Zoekresultaten - Carlo Berzuini

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  1. 1
    A Bayesian approach to Mendelian randomization with multiple pleiotropic variants

    A Bayesian approach to Mendelian randomization with multiple pleiotropic variants door Carlo Berzuini, Hui Guo, Stephen Burgess, Luisa Bernardinelli

    Gepubliceerd in 2018
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  2. 2
    Women’s Pregnancy Life History and Alzheimer’s Risk: Can Immunoregulation Explain the Link?

    Women’s Pregnancy Life History and Alzheimer’s Risk: Can Immunoregulation Explain the Link? door Molly Fox, Carlo Berzuini, Leslie A. Knapp, Laura M. Glynn

    Gepubliceerd in 2018
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  3. 3
    Sensitivity to pain expectations: A Bayesian model of individual differences

    Sensitivity to pain expectations: A Bayesian model of individual differences door Robert E. Hoskin, Carlo Berzuini, D. Acosta-Kane, Wael El‐Deredy, Hui Guo, Deborah Talmi

    Gepubliceerd in 2018
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  4. 4
    Genetic association between NLRP3 variants and Crohnʼs disease does not replicate in a large UK panel

    Genetic association between NLRP3 variants and Crohnʼs disease does not replicate in a large UK panel door Gregory J. Lewis, Dunecan Massey, Hu Zhang, Francesca Bredin, Mark Tremelling, James Lee, Carlo Berzuini, Miles Parkes

    Gepubliceerd in 2010
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  5. 5
    Contribution of TNFSF15 gene variants to Crohnʼs disease susceptibility confirmed in UK population

    Contribution of TNFSF15 gene variants to Crohnʼs disease susceptibility confirmed in UK population door Mark Tremelling, Carlo Berzuini, Dunecan Massey, Francesca Bredin, C.J. Price, Claire Dawson, Sheila Bingham, Miles Parkes

    Gepubliceerd in 2008
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  6. 6
    Endothelial Nitric Oxide Synthase Polymorphisms Are Associated With Type 2 Diabetes and the Insulin Resistance Syndrome

    Endothelial Nitric Oxide Synthase Polymorphisms Are Associated With Type 2 Diabetes and the Insulin Resistance Syndrome door Lucilla D. Monti, Cristina Barlassina, Lorena Citterio, Elena Galluccio, Carlo Berzuini, Emanuela Setola, G. Valsecchi, Pietro Lucotti, G. Pozza, Luisa Bernardinelli, Giorgio Casari, PierMarco Piatti

    Gepubliceerd in 2003
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  7. 7
    The Combination of Circulating Ang1 and Tie2 Levels Predicts Progression-Free Survival Advantage in Bevacizumab-Treated Patients with Ovarian Cancer

    The Combination of Circulating Ang1 and Tie2 Levels Predicts Progression-Free Survival Advantage in Bevacizumab-Treated Patients with Ovarian Cancer door Alison Backen, Andrew G. Renehan, Andrew R. Clamp, Carlo Berzuini, Cong Zhou, Amit M. Oza, Selina Bannoo, Stefan Scherer, Rosamonde E. Banks, Caroline Dive, Gordon C. Jayson

    Gepubliceerd in 2014
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  8. 8
    Mapping the platelet profile for functional genomic studies and demonstration of the effect size of the GP6 locus

    Mapping the platelet profile for functional genomic studies and demonstration of the effect size of the GP6 locus door Chris I. Jones, Stephen F. Garner, Will Angenent, Adam S. Bernard, Carlo Berzuini, Philippa Burns, Richard W. Farndale, John Hogwood, Angela Rankin, Jonathan Stephens, Brian D. M. Tom, J. Walton, Frank Dudbridge, Willem H. Ouwehand, Alison H. Goodall

    Gepubliceerd in 2007
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  9. 9
    IL23R Variation Determines Susceptibility But Not Disease Phenotype in Inflammatory Bowel Disease

    IL23R Variation Determines Susceptibility But Not Disease Phenotype in Inflammatory Bowel Disease door Mark Tremelling, Fraser Cummings, Sheila Fisher, John Mansfield, Rhian Gwilliam, Andrew Keniry, Elaine R. Nimmo, Hazel E. Drummond, Clive M. Onnie, Natalie J. Prescott, Jeremy Sanderson, Francesca Bredin, Carlo Berzuini, Alastair Forbes, Cathryn M. Lewis, Lon R. Cardon, Panos Deloukas, Derek P. Jewell, Christopher G. Mathew, Miles Parkes, Jack Satsangi

    Gepubliceerd in 2007
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  10. 10
    Molecular insights into genome-wide association studies of chronic kidney disease-defining traits

