A longitudinal study highlights shared aspects of the transcriptomic response to cardiogenic and septic shock

por Braga, Daniele, Barcella, Matteo, Herpain, Antoine, Aletti, Federico, Kistler, Erik B., Bollen Pinto, Bernardo, Bendjelid, Karim, Barlassina, Cristina
Publicado 2019

Self-renewal and phenotypic conversion are the main physiological responses of macrophages to the endogenous estrogen surge

por Pepe, Giovanna, Braga, Daniele, Renzi, Tiziana A., Villa, Alessandro, Bolego, Chiara, D’Avila, Francesca, Barlassina, Cristina, Maggi, Adriana, Locati, Massimo, Vegeto, Elisabetta
Publicado 2017

Identification of a transcriptome profile associated with improvement of organ function in septic shock patients after early supportive therapy

por Barcella, Matteo, Bollen Pinto, Bernardo, Braga, Daniele, D’Avila, Francesca, Tagliaferri, Federico, Cazalis, Marie-Angelique, Monneret, Guillaume, Herpain, Antoine, Bendjelid, Karim, Barlassina, Cristina
Publicado 2018

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

por Calzari, Luciano, Barcella, Matteo, Alari, Valentina, Braga, Daniele, Muñoz-Viana, Rafael, Barlassina, Cristina, Finelli, Palma, Gervasini, Cristina, Barco, Angel, Russo, Silvia, Larizza, Lidia
Publicado 2020

Genes Involved in Vasoconstriction and Vasodilation System Affect Salt-Sensitive Hypertension

por Citterio, Lorena, Simonini, Marco, Zagato, Laura, Salvi, Erika, Delli Carpini, Simona, Lanzani, Chiara, Messaggio, Elisabetta, Casamassima, Nunzia, Frau, Francesca, D'Avila, Francesca, Cusi, Daniele, Barlassina, Cristina, Manunta, Paolo
Publicado 2011

Sardinians Genetic Background Explained by Runs of Homozygosity and Genomic Regions under Positive Selection

por Di Gaetano, Cornelia, Fiorito, Giovanni, Ortu, Maria Francesca, Rosa, Fabio, Guarrera, Simonetta, Pardini, Barbara, Cusi, Daniele, Frau, Francesca, Barlassina, Cristina, Troffa, Chiara, Argiolas, Giuseppe, Zaninello, Roberta, Fresu, Giovanni, Glorioso, Nicola, Piazza, Alberto, Matullo, Giuseppe
Publicado 2014

Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components

por Maj, Carlo, Salvi, Erika, Citterio, Lorena, Borisov, Oleg, Simonini, Marco, Glorioso, Valeria, Barlassina, Cristina, Glorioso, Nicola, Thijs, Lutgarde, Kuznetsova, Tatiana, Cappuccio, Francesco P., Zhang, Zhen-Yu, Staessen, Jan A., Cusi, Daniele, Lanzani, Chiara, Manunta, Paolo
Publicado 2022

Application of an Exploratory Knowledge-Discovery Pipeline Based on Machine Learning to Multi-Scale OMICS Data to Characterise Myocardial Injury in a Cohort of Patients with Septic...

por Bollen Pinto, Bernardo, Ribas Ripoll, Vicent, Subías-Beltrán, Paula, Herpain, Antoine, Barlassina, Cristina, Oliveira, Eliandre, Pastorelli, Roberta, Braga, Daniele, Barcella, Matteo, Subirats, Laia, Bauzá-Martinez, Julia, Odena, Antonia, Ferrario, Manuela, Baselli, Giuseppe, Aletti, Federico, Bendjelid, Karim
Publicado 2021

Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy

por D’Avila, Francesca, Meregalli, Mirella, Lupoli, Sara, Barcella, Matteo, Orro, Alessandro, De Santis, Francesca, Sitzia, Clementina, Farini, Andrea, D’Ursi, Pasqualina, Erratico, Silvia, Cristofani, Riccardo, Milanesi, Luciano, Braga, Daniele, Cusi, Daniele, Poletti, Angelo, Barlassina, Cristina, Torrente, Yvan
Publicado 2016

An Overview of the Genetic Structure within the Italian Population from Genome-Wide Data

por Di Gaetano, Cornelia, Voglino, Floriana, Guarrera, Simonetta, Fiorito, Giovanni, Rosa, Fabio, Di Blasio, Anna Maria, Manzini, Paola, Dianzani, Irma, Betti, Marta, Cusi, Daniele, Frau, Francesca, Barlassina, Cristina, Mirabelli, Dario, Magnani, Corrado, Glorioso, Nicola, Bonassi, Stefano, Piazza, Alberto, Matullo, Giuseppe
Publicado 2012

Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study

por Rizzi, Federica, Conti, Costanza, Dogliotti, Elena, Terranegra, Annalisa, Salvi, Erika, Braga, Daniele, Ricca, Flavia, Lupoli, Sara, Mingione, Alessandra, Pivari, Francesca, Brasacchio, Caterina, Barcella, Matteo, Chittani, Martina, D’Avila, Francesca, Turiel, Maurizio, Lazzaroni, Monica, Soldati, Laura, Cusi, Daniele, Barlassina, Cristina
Publicado 2016

gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML

por Rainero, Alessia, Angaroni, Fabrizio, D’Avila, Francesca, Conti, Andrea, Pirrone, Cristina, Micheloni, Giovanni, Tararà, Lucia, Millefanti, Giorgia, Maserati, Emanuela, Valli, Roberto, Spinelli, Orietta, Buklijas, Ksenija, Michelato, Anna, Casalone, Rosario, Barlassina, Cristina, Barcella, Matteo, Sirchia, Silvia, Piscitelli, Eleonora, Caccia, Massimo, Porta, Giovanni
Publicado 2018

