RIMOLDI, VALERIA
RIMOLDI, VALERIA
Universita' degli Studi di MILANO
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency
2007 C. Bozzao, V. Rimoldi, R. Asselta, M. Landau, R. Ghiotto, M.L. Tenchini, R. De Cristofaro, G. Castaman, S. Duga
Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency
2009 S. Spena, R. Asselta, S. Caccia, V. Rimoldi, S.H. Giacomelli, A. Tagliaferri, F. Peyvandi, G. Castaman, S. Duga
Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease
2009 I. Guella, V. Rimoldi, R. Asselta, D. Ardissino, M. Francolini, N. Martinelli, D. Girelli, F. Peyvandi, M. Tubaro, P.A. Merlini, P.M. Mannucci, S. Duga
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation FXI isoform
2008 V. Rimoldi, I. Guella, R. Asselta, R. De Cristofaro, F. Peyvandi, P.M. Mannucci, S. Duga
Characterization of productive and unproductive mRNA splicings in F11 : identification of a novel coagulation isoform
2006 R. Asselta, I. Guella, V. Rimoldi, M. Malcovati, M.L. Tenchini, S. Duga
Characterization of the F11 alternative splicing pattern : identification of a novel coagulation FXI isoform
2007 I. Guella, R. Asselta, V. Rimoldi, M.L. Tenchini, S. Duga
Characterization of the genetic basis of FXI deficiency in fourteen unrelated patients
2009 V. Rimoldi, I. Guella, S. Spena, N. Ciavarella, F. Peyvandi, R. Asselta, P.M. Mannucci, S. Duga
Characterization of the genetic basis of FXI deficiency in two Turkish patients
2010 E. Berber, V. Rimoldi, S. Usluer, S. Aksu, Y. Pekçelen, S.H. Çağlayan, S. Duga
Detailed stratified GWAS analysis for severe COVID-19 in four European populations
2022 F. Degenhardt, D. Ellinghaus, S. Juzenas, J. Lerga-Jaso, M. Wendorff, D. Maya-Miles, F. Uellendahl-Werth, H. Elabd, M.C. Rühlemann, J. Arora, O. Özer, O.B. Lenning, R. Myhre, M.S. Vadla, E.M. Wacker, L. Wienbrandt, A.B. Ortiz, A. Salazar, A.G. Chercoles, A. Palom, A. Ruiz, A. Garcia-Fernandez, A. Blanco-Grau, A. Mantovani, A. Zanella, A.R. Holten, A. Mayer, A. Bandera, A. Cherubini, A. Protti, A. Aghemo, A. Gerussi, A. Ramirez, A. Braun, A. Nebel, A. Barreira, A. Lleo, A. Teles, A.B. Kildal, A. Biondi, A. Caballero-Garralda, A. Ganna, A. Gori, A. Glück, A. Lind, A. Tanck, A. Hinney, A.C. Nolla, A.L. Fracanzani, A. Peschuck, A. Cavallero, A.M. Dyrhol-Riise, A. Ruello, A. Julià, A. Muscatello, A. Pesenti, A. Voza, A. Rando-Segura, A. Solier, A. Schmidt, B. Cortes, B. Mateos, B. Nafria-Jimenez, B. Schaefer, B. Jensen, C. Bellinghausen, C. Maj, C. Ferrando, C. Horra, C. Quereda, C. Skurk, C. Thibeault, C. Scollo, C. Herr, C.D. Spinner, C. Gassner, C. Lange, C. Hu, C. Paccapelo, C. Lehmann, C. Angelini, C. Cappadona, C. Azuure, C. Bianco, C. Cea, C. Sancho, D.A.L. Hoff, D. Galimberti, D. Prati, D. Haschka, D. Jiménez, D. Pestaña, D. Toapanta, E. Muñiz-Diaz, E. Azzolini, E. Sandoval, E. Binatti, E. Scarpini, E.T. Helbig, E. Casalone, E. Urrechaga, E.M. Paraboschi, E. Pontali, E. Reverter, E.J. Calderón, E. Navas, E. Solligård, E. Contro, E. Arana-Arri, F. Aziz, F. Garcia, F.G. Sánchez, F. Ceriotti, F. Martinelli-Boneschi, F. Peyvandi, F. Kurth, F. Blasi, F. Malvestiti, F.J. Medrano, F. Mesonero, F. Rodriguez-Frias, F. Hanses, F. Müller, G. Hemmrich-Stanisak, G. Bellani, G. Grasselli, G. Pezzoli, G. Costantino, G. Albano, G. Cardamone, G. Bellelli, G. Citerio, G. Foti, G. Lamorte, G. Matullo, G. Baselli, H. Kurihara, H. Neb, I. My, I. Kurth, I. Hernández, I. Pink, I. Rojas, I. Galván-Femenia, J.C. Holter, J.E. Afset, J. Heyckendorf, J. Kässens, J.K. Damås, J. Rybniker, J. Altmüller, J. Ampuero, J. Martín, J. Erdmann, J.M. Banales, J.R. Badia, J. Dopazo, J. Schneider, J. Bergan, J. Barretina, J. Walter, J.H. Quero, J. Goikoetxea, J. Delgado, J.M. Guerrero, J. Fazaal, J. Kraft, J. Schröder, K. Risnes, K. Banasik, K.E. Müller, K.I. Gaede, K. Garcia-Etxebarria, K. Tonby, L. Heggelund, L. Izquierdo-Sanchez, L.R. Bettini, L. Sumoy, L.E. Sander, L.J. Lippert, L. Terranova, L. Nkambule, L. Knopp, L.T. Gustad, L. Garbarino, L. Santoro, L. Téllez, L. Roade, M. Ostadreza, M. Intxausti, M. Kogevinas, M. Riveiro-Barciela, M.M. Berger, M. Schaefer, M.E.K. Niemi, M.A. Gutiérrez-Stampa, M. Carrabba, M.E. Figuera