Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Seraya Maouche"'
Autor:
Jonas Carlsson Almlöf, Per Lundmark, Anders Lundmark, Bing Ge, Seraya Maouche, Harald H H Göring, Ulrika Liljedahl, Camilla Enström, Jessy Brocheton, Carole Proust, Tiphaine Godefroy, Jennifer G Sambrook, Jennifer Jolley, Abigail Crisp-Hihn, Nicola Foad, Heather Lloyd-Jones, Jonathan Stephens, Rhian Gwilliam, Catherine M Rice, Christian Hengstenberg, Nilesh J Samani, Jeanette Erdmann, Heribert Schunkert, Tomi Pastinen, Panos Deloukas, Alison H Goodall, Willem H Ouwehand, François Cambien, Ann-Christine Syvänen
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
A large number of genome-wide association studies have been performed during the past five years to identify associations between SNPs and human complex diseases and traits. The assignment of a functional role for the identified disease-associated SN
Externí odkaz:
https://doaj.org/article/d0a286581c23430fa9c2b3d1ada6f11f
Autor:
Maxime Rotival, Tanja Zeller, Philipp S Wild, Seraya Maouche, Silke Szymczak, Arne Schillert, Raphaele Castagné, Arne Deiseroth, Carole Proust, Jessy Brocheton, Tiphaine Godefroy, Claire Perret, Marine Germain, Medea Eleftheriadis, Christoph R Sinning, Renate B Schnabel, Edith Lubos, Karl J Lackner, Heidi Rossmann, Thomas Münzel, Augusto Rendon, Cardiogenics Consortium, Jeanette Erdmann, Panos Deloukas, Christian Hengstenberg, Patrick Diemert, Gilles Montalescot, Willem H Ouwehand, Nilesh J Samani, Heribert Schunkert, David-Alexandre Tregouet, Andreas Ziegler, Alison H Goodall, François Cambien, Laurence Tiret, Stefan Blankenberg
Publikováno v:
PLoS Genetics, Vol 7, Iss 12, p e1002367 (2011)
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://doaj.org/article/1a2e314eb5264c0da8eb2cd82c7bb6eb
Autor:
Tanja Zeller, Philipp Wild, Silke Szymczak, Maxime Rotival, Arne Schillert, Raphaele Castagne, Seraya Maouche, Marine Germain, Karl Lackner, Heidi Rossmann, Medea Eleftheriadis, Christoph R Sinning, Renate B Schnabel, Edith Lubos, Detlev Mennerich, Werner Rust, Claire Perret, Carole Proust, Viviane Nicaud, Joseph Loscalzo, Norbert Hübner, David Tregouet, Thomas Münzel, Andreas Ziegler, Laurence Tiret, Stefan Blankenberg, François Cambien
Publikováno v:
PLoS ONE, Vol 5, Iss 5, p e10693 (2010)
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
Externí odkaz:
https://doaj.org/article/ddff369ae95d407899dfaa35e1952af6
Autor:
Seraya Maouche
Publikováno v:
Seraya Maouche
Emerging technologies (ET) are novel and relatively fast-growing technologies that can have massive socio-economic impact and bring new ethical and regulatory challenges. Although they cannot be co...
