Role of Vitamin D Receptor Activators in Cardio-Renal Syndromes von Cozzolino, Mario, MD, PhD, Bruschetta, Elena, MD, Stucchi, Andrea, MD, Ronco, Claudio, MD, Cusi, Daniele, MD

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Renal lithium clearance in the different stages of hypertension von Niutta, Enrico, Barlassina, Cristina, Colombo, Roberto, Dossi, Fiorella, Pellizzoni, Manuela, Cusi, Daniele M, Cesana, Bruno, Bianchi, Giuseppe

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19 Two point mutations within the adducin genes are responsible for variation in blood pressure, kidney and erythrocyte size: a new mechanism for genetic hypertension von Bianchi, Giuseppe, Tripodi, G., Casari, G., Modica, R., Torielli, Lucia, Salardi, Sergio, Barber, B. R., Cusi, Daniele M., Ferrandi, Mara, Ferrari, Patrizia

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Setting Priorities for Optimizing Vascular Access Decision Making--An International Survey of Patients and Clinicians von van der Veer, Sabine N, Haller, Maria C, Pittens, Carina A C M, Broerse, Jacqueline, Castledine, Clare, Gallieni, Maurizio, Inston, Nicholas, Marti Monros, Anna, Peek, Niels, van Biesen, Wim

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Effects of dietary phosphate on adynamic bone disease in rats with chronic kidney disease--role of sclerostin? von Ferreira, Juliana C, Ferrari, Guaraciaba O, Neves, Katia R, Cavallari, Raquel T, Dominguez, Wagner V, Dos Reis, Luciene M, Graciolli, Fabiana G, Oliveira, Elizabeth C, Liu, Shiguang, Sabbagh, Yves, Jorgetti, Vanda, Schiavi, Susan, Moysés, Rosa M A

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A magnesium based phosphate binder reduces vascular calcification without affecting bone in chronic renal failure rats von Neven, Ellen, De Schutter, Tineke M, Dams, Geert, Gundlach, Kristina, Steppan, Sonja, Büchel, Janine, Passlick-Deetjen, Jutta, D'Haese, Patrick C, Behets, Geert J

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Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility von Patsopoulos, Nikolaos A., Baranzini, Sergio E., Santaniello, Adam, Shoostari, Parisa, Cotsapas, Chris, Wong, Garrett, Beecham, Ashley H., James, Tojo, Replogle, Joseph, Vlachos, Ioannis S., McCabe, Cristin, Pers, Tune H., Brandes, Aaron, White, Charles, Keenan, Brendan, Cimpean, Maria, Winn, Phoebe, Panteliadis, Ioannis-Pavlos, Robbins, Allison, Andlauer, Till F. M., Zarzycki, Onigiusz, Dubois, Bénédicte, Goris, An, Søndergaard, Helle Bach, Sellebjerg, Finn, Sorensen, Per Soelberg, Ullum, Henrik, Thørner, Lise Wegner, Saarela, Janna, Cournu-Rebeix, Isabelle, Damotte, Vincent, Fontaine, Bertrand, Guillot-Noel, Lena, Lathrop, Mark, Vukusic, Sandra, Berthele, Achim, Pongratz, Viola, Buck, Dorothea, Gasperi, Christiane, Graetz, Christiane, Grummel, Verena, Hemmer, Bernhard, Hoshi, Muni, Knier, Benjamin, Korn, Thomas, Lill, Christina M., Luessi, Felix, Mühlau, Mark, Zipp, Frauke, Dardiotis, Efthimios, Agliardi, Cristina, Amoroso, Antonio, Barizzone, Nadia, Benedetti, Maria D., Bernardinelli, Luisa, Cavalla, Paola, Clarelli, Ferdinando, Comi, Giancarlo, Cusi, Daniele, Esposito, Federica, Ferrè, Laura, Galimberti, Daniela, Guaschino, Clara, Leone, Maurizio A., Martinelli, Vittorio, Moiola, Lucia, Salvetti, Marco, Sorosina, Melissa, Vecchio, Domizia, Zauli, Andrea, Santoro, Silvia, Mancini, Nicasio, Zuccalà, Miriam, Mescheriakova, Julia, van Duijn, Cornelia, Bos, Steffan D., Celius, Elisabeth G., Spurkland, Anne, Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Bomfim, Izaura L., Gomez-Cabrero, David, Hillert, Jan, Jagodic, Maja, Lindén, Magdalena, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mirela, Baker, Amie, Ban, Maria, Hawkins, Clive, Hysi, Pirro, Kalra, Seema, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Molyneux, Paul, Neville, Matthew

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Copy Number Variations and Cognitive Phenotypes in Unselected Populations von Männik, Katrin, Mägi, Reedik, Macé, Aurélien, Cole, Ben, Guyatt, Anna L, Shihab, Hashem A, Maillard, Anne M, Alavere, Helene, Kolk, Anneli, Reigo, Anu, Mihailov, Evelin, Leitsalu, Liis, Ferreira, Anne-Maud, Nõukas, Margit, Teumer, Alexander, Salvi, Erika, Cusi, Daniele, McGue, Matt, Iacono, William G, Gaunt, Tom R, Beckmann, Jacques S, Jacquemont, Sébastien, Kutalik, Zoltán, Pankratz, Nathan, Timpson, Nicholas, Metspalu, Andres, Reymond, Alexandre

