Resultados da pesquisa - Sophie Garnier
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Arterial Stiffness and Chronic Kidney Disease Por Anne‐Sophie Garnier, Marie Briet
Publicado em 2015Artigo -
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Contribution of 18 F-fluorocholine PET-CT to the preoperative localisation of parathyroid adenoma for the treatment of primary hyperparathyroidism Por Sophie Garnier, Clémentine Maheo, G. Potard, M. Cavarec, N. Roudaut, Philippe Thuillier, R. Marianowski, Ronan Abgral, J Leclère
Publicado em 2025Artigo -
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Humoral response to a third injection of BNT162b2 vaccine in patients on maintenance haemodialysis Por Marine Dekervel, Nicolás Henry, Massimo Torreggiani, Lise-Marie Pouteau, Jean-Paul Imiela, Chloé Mellaza, Anne‐Sophie Garnier, A. Dujardin, Marine Asfar, Alexandra Ducancelle, Axelle Paquin, Sophie Blanchi, Virginie Besson, Giorgina Barbara Piccoli, Jean‐François Augusto
Publicado em 2021Artigo -
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A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus Por Elisabet Svenungsson, Jan-Ακε Gustafsson, Dag Leonard, Johanna K. Sandling, Iva Gunnarsson, Gunnel Nordmark, Andreas Jönsen, Anders Bengtsson, G Sturfelt, Solbritt Rantapää‐Dahlqvist, Kerstin Elvin, Ulf Sundin, Sophie Garnier, Julia F. Simard, Snævar Sigurðsson, Leonid Padyukov, Ann-Christine Syvänen, Lars Rönnblom
Publicado em 2009Artigo -
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Genome-Wide Haplotype Analysis of Cis Expression Quantitative Trait Loci in Monocytes Por Sophie Garnier, Vinh Trương, Jessy Brocheton, Tanja Zeller, Maxime Rovital, Philipp S. Wild, Andreas Ziegler, Thomas Münzel, Laurence Tiret, Stefan Blankenberg, Panos Deloukas, Jeanette Erdmann, Christian Hengstenberg, Nilesh J. Samani, Heribert Schunkert, Willem H. Ouwehand, Alison H. Goodall, François Cambien, David‐Alexandre Trégouët
Publicado em 2013Artigo -
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A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5 Por Snævar Sigurðsson, Gunnel Nordmark, Sophie Garnier, Elin Grundberg, Tony Kwan, Ola Nilsson, Maija‐Leena Eloranta, Iva Gunnarsson, Elisabet Svenungsson, Gunnar Sturfelt, Anders Bengtsson, Andreas Jönsen, Lennart Truedsson, Solbritt Rantapää‐Dahlqvist, Catharina Eriksson, G. Alm, H.H.H. Göring, Tomi Pastinen, A-C Syvänen, L. Ronnblom
Publicado em 2008Artigo -
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A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE Por Johanna K. Sandling, Sophie Garnier, Snævar Sigurðsson, Chuan Wang, Gunnel Nordmark, Iva Gunnarsson, Elisabet Svenungsson, Leonid Padyukov, Gunnar Sturfelt, Andreas Jönsen, Anders A Bengtsson, Lennart Truedsson, Catharina Eriksson, Solbritt Rantapää‐Dahlqvist, Anders Mälarstig, Rona J. Strawbridge, Anders Hamsten, Lindsey A. Criswell, Robert Graham, Timothy W. Behrens, Maija‐Leena Eloranta, Gunnar V. Alm, Lars Rönnblom, Ann‐Christine Syvänen
Publicado em 2010Revisão -
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Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated LRRK2 Locus Por Daniah Trabzuni, Mina Ryten, Warren Emmett, Adaikalavan Ramasamy, Karl J. Lackner, Tanja Zeller, Robert Walker, Colin Smith, Patrick A. Lewis, Adamantios Mamais, Rohan de Silva, Jana Vandrovcová, Dena G. Hernandez, Michael A. Nalls, Manu Sharma, Sophie Garnier, Suzanne Lesage, Javier Simón‐Sánchez, Thomas Gasser, Peter Heutink, Alexis Brice, Andrew Singleton, Huaibin Cai, Eric E. Schadt, Nicholas Wood, Rina Bandopadhyay, Michael E. Weale, John Hardy, Vincent Plagnol
