RUBINO, Elisa

RUBINO, Elisa  

NEUROSCIENZE "RITA LEVI MONTALCINI"  

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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers 2018 Zhang M, Ferrari R, Tartaglia MC, Keith J, Surace EI, Wolf U, Sato C, Grinberg M, Liang Y, Xi Z, Dupont K, McGoldrick P, Weichert A, McKeever PM, Schneider R, McCorkindale MD, Manzoni C, Rademakers R, Graff-Radford NR, Dickson DW, Parisi JE, Boeve BF, Petersen RC, Miller BL, Seeley WW, van Swieten JC, van Rooij J, Pijnenburg Y, van der Zee J, Van Broeckhoven C, Le Ber I, Van Deerlin V, Suh E, Rohrer JD, Mead S, Graff C, Öijerstedt L, Pickering-Brown S, Rollinson S, Rossi G, Tagliavini F, Brooks WS, Dobson-Stone C, Halliday GM, Hodges JR, Piguet O, Binetti G, Benussi L, Ghidoni R, Nacmias B, Sorbi S, Bruni AC, Galimberti D, Scarpini E, Rainero I, Rubino E, Clarimon J, Lleó A, Ruiz A, Hernández I, Pastor P, Diez-Fairen M, Borroni B, Pasquier F, Deramecourt V, Lebouvier T, Perneczky R, Diehl-Schmid J, Grafman J, Huey ED, Mayeux R, Nalls MA, Hernandez D, Singleton A, Momeni P, Zeng Z, Hardy J, Robertson J, Zinman L, Rogaeva E; International FTD-Genomics Consortium (Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JBJ, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Albani D, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Wald Ouml ML, Nilsson K, Nilsson C, Mackenzie IRA, Hsiung GR, Mann DMA, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, Pastor P, Razquin C, Ortega-Cubero S, Alonso E, Perneczky R, Diehl-Schmid J, Alexopoulos P, Kurz A, Rainero I, Rubino E, Pinessi L, Rogaeva E, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JCM, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Van Broeckhoven C, Cappa SF, Leber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Grazia Spillantini M, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Elena Conidi M, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EGP, Seelaar H, Pijnenburg YAL, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebouvier T, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P.)
A functional polymorphism of the interleukin-6 gene influences the psychiatry comorbidity of migraine 2009 Rainero I; Rubino E; Negro E; Gallone S; Fenoglio P; Binello E; Gentile S; Vaula G; Pinessi L
A genome-wide linkage scan of a new italian family confirms the presence of several loci influencing migraine without aura 2008 Rainero I; Rubino E; Pinessi L; Rogaeva E; St.George-Hyslop P
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia 2015 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
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity 2019 van der Lee, Sven J; Conway, Olivia J; Jansen, Iris; Carrasquillo, Minerva M; Kleineidam, Luca; van den Akker, Erik; Hernández, Isabel; van Eijk, Kristel R; Stringa, Najada; Chen, Jason A; Zettergren, Anna; Andlauer, Till F M; Diez-Fairen, Monica; Simon-Sanchez, Javier; Lleó, Alberto; Zetterberg, Henrik; Nygaard, Marianne; Blauwendraat, Cornelis; Savage, Jeanne E; Mengel-From, Jonas; Moreno-Grau, Sonia; Wagner, Michael; Fortea, Juan; Keogh, Michael J; Blennow, Kaj; Skoog, Ingmar; Friese, Manuel A; Pletnikova, Olga; Zulaica, Miren; Lage, Carmen; de Rojas, Itziar; Riedel-Heller, Steffi; Illán-Gala, Ignacio; Wei, Wei; Jeune, Bernard; Orellana, Adelina; Then Bergh, Florian; Wang, Xue; Hulsman, Marc; Beker, Nina; Tesi, Niccolo; Morris, Christopher M; Indakoetxea, Begoña; Collij, Lyduine E; Scherer, Martin; Morenas-Rodríguez, Estrella; IFGC; Raffaele Ferrari,Dena G. Hernandez, Michael A. Nalls, Jonathan D. Rohrer, AdaikalavanRamasamy, John B.J. Kwok, Carol Dobson-Stone, William S. Brooks, PeterR. Schofield, Glenda M. Halliday, John R. Hodges, Olivier Piguet, LaurenBartley, Elizabeth