Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Martina Graßl"'
Autor:
Klaus Stark, Ulrike B Esslinger, Wibke Reinhard, George Petrov, Thomas Winkler, Michel Komajda, Richard Isnard, Philippe Charron, Eric Villard, François Cambien, Laurence Tiret, Marie-Claude Aumont, Olivier Dubourg, Jean-Noël Trochu, Laurent Fauchier, Pascal Degroote, Anette Richter, Bernhard Maisch, Thomas Wichter, Christa Zollbrecht, Martina Grassl, Heribert Schunkert, Patrick Linsel-Nitschke, Jeanette Erdmann, Jens Baumert, Thomas Illig, Norman Klopp, H-Erich Wichmann, Christa Meisinger, Wolfgang Koenig, Peter Lichtner, Thomas Meitinger, Arne Schillert, Inke R König, Roland Hetzer, Iris M Heid, Vera Regitz-Zagrosek, Christian Hengstenberg
Publikováno v:
PLoS Genetics, Vol 6, Iss 10, p e1001167 (2010)
Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations located mostly in genes encoding structural and sarcomeric proteins. However, strong evidence su
Externí odkaz:
https://doaj.org/article/56e0d4b0c2df4726aa00ecb1f26bdf14
Autor:
J Brent Richards, Dawn Waterworth, Stephen O'Rahilly, Marie-France Hivert, Ruth J F Loos, John R B Perry, Toshiko Tanaka, Nicholas John Timpson, Robert K Semple, Nicole Soranzo, Kijoung Song, Nuno Rocha, Elin Grundberg, Josée Dupuis, Jose C Florez, Claudia Langenberg, Inga Prokopenko, Richa Saxena, Robert Sladek, Yurii Aulchenko, David Evans, Gerard Waeber, Jeanette Erdmann, Mary-Susan Burnett, Naveed Sattar, Joseph Devaney, Christina Willenborg, Aroon Hingorani, Jaquelin C M Witteman, Peter Vollenweider, Beate Glaser, Christian Hengstenberg, Luigi Ferrucci, David Melzer, Klaus Stark, John Deanfield, Janina Winogradow, Martina Grassl, Alistair S Hall, Josephine M Egan, John R Thompson, Sally L Ricketts, Inke R König, Wibke Reinhard, Scott Grundy, H-Erich Wichmann, Phil Barter, Robert Mahley, Y Antero Kesaniemi, Daniel J Rader, Muredach P Reilly, Stephen E Epstein, Alexandre F R Stewart, Cornelia M Van Duijn, Heribert Schunkert, Keith Burling, Panos Deloukas, Tomi Pastinen, Nilesh J Samani, Ruth McPherson, George Davey Smith, Timothy M Frayling, Nicholas J Wareham, James B Meigs, Vincent Mooser, Tim D Spector, GIANT Consortium
Publikováno v:
PLoS Genetics, Vol 5, Iss 12, p e1000768 (2009)
The adipocyte-derived protein adiponectin is highly heritable and inversely associated with risk of type 2 diabetes mellitus (T2D) and coronary heart disease (CHD). We meta-analyzed 3 genome-wide association studies for circulating adiponectin levels
Externí odkaz:
https://doaj.org/article/5ebadbaada2a4a9caf70475a98073cf4
Autor:
Klaus Stark, Wibke Reinhard, Martina Grassl, Jeanette Erdmann, Heribert Schunkert, Thomas Illig, Christian Hengstenberg
Publikováno v:
PLoS ONE, Vol 4, Iss 11, p e7729 (2009)
BACKGROUND:Recently, a large meta-analysis including over 28,000 participants identified nine different loci with association to serum uric acid (UA) levels. Since elevated serum UA levels potentially cause gout and are a possible risk factor for cor
