Cetacean sensitivity and threats analysis to assess effectiveness of protection measures: an example of integrated approach for cetacean conservation in the Bonifacio Bouches von Campana, I., Angeletti, D., Giovani, G., Paraboschi, M., Arcangeli, A.

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Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis von Paraboschi, Elvezia M, Rimoldi, Valeria, Soldà, Giulia, Tabaglio, Tommaso, Dall'Osso, Claudia, Saba, Elena, Vigliano, Marco, Salviati, Alessandro, Leone, Maurizio, Benedetti, Maria D, Fornasari, Diego, Saarela, Janna, De Jager, Philip L, Patsopoulos, Nikolaos A, D'Alfonso, Sandra, Gemmati, Donato, Duga, Stefano, Asselta, Rosanna

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Turtles on the trash track: loggerhead turtles exposed to floating plastic in the Mediterranean Sea von Arcangeli, A, Maffucci, F, Atzori, F, Azzolin, M, Campana, I, Carosso, L, Crosti, R, Frau, F, David, L, Di-Méglio, N, Roul, M, Gregorietti, M, Mazzucato, V, Pellegrino, G, Giacoletti, A, Paraboschi, M, Zampollo, A, de Lucia, GA, Hochscheid, S

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Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis von Cardamone, Giulia, Paraboschi, Elvezia M, Soldà, Giulia, Cantoni, Claudia, Supino, Domenico, Piccio, Laura, Duga, Stefano, Asselta, Rosanna

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Nonenzymatic Polymerization into Long Linear RNA Templated by Liquid Crystal Self-Assembly von Todisco, Marco, Fraccia, Tommaso P, Smith, Greg P, Corno, Andrea, Bethge, Lucas, Klussmann, Sven, Paraboschi, Elvezia M, Asselta, Rosanna, Colombo, Diego, Zanchetta, Giuliano, Clark, Noel A, Bellini, Tommaso

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Functional and clinical implications of genetic structure in 1686 Italian exomes von Birolo, Giovanni, Aneli, Serena, Di Gaetano, Cornelia, Cugliari, Giovanni, Russo, Alessia, Allione, Alessandra, Casalone, Elisabetta, Giorgio, Elisa, Paraboschi, Elvezia M., Ardissino, Diego, Duga, Stefano, Asselta, Rosanna, Matullo, Giuseppe

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Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis von Cagliani, Rachele, Fumagalli, Matteo, Guerini, Franca R., Riva, Stefania, Galimberti, Daniela, Comi, Giacomo P., Agliardi, Cristina, Scarpini, Elio, Pozzoli, Uberto, Forni, Diego, Caputo, Domenico, Asselta, Rosanna, Biasin, Mara, Paraboschi, Elvezia M., Bresolin, Nereo, Clerici, Mario, Sironi, Manuela

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Molecular investigation of 41 patients affected by coagulation factor XI deficiency von Rimoldi, V., Paraboschi, E. M., Menegatti, M., Peyvandi, F., Salomon, O., Duga, S., Asselta, R.

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Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay von Nuzzo, F., Paraboschi, E. M., Straniero, L., Pavlova, A., Duga, S., Castoldi, E.

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Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women von Biguzzi, E., Franchi, F., Acaia, B., Ossola, W., Nava, U., Paraboschi, E. M., Asselta, R., Peyvandi, F.

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Genomewide Association Study of Severe Covid-19 with Respiratory Failure von Ellinghaus, David, Degenhardt, Frauke, Bujanda, Luis, Buti, Maria, Albillos, Agustín, Invernizzi, Pietro, Fernández, Javier, Prati, Daniele, Baselli, Guido, Asselta, Rosanna, Grimsrud, Marit M, Milani, Chiara, Aziz, Fátima, Kässens, Jan, May, Sandra, Wendorff, Mareike, Wienbrandt, Lars, Uellendahl-Werth, Florian, Zheng, Tenghao, Yi, Xiaoli, de Pablo, Raúl, Chercoles, Adolfo G, Palom, Adriana, Garcia-Fernandez, Alba-Estela, Rodriguez-Frias, Francisco, Zanella, Alberto, Bandera, Alessandra, Protti, Alessandro, Aghemo, Alessio, Lleo, Ana, Biondi, Andrea, Caballero-Garralda, Andrea, Gori, Andrea, Tanck, Anja, Carreras Nolla, Anna, Latiano, Anna, Fracanzani, Anna Ludovica, Peschuck, Anna, Julià, Antonio, Pesenti, Antonio, Voza, Antonio, Jiménez, David, Mateos, Beatriz, Nafria Jimenez, Beatriz, Quereda, Carmen, Paccapelo, Cinzia, Gassner, Christoph, Angelini, Claudio, Cea, Cristina, Solier, Aurora, Pestaña, David, Muñiz-Diaz, Eduardo, Sandoval, Elena, Paraboschi, Elvezia M, Navas, Enrique, García Sánchez, Félix, Ceriotti, Ferruccio, Martinelli-Boneschi, Filippo, Peyvandi, Flora, Blasi, Francesco, Téllez, Luis, Blanco-Grau, Albert, Hemmrich-Stanisak, Georg, Grasselli, Giacomo, Costantino, Giorgio, Cardamone, Giulia, Foti, Giuseppe, Aneli, Serena, Kurihara, Hayato, ElAbd, Hesham, My, Ilaria, Galván-Femenia, Iván, Martín, Javier, Erdmann, Jeanette, Ferrusquía-Acosta, Jose, Garcia-Etxebarria, Koldo, Izquierdo-Sanchez, Laura, Bettini, Laura R, Sumoy, Lauro, Terranova, Leonardo, Moreira, Leticia, Santoro, Luigi, Scudeller, Luigia, Mesonero, Francisco, Roade, Luisa, Rühlemann, Malte C, Schaefer, Marco, Carrabba, Maria, Riveiro-Barciela, Mar, Figuera Basso, Maria E, Valsecchi, Maria G, Hernandez-Tejero, María, Acosta-Herrera, Marialbert, D'Angiò, Mariella, Baldini, Marina, Cazzaniga, Marina, Schulzky, Martin, Cecconi, Maurizio, Wittig, Michael, Ciccarelli, Michele