Thompson, Eric Haan, Isabel Hernández, Agustín Ruiz,Mercè Boada, Barbara Borroni, Alessandro Padovani, Carlos Cruchaga,Nigel J. Cairns, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, GianluigiForloni, Daniela Galimberti, Chiara Fenoglio, Maria Serpente, Elio Scarpini,Jordi Clarimón, Alberto Lleó, Rafael Blesa, Maria Landqvist Waldö, KarinNilsson, Christer Nilsson, Ian R.A. Mackenzie, Ging-Yuek R. Hsiung, DavidM.A. Mann, Jordan Grafman, Christopher M. Morris, Johannes Attems,Timothy D. Griffiths, Ian G. McKeith, Alan J. Thomas, P. Pietrini, Edward D.Huey, Eric M. Wassermann, Atik Baborie, Evelyn Jaros, Michael C. Tierney,Pau Pastor, Cristina Razquin, Sara Ortega-Cubero, Elena Alonso, RobertPerneczky, Janine Diehl-Schmid, Panagiotis Alexopoulos, Alexander Kurz,Innocenzo Rainero, Elisa Rubino, Lorenzo Pinessi, Ekaterina Rogaeva, PeterSt. George-Hyslop, Giacomina Rossi, Fabrizio Tagliavini, Giorgio Giaccone,James B. Rowe, Johannes C.M. Schlachetzki, James Uphill, John Collinge,Simon Mead, Adrian Danek, Vivianna M. Van Deerlin, Murray Grossman,John Q. Trojanowski, Julie van der Zee, William Deschamps, Tim VanLangenhove, Marc Cruts, Christine Van Broeckhoven, Stefano F. Cappa,Isabelle Le Ber, Didier Hannequin, Véronique Golfier, Martine Vercelletto,Alexis Brice, Benedetta Nacmias, Sandro Sorbi, Silvia Bagnoli, Irene Piaceri,Jørgen E. Nielsen, Lena E. Hjermind, Matthias Riemenschneider, ManuelMayhaus, Bernd Ibach, Gilles Gasparoni, Sabrina Pichler, Wei Gu, Martin N.Rossor, Nick C. Fox, Jason D. Warren, Maria Grazia Spillantini, Huw R.Morris, Patrizia Rizzu, Peter Heutink, Julie S. Snowden, Sara Rollinson, AnnaRichardson, Alexander Gerhard, Amalia C. Bruni, Raffaele Maletta, Fran-cesca Frangipane, Chiara Cupidi, Livia Bernardi, Maria Anfossi, Maura Gallo,Maria Elena Conidi, Nicoletta Smirne, Rosa Rademakers, Matt Baker,Dennis W. Dickson, Neill R. Graff-Radford, Ronald C. Petersen, DavidKnopman, Keith A. Josephs, Bradley F. Boeve, Joseph E. Parisi, William W.Seeley, Bruce L. Miller, Anna M. Karydas, Howard Rosen, John C. vanSwieten, Elise G.P. Dopper, Harro Seelaar, Yolande A.L. Pijnenburg, PhilipScheltens, Giancarlo Logroscino, Rosa Capozzo, Valeria Novelli, Annibale A.Puca, Massimo Franceschi, Alfredo Postiglione, Graziella Milan, PaoloSorrentino, Mark Kristiansen, Huei-Hsin Chiang, Caroline Graff, FlorencePasquier, Adeline Rollin, Vincent Deramecourt, Florence Lebert, DimitriosKapogiannis, Luigi Ferrucci, Stuart Pickering-Brown, Andrew B. Singleton,John Hardy, Parastoo Momeni; Ironside, James W; van Berckel, Bart N M; Alcolea, Daniel; Wiendl, Heinz; Strickland, Samantha L; Pastor, Pau; Rodríguez Rodríguez, Eloy; Boeve, Bradley F; Petersen, Ronald C; Ferman, Tanis J; van Gerpen, Jay A; Reinders, Marcel J T; Uitti, Ryan J; Tárraga, Lluís; Maier, Wolfgang; Dols-Icardo, Oriol; Kawalia, Amit; Dalmasso, Maria Carolina; Boada, Mercè; Zettl, Uwe K; van Schoor, Natasja M; Beekman, Marian; Allen, Mariet; Masliah, Eliezer; de Munain, Adolfo López; Pantelyat, Alexander; Wszolek, Zbigniew K; Ross, Owen A; Dickson, Dennis W; Graff-Radford, Neill R; Knopman, David; Rademakers, Rosa; Lemstra, Afina W; Pijnenburg, Yolande A L; Scheltens, Philip; Gasser, Thomas; Chinnery, Patrick F; Hemmer, Bernhard; Huisman, Martijn A; Troncoso, Juan; Moreno, Fermin; Nohr, Ellen A; Sørensen, Thorkild I A; Heutink, Peter; Sánchez-Juan, Pascual; Posthuma, Danielle; Clarimón, Jordi; Christensen, Kaare; Ertekin-Taner, Nilüfer; Scholz, Sonja W; Ramirez, Alfredo; Ruiz, Agustín; Slagboom, Eline; van der Flier, Wiesje M; Holstege, Henne
A novel neurocognitive approach for placebo analgesia in neurocognitive disorders 2019 Palermo S.; Rainero I.; Stanziano M.; Vase L.; D'Agata F.; Rubino E.; Fonio P.; Sardanelli F.; Amanzio M.