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Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis von 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

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A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia von Palluzzi, Fernando, Ferrari, Raffaele, Graziano, Francesca, Novelli, Valeria, Rossi, Giacomina, Galimberti, Daniela, Rainero, Innocenzo, Benussi, Luisa, Nacmias, Benedetta, Bruni, Amalia C, Cusi, Daniele, Salvi, Erika, Borroni, Barbara, Grassi, Mario

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Classical HLA-DRB1 and DPB1 alleles account for HLA associations with primary biliary cirrhosis von Invernizzi, P, Ransom, M, Raychaudhuri, S, Kosoy, R, Lleo, A, Shigeta, R, Franke, A, Bossa, F, Amos, C I, Gregersen, P K, Siminovitch, K A, Cusi, D, de Bakker, P I W, Podda, M, Gershwin, M E, Seldin, M F

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Quality control and conduct of genome-wide association meta-analyses von Winkler, Thomas W, Day, Felix R, Croteau-Chonka, Damien C, Wood, Andrew R, Locke, Adam E, Mägi, Reedik, Ferreira, Teresa, Fall, Tove, Graff, Mariaelisa, Justice, Anne E, Luan, Jian'an, Gustafsson, Stefan, Randall, Joshua C, Vedantam, Sailaja, Workalemahu, Tsegaselassie, Kilpeläinen, Tuomas O, Scherag, André, Esko, Tonu, Kutalik, Zoltán, Heid, Iris M, Loos, Ruth J F

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Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis von Noyce, Alastair J., Hemani, Gibran, Mora, Gabriele, Bartolomei, Ilaria, Benigni, Michele, Borghero, Giuseppe, Brunetti, Maura, Calvo, Andrea, Cammarosano, Stefania, Cannas, Antonino, Caponnetto, Claudia, Casale, Federico, Cavallaro, Sebastiano, Chiò, Adriano, Colletti, Tiziana, Conforti, Francesca L., Conte, Amelia, Corrado, Lucia, Costantino, Emanuela, D'Alfonso, Sandra, Femiano, Cinzia, Ferrarese, Carlo, Fini, Nicola, Floris, Gianluca, Grassano, Maurizio, Lattante, Serena, Logroscino, Giancarlo, Loi, Daniela, Mancardi, Gianluigi, Mandich, Paola, Manera, Umberto, Marinou, Kalliopi, Marrali, Giuseppe, Marrosu, Maria Giovanna, Mazzini, Letizia, Melis, Maurizio, Messina, Sonia, Mora, Gabriele, Occhineri, Patrizia, Origone, Paola, Pani, Carla, Petrucci, Antonio, Pirisi, Angelo, Restagno, Gabriella, Ricci, Claudia, Riva, Nilo, Sabatelli, Mario, Santarelli, Marialuisa, Spataro, Rossella, Tanel, Raffaella, Tremolizzo, Lucio, Volanti, Paolo, Zollino, Marcella, Arepalli, Sampath, Bowser, Robert, Broach, James, Camu, William, Chia, Ruth, Chiò, Adriano, Ding, Jinhui, Dunckley, Travis L., Eicher, John D., Faghri, Faraz, Feldman, Eva, Fratta, Pietro, Geiger, Joshua T., Gerhard, Glenn, Hardy, John, Harms, Matthew B., Heiman‐Patterson, Terry D., Kamel, Freya, MacGowan, Daniel J.L., Maragakis, Nicholas J., Murphy, Natalie A., Myllykangas, Liisa, Nalls, Mike A., Nicolas, Aude, Orrell, Richard W., Pamphlett, Roger, Pickering‐Brown, Stuart, Pioro, Erik, Pliner, Hannah A., Pulst, Stefan M., Ravits, John M., Rothstein, Jeffrey D., Salvi, Erika, Sendtner, Michael, Simmons, Zachary, Stone, David C., Sulkava, Raimo, Troncoso, Juan C., Van Damme, Philip, Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Zinman, Lorne, Tienari, Pentti J., Stone, David J., Nalls, Mike A., Singleton, Andrew B., Traynor, Bryan J.