Externí odkaz:
https://doaj.org/article/fa6ced385253466c827a17e7c22e7e3d
Publikováno v:
BioProcessing Journal. 15:8-15
Autor:
Thomas Langmann, Martina Grassl, Regina Höcherl, Christa Zollbrecht, S. Fenk, Ute Hubauer, Wibke Reinhard, Klaus Stark, Stefanie Ebert, Ulrike B. Esslinger, Christian Hengstenberg
Publikováno v:
Atherosclerosis. 227:244-249
Objective Genome-wide association studies identified a risk haplotype on chromosome 9p21.3 to be associated with coronary artery disease (CAD) and myocardial infarction (MI). Since this region does not contain a clear candidate gene with known pathop
Autor:
François Cambien, Anette Richter, Bernhard Maisch, Christa Zollbrecht, Laurence Tiret, Klaus Stark, Christa Meisinger, Jeanette Erdmann, Thomas Meitinger, Jean-Noël Trochu, Marie-Claude Aumont, Wolfgang Koenig, Laurent Fauchier, Arne Schillert, Peter Lichtner, Martina Grassl, Norman Klopp, Jens Baumert, Iris M. Heid, Vera Regitz-Zagrosek, Pascal DeGroote, Inke R. König, Philippe Charron, Patrick Linsel-Nitschke, Thomas Illig, Eric Villard, Roland Hetzer, Ulrike B. Esslinger, Thomas Wichter, Michel Komajda, Christian Hengstenberg, Thomas W. Winkler, Richard Isnard, Wibke Reinhard, H.-Erich Wichmann, Olivier Dubourg, Heribert Schunkert, George Petrov
Publikováno v:
PLoS Genetics, Vol 6, Iss 10, p e1001167 (2010)
PLoS Genetics
PLoS Genetics, 2010, 6 (10), pp.e1001167. ⟨10.1371/journal.pgen.1001167⟩
Scopus-Elsevier
PLoS Genet. 6:e1001167 (2010)
PLoS Genetics
PLoS Genetics, 2010, 6 (10), pp.e1001167. ⟨10.1371/journal.pgen.1001167⟩
Scopus-Elsevier
PLoS Genet. 6:e1001167 (2010)
Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations located mostly in genes encoding structural and sarcomeric proteins. However, strong evidence su
Autor:
Gérard Waeber, Robert Sladek, Nicholas J. Timpson, Luigi Ferrucci, James B. Meigs, David M. Evans, Marie-France Hivert, George Davey Smith, John E. Deanfield, J. Brent Richards, Joseph M. Devaney, Beate Glaser, Toshiko Tanaka, Ruth J. F. Loos, Claudia Langenberg, Christina Willenborg, Christian Hengstenberg, Stephen O'Rahilly, Peter Vollenweider, Klaus Stark, John R. B. Perry, Jaquelin C. M. Witteman, Vincent Mooser, Ruth McPherson, Sally L. Ricketts, Nuno Rocha, Naveed Sattar, Muredach P. Reilly, Scott M. Grundy, Elin Grundberg, Alexandre F.R. Stewart, Keith Burling, Janina Winogradow, Robert K. Semple, Nicole Soranzo, Stephen E. Epstein, Martina Grassl, Mary-Susan Burnett, Robert W. Mahley, John R. Thompson, Nicholas J. Wareham, Josée Dupuis, David Melzer, Richa Saxena, Yurii S. Aulchenko, Panos Deloukas, Josephine M. Egan, Jose C. Florez, H-Erich Wichmann, Wibke Reinhard, Tim D. Spector, Dawn M. Waterworth, Daniel J. Rader, Cornelia M. van Duijn, Nilesh J. Samani, Inke R. König, Inga Prokopenko, Aroon D. Hingorani, Tomi Pastinen, Timothy M. Frayling, Heribert Schunkert, Y. Antero Kesäniemi, Phil Barter, Kijoung Song, Jeanette Erdmann, Alistair S. Hall
