Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Medea S. Eleftheriadis"'
A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease
Autor:
Juergen Schrezenmeir, Heidi Rossmann, Joshua C. Bis, Tanja Zeller, Heinz Erich Wichmann, Sandra Wilde, Jeanette Erdmann, Serkalem Demissie, Wibke Reinhard, Roberto Elosua, Arne Schillert, Vilmundur Gudnason, Albert Hofman, Sekar Kathiresan, Philipp S. Wild, Christoph Bickel, François Cambien, Stefan Schreiber, Mary Susan Burnett, Eric Boerwinkle, Klaus Stark, Nour Eddine El Mokthari, Stefan Blankenberg, Mingyao Li, Veikko Salomaa, Medea S. Eleftheriadis, Marcus E. Kleber, Dominique Arveiler, Alun Evans, Kaisa Silander, Jarmo Virtamo, Michael M. Hoffmann, Arne Schäfer, Andreas Ziegler, Patrick Diemert, Till Keller, Aaron R. Folsom, Peter S. Braund, Annette Peters, Karl J. Lackner, Nehal N. Mehta, Stephen M. Schwartz, Nilesh J. Samani, Inke R. König, Heribert Schunkert, Renate B. Schnabel, Jens Baumert, L. Adrienne Cupples, André G. Uitterlinden, Tamara B. Harris, Muredach P. Reilly, Per-Gunnar Wiklund, Hans J. Rupprecht, Maja Barbalić, Jaqueline C M Witteman, Frank Kee, Jean Ferrières, Edith Lubos, Hendrik B. Sager, David S. Siscovick, Liming Qu, Norman Klopp, Daniel J. Rader, Thomas Münzel, Joseph M. Devaney, Hakon Hakonarson, Benjamin F. Voight, Stephen E. Epstein, Emmanuelle Yon, Albert V. Smith, Silke Szymczak, Claire Perret, Christoph Sinning, Diana Rubin, Maryam Kavousi, David Altshuler, Laurence Tiret, Carole Proust, Christopher J. O'Donnell, John R. Thompson, Winfried März, Olli Saarela, Arne Deiseroth, Thomas Illig, Philippe Amouyel, Christian Hengstenberg, Olle Melander, Kari Kuulasmaa, Alistair S. Hall
Publikováno v:
Circulation: Cardiovascular Genetics
Wild, P S, Zeller, T, Schillert, A, Kee, F & Evans, A 2011, ' A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease ', Circulation. Cardiovascular genetics, vol. 4, no. 4, pp. 403-412 . https://doi.org/10.1161/CIRCGENETICS.110.958728
Circulation-cardiovascular genetics, 4(4), 403-U203. Lippincott Williams & Wilkins
Wild, P S, Zeller, T, Schillert, A, Kee, F & Evans, A 2011, ' A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease ', Circulation. Cardiovascular genetics, vol. 4, no. 4, pp. 403-412 . https://doi.org/10.1161/CIRCGENETICS.110.958728
Circulation-cardiovascular genetics, 4(4), 403-U203. Lippincott Williams & Wilkins
Background— eQTL analyses are important to improve the understanding of genetic association results. We performed a genome-wide association and global gene expression study to identify functionally relevant variants affecting the risk of coronary a
Autor:
Philipp S. Wild, Stergios Tzikas, Felix Post, Laurence Tiret, Christoph Bickel, Meike Fröhlich, Ewa Czyz, Thomas Münzel, Till Keller, Stefan Blankenberg, Stephan Baldus, Dirk Peetz, Renate B. Schnabel, Edith Lubos, Nicole Jachmann, Alexander Röth, Ascan Warnholtz, Viviane Nicaud, Sabine Genth-Zotz, Medea S. Eleftheriadis, Tanja Zeller, Karl J. Lackner, Christoph Sinning
Publikováno v:
New England Journal of Medicine. 361:868-877
BACKGROUND Cardiac troponin testing is central to the diagnosis of acute myocardial infarction. We evaluated a sensitive troponin I assay for the early diagnosis and risk stratification of myocardial infarction. METHODS In a multicenter study, we det
Autor:
Wolfgang Koenig, E J Benjamin, Christian Herder, Philipp S. Wild, Barbara Thorand, Christian P. Müller, Tina Haase, Thomas Münzel, Carole Proust, Jens Baumert, Jasmin Krause, Carola Marzi, Melanie Waldenberger, Karl J. Lackner, Renate B. Schnabel, Tanja Zeller, Denise Lau, Annette Peters, Medea S. Eleftheriadis, Ole Pless, Josée Dupuis, Sonja Zeilinger, Konstantin Strauch, Simon Zeller, Stefan Blankenberg, Laurence Tiret, Andreas Ziegler, Holger Prokisch, Helene Riess