Autor:
Seraya Maouche, Heribert Schunkert
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 32:170-181
Atherosclerotic diseases, including coronary artery disease (CAD) and myocardial infarction (MI), are the leading causes of death in the world. The genetic basis of CAD and MI, which are caused by multiple interacting endogenous and exogenous factors
Autor:
Benjamin F. Voight, Andrew D. Morris, G. Kees Hovingh, Anthony J. Balmforth, Hanneke Basart, Alistair S. Hall, Dominique Gauguier, Bok Ghee Han, Martina Müller-Nurasyid, Sarah Parish, Jarmo Virtamo, Christa Meisinger, Peter Wagner, George Dedoussis, Philipp S. Wild, Kari Stefansson, Jean-Baptiste Cazier, Kathleen Stirrups, Jiyoung Lee, Adrienne Cupples, Stavroula Kanoni, Danish Saleheen, Christian Hengstenberg, Svati H. Shah, Panos Deloukas, Anuj Goel, Stefan Blankenberg, Sian Tsung Tan, Alison H. Goodall, Tõnu Esko, Eric Boerwinkle, Gudmundur Thorgeirsson, Peter S. Braund, Joshua W. Knowles, Olle Melander, C. Ellen van der Schoot, Silke Rosinger, Maria Dimitriou, Wolfgang Koenig, Michael Boehnke, François Cambien, Per Lundmark, Dmitry Shungin, Wolfgang Kratzer, Pierre Zalloua, Reijo Laaksonen, Jean Ferrières, Villi Gudnason, Thorsten Kessler, Daniel J. Rader, Niclas Eriksson, Dominique Arveiler, Natalie R. van Zuydam, Kari Kuulasmaa, N. William Rayner, Sarah E. Hunt, Gudmar Thorleifsson, Jeanette Erdmann, Samuli Ripatti, Tsun-Po Yang, George A. Wells, Terho Lehtimäki, Kjell Nikus, Pierre Fontanillas, Jorg Hager, Martin Farrall, Jemma C. Hopewell, Frank Kee, Juha Sinisalo, Christopher J. O'Donnell, Asif Rasheed, Mika Kähönen, Genovefa Kolovou, Seraya Maouche, Suzanne Rafelt, Cordelia Langford, Winfried März, Leo-Pekka Lyytikäinen, Christina Willenborg, Weihua Zhang, Kati Kristiansson, Hyo-Soo Kim, Weang K. Ho, Jeong E. Park, Mohan U. Sivananthan, Moritz P. Rumpf, Markku Laakso, Klaus Stark, Philippe Amouyel, Paul W. Franks, Andres Metspalu, Anders Franco-Cereceda, Manjinder S. Sandhu, Nour Eddine El Mokhtari, Nicholas J. Wareham, Robert Roberts, Veikko Salomaa, Thomas Illig, Tomi Pastinen, Robert Clarke, Christof Burgdorf, Leif Groop, Devin Absher, Yangsoo Jang, Mark I. McCarthy, Bernhard O. Boehm, Per Eriksson, Nilesh J. Samani, Inke R. König, Stefan Schreiber, Karin Leander, Simone Claudi-Boehm, Ci Song, Benjamin A. Goldstein, Stephen E. Epstein, Andreas Ziegler, Stanley L. Hazen, Arne Schäfer, Elin Grundberg, Sekar Kathiresan, John R. Thompson, Unnur Thorsteinsdottir, Muredach P. Reilly, Heribert Schunkert, Rory Collins, Thomas Quertermous, Jong-Young Lee, John Danesh, John C. Chambers, Marco M Ferrario, Carlos Iribarren, Claudia Langenberg, Hilma Holm, Rona J. Strawbridge, Alan S. Go, Cristen J. Willer, Ron Do, Emmi Tikkanen, Abbas Dehghan, Evelin Mihailov, Lindsay L. Waite, Patrick Diemert, Willem H. Ouwehand, Eric E. Schadt, Diana Rubin, David Altshuler, Marcus E. Kleber, Markus Perola, Alexandre F.R. Stewart, Jaspal S. Kooner, Themistocles L. Assimes, Inês Barroso, Bruna Gigante, Göran Hallmans, Marja-Liisa Lokki, Aki S. Havulinna, Anders Hamsten, Agneta Siegbahn, Lasse Folkersen, Erik Ingelsson, Martina E. Zimmermann, Colin N. A. Palmer, Paolo Brambilla, Ann-Christine Syvänen, Alun Evans, Åsa Johansson, John F. Peden, Alex S. F. Doney, Hugh Watkins, Johanna Kuusisto, Anders Lundmark, David G. Cox, Hyun Min Kang, Lars Lind, Krista Fischer, Markku S. Nieminen, Annette Peters, Norman Klopp, Stefan Gustafsson, Lars Wallentin, Nancy L. Pedersen, David-Alexandre Trégouët, Ulf de Faire
