The Perception of Instability and Legitimacy of Status Differences Enhances the Infrahumanization Bias among High Status Groups

od Mosso, Cristina, Russo, Silvia
izdano v Eur J Psychol (2019)

A Democratic Emergency After a Health Emergency? Exposure to COVID‐19, Perceived Economic Threat and Support for Anti‐Democratic Political Systems

od Roccato, Michele, Cavazza, Nicoletta, Colloca, Pasquale, Russo, Silvia
izdano v Soc Sci Q (2020)

The Lasting Effects of the COVID‐19 Pandemic on Support for Anti‐Democratic Political Systems: A Six‐Month Longitudinal Study

od Roccato, Michele, Russo, Silvia, Colloca, Pasquale, Cavazza, Nicoletta
izdano v Soc Sci Q (2021)

The Drop That Spilled the Cup: Acute Myocardial Infarction in a Young Woman with Underlying Thrombophilic Polymorphisms and Oral Contraceptive Use

od Russo, Nunzio, Franzì, Enrico, Capilli, Gianfranco, Patané, Anella Antonietta, Russo, Silvia Paola, Evola, Rosario
izdano v Case Rep Cardiol (2014)

Recurrence and Familial Inheritance of Intronic NIPBL Pathogenic Variant Associated With Mild CdLS

od Masciadri, Maura, Ficcadenti, Anna, Milani, Donatella, Cogliati, Francesca, Divizia, Maria Teresa, Larizza, Lidia, Russo, Silvia
izdano v Front Neurol (2018)

Recombinant Chromosome 7 Driven by Maternal Chromosome 7 Pericentric Inversion in a Girl with Features of Silver-Russell Syndrome

od Catusi, Ilaria, Bonati, Maria Teresa, Mainini, Ester, Russo, Silvia, Orlandini, Eleonora, Larizza, Lidia, Recalcati, Maria Paola
izdano v Int J Mol Sci (2020)

PBMC of Multiple Sclerosis Patients Show Deregulation of OPA1 Processing Associated with Increased ROS and PHB2 Protein Levels

od De Rasmo, Domenico, Ferretta, Anna, Russo, Silvia, Ruggieri, Maddalena, Lasorella, Piergiorgio, Paolicelli, Damiano, Trojano, Maria, Signorile, Anna
izdano v Biomedicines (2020)

Familial intragenic duplication of ANKRD11 underlying three patients of KBG syndrome

od Crippa, Milena, Rusconi, Daniela, Castronovo, Chiara, Bestetti, Ilaria, Russo, Silvia, Cereda, Anna, Selicorni, Angelo, Larizza, Lidia, Finelli, Palma
izdano v Mol Cytogenet (2015)

Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy

od D'Apice, Maria Rosaria, Gambardella, Stefano, Bengala, Mario, Russo, Silvia, Nardone, Anna Maria, Lucidi, Vincenzina, Sangiuolo, Federica, Novelli, Giuseppe
Izdano 2004

The Steady-State Serum Concentration of Genistein Aglycone Is Affected by Formulation: A Bioequivalence Study of Bone Products

od Bitto, Alessandra, Burnett, Bruce P., Polito, Francesca, Russo, Silvia, D'Anna, Rosario, Pillai, Lakshmi, Squadrito, Francesco, Altavilla, Domenica, Levy, Robert M.
Izdano 2013

Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains

od Monk, David, Morales, Joannella, den Dunnen, Johan T., Russo, Silvia, Court, Franck, Prawitt, Dirk, Eggermann, Thomas, Beygo, Jasmin, Buiting, Karin, Tümer, Zeynep
izdano v Epigenetics (2018)

Taurine Administration Recovers Motor and Learning Deficits in an Angelman Syndrome Mouse Model

od Guzzetti, Sara, Calzari, Luciano, Buccarello, Lucia, Cesari, Valentina, Toschi, Ivan, Cattaldo, Stefania, Mauro, Alessandro, Pregnolato, Francesca, Mazzola, Silvia Michela, Russo, Silvia
izdano v Int J Mol Sci (2018)

Mitochondrial Dynamics of Proximal Tubular Epithelial Cells in Nephropathic Cystinosis

od De Rasmo, Domenico, Signorile, Anna, De Leo, Ester, Polishchuk, Elena V., Ferretta, Anna, Raso, Roberto, Russo, Silvia, Polishchuk, Roman, Emma, Francesco, Bellomo, Francesco
izdano v Int J Mol Sci (2019)

Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation

od Calzari, Luciano, Barcella, Matteo, Alari, Valentina, Braga, Daniele, Muñoz-Viana, Rafael, Barlassina, Cristina, Finelli, Palma, Gervasini, Cristina, Barco, Angel, Russo, Silvia, Larizza, Lidia
izdano v Mol Neurobiol (2020)

Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controls

od Parenti, Ilaria, Rovina, Davide, Masciadri, Maura, Cereda, Anna, Azzollini, Jacopo, Picinelli, Chiara, Limongelli, Giuseppe, Finelli, Palma, Selicorni, Angelo, Russo, Silvia, Gervasini, Cristina, Larizza, Lidia
Izdano 2014

Genomic imbalances in patients with a clinical presentation in the spectrum of Cornelia de Lange syndrome

od Gervasini, Cristina, Picinelli, Chiara, Azzollini, Jacopo, Rusconi, Daniela, Masciadri, Maura, Cereda, Anna, Marzocchi, Cinzia, Zampino, Giuseppe, Selicorni, Angelo, Tenconi, Romano, Russo, Silvia, Larizza, Lidia, Finelli, Palma
Izdano 2013

Intragenic and large NIPBL rearrangements revealed by MLPA in Cornelia de Lange patients

od Russo, Silvia, Masciadri, Maura, Gervasini, Cristina, Azzollini, Jacopo, Cereda, Anna, Zampino, Giuseppe, Haas, Oskar, Scarano, Gioacchino, Di Rocco, Maja, Finelli, Palma, Tenconi, Romano, Selicorni, Angelo, Larizza, Lidia
Izdano 2012

A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation

od Demond, Hannah, Anvar, Zahra, Jahromi, Bahia Namavar, Sparago, Angela, Verma, Ankit, Davari, Maryam, Calzari, Luciano, Russo, Silvia, Jahromi, Mojgan Akbarzadeh, Monk, David, Andrews, Simon, Riccio, Andrea, Kelsey, Gavin
izdano v Genome Med (2019)

Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance

od Cubellis, Maria Vittoria, Pignata, Laura, Verma, Ankit, Sparago, Angela, Del Prete, Rosita, Monticelli, Maria, Calzari, Luciano, Antona, Vincenzo, Melis, Daniela, Tenconi, Romano, Russo, Silvia, Cerrato, Flavia, Riccio, Andrea
izdano v Clin Epigenetics (2020)

Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features

od Cirello, Valentina, Giorgini, Valentina, Castronovo, Chiara, Marelli, Susan, Mainini, Ester, Sironi, Alessandra, Recalcati, Maria Paola, Pessina, Marco, Giardino, Daniela, Larizza, Lidia, Persani, Luca, Finelli, Palma, Russo, Silvia, Fugazzola, Laura
izdano v Front Genet (2018)