Publicado em 2013Artigo -
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Linkage proof for <i>PTPN22</i> , a rheumatoid arthritis susceptibility gene and a human autoimmunity gene Por Laëtitia Michou, Sandra Lasbleiz, Anne‐Christine Rat, Paola Migliorini, Alejandro Balsa, R. Westhovens, Pilar Barrera, Helena Alves, Céline Pierlot, Elodie Glikmans, Sophie Garnier, J Dausset, Carlos Vaz, Manuela Fernandes, Élisabeth Petit, Isabelle Lemaire, Dora Pascual‐Salcedo, Stefano Bombardieri, J. Dequeker, Timothy R. D. J. Radstake, Piet L. C. M. van Riel, Leo van de Putte, Antonio Lopes-Vaz, Bernard Prum, Thomas Bardin, Philippe Dieudé, François Cornélis
Publicado em 2007Artigo -
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Association of Systemic Lupus Erythematosus with<i>C8orf13–BLK</i>and<i>ITGAM–ITGAX</i> Por Geoffrey Hom, Robert Graham, Barmak Modrek, Robert P. Kimberly, Ward Ortmann, Sophie Garnier, Annette T. Lee, Sharon A. Chung, Ricardo C. Ferreira, P.V. Krishna Pant, Dennis G. Ballinger, Roman Kosoy, F. Yesim Demirci, M. Ilyas Kamboh, Amy Kao, Chao Tian, Iva Gunnarsson, Anders Bengtsson, Solbritt Rantapää‐Dahlqvist, Michelle Petri, Susan Manzi, Michael F. Seldin, Lars Rönnblom, Ann Christine Syvänen, Lindsey A. Criswell, Peter K. Gregersen, Timothy W. Behrens
Publicado em 2008Artigo -
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Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy Por Ulrike Esslinger, Sophie Garnier, Agathe Korniat, Carole Proust, Georgios Kararigas, Martina Müller‐Nurasyid, Jean‐Philippe Empana, Michael P. Morley, Claire Perret, Klaus Stark, Alexander G. Bick, Sanjay Prasad, Jennifer Kriebel, Jin Li, Laurence Tiret, Konstantin Strauch, Declan P. O’Regan, Kenneth B. Marguiles, J. G. Seidman, Pierre Boutouyrie, Patrick Lacolley, Xavier Jouven, Christian Hengstenberg, Michel Komajda, Hákon Hákonarson, Richard Isnard, Eloisa Arbustini, Harald Grallert, Stuart A. Cook, Christine E. Seidman, Vera Regitz‐Zagrosek, Thomas P. Cappola, Philippe Charron, François Cambien, Eric Villard
Publicado em 2017Artigo -
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Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience Por Sean J. Jurgens, Joel Rämö, Daria R. Kramarenko, Leonoor F. J. M. Wijdeveld, Jan Haas, Mark Chaffin, Sophie Garnier, Liam Gaziano, Lu‐Chen Weng, Alex Lipov, Sean L. Zheng, Albert Henry, Jennifer E. Huffman, Saketh Challa, Frank Rühle, Carmen Diaz Verdugo, Christian Krijger Juárez, Shinwan Kany, Constance A. van Orsouw, Kiran J. Biddinger, Edwin Poel, Amanda L. Elliott, Xin Wang, Catherine Francis, Richard Ruan, Satoshi Koyama, Leander Beekman, Dominic S. Zimmerman, Jean‐François Deleuze, Eric Villard, David‐Alexandre Trégouët, Richard Isnard, D.I. Boomsma, Eco J. C. de Geus, Rafik Tadros, Yigal M. Pinto, Arthur A.M. Wilde, Jouke‐Jan Hottenga, Juha Sinisalo, Teemu Niiranen, Roddy Walsh, Amand F. Schmidt, Seung Hoan Choi, Kyong‐Mi Chang, Philip S. Tsao, Paul M. Matthews, James S. Ware, R. Thomas Lumbers, Saskia van der Crabben, Jari A. Laukkanen, Aarno Palotie, Ahmad S. Amin, Philippe Charron, Benjamin Meder, Patrick T. Ellinor, Mark J. Daly, Krishna G. Aragam, Connie R. Bezzina
Publicado em 2024Artigo -