Publikováno v:
Nature Genetics
Nature Genetics; Vol 45
Nature genetics, 45(1), 25-33. Nature Publishing Group
Deloukas, P, Kanoni, S, Willenborg, C, Farrall, M, Assimes, T L, Thompson, J R, Ingelsson, E, Saleheen, D, Erdmann, J, Goldstein, B A, Stirrups, K, König, I R, Cazier, J B, Johansson, Å, Hall, A S, Lee, J Y, Willer, C J, Chambers, J C, Esko, T, Folkersen, L, Goel, A, Grundberg, E, Havulinna, A S, Ho, W K, Hopewell, J C, Eriksson, N, Kleber, M E, Kristiansson, K, Lundmark, P, Lyytikäinen, L P, Rafelt, S, Shungin, D, Strawbridge, R J, Thorleifsson, G, Tikkanen, E, Van Zuydam, N, Voight, B F, Waite, L L, Zhang, W, Ziegler, A, Absher, D, Altshuler, D, Balmforth, A J, Barroso, I, Braund, P S, Burgdorf, C, Claudi-Boehm, S, Cox, D, Dimitriou, M, Do, R, Doney, A S F, El Mokhtari, N, Eriksson, P, Fischer, K, Fontanillas, P, Franco-Cereceda, A, Gigante, B, Groop, L, Gustafsson, S, Hager, J, Hallmans, G, Han, B G, Hunt, S E, Kang, H M, Illig, T, Kessler, T, Knowles, J W, Kolovou, G, Kuusisto, J, Langenberg, C, Langford, C, Leander, K, Lokki, M L, Lundmark, A, McCarthy, M I, Meisinger, C, Melander, O, Mihailov, E, Maouche, S, Morris, A D, Müller-Nurasyid, M, Nikus, K, Peden, J F, Rayner, N W, Rasheed, A, Rosinger, S, Rubin, D, Rumpf, M P, Schäfer, A, Sivananthan, M, Song, C, Stewart, A F R, Tan, S T, Thorgeirsson, G, Van Der Schoot, C E, Wagner, P J, Wells, G A, Wild, P S, Yang, T P, Amouyel, P, Arveiler, D, Basart, H, Boehnke, M, Boerwinkle, E, Brambilla, P, Cambien, F, Cupples, A L, De Faire, U, Dehghan, A, Diemert, P, Epstein, S E, Evans, A, Ferrario, M M, Ferrières, J, Gauguier, D, Go, A S, Goodall, A H, Gudnason, V, Hazen, S L, Holm, H, Iribarren, C, Jang, Y, Kähönen, M, Kee, F, Kim, H S, Klopp, N, Koenig, W, Kratzer, W, Kuulasmaa, K, Laakso, M, Laaksonen, R, Lee, J Y, Lind, L, Ouwehand, W H, Parish, S, Park, J E, Pedersen, N L, Peters, A, Quertermous, T, Rader, D J, Salomaa, V, Schadt, E, Shah, S H, Sinisalo, J, Stark, K, Stefansson, K, Trégouët, D A, Virtamo, J, Wallentin, L, Wareham, N, Zimmermann, M E, Nieminen, M S, Hengstenberg, C, Sandhu, M S, Pastinen, T, Syvänen, A C, Hovingh, G K, Dedoussis, G, Franks, P W, Lehtimäki, T, Metspalu, A, Zalloua, P A, Siegbahn, A, Schreiber, S, Ripatti, S, Blankenberg, S S, Perola, M, Clarke, R, Boehm, B O, O'Donnell, C, Reilly, M P, März, W, Collins, R, Kathiresan, S, Hamsten, A, Kooner, J S, Thorsteinsdottir, U, Danesh, J, Palmer, C N A, Roberts, R, Watkins, H, Schunkert, H & Samani, N J 2013, ' Large-scale association analysis identifies new risk loci for coronary artery disease ', Nature Genetics, vol. 45, no. 1, pp. 25-33 . https://doi.org/10.1038/ng.2480
Nature Genetics; Vol 45
Nature genetics, 45(1), 25-33. Nature Publishing Group
