jonsson, P V; Holmes, C; St George-Hyslop, P H; Boada, M; Passmore, P; Wendland, J R; Schmidt, R; Morgan, K; Winslow, A R; Powell, J F; Carasquillo, M; Younkin, S G; Jakobsdóttir, J; Kauwe, J S K; Wilhelmsen, K C; Rujescu, D; Nöthen, M M; Hofman, A; Jones, L; Haines, J L; Psaty, B M; Van Broeckhoven, C; Holmans, P; Launer, L J; Mayeux, R; Sorbi, S; Nacmias, B; Lathrop, M; Goate, A M; Escott-Price, V; Seshadri, S; Pericak-Vance, M A; Amouyel, P; Williams, J; van Duijn, C M; Schellenberg, G D; Farrer, L A
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene
1992 Vaula G.; Mortilla M.; Tupler R.; Lukiw W.; Tanzi R.; Nee L.; Polinsky R.; Foncin J.-F.; Bruni A.C.; Montesi M.P.; Sorbi S.; St George-Hyslop P.
A novel PS-1 mutation in an Italian AD family with psychotic symptoms at onset
2000 Tedde A.; Nacmias B.; Forleo P.; Piccini C.; Bracco L.; Piacentini S.; Sorbi S.
A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats
2013 van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study
2021 Bergström, Sofia; Öijerstedt, Linn; Remnestål, Julia; Olofsson, Jennie; Ullgren, Abbe; Seelaar, Harro; van Swieten, John C; Synofzik, Matthis; Sanchez-Valle, Raquel; Moreno, Fermin; Finger, Elizabeth; Masellis, Mario; Tartaglia, Carmela; Vandenberghe, Rik; Laforce, Robert; Galimberti, Daniela; Borroni, Barbara; Butler, Chris R; Gerhard, Alexander; Ducharme, Simon; Rohrer, Jonathan D; Sorbi, Sandro; Nacmias, Benedetta; Månberg, Anna; Graff, Caroline; Nilsson, Peter; Ferrari, Camilla
A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians
2014 Fabio Coppedè;Pierpaola Tannorella;Gloria Tognoni;Silvia Bagnoli;Paolo Bongioanni;Benedetta Nacmias;Gabriele Siciliano;Sandro Sorbi;Ubaldo Bonuccelli;Lucia Migliore
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| "Alpha2 macroglobulin and Alzheimer's disease" | 1999 | ROGAEVA E.; S. SORBI; ST GEORGE-HYSLOP P.H.; FARRR L.A; PERICAK-VANCE M.A | |
| "Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity" | 1998 | ROGAEVA E; PREMKUMAR S.; SONG Y.S.; S. SORBI; BRINDLE N | |
| "stato dell'arte" della ricerca | 2012 | Sorbi S; Bagnoli S; Piaceri I; Ferrari C; Lombardi G; Nacmias B | |
| 5-HT2A promoter polymorphism in anorexia nervosa. | 1998 | S. Sorbi; B. Nacmias; A. Tedde; V. Ricca; B. Mezzani; C. M. Rotella | |
| 5-HT2A receptor gene polymorphism and eating disorders. | 2002 | Ricca V; Nacmias B; Cellini E; Di Bernardo M; Rotella CM; Sorbi S. | |
| 5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa | 1999 | Nacmias B; Ricca V; Tedde A; Mezzani B; Rotella CM; Sorbi S. | |
| A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers | 2018 | 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 | |
| A case of limbic encephalitis evolving into a frontotemporal dementia-like picture | 2019 | Lombardi G.; Mata S.; Berti V.; Padiglioni S.; Ginestroni A.; Piaceri I.; Bagnoli S.; Nacmias B.; De Cristofaro M.T.; Pupi A.; Sorbi S. | |
| A comparison of unawareness in frontotemporal dementia and Alzheimer's disease. | 2008 | E. Salmon; D. Perani; F. Collette; D. Feyers; E. Kalbe; V. Holthoff; S. Sorbi; K. Herholz | |