    Molecular insights into genome-wide association studies of chronic kidney disease-defining traits door Xiaoguang Xu, James Eales, Artur Akbarov, Hui Guo, Lorenz K. Becker, David Talavera, Fehzan Ashraf, Jabran Nawaz, Sanjeev Pramanik, John Bowes, Xiao Jiang, John Dormer, Matthew Denniff, Andrzej Antczak, Monika Szulińska, Ingrid Wise, Priscilla R. Prestes, Maciej Głyda, Paweł Bogdański, E Zukowska-Szczechowska, Carlo Berzuini, Adrian S. Woolf, Nilesh J. Samani, Fadi J. Charchar, Maciej Tomaszewski

    Gepubliceerd in 2018
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  11. 11
    Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction

    Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction door Diego Ardissino, Carlo Berzuini, Piera Angelica Merlini, Pier Mannuccio Mannucci, Aarti Surti, Noël P. Burtt, Benjamin F. Voight, Marco Tubaro, Flora Peyvandi, M. Spreafico, Patrizia Celli, Daniela Lina, Maria Francesca Notarangelo, Maurizio Ferrario, Raffaela Fetiveau, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Nicola Marziliano, Pietro Zonzin, Francesco Mauri, Alberto Piazza, Luisa Foco, Luisa Bernardinelli, David Altshuler, Sekar Kathiresan

    Gepubliceerd in 2011
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  12. 12
    Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease

    Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease door Sheila Fisher, Mark Tremelling, Carl A. Anderson, Rhian Gwilliam, Suzannah Bumpstead, Natalie J. Prescott, Elaine R. Nimmo, Dunecan Massey, Carlo Berzuini, C. Mark Johnson, Jeffrey C. Barrett, Fraser Cummings, Hazel E. Drummond, Charlie W. Lees, Clive M. Onnie, Catherine Hanson, Katarzyna Błaszczyk, Michael Inouye, Philip Ewels, Rathi Ravindrarajah, Andrew Keniry, Sarah Hunt, Martyn Carter, Nick Watkins, Willem H. Ouwehand, Cathryn M. Lewis, Lon R. Cardon, Alan Lobo, Alastair Forbes, Jeremy Sanderson, Derek P. Jewell, John Mansfield, Panos Deloukas, Christopher G. Mathew, Miles Parkes, Jack Satsangi

    Gepubliceerd in 2008
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  13. 13
    Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney

    Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney door James Eales, Xiao Jiang, Xiaoguang Xu, Sushant Saluja, Artur Akbarov, Eddie Cano-Gamez, Michelle Mcnulty, Chris Finan, Hui Guo, Wojciech Wystrychowski, Monika Szulińska, Huw B. Thomas, Sanjeev Pramanik, Sandesh Chopade, Priscilla R. Prestes, Ingrid Wise, Εvangelos Εvangelou, Mahan Salehi, Yusif Shakanti, Mikael Ekholm, Matthew Denniff, Alicja Nazgiewicz, Felix Eichinger, Bradley Godfrey, Andrzej Antczak, Maciej Głyda, Robert Król, Stephen Eyre, Jason L. Brown, Carlo Berzuini, John Bowes, Mark J. Caulfield, E Zukowska-Szczechowska, Joanna Żywiec, Paweł Bogdański, Matthias Kretzler, Adrian S. Woolf, David Talavera, Bernard Keavney, Pasquale Maffia, Tomasz J. Guzik, Raymond T. O’Keefe, Gosia Trynka, Nilesh J. Samani, Aroon D. Hingorani, Matthew G. Sampson, Andrew P. Morris, Fadi J. Charchar, Maciej Tomaszewski

    Gepubliceerd in 2021
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  14. 14
    Association Between Variants of PRDM1 and NDP52 and Crohn's Disease, Based on Exome Sequencing and Functional Studies

    Association Between Variants of PRDM1 and NDP52 and Crohn's Disease, Based on Exome Sequencing and Functional Studies door David Ellinghaus, Hu Zhang, Sebastian Zeißig, Simone Lipinski, Andreas Till, Tao Jiang, Björn Stade, Yana Bromberg, Eva Ellinghaus, Andreas Keller, Manuel A. Rivas, Jurgita Skiecevičienė, Nadezhda T. Doncheva, Xiao Liu, Qing Liu, Fuman Jiang, Michael Förster, Gabriele Mayr, Mario Albrecht, Robert Häsler, Bernhard O. Boehm, Jane Goodall, Carlo Berzuini, James Lee, Vibeke Andersen, Ulla Vogel, Limas Kupčinskas, Manfred Kayser, Michael Krawczak, Susanna Nikolaus, Rinse K. Weersma, Cyriel Y. Ponsioen, Miquel Sans, Cisca Wijmenga, David P. Strachan, Wendy L. McArdle, Séverine Vermeire, Paul Rutgeerts, Jeremy Sanderson, Christopher G. Mathew, Morten H. Vatn, Jun Wang, Markus M. Nöthen, Richard H. Duerr, Carsten Büning, Stephan Brand, Jürgen Glas, Juliane Winkelmann, Thomas Illig, Anna Latiano, Vito Annese, Jonas Halfvarson, Mauro D’Amato, Mark J. Daly, Michael Nothnagel, Tom H. Karlsen, Suresh Subramani, Philip Rosenstiel, Stefan Schreiber, Miles Parkes, André Franke