Deloukas, P, Kanoni, S, Willenborg, C, Farrall, M, Assimes, T L, Thompson, J R, Ingelsson, E, Saleheen, D, Erdmann, J, Goldstein, B A, Stirrups, K, König, I R, Cazier, J B, Johansson, Å, Hall, A S, Lee, J Y, Willer, C J, Chambers, J C, Esko, T, Folkersen, L, Goel, A, Grundberg, E, Havulinna, A S, Ho, W K, Hopewell, J C, Eriksson, N, Kleber, M E, Kristiansson, K, Lundmark, P, Lyytikäinen, L P, Rafelt, S, Shungin, D, Strawbridge, R J, Thorleifsson, G, Tikkanen, E, Van Zuydam, N, Voight, B F, Waite, L L, Zhang, W, Ziegler, A, Absher, D, Altshuler, D, Balmforth, A J, Barroso, I, Braund, P S, Burgdorf, C, Claudi-Boehm, S, Cox, D, Dimitriou, M, Do, R, Doney, A S F, El Mokhtari, N, Eriksson, P, Fischer, K, Fontanillas, P, Franco-Cereceda, A, Gigante, B, Groop, L, Gustafsson, S, Hager, J, Hallmans, G, Han, B G, Hunt, S E, Kang, H M, Illig, T, Kessler, T, Knowles, J W, Kolovou, G, Kuusisto, J, Langenberg, C, Langford, C, Leander, K, Lokki, M L, Lundmark, A, McCarthy, M I, Meisinger, C, Melander, O, Mihailov, E, Maouche, S, Morris, A D, Müller-Nurasyid, M, Nikus, K, Peden, J F, Rayner, N W, Rasheed, A, Rosinger, S, Rubin, D, Rumpf, M P, Schäfer, A, Sivananthan, M, Song, C, Stewart, A F R, Tan, S T, Thorgeirsson, G, Van Der Schoot, C E, Wagner, P J, Wells, G A, Wild, P S, Yang, T P, Amouyel, P, Arveiler, D, Basart, H, Boehnke, M, Boerwinkle, E, Brambilla, P, Cambien, F, Cupples, A L, De Faire, U, Dehghan, A, Diemert, P, Epstein, S E, Evans, A, Ferrario, M M, Ferrières, J, Gauguier, D, Go, A S, Goodall, A H, Gudnason, V, Hazen, S L, Holm, H, Iribarren, C, Jang, Y, Kähönen, M, Kee, F, Kim, H S, Klopp, N, Koenig, W, Kratzer, W, Kuulasmaa, K, Laakso, M, Laaksonen, R, Lee, J Y, Lind, L, Ouwehand, W H, Parish, S, Park, J E, Pedersen, N L, Peters, A, Quertermous, T, Rader, D J, Salomaa, V, Schadt, E, Shah, S H, Sinisalo, J, Stark, K, Stefansson, K, Trégouët, D A, Virtamo, J, Wallentin, L, Wareham, N, Zimmermann, M E, Nieminen, M S, Hengstenberg, C, Sandhu, M S, Pastinen, T, Syvänen, A C, Hovingh, G K, Dedoussis, G, Franks, P W, Lehtimäki, T, Metspalu, A, Zalloua, P A, Siegbahn, A, Schreiber, S, Ripatti, S, Blankenberg, S S, Perola, M, Clarke, R, Boehm, B O, O'Donnell, C, Reilly, M P, März, W, Collins, R, Kathiresan, S, Hamsten, A, Kooner, J S, Thorsteinsdottir, U, Danesh, J, Palmer, C N A, Roberts, R, Watkins, H, Schunkert, H & Samani, N J 2013, ' Large-scale association analysis identifies new risk loci for coronary artery disease ', Nature Genetics, vol. 45, no. 1, pp. 25-33 . https://doi.org/10.1038/ng.2480
Coronary artery disease (CAD) is the commonest cause of death. Here, we report an association analysis in 63,746 CAD cases and 130,681 controls identifying 15 loci reaching genome-wide significance, taking the number of susceptibility loci for CAD to
Autor:
Hervé Durand, Fabien Koskas, Vincent Braunersreuther, François Mach, Alexei Gratchev, Seraya Maouche, Julia Kzhyshkowska, Gilles Le Naour, Ewa Ninio, Isabelle Brocheriou
Publikováno v:
Atherosclerosis; Vol 214