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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk von Patsopoulos, Nikolaos A., Beecham, Ashley H., Goris, An, Dubois, Bénédicte, D’hooghe, Marie B., Van Damme, Philip, Søndergaard, Helle Bach, Sellebjerg, Finn, Ullum, Henrik, Thørner, Lise W., Werge, Thomas, Damotte, Vincent, Fontaine, Bertrand, Lathrop, Mark, Gourraud, Pierre-Antoine, Pongratz, Viola, Gasperi, Christiane, Bayas, Antonios, Heesen, Christoph, Linker, Ralf, Paul, Friedemann, Stangel, Martin, Tackenberg, Björn, Bergh, Florian Then, Wildemann, Brigitte, Tumani, Hayrettin, Gold, Ralf, Grummel, Verena, Knier, Benjamin, Lill, Christina M., Dardiotis, Efthimios, Agliardi, Cristina, Barizzone, Nadia, Mascia, Elisabetta, Bernardinelli, Luisa, Cusi, Daniele, Ferrè, Laura, Comi, Cristoforo, Galimberti, Daniela, Leone, Maurizio A., Mescheriakova, Julia, Hintzen, Rogier, van Duijn, Cornelia, Teunissen, Charlotte E., Bos, Steffan D., Myhr, Kjell-Morten, Celius, Elisabeth G., Lie, Benedicte A., Comabella, Manuel, Montalban, Xavier, Alfredsson, Lars, Stridh, Pernilla, Hillert, Jan, Piehl, Fredrik, Jelčić, Ilijas, Martin, Roland, Sospedra, Mireia, Hawkins, Clive, Hysi, Pirro, Karpe, Fredrik, Khadake, Jyoti, Lachance, Genevieve, Neville, Matthew, Santaniello, Adam, Caillier, Stacy J., Calabresi, Peter A., Cross, Anne, Davis, Mary F., de Bakker, Paul I.W., Delgado, Silvia, Dembele, Marieme, Edwards, Keith, Fitzgerald, Kathryn C., Hakonarson, Hakon, Konidari, Ioanna, Lathi, Ellen, Manrique, Clara P., Pericak-Vance, Margaret A., Piccio, Laura, Schaefer, Cathy, McCabe, Cristin, Hadjigeorgiou, Georgios, Taylor, Bruce, Tajouri, Lotti, Charlesworth, Jac, Booth, David R., Harbo, Hanne F., Ivinson, Adrian J., Hauser, Stephen L., Compston, Alastair, Stewart, Graeme, Zipp, Frauke, Barcellos, Lisa F., Baranzini, Sergio E., Martinelli-Boneschi, Filippo, Ziegler, Andreas, McCauley, Jacob L., Sawcer, Stephen J., De Jager, Philip L., Kockum, Ingrid

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

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Xanthine oxidase gene variants and their association with blood pressure and incident hypertension: a population study von Scheepers, Lieke E.J.M, Wei, Fang-Fei, Stolarz-Skrzypek, Katarzyna, Malyutina, Sofia, Tikhonoff, Valérie, Thijs, Lutgarde, Salvi, Erika, Barlassina, Cristina, Filipovský, Jan, Casiglia, Edoardo, Nikitin, Yuri, Kawecka-Jaszcz, Kalina, Manunta, Paolo, Cusi, Daniele, Boonen, Annelies, Staessen, Jan A, Arts, Ilja C.W

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Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 a... von Juran, Brian D, Hirschfield, Gideon M, Invernizzi, Pietro, Atkinson, Elizabeth J, Li, Yafang, Xie, Gang, Kosoy, Roman, Ransom, Michael, Sun, Ye, Bianchi, Ilaria, Schlicht, Erik M, Lleo, Ana, Coltescu, Catalina, Bernuzzi, Francesca, Podda, Mauro, Lammert, Craig, Shigeta, Russell, Chan, Landon L, Balschun, Tobias, Marconi, Maurizio, Cusi, Daniele, Heathcote, E Jenny, Mason, Andrew L, Myers, Robert P, Milkiewicz, Piotr, Odin, Joseph A, Luketic, Velimir A, Bacon, Bruce R, Bodenheimer, Jr, Henry C, Liakina, Valentina, Vincent, Catherine, Levy, Cynthia, Franke, Andre, Gregersen, Peter K, Bossa, Fabrizio, Gershwin, M Eric, deAndrade, Mariza, Amos, Christopher I, Lazaridis, Konstantinos N, Seldin, Michael F, Siminovitch, Katherine A

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TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives von Chittani, Martina, Zaninello, Roberta, Lanzani, Chiara, Frau, Francesca, Ortu, Maria F, Salvi, Erika, Fresu, Giovanni, Citterio, Lorena, Braga, Daniele, Piras, Daniela A, Carpini, Simona Delli, Velayutham, Dinesh, Simonini, Marco, Argiolas, Giuseppe, Pozzoli, Simona, Troffa, Chiara, Glorioso, Valeria, Kontula, Kimmo K, Hiltunen, Timo P, Donner, Kati M, Turner, Stephen T, Boerwinkle, Eric, Chapman, Arlene B, Padmanabhan, Sandosh, Dominiczak, Anna F, Melander, Olle, Johnson, Julie A, Cooper-Dehoff, Rhonda M, Gong, Yan, Rivera, Natalia V, Condorelli, Gianluigi, Trimarco, Bruno, Manunta, Paolo, Cusi, Daniele, Glorioso, Nicola, Barlassina, Cristina

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Left Ventricular Mass, Stroke Volume, and Ouabain-Like Factor in Essential Hypertension von Manunta, Paolo, Stella, Paola, Rivera, Rodolfo, Ciurlino, Daniele, Cusi, Daniele, Ferrandi, Mara, Hamlyn, John M, Bianchi, Giuseppe

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Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients von 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

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