Publikováno v:
PLoS Genetics (print), 5(12). Public Library of Science
Scopus-Elsevier
PLoS Genetics, Vol 5, Iss 12, p e1000768 (2009)
PLoS Genetics
PLoS genetics
PLoS Genetics, vol. 5, no. 12, pp. 1000768
e1000768
PLoS Genetics; Vol 5
Scopus-Elsevier
PLoS Genetics, Vol 5, Iss 12, p e1000768 (2009)
PLoS Genetics
PLoS genetics
PLoS Genetics, vol. 5, no. 12, pp. 1000768
e1000768
PLoS Genetics; Vol 5
The adipocyte-derived protein adiponectin is highly heritable and inversely associated with risk of type 2 diabetes mellitus (T2D) and coronary heart disease (CHD). We meta-analyzed 3 genome-wide association studies for circulating adiponectin levels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad2548b3c8b2a671f64949d2a2bb0676
https://pure.eur.nl/en/publications/e3e13dea-74a7-4074-8b19-9debd7ad67ff
https://pure.eur.nl/en/publications/e3e13dea-74a7-4074-8b19-9debd7ad67ff
Autor:
Wibke Reinhard, Klaus Stark, Christian Hengstenberg, Jeanette Erdmann, Heribert Schunkert, Thomas Illig, Martina Grassl
Publikováno v:
PLoS ONE, Vol 4, Iss 11, p e7729 (2009)
PLoS ONE 4:e7729 (2009)
PLoS ONE
PLoS ONE 4:e7729 (2009)
PLoS ONE
Background Recently, a large meta-analysis including over 28,000 participants identified nine different loci with association to serum uric acid (UA) levels. Since elevated serum UA levels potentially cause gout and are a possible risk factor for cor
Autor:
Thomas M. Morgan, Stephen P. Fortmann, Daniel B. Mirel, Christopher W. Knouff, Willem H. Ouwehand, Sekar Kathiresan, Dawn M. Waterworth, Ingo Ruczinski, Lewis C. Becker, Candace Guiducci, Alan S. Go, Brian G. Kral, Nicola Martinelli, Diane M. Becker, Ron Do, Michael Scholz, Gudmundur Thorgeirsson, Wibke Reinhard, J. Enrique Herrera, Themistocles L. Assimes, Mary Susan Burnett, Liming Qu, Pier Franco Pignatti, Hakon Hakonarson, Rosanna Asselta, Jean Yee, Stefano Duga, Rasika A. Mathias, M Walker, David M. Nathan, Gavin Lucas, Alexander F. Wilson, Roberto Elosua, Richard M. Myers, Martina Grassl, Leena Peltonen, Christa Meisinger, James C. Engert, Stephen E. Epstein, Wolfgang Lieb, Peter S. Braund, H.-Erich Wichmann, Benjamin J. Wright, Patrick Linsel-Nitschke, Mingyao Li, Stefan Schreiber, Klaus Berger, Gordon H. Williams, Alistair S. Hall, Karl Andersen, Jeanette Erdmann, Lisa R. Yanek, Andreas Ziegler, Nauder Faraday, Marcus Fischer, Stephen G. Ball, Yechiel Friedlander, Veikko Salomaa, Stephen M. Schwartz, Bhoom Suktitipat, Joseph M. Devaney, Klaus Stark, Panos Deloukas, Ron Waksman, Changchun Xie, Thomas Scheffold, Michael Preuss, Robert L. Wilensky, François Cambien, Devin Absher, Janina Winogradow, Yoonhee Kim, Andreas Huge, Unnur Thorsteinsdottir, Muredach P. Reilly, Christina Willenborg, Joan Sala, David S. Siscovick, Pascal P. McKeown, Joseph M. Lindsay, Gudmar Thorleifsson, Kenneth M. Kent, Daniel J. Rader, James B. Meigs, Benjamin F. Voight, John R. Thompson, Christopher B. Granger, Elisabetta Trabetti, Vincent Mooser, Stephen Sidney, Neil Risch, Domenico Girelli, Atif Qasim, John A. Spertus, Mark J. Daly, Shaun Purcell, Aki S. Havulinna, David Altshuler, Kari Stefansson, Dhananjay Vaidya, Carlos Iribarren, Christian Hengstenberg, Svati H. Shah, Rafael Ramos, Olle Melander, Mark A. Hlatky, Christopher Patterson, Anthony J. Balmforth, Giovanni Malerba, Calum A. MacRae, Melissa Parkin, William H. Matthai, Christopher J. O'Donnell, Jaume Marrugat, Kiran Musunuru, Monika Stoll, Anika Grosshennig, Augusto D. Pichard, Lowell F. Satler, Hua Tang, Joel N. Hirschhorn, Nilesh J. Samani, Inke R. König, Sandra Eifert, Joshua W. Knowles, Sonia S. Anand, Heribert Schunkert, Thomas Quertermous, Hilma Holm, Isaac Subirana, Oliviero Olivieri
Publikováno v:
Assimes, T L, Holm, H, Kathiresan, S, Reilly, M P, Thorleifsson, G, Voight, B F, Erdmann, J, Willenborg, C, Vaidya, D, Xie, C C, Patterson, C, Morgan, T M, Burnett, M S, Li, M Y, Hlatky, M A, Knowles, J W, Thompson, J R, Absher, D, Iribarren, C, Go, A, Fortmann, S P, Sidney, S, Risch, N, Tang, H, Myers, R M, Berger, K, Stoll, M, Shah, S H, Thorgeirsson, G, Andersen, K, Havulinna, A S, Herrera, J E, Faraday, N, Kim, Y, Kral, B G, Mathias, R A, Ruczinski, I, Suktitipat, B, Wilson, A F, Yanek, L R, Becker, L C, Linsel-Nitschke, P, Lieb, W, Konig, I R, Hengstenberg, C, Fischer, M, Stark, K, Reinhard, W, Winogradow, J, Grassl, M, Grosshennig, A, Preuss, M, Schreiber, S, Wichmann, H E, Meisinger, C, Yee, J, Friedlander, Y, Do, R, Meigs, J B, Williams, G, Nathan, D M, MacRae, C A, Qu, L M, Wilensky, R L, Matthai, W H, Qasim, A N, Hakonarson, H, Pichard, A D, Kent, K M, Satler, L, Lindsay, J M, Waksman, R, Knouff, C W, Waterworth, D M, Walker, M C, Mooser, V E, Marrugat, J, Lucas, G, Subirana, I, Sala, J, Ramos, R, Martinelli, N, Olivieri, O, Trabetti, E, Malerba, G, Pignatti, P F, Guiducci, C, Mirel, D, Parkin, M, Hirschhorn, J N, Asselta, R, Duga, S, Musunuru, K, Daly, M J, Purcell, S, Eifert, S, Braund, P S, Wright, B J, Balmforth, A J, Ball, S G, Ouwehand, W H, Deloukas, P, Scholz, M, Cambien, F, Huge, A, Scheffold, T, Salomaa, V, Girelli, D, Granger, C B, Peltonen, L, McKeown, P, Altshuler, D, Melander, O, Devaney, J M, Epstein, S E, Rader, D J, Elosua, R, Engert, J C, Anand, S S, Hall, A S, Ziegler, A, O'Donnell, C J, Spertus, J A, Siscovick, D, Schwartz, S M, Becker, D, Thorsteinsdottir, U, Stefansson, K, Schunkert, H, Samani, N J & Quertermous, T 2010, ' Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies ' Journal of the American College of Cardiology, vol. 56, no. 19, pp. 1552-1563 . DOI: 10.1016/j.jacc.2010.06.022
Objectives We sought to replicate the association between the kinesin-like protein 6 (KIF6) Trp719Arg polymorphism (rs20455), and clinical coronary artery disease (CAD). Background Recent prospective studies suggest that carriers of the 719Arg allele