| A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia | 2022 | van der Ende, Emma L; Bron, Esther E; Poos, Jackie M; Jiskoot, Lize C; Panman, Jessica L; Papma, Janne M; Meeter, Lieke H; Dopper, Elise G P; Wilke, Carlo; Synofzik, Matthis; Heller, Carolin; Swift, Imogen J; Sogorb-Esteve, Aitana; Bouzigues, Arabella; Borroni, Barbara; Sanchez-Valle, Raquel; Moreno, Fermin; Graff, Caroline; Laforce, Robert; Galimberti, Daniela; Masellis, Mario; Tartaglia, Maria Carmela; Finger, Elizabeth; Vandenberghe, Rik; Rowe, James B; de Mendonça, Alexandre; Tagliavini, Fabrizio; Santana, Isabel; Ducharme, Simon; Butler, Christopher R; Gerhard, Alexander; Levin, Johannes; Danek, Adrian; Otto, Markus; Pijnenburg, Yolande A L; Sorbi, Sandro; Zetterberg, Henrik; Niessen, Wiro J; Rohrer, Jonathan D; Klein, Stefan; van Swieten, John C; Venkatraghavan, Vikram; Seelaar, Harro; Afonso, Sónia; Almeida, Maria Rosario; Anderl-Straub, Sarah; Andersson, Christin; Antonell, Anna; Archetti, Silvana; Arighi, Andrea; Balasa, Mircea; Barandiaran, Myriam; Bargalló, Nuria; Bartha, Robart; Bender, Benjamin; Benussi, Alberto; Benussi, Luisa; Bessi, Valentina; Binetti, Giuliano; Black, Sandra; Bocchetta, Martina; Borrego-Ecija, Sergi; Bras, Jose; Bruffaerts, Rose; Cañada, Marta; Cantoni, Valentina; Caroppo, Paola; Cash, David; Castelo-Branco, Miguel; Convery, Rhian; Cope, Thomas; Di Fede, Giuseppe; Díez, Alina; Duro, Diana; Fenoglio, Chiara; Ferrari, Camilla; Ferreira, Catarina B; Fox, Nick; Freedman, Morris; Fumagalli, Giorgio; Gabilondo, Alazne; Gasparotti, Roberto; Gauthier, Serge; Gazzina, Stefano; Giaccone, Giorgio; Gorostidi, Ana; Greaves, Caroline; Guerreiro, Rita; Hoegen, Tobias; Indakoetxea, Begoña; Jelic, Vesna; Karnath, Hans-Otto; Keren, Ron; Langheinrich, Tobias; Leitão, Maria João; Lladó, Albert; Lombardi, Gemma; Loosli, Sandra; Maruta, Carolina; Mead, Simon; Miltenberger, Gabriel; van Minkelen, Rick; Mitchell, Sara; Moore, Katrina; Nacmias, Benedetta; Nicholas, Jennifer; Öijerstedt, Linn; Olives, Jaume; Ourselin, Sebastien; Padovani, Alessandro; Peakman, Georgia; Pievani, Michela; Pijnenburg, Yolande; Polito, Cristina; Premi, Enrico; Prioni, Sara; Prix, Catharina; Rademakers, Rosa; Redaelli, Veronica; Rittman, Tim; Rogaeva, Ekaterina; Rosa-Neto, Pedro; Rossi, Giacomina; Rosser, Martin; Santiago, Beatriz; Scarpini, Elio; Schönecker, Sonja; Semler, Elisa; Shafei, Rachelle; Shoesmith, Christen; Tábuas-Pereira, Miguel; Tainta, Mikel; Taipa, Ricardo; Tang-Wai, David; Thomas, David L; Thompson, Paul; Thonberg, Hakan; Timberlake, Carolyn; Tiraboschi, Pietro; Todd, Emily; Van Damme, Philip; Vandenbulcke, Mathieu; Veldsman, Michele; Verdelho, Ana; Villanua, Jorge; Warren, Jason; Woollacott, Ione; Wlasich, Elisabeth; Zulaica, Miren | |
| A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. | 2002 | Elena Cellini; Silvia Piacentini; Benedetta Nacmias; Paolo Forleo; Andrea Tedde; Silvia Bagnoli; Monica Ciantelli; Sandro Sorbi | |
| A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. | 2014 | Fogh, I; Ratti, A; Gelleram, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, L; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, FL; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, AM; Signorini, S; Shatunov, A; Jones, A; Shaw, PJ; Morrison, KE; Farmer, AE; Van Damme, P; Robberecht, W; Chiò, A; Traynor, BJ; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, PM; Leigh, NP; Glass, JD; Overste, D; Diekstra, FP; Veldink, JH; van Es, MA; Shaw, CE; Weale, ME; Lewis, CM; Williams, J; Brown, RH; Landers, JE; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, GP; D'Alfonso, S; van den Berg, LH; Taroni, F; Al-Chalabi, A; Powell, J; Silani, V; the SLAGEN Consortium and Collaborators | |