Basso, M.G. Valsecchi, M. Hernandez-Tejero, M.J.G.T. Vehreschild, M. Manunta, M. Acosta-Herrera, M. D'Angiò, M. Baldini, M. Cazzaniga, M.M. Grimsrud, M. Cornberg, M.M. Nöthen, M. Marquié, M. Castoldi, M. Cordioli, M. Cecconi, M. D'Amato, M. Augustin, M. Tomasi, M. Boada, M. Dreher, M.J. Seilmaier, M. Joannidis, M. Wittig, M. Mazzocco, M. Ciccarelli, M. Rodríguez-Gandía, M. Bocciolone, M. Miozzo, N.I. Ayo, N. Blay, N. Chueca, N. Montano, N. Braun, N. Ludwig, N. Marx, N. Martínez, O.A. Cornely, O. Witzke, O. Palmieri, P. Faverio, P. Preatoni, P. Bonfanti, P. Omodei, P. Tentorio, P. Castro, P.M. Rodrigues, P.P. España, P. Hoffmann, P. Rosenstiel, P. Schommers, P. Suwalski, R. Pablo, R. Ferrer, R. Bals, R. Gualtierotti, R. Gallego-Durán, R. Nieto, R. Carpani, R. Morilla, S. Badalamenti, S. Haider, S. Ciesek, S. May, S. Bombace, S. Marsal, S. Pigazzini, S. Klein, S. Pelusi, S. Wilfling, S. Bosari, S. Volland, S. Brunak, S. Raychaudhuri, S. Schreiber, S. Heilmann-Heimbach, S. Aliberti, S. Ripke, S. Dudman, T. Wesse, T. Zheng, T. Bahmer, T. Eggermann, T. Illig, T. Brenner, T. Pumarola, T. Feldt, T. Folseraas, T.G. Cejudo, U. Landmesser, U. Protzer, U. Hehr, V. Rimoldi, V. Monzani, V. Skogen, V. Keitel, V. Kopfnagel, V. Friaza, V. Andrade, V. Moreno, W. Albrecht, W. Peter, W. Poller, X. Farre, X. Yi, X. Wang, Y. Khodamoradi, Z. Karadeniz, A. Latiano, S. Goerg, P. Bacher, P. Koehler, F. Tran, H. Zoller, E.C. Schulte, B. Heidecker, K.U. Ludwig, J. Fernández, M. Romero-Gómez, A. Albillos, P. Invernizzi, M. Buti, S. Duga, L. Bujanda, J.R. Hov, T.L. Lenz, R. Asselta, R. Cid, L. Valenti, T.H. Karlsen, M. Cáceres, A. Franke
DNAJC12 and dopa-responsive nonprogressive parkinsonism
2017 L. Straniero, I. Guella, R. Cilia, L. Parkkinen, V. Rimoldi, A. Young, R. Asselta, G. Soldã , V. Sossi, A.J. Stoessl, A. Priori, K. Nishioka, N. Hattori, J. Follett, A. Rajput, N. Blau, G. Pezzoli, M.J. Farrer, S. Goldwurm, A.H. Rajput, S. Duga
Dowregulation of the oxytocin receptor after ligand binding
2005 S. Sertic, A. Reversi, V. Rimoldi, B. Chini
Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript
2013 V. Rimoldi, G. Soldà, R. Asselta, S. Spena, C. Stuani, E. Buratti, S. Duga
Effects of cholesterol manipulation on the signaling of the human oxytocin receptor
2006 A. Reversi, V. Rimoldi, S. Brambillasca, B. Chini
Evidence of Liquid Crystal–Assisted Abiotic Ligation of Nucleic Acids
2015 T.P. Fraccia, G. Zanchetta, V. Rimoldi, N.A. Clark, T. Bellini
Exploring the global landscape of genetic variation in coagulation factor XI deficiency
2017 R. Asselta, E.M. Paraboschi, V. Rimoldi, M. Menegatti, F. Peyvandi, O. Salomon, S. Duga
Functional analysis of missense mutations in the Myocyte Enhancer Factor 2A (MEF2A) gene do not support their causal role in the pathogenesis of myocardial infarction
2008 I. Guella, V. Rimoldi, P.A. Merlini, R. Asselta, E.M. Paraboschi, M. Francolini, F. Peyvandi, D. Ardissino, P.M. Mannucci, S. Duga
Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II
2014 V. Rimoldi, L. Straniero, R. Asselta, L. Mauri, E. Manfredini, S. Penco, G.P. Gesu, A. Del Longo, E. Piozzi, G. Soldà, P. Primignani
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis
2014 E.M. Paraboschi, V. Rimoldi, G. Soldà, T. Tabaglio, C. Dall'Osso, E. Saba, M. Vigliano, A. Salviati, M. Leone, M.D. Benedetti, D. Fornasari, J. Saarela, P.L. De Jager, N.A. Patsopoulos, S. D'Alfonso, D. Gemmati, S. Duga, R. Asselta
Gene regulation in the pathogenesis of angioedema due to inherited c1 inhibitor deficiency (hereditary angioedema)
2009 M. Cicardi, A. Zanichelli, E. Bonanni, C. Suffritti, L. Maggioni, S. Caccia, R. Russo, Y. Zhi, S. Duga, R. Asselta, V. Rimoldi, G. Castellano
Gene regulation in the pathogenesis of inherited C1-inhibitor deficiency (Hereditary Angioedema)
2011 S. Caccia, V. Rimoldi, R. Asselta, G.M. Soldà, E. Bonanni, R. Russo, S. Duga, M. Cicardi