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Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency von PARABOSCHI, E. M., KAYIRAN, S. M., ÖZBEK, N., GÜRAKAN, B., PEYVANDI, F., GUELLA, I., DUGA, S., ASSELTA, R.

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Genetic association and altered gene expression of mir-155 in multiple sclerosis patients von Paraboschi, Elvezia Maria, Soldà, Giulia, Gemmati, Donato, Orioli, Elisa, Zeri, Giulia, Benedetti, Maria Donata, Salviati, Alessandro, Barizzone, Nadia, Leone, Maurizio, Duga, Stefano, Asselta, Rosanna

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Identification of the first Alu-mediated large deletion involving the F5 gene in a compound heterozygous patient with severe factor V deficiency von Guella, Ilaria, Paraboschi, Elvezia Maria, van Schalkwyk, Willem A., Asselta, Rosanna, Duga, Stefano

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X chromosome contribution to the genetic architecture of primary biliary cholangitis von Asselta, R, Paraboschi, EM, Gerussi, A, Cordell, HJ, Mells, GF, Sandford, RN, Jones, DE, Nakamura, M, Ueno, K, Hitomi, Y, Kawashima, M, Nishida, N, Tokunaga, K, Nagasaki, M, Tanaka, A, Tang, R, Li, Z, Shi, Y, Liu, X, Xiong, M, Hirschfield, G, Siminovitch, KA, Canadian-US PBC Consortium, Italian PBC Genetics Study Group, UK-PBC Consortium, Japan PBC-GWAS Consortium, Carbone, M, Cardamone, G, Duga, S, Gershwin, ME, Seldin, MF, Invernizzi, P

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Molecular characterization of three novel splicing mutations causing factor V deficiency and analysis of the F5 gene splicing pattern von Dall'Osso, Claudia, Guella, Ilaria, Duga, Stefano, Locatelli, Nadia, Paraboschi, Elvezia Maria, Spreafico, Marta, Afrasiabi, Abdolreza, Pechlaner, Christoph, Peyvandi, Flora, Tenchini, Maria Luisa, Asselta, Rosanna

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Les bords de Marne

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X Chromosome Contribution to the Genetic Architecture of Primary Biliary Cholangitis von Asselta, Rosanna, Paraboschi, Elvezia M, Gerussi, Alessio, Cordell, Heather J, Mells, George F, Sandford, Richard N, Jones, David E, Nakamura, Minoru, Ueno, Kazuko, Hitomi, Yuki, Kawashima, Minae, Nishida, Nao, Tokunaga, Katsushi, Nagasaki, Masao, Tanaka, Atsushi, Tang, Ruqi, Li, Zhiqiang, Shi, Yongyong, Liu, Xiangdong, Xiong, Ma, Hirschfield, Gideon, Siminovitch, Katherine A, Carbone, Marco, Cardamone, Giulia, Duga, Stefano, Gershwin, M Eric, Seldin, Michael F, Invernizzi, Pietro

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Link to Dataset related to article "Interpreting Non-coding Genetic Variation in Multiple Sclerosis Genome-Wide Associated Regions" von Paraboschi, EM, Cardamone, G, Solda', Giulia Maria Emilia Antonietta, Duga, Stefano, Asselta, Rosanna

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Conversation analysis, psychopathology and subjective experience in patients with schizophrenia von Lucarini, V., Cangemi, F., Paraboschi, F., Lucchese, J., Daniel, B., Marchesi, C., Tonna, M.

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