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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23 Por Sophie Garnier, Magdaléna Harakaľová, Stefan Weiß, Michal Mokrý, Vera Regitz‐Zagrosek, Christian Hengstenberg, Thomas P. Cappola, Richard Isnard, Eloisa Arbustini, Stuart A. Cook, Jessica van Setten, Jorg J. A. Calis, Hákon Hákonarson, Michael P. Morley, Klaus Stark, Sanjay Prasad, Jin Li, Declan P. O’Regan, Maurizia Grasso, Martina Müller‐Nurasyid, Thomas Meitinger, Jean‐Philippe Empana, Konstantin Strauch, Mélanie Waldenberger, Kenneth B. Marguiles, Christine E. Seidman, Georgios Kararigas, Benjamin Meder, Jan Haas, Pierre Boutouyrie, Patrick Lacolley, Xavier Jouven, Jeanette Erdmann, Stefan Blankenberg, Thomas Wichter, Volker Ruppert, Luigi Tavazzi, Olivier Dubourg, Gérard Roizès, Richard Dorent, Pascal de Groote, Laurent Fauchier, Jean‐Noël Trochu, Jean‐François Aupetit, Zofia T. Bilińska, Marine Germain, Uwe Völker, Daiane Hemerich, Ibticem Raji, Delphine Bacq‐Daian, Carole Proust, Paloma Remior, Manuel Gómez‐Bueno, Kristin Lehnert, Renée G. C. Maas, Robert Olaso, Ganapathi Varma Saripella, Stephan B. Felix, Steven McGinn, Laëtitia Duboscq-Bidot, Alain van Mil, Céline Besse, Vincent Fontaine, Hélène Blanché, Flavie Ader, Brendan J. Keating, Angélique Curjol, Anne Boland, Michel Komajda, François Cambien, Jean‐François Deleuze, Marcus Dörr, Folkert W. Asselbergs, Eric Villard, David‐Alexandre Trégouët, Philippe Charron
Publicado em 2021Artigo -
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Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease Por William J. Young, Jeffrey Haessler, Jan Walter Benjamins, L. Repetto, Jie Yao, Aaron Isaacs, Andrew R. Harper, Julia Ramírez, Sophie Garnier, Stefan van Duijvenboden, Antoine Baldassari, Maria Pina Concas, ThuyVy Duong, Luisa Foco, Jonas L. Isaksen, Hao Mei, Raymond Noordam, Casia Nursyifa, Anne Richmond, Meddly L. Santolalla, Colleen M. Sitlani, Negin Soroush, Sébastien Thériault, Stella Trompet, Stefanie Aeschbacher, Fariba Ahmadizar, Álvaro Alonso, Jennifer A. Brody, Archie Campbell, Adolfo Correa, Dawood Darbar, Antonio De Luca, Jean‐François Deleuze, Christina Ellervik, Christian Fuchsberger, Anuj Goel, Christopher Grace, Xiuqing Guo, Torben Hansen, Susan R. Heckbert, Rebecca D. Jackson, Jan A. Kors, Maria Fernanda Lima‐Costa, Allan Linneberg, Peter W. Macfarlane, Alanna C. Morrison, Pau Navarro, David J. Porteous, Peter P. Pramstaller, Alexander P. Reiner, Lorenz Risch, Ulrich Schotten, Xia Shen, Gianfranco Sinagra, Elsayed Z. Soliman, Monika Stoll, Eduardo Tarazona‐Santos, Andrew Tinker, Katerina Trajanoska, Eric Villard, Helen R. Warren, Eric A. Whitsel, Kerri L. Wiggins, Dan E. Arking, Christy L. Avery, David Conen, Giorgia Girotto, Niels Grarup, Caroline Hayward, J. Wouter Jukema, Dennis O. Mook‐Kanamori, Morten S. Olesen, Sandosh Padmanabhan, Bruce M. Psaty, Cristian Pattaro, Antônio Luiz Pinho Ribeiro, Jerome I. Rotter, Bruno H. Stricker, Pim van der Harst, Cornelia M. van Duijn, Niek Verweij, James G. Wilson, Michele Orini, Philippe Charron, Hugh Watkins, Charles Kooperberg, Henry J. Lin, James F. Wilson, Jørgen K. Kanters, Nona Sotoodehnia, Borbála Mifsud, Pier D. Lambiase, Larisa G. Tereshchenko, Patricia B. Munroe
Publicado em 2023Artigo
Ferramentas de pesquisa:
Assuntos relacionados
Medicine
Internal medicine
Biology
Gene
Genetics
Genotype
Single-nucleotide polymorphism
Immunology
Allele
Disease
Environmental health
Genetic association
Genome-wide association study
Population
Quantitative trait locus
Cardiology
Cardiomyopathy
Dilated cardiomyopathy
Heart failure
Allele frequency
Antibody
Candidate gene
Expression quantitative trait loci
Genetic architecture
Haplotype
IRF5
Interferon regulatory factors
Linkage disequilibrium
Locus (genetics)
Mutation