Publikováno v:
Circ. Cardiovasc. Genet. 8, 717-726 (2015)
Background— Interleukin-18 (IL-18) is a pleiotropic cytokine centrally involved in the cytokine cascade with complex immunomodulatory functions in innate and acquired immunity. Circulating IL-18 concentrations are associated with type 2 diabetes me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bf59de578cce16513fc296fb880c000
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=46794
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=46794
Autor:
Renate B. Schnabel, Stefan Blankenberg, Karl J. Lackner, Andreas Schulz, Philipp S. Wild, Thomas Münzel, Ascan Warnholtz, Edith Lubos, Stephanie Herkenhoff, Christoph Sinning, Sandra Wilde, Tanja Zeller, Tommaso Gori, Medea S. Eleftheriadis
Publikováno v:
Circulation. Cardiovascular imaging. 4(4)
Background— Several methods of noninvasive vascular function testing have been suggested for cardiovascular risk screening in the community. A direct comparison of the different methods and their relation to classical cardiovascular risk factors in
Autor:
Heidi Rossmann, Andreas Ziegler, Patrick Diemert, Willem H. Ouwehand, Claire Perret, Philipp S. Wild, Augusto Rendon, Raphaële Castagné, François Cambien, Christian Hengstenberg, Medea S. Eleftheriadis, C. Sinning, Maxime Rotival, Arne Schillert, Panos Deloukas, Renate B. Schnabel, Edith Lubos, Tiphaine Godefroy, Marine Germain, Laurence Tiret, Silke Szymczak, Seraya Maouche, Heribert Schunkert, Carole Proust, David-Alexandre Trégouët, Stefan Blankenberg, Tanja Zeller, Jeanette Erdmann, Thomas Münzel, Alison H. Goodall, Karl J. Lackner, Jessy Brocheton, Arne Deiseroth, Nilesh J. Samani, Gilles Montalescot
Publikováno v:
PLoS Genetics
PLoS Genetics, Public Library of Science, 2011, 7 (12), pp.e1002367. ⟨10.1371/journal.pgen.1002367⟩
PLoS Genetics, Vol 7, Iss 12, p e1002367 (2011)
PLoS Genetics, 2011, 7 (12), pp.e1002367. ⟨10.1371/journal.pgen.1002367⟩
PLoS Genetics, Public Library of Science, 2011, 7 (12), pp.e1002367. ⟨10.1371/journal.pgen.1002367⟩
PLoS Genetics, Vol 7, Iss 12, p e1002367 (2011)
PLoS Genetics, 2011, 7 (12), pp.e1002367. ⟨10.1371/journal.pgen.1002367⟩
One major expectation from the transcriptome in humans is to characterize the biological basis of associations identified by genome-wide association studies. So far, few cis expression quantitative trait loci (eQTLs) have been reliably related to dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::797cb52b84783b5600b4bbad69728df8
https://www.hal.inserm.fr/inserm-00711658
https://www.hal.inserm.fr/inserm-00711658
Autor:
Silke Szymczak, Seraya Maouche, Stefan Blankenberg, Edith Lubos, David-Alexandre Trégouët, Philipp S. Wild, Claire Perret, François Cambien, Detlev Mennerich, Andreas Ziegler, Medea S. Eleftheriadis, Heidi Rossmann, Arne Schillert, Tanja Zeller, Maxime Rotival, Raphaële Castagné, C. Sinning, Karl J. Lackner, Werner Rust, Norbert Hubner, Laurence Tiret, Viviane Nicaud, Renate B. Schnabel, Joseph Loscalzo, Marine Germain, Carole Proust, Thomas Münzel
Publikováno v:
PLoS ONE, Vol 5, Iss 5, p e10693 (2010)
PLoS ONE
PLoS ONE
BACKGROUND: Variability of gene expression in human may link gene sequence variability and phenotypes; however, non-genetic variations, alone or in combination with genetics, may also influence expression traits and have a critical role in physiologi