α- and β-Adducin polymorphisms affect podocyte proteins and proteinuria in rodents and decline of renal function in human IgA nephropathy

por Ferrandi, Mara, Cusi, Daniele, Molinari, Isabella, Del Vecchio, Lucia, Barlassina, Cristina, Rastaldi, Maria Pia, Schena, Francesco Paolo, Macciardi, Fabio, Marcantoni, Carmelita, Roccatello, Dario, Peters, Luanne L., Armelloni, Silvia, Min, Li, Giardino, Laura, Mattinzoli, Deborah, Camisasca, Claudio, Palazzo, Fiorentina, Manunta, Paolo, Ferrari, Patrizia, Bianchi, Giuseppe
Publicado 2009

ShockOmics: multiscale approach to the identification of molecular biomarkers in acute heart failure induced by shock

por Aletti, Federico, Conti, Costanza, Ferrario, Manuela, Ribas, Vicent, Bollen Pinto, Bernardo, Herpain, Antoine, Post, Emiel, Romay Medina, Eduardo, Barlassina, Cristina, de Oliveira, Eliandre, Pastorelli, Roberta, Tedeschi, Gabriella, Ristagno, Giuseppe, Taccone, Fabio S., Schmid-Schönbein, Geert W., Ferrer, Ricard, De Backer, Daniel, Bendjelid, Karim, Baselli, Giuseppe
Publicado 2016

PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population

por Yang, Wen-Yi, Petit, Thibault, Cauwenberghs, Nicholas, Zhang, Zhen-Yu, Sheng, Chang-Sheng, Thijs, Lutgarde, Salvi, Erika, Izzi, Benedetta, Vandenbriele, Christophe, Wei, Fang-Fei, Gu, Yu-Mei, Jacobs, Lotte, Citterio, Lorena, Delli Carpini, Simona, Barlassina, Cristina, Cusi, Daniele, Hoylaerts, Marc F., Verhamme, Peter, Kuznetsova, Tatiana, Staessen, Jan A.
Publicado 2017

Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population

por Yang, Wen-Yi, Petit, Thibault, Thijs, Lutgarde, Zhang, Zhen-Yu, Jacobs, Lotte, Hara, Azusa, Wei, Fang-Fei, Salvi, Erika, Citterio, Lorena, Delli Carpini, Simona, Gu, Yu-Mei, Knez, Judita, Cauwenberghs, Nicholas, Barcella, Matteo, Barlassina, Cristina, Manunta, Paolo, Coppiello, Giulia, Aranguren, Xabier L., Kuznetsova, Tatiana, Cusi, Daniele, Verhamme, Peter, Luttun, Aernout, Staessen, Jan A.
Publicado 2015

Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

por Sorosina, Melissa, Barizzone, Nadia, Clarelli, Ferdinando, Anand, Santosh, Lupoli, Sara, Salvi, Erika, Mangano, Eleonora, Bordoni, Roberta, Roostaei, Tina, Mascia, Elisabetta, Zuccalà, Miriam, Vecchio, Domizia, Cavalla, Paola, Santoro, Silvia, Ferrè, Laura, Zollo, Alen, Barlassina, Cristina, Cusi, Daniele, Martinelli, Vittorio, Comi, Giancarlo, Leone, Maurizio, Filippi, Massimo, Patsopoulos, Nikolaos A., De Jager, Philip L., De Bellis, Gianluca, Esposito, Federica, D’Alfonso, Sandra, Martinelli Boneschi, Filippo
Publicado 2022

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

por Sorosina, Melissa, Barizzone, Nadia, Clarelli, Ferdinando, Anand, Santosh, Lupoli, Sara, Salvi, Erika, Mangano, Eleonora, Bordoni, Roberta, Roostaei, Tina, Mascia, Elisabetta, Zuccalà, Miriam, Vecchio, Domizia, Cavalla, Paola, Santoro, Silvia, Ferrè, Laura, Zollo, Alen, Barlassina, Cristina, Cusi, Daniele, Martinelli, Vittorio, Comi, Giancarlo, Leone, Maurizio, Filippi, Massimo, Patsopoulos, Nikolaos A., De Jager, Philip L., De Bellis, Gianluca, Esposito, Federica, D’Alfonso, Sandra, Martinelli Boneschi, Filippo
Publicado 2022

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

por 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
Publicado 2015

PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance

por Kiando, Soto Romuald, Tucker, Nathan R., Castro-Vega, Luis-Jaime, Katz, Alexander, D’Escamard, Valentina, Tréard, Cyrielle, Fraher, Daniel, Albuisson, Juliette, Kadian-Dodov, Daniella, Ye, Zi, Austin, Erin, Yang, Min-Lee, Hunker, Kristina, Barlassina, Cristina, Cusi, Daniele, Galan, Pilar, Empana, Jean-Philippe, Jouven, Xavier, Gimenez-Roqueplo, Anne-Paule, Bruneval, Patrick, Hyun Kim, Esther Soo, Olin, Jeffrey W., Gornik, Heather L., Azizi, Michel, Plouin, Pierre-François, Ellinor, Patrick T., Kullo, Iftikhar J., Milan, David J., Ganesh, Santhi K., Boutouyrie, Pierre, Kovacic, Jason C., Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Publicado 2016