A Novel Channelopathy in Pulmonary Arterial Hypertension
Ma, Lijiang, Roman-Campos, Danilo, Austin, Eric D, Eyries, Mélanie, Sampson, Kevin S, Soubrier, Florent, Germain, Marine, Trégouët, David-Alexandre, Borczuk, Alain, Rosenzweig, Erika Berman, Girerd, Barbara, Montani, David, Humbert, Marc, Loyd, James E, Kass, Robert S, Chung, Wendy K
Published in The New England journal of medicine (25.07.2013)
Published in The New England journal of medicine (25.07.2013)
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GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis
Megy, Karyn, Downes, Kate, Morel-Kopp, Marie-Christine, Bastida, José M, Brooks, Shannon, Bury, Loredana, Leinoe, Eva, Gomez, Keith, Morgan, Neil V, Othman, Maha, Ouwehand, Willem H, Perez Botero, Juliana, Rivera, José, Schulze, Harald, Trégouët, David-Alexandre, Freson, Kathleen
Published in Journal of thrombosis and haemostasis (01.10.2021)
Published in Journal of thrombosis and haemostasis (01.10.2021)
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Effects of Genetically Determined Iron Status on Risk of Venous Thromboembolism and Carotid Atherosclerotic Disease: A Mendelian Randomization Study
Gill, Dipender, Brewer, Christopher F, Monori, Grace, Trégouët, David-Alexandre, Franceschini, Nora, Giambartolomei, Claudia, Tzoulaki, Ioanna, Dehghan, Abbas
Published in Journal of the American Heart Association (06.08.2019)
Published in Journal of the American Heart Association (06.08.2019)
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DNA methylation and body-mass index: a genome-wide analysis
Dick, Katherine J, PhD, Nelson, Christopher P, PhD, Tsaprouni, Loukia, PhD, Sandling, Johanna K, PhD, Aïssi, Dylan, MSc, Wahl, Simone, MSc, Meduri, Eshwar, PhD, Morange, Pierre-Emmanuel, Prof, Gagnon, France, PhD, Grallert, Harald, PhD, Waldenberger, Melanie, PhD, Peters, Annette, Prof, Erdmann, Jeanette, Prof, Hengstenberg, Christian, Prof, Cambien, Francois, Prof, Goodall, Alison H, Prof, Ouwehand, Willem H, Prof, Schunkert, Heribert, Prof, Thompson, John R, Prof, Spector, Tim D, FRCP, Gieger, Christian, PhD, Trégouët, David-Alexandre, PhD, Deloukas, Panos, Prof, Samani, Nilesh J, Prof
Published in The Lancet (British edition) (07.06.2014)
Published in The Lancet (British edition) (07.06.2014)
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Anti-integrin αv therapy improves cardiac fibrosis after myocardial infarction by blunting cardiac PW1+ stromal cells
Bouvet, Marion