The Effect of Paricalcitol on Vascular Calcification and Cardiovascular Disease in Uremia: Beyond PTH Control

by Cozzolino, Mario, Mehmeti, Florjan, Ciceri, Paola, Volpi, Elisa, Stucchi, Andrea, Brenna, Irene, Cusi, Daniele
Published 2011

Calcium-sensing receptor and calcium kidney stones

by Vezzoli, Giuseppe, Terranegra, Annalisa, Rainone, Francesco, Arcidiacono, Teresa, Cozzolino, Mario, Aloia, Andrea, Dogliotti, Elena, Cusi, Daniele, Soldati, Laura
Published 2011

Nutrition in calcium nephrolithiasis

by Dogliotti, Elena, Vezzoli, Giuseppe, Nouvenne, Antonio, Meschi, Tiziana, Terranegra, Annalisa, Mingione, Alessandra, Brasacchio, Caterina, Raspini, Benedetta, Cusi, Daniele, Soldati, Laura
Published 2013

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

by 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
Published 2011

Relevance of Mediterranean diet and glucose metabolism for nephrolithiasis in obese subjects

by Soldati, Laura, Bertoli, Simona, Terranegra, Annalisa, Brasacchio, Caterina, Mingione, Alessandra, Dogliotti, Elena, Raspini, Benedetta, Leone, Alessandro, Frau, Francesca, Vignati, Laila, Spadafranca, Angela, Vezzoli, Giuseppe, Cusi, Daniele, Battezzati, Alberto
Published 2014

Classical HLA-DRB1 and DPB1 Alleles Account for HLA Associations with Primary Biliary Cirrhosis

by Invernizzi, Pietro, Ransom, Michael, Raychaudhuri, Soumya, Kosoy, Roman, Lleo, Ana, Shigeta, Russell, Franke, Andre, Bossa, Fabrizio, Amos, Christopher I., Gregersen, Peter K., Siminovitch, Katherine A., Cusi, Daniele, de Bakker, Paul I.W., Podda, Mauro, Gershwin, M. Eric, Seldin, Michael F.
Published 2012

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

by 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
Published 2012

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

by 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
Published 2014

Left ventricular diastolic function associated with common genetic variation in ATP12A in a general population

by Knez, Judita, Salvi, Erika, Tikhonoff, Valérie, Stolarz-Skrzypek, Katarzyna, Ryabikov, Andrew, Thijs, Lutgarde, Braga, Daniele, Kloch-Badelek, Malgorzata, Malyutina, Sofia, Casiglia, Edoardo, Czarnecka, Danuta, Kawecka-Jaszcz, Kalina, Cusi, Daniele, Nawrot, Tim, Staessen, Jan A, Kuznetsova, Tatiana
Published 2014

Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort

by Landini, Martina, Merelli, Ivan, Raggi, M. Elisabetta, Galluccio, Nadia, Ciceri, Francesca, Bonfanti, Arianna, Camposeo, Serena, Massagli, Angelo, Villa, Laura, Salvi, Erika, Cusi, Daniele, Molteni, Massimo, Milanesi, Luciano, Marabotti, Anna, Mezzelani, Alessandra
Published 2016

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

by 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
Published 2016

Identification of NF-κB and PLCL2 as new susceptibility genes and highlights on a potential role of IRF8 through interferon signature modulation in systemic sclerosis

by Arismendi, Maria, Giraud, Matthieu, Ruzehaji, Nadira, Dieudé, Philippe, Koumakis, Eugenie, Ruiz, Barbara, Airo, Paolo, Cusi, Daniele, Matucci-Cerinic, Marco, Salvi, Erika, Cuomo, Giovanna, Hachulla, Eric, Diot, Elisabeth, Caramaschi, Paola, Riccieri, Valeria, Avouac, Jérôme, Kayser, Cristiane, Allanore, Yannick
Published 2015

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

by 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
Published 2016

Association of Genetic Markers with CSF Oligoclonal Bands in Multiple Sclerosis Patients

by Leone, Maurizio A., Barizzone, Nadia, Esposito, Federica, Lucenti, Ausiliatrice, Harbo, Hanne F., Goris, An, Kockum, Ingrid, Oturai, Annette Bang, Celius, Elisabeth Gulowsen, Mero, Inger L., Dubois, Bénédicte, Olsson, Tomas, Søndergaard, Helle Bach, Cusi, Daniele, Lupoli, Sara, Andreassen, Bettina Kulle, Myhr, Kjell-Morten, Guerini, Franca R., Comi, Giancarlo, Martinelli-Boneschi, Filippo, D'Alfonso, Sandra
Published 2013

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

by 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.
Published 2015

International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

by Cordell, Heather J., Han, Younghun, Mells, George F., Li, Yafang, Hirschfield, Gideon M., Greene, Casey S., Xie, Gang, Juran, Brian D., Zhu, Dakai, Qian, David C., Floyd, James A. B., Morley, Katherine I., Prati, Daniele, Lleo, Ana, Cusi, Daniele, Gershwin, M. Eric, Anderson, Carl A., Lazaridis, Konstantinos N., Invernizzi, Pietro, Seldin, Michael F., Sandford, Richard N., Amos, Christopher I., Siminovitch, Katherine A.
Published 2015

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

by 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
Published 2015

Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis

by Kiryluk, Krzysztof, Li, Yifu, Sanna-Cherchi, Simone, Rohanizadegan, Mersedeh, Suzuki, Hitoshi, Eitner, Frank, Snyder, Holly J., Choi, Murim, Hou, Ping, Scolari, Francesco, Izzi, Claudia, Gigante, Maddalena, Gesualdo, Loreto, Savoldi, Silvana, Amoroso, Antonio, Cusi, Daniele, Zamboli, Pasquale, Julian, Bruce A., Novak, Jan, Wyatt, Robert J., Mucha, Krzysztof, Perola, Markus, Kristiansson, Kati, Viktorin, Alexander, Magnusson, Patrik K., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boland, Anne, Metzger, Marie, Thibaudin, Lise, Wanner, Christoph, Jager, Kitty J., Goto, Shin, Maixnerova, Dita, Karnib, Hussein H., Nagy, Judit, Panzer, Ulf, Xie, Jingyuan, Chen, Nan, Tesar, Vladimir, Narita, Ichiei, Berthoux, Francois, Floege, Jürgen, Stengel, Benedicte, Zhang, Hong, Lifton, Richard P., Gharavi, Ali G.
Published 2012

Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis

by Allanore, Yannick, Saad, Mohamad, Dieudé, Philippe, Avouac, Jérôme, Distler, Jorg H. W., Amouyel, Philippe, Matucci-Cerinic, Marco, Riemekasten, Gabriella, Airo, Paolo, Melchers, Inga, Hachulla, Eric, Cusi, Daniele, Wichmann, H.-Erich, Wipff, Julien, Lambert, Jean-Charles, Hunzelmann, Nicolas, Tiev, Kiet, Caramaschi, Paola, Diot, Elisabeth, Kowal-Bielecka, Otylia, Valentini, Gabriele, Mouthon, Luc, Czirják, László, Damjanov, Nemanja, Salvi, Erika, Conti, Costanza, Müller, Martina, Müller-Ladner, Ulf, Riccieri, Valeria, Ruiz, Barbara, Cracowski, Jean-Luc, Letenneur, Luc, Dupuy, Anne Marie, Meyer, Oliver, Kahan, André, Munnich, Arnold, Boileau, Catherine, Martinez, Maria
Published 2011

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

by 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
Published 2016