| A new paraplegin mutation in a patient with primary progressive multiple sclerosis | 2020 | Bellinvia A.; Pasto L.; Niccolai C.; Tessa A.; Carrai R.; Martinelli C.; Moretti M.; Amato M.P.; Santorelli F.M.; Sorbi S.; Mata S. | |
| A new social-family model for eating disorders: A European multicentre project using a case-control design | 2015 | Krug, Isabel; Fuller-Tyszkiewicz, Matthew; Anderluh, Marija; Bellodi, Laura; Bagnoli, Silvia; Collier, David; Fernandez-Aranda, Fernando; Karwautz, Andreas; Mitchell, Sarah; Nacmias, Benedetta; Ricca, Valdo; Sorbi, Sandro; Tchanuria, Kate; Wagner, Gudrun; Treasure, Janet; Micali, Nadia | |
| A novel Alzheimer disease locus located near the gene encoding tau protein | 2016 | Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M; Lambert, J-C; Chung, J; Naj, A C; Kunkle, B W; Wang, L-S; Bis, J C; Bellenguez, C; Harold, D; Lunetta, K L; Destefano, A L; Grenier-Boley, B; Sims, R; Beecham, G W; Smith, A V; Chouraki, V; Hamilton-Nelson, K L; Ikram, M A; Fievet, N; Denning, N; Martin, E R; Schmidt, H; Kamatani, Y; Dunstan, M L; Valladares, O; Laza, A R; Zelenika, D; Ramirez, A; Foroud, T M; Choi, S-H; Boland, A; Becker, T; Kukull, W A; van der Lee, S J; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, A L; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, D A; Amin, N; Berr, C; Tsolaki, Magda; Buxbaum, J D; Lopez, O L; Deramecourt, V; Fox, N C; Cantwell, L B; Tárraga, L; Dufouil, C; Hardy, J; Crane, P K; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, T H; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, J-F; Hampel, H; Kamboh, M I; de Bruijn, R F A G; Tzourio, C; Pastor, P; Larson, E B; Rotter, J I; O'Donovan, M C; Montine, T J; Nalls, M A; Mead, S; Reiman, E M; Jonsson, P V; Holmes, C; St George-Hyslop, P H; Boada, M; Passmore, P; Wendland, J R; Schmidt, R; Morgan, K; Winslow, A R; Powell, J F; Carasquillo, M; Younkin, S G; Jakobsdóttir, J; Kauwe, J S K; Wilhelmsen, K C; Rujescu, D; Nöthen, M M; Hofman, A; Jones, L; Haines, J L; Psaty, B M; Van Broeckhoven, C; Holmans, P; Launer, L J; Mayeux, R; Sorbi, S; Nacmias, B; Lathrop, M; Goate, A M; Escott-Price, V; Seshadri, S; Pericak-Vance, M A; Amouyel, P; Williams, J; van Duijn, C M; Schellenberg, G D; Farrer, L A | |
| A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene | 1992 | Vaula G.; Mortilla M.; Tupler R.; Lukiw W.; Tanzi R.; Nee L.; Polinsky R.; Foncin J.-F.; Bruni A.C.; Montesi M.P.; Sorbi S.; St George-Hyslop P. | |
| A novel PS-1 mutation in an Italian AD family with psychotic symptoms at onset | 2000 | Tedde A.; Nacmias B.; Forleo P.; Piccini C.; Bracco L.; Piacentini S.; Sorbi S. | |
| A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats | 2013 | van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P | |
| A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study | 2021 | Bergström, Sofia; Öijerstedt, Linn; Remnestål, Julia; Olofsson, Jennie; Ullgren, Abbe; Seelaar, Harro; van Swieten, John C; Synofzik, Matthis; Sanchez-Valle, Raquel; Moreno, Fermin; Finger, Elizabeth; Masellis, Mario; Tartaglia, Carmela; Vandenberghe, Rik; Laforce, Robert; Galimberti, Daniela; Borroni, Barbara; Butler, Chris R; Gerhard, Alexander; Ducharme, Simon; Rohrer, Jonathan D; Sorbi, Sandro; Nacmias, Benedetta; Månberg, Anna; Graff, Caroline; Nilsson, Peter; Ferrari, Camilla | |
| A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians | 2014 | Fabio Coppedè;Pierpaola Tannorella;Gloria Tognoni;Silvia Bagnoli;Paolo Bongioanni;Benedetta Nacmias;Gabriele Siciliano;Sandro Sorbi;Ubaldo Bonuccelli;Lucia Migliore |