A Novel PSEN1 Variant Leading to Posterior Cortical Atrophy: A Case Report 2023 Roveta, Fausto; Marcinnò, Andrea; Grassini, Alberto; Ferrandes, Fabio; Cermelli, Aurora; Boschi, Silvia; Gallone, Salvatore; Atzori, Cristiana; Imperiale, Daniele; Dentelli, Patrizia; Pasini, Barbara; Brusco, Alfredo; Rubino, Elisa; Rainero, Innocenzo
A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache 2004 RAINERO I; GALLONE S; VALFRÈ W; FERRERO M; ANGILELLA G; RIVOIRO C; RUBINO E; DE MARTINO P; SAVI L; FERRONE M; PINESSI L
A review of the recent advances in neuroimaging of frontotemporal lobar degeneration 2017 D'Agata, Federico; Orsi, Laura; Cicerale, Alessandro; Rubino, Elisa; Rainero, Innocenzo; Bergui, Mauro; Pinessi, Lorenzo
A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10 2017 Giorgio, Elisa; Rubino, Elisa; Bruselles, Alessandro; Pizzi, Simone; Rainero, Innocenzo; Duca, Sergio; Sirchia, Fabio; Pasini, Barbara; Tartaglia, Marco; Brusco, Alfredo
Absence of TARDBP Gene Mutations in an Italian Series of Patients with Frontotemporal Lobar Degeneration 2009 Salvatore Gallone; Maria Teresa Giordana; Elio Scarpini; Innocenzo Rainero; Elisa Rubino; Pierpaola Fenoglio; Daniela Galimberti; Silvia Grifoni; Eliana Venturelli; Pier Luigi Acutis; Silvia Peletto; Maria Grazia Maniaci; Patrizia Ferrero; Michela Zotta; Lorenzo Pinessi
Analysis of CHCHD2 and CHCHD10 genes in patients with Parkinson’s disease and mitochondrial myopathy. 2017 E. Rubino; S. Boschi; M. Zhang; L. Brusa; F. Govone; A. Vacca; A. Gai; L. Lopiano; E. Rogaeva; T. Mongini; M. Giordana; I. Rainero;
Analysis of the DNA methylation pattern of the promoter region of calcitonin gene-related peptide 1 gene in patients with episodic migraine: An exploratory case-control study 2022 Rubino E.; Boschi S.; Giorgio E.; Pozzi E.; Marcinno' A.; Gallo E.; Roveta F.; Grassini A.; Brusco A.; Rainero I.
Antiepileptic drugs in migraine prophylaxis 2005 Gentile S; Lo Giudice R; Rainero I; Rubino E; Magaudda A; Pinessi L
APOE Gene Polymorphisms and Frontotemporal Dementia: A Meta-Analysis 2009 Rubino E; Rainero I; Ferrero M; Vaula G; Gentile S; Valfre' W; De Martino P; Negro E; Pinessi L
Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: A meta-analysis. 2013 Rubino E; Vacca A; Govone F; De Martino P; Pinessi L; Rainero I
Aquaporin 4 gene and migraine: an association study 2008 Rubino E; Rainero I; Gallone S; Valfrè W; Berra E; Pinessi L
Assessing the prevalence of KCNK18 (TRESK) gene mutations in Italian patients with migraine 2012 Rainero I; Rubino E; Gallone S; Fenoglio P; Zavarise P; Carli D; Boschi S; Pinessi L; Dalla Volta G
Association analyses of genetic variants of the HCTR1 gene in migraine 2009 Rubino E; Rainero I; Gallone S; Fenoglio P; Negro E; Savi L; Pinessi L
Association between Alzheimer's Disease and the hypocretin receptor 2 gene 2011 Rainero I; Rubino E; Galimberti D; Gallone S; Fenoglio P; Fenoglio C; Scarpini E; Pinessi L