    Gepubliceerd in 2013
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  15. 15
    No Evidence of Association Between Prothrombotic Gene Polymorphisms and the Development of Acute Myocardial Infarction at a Young Age

    No Evidence of Association Between Prothrombotic Gene Polymorphisms and the Development of Acute Myocardial Infarction at a Young Age door Pier Mannuccio Mannucci, Pier Angelica Merlini, Diego Ardissino, C. Barzuini, Francesco Bernardi, Luisa Bernardinelli, Claudio Cavallini, Patrizia Celli, G Corsini, Maurizio Ferrario, Raffaela Fetiveau, Michele Galli, Alberto Piazza, F Ribichini, Elisabetta Sacchi, Marco Tubaro, Pietro Zonzin, Carlo Berzuini, Luisa Foco, L. Tagliabue, Marzia Menegatti, Flora Peyvandi, Alessandra Repetto, Umberto Canosi, V. Cucci, Silvia Buratti, S. Fondazione, M. Ponzetta, Massimo Rinuncini, M. Spolverato, A Vetrano, Marco Lamponi, L. Cacciavillani, Christel Castelli, A. Colizzi, N Pagnoni, Elisabetta Colombi, D. Covini, Gemma Viola Fantini, Claudio Dodi, P Paoloni, I. Maoddi, G. Bardelli, Michele Azzarito, M. Beciani, F. Tettamanti, M. Caccia, P. Massoli, R Pozzi, F Pecchio, Peter Barberis, Marco Giudice, R. Di Giovanbattista, B. Mazzocco, G.B. Gaeta, Maurizio Margaglione, P Diotallevi, Alessandro Salvioni, S. Biancoli, Andrea Rosi, Elena Milanesi, Simonetta Span, Antonino Saccà, Alessandra Maugeri, D Scorzoni, Michela Maffi, G. A. Dei Tos, P. P. Cannarozzo, R. Vandelli, M. Fici, A. Tempesta, G. R. Lucchi, G Ricci, D Baragli, D. Laiso, L. Garzaro, Raffaella Vaninetti, Gaia Cattadori, Anna Picozzi, R Petacchi, Cecilia Berardi, Vincenzo Guiducci, Oscar Gaddi, N. Franco, E Buia, Franco Fedeli, Francesco Barillà, Luigi Irace, S. M. Sarracino, N. De Giorgio, G. Scalera, Maurizio Elia, P. Sabella, A.M. Previtera, G. Di Tano, Bruno Francaviglia, Giovanni Contini, F. Del Nevo, Pietro Agricola

    Gepubliceerd in 2003
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  16. 16
    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants door Sekar Kathiresan, Benjamin F. Voight, Shaun Purcell, Kiran Musunuru, Diego Ardissino, Pier M Mannucci, Sonia Anand, James C. Engert, Nilesh J Samani, Heribert Schunkert, Jeanette Erdmann, Muredach P. Reilly, Daniel J. Rader, Thomas Morgan, John A. Spertus, Monika Stoll, Domenico Girelli, Pascal McKeown, Chris C Patterson, David S Siscovick, Christopher J O'Donnell, Roberto Elosúa, Leena Peltonen, Veikko Salomaa, Stephen M Schwartz, Olle Melander, David Altshuler, Pier Angelica Merlini, Carlo Berzuini, Luisa Bernardinelli, Flora Peyvandi, Marco Tubaro, Patrizia Celli, Maurizio Ferrario, Raffaela Fetiveau, Nicola Marziliano, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Pietro Zonzin, Alberto Piazza, Jean Yee, Yechiel Friedlander, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, James B Meigs, Gordon Williams, David M Nathan, Calum A. MacRae, Aki S Havulinna, Göran Berglund, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Marta Spreafico, Mark Daly, James Nemesh, Joshua M. Korn, Steven A. McCarroll, Aarti Surti, Candace Guiducci, Lauren Gianniny, Daniel B. Mirel, Melissa Parkin, Noël P. Burtt, Stacey B. Gabriel, John R Thompson, Peter S. Braund, Benjamin J. Wright, Anthony J Balmforth, Stephen G. Ball, Alistair S. Hall, Patrick Linsel‐Nitschke, Wolfgang Lieb, Andreas Ziegler, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Anika Grosshennig, Michael Preuß, H‐Erich Wichmann, Stefan Schreiber, Willem H. Ouwehand, Panos Deloukas, Michael Scholz, Francois Cambien, Mingyao Li, Zhen Chen, Robert Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Joe Devaney, Mary-Susan Burnett

    Gepubliceerd in 2009
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