Objectives We characterized the transcriptional profiles of GM-CSF- (GM-MO) and M-CSF-induced macrophages (M-MO) and investigated in situ a subset of differentially expressed genes in human and mouse atherosclerotic lesions. Methods and results Using
Autor:
Kristell Wanherdrick, Sonia-Athina Karabina, Gérard Lambeau, Rajai Atout, Ewa Ninio, Seraya Maouche, François Cambien, Sarah Gora
Publikováno v:
FASEB Journal
FASEB Journal, 2010, 24 (9), pp.3284-3297 ⟨10.1096/fj.09-146852⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2010, 24 (9), pp.3284-3297 ⟨10.1096/fj.09-146852⟩
FASEB Journal, 2010, 24 (9), pp.3284-3297 ⟨10.1096/fj.09-146852⟩
FASEB Journal, Federation of American Society of Experimental Biology, 2010, 24 (9), pp.3284-3297 ⟨10.1096/fj.09-146852⟩
International audience; Secreted phospholipases A2 (sPLA2s) are present in atherosclerotic plaques and are now considered novel attractive therapeutic targets and potential biomarkers as they contribute to the development of atherosclerosis through l
Autor:
Per Lundmark, Abigail Crisp-Hihn, Seraya Maouche, Tiphaine Godefroy, Harald H H Göring, Nilesh J. Samani, Anders Lundmark, Carole Proust, Jonathan Stephens, François Cambien, Jessy Brocheton, Bing Ge, Nicola S. Foad, Heribert Schunkert, Ulrika Liljedahl, Tomi Pastinen, Panos Deloukas, Camilla Enström, Jennifer Jolley, Rhian Gwilliam, Heather Lloyd-Jones, Ann-Christine Syvänen, Alison H. Goodall, Jonas Carlsson Almlöf, Jeanette Erdmann, Willem H. Ouwehand, Jennifer G. Sambrook, Catherine M. Rice, Christian Hengstenberg
Publikováno v:
PLoS ONE; Vol 7
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52260 (2012)
A large number of genome-wide association studies have been performed during the past five years to identify associations between SNPs and human complex diseases and traits. The assignment of a functional role for the identified disease-associated SN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c26502286334aa82a5f081f2917b2ea
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-195164
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-195164
Autor:
Nicolas Greliche, Tanja Zeller, Philipp S. Wild, Maxime Rotival, Arne Schillert, Andreas Ziegler, Tony Attwood, Belz Stephanie, Peter Braund, Jessy Brocheton, Jason Cooper, Abi Crisp-Hihn, Patrick (formerly Linsel-Nitschke) Diemert, Nicola Foad, Tiphaine Godefroy, Jay Gracey, Emma Gray, Rhian Gwilliams, Susanne Heimerl, Jennifer Jolley, Unni Krishnan, Heather Lloyd-Jones, Ulrika Liljedahl, Ingrid Lugauer, Per Lundmark, Seraya Maouche, Jasbir S Moore, Montalescot Gilles, David Muir, Elizabeth Murray, Chris P Nelson, Jessica Neudert, David Niblett, Karen O.Leary, Helen Pollard, Carole Proust, Angela Rankin, Augusto Rendon, Catherine M Rice, Hendrik Sager, Jennifer Sambrook, Schmitz Gerd, Michael Scholz, Laura Schroeder, Jonathan Stephens, Ann-Christine Syvannen, Stefanie (formerlyGulde) Tennstedt, Chris Wallace
Publikováno v:
PLoS ONE, Vol 7, Iss 10 (2012)
PLoS ONE
PLoS ONE
There was an error in the author byline. The correct byline is: Nicolas Greliche1,2, Tanja Zeller3, Philipp S. Wild4, Maxime Rotival1¤, Arne Schillert5, Andreas Ziegler5, the Cardiogenics Consortium¶, Panos Deloukas6, Jeanette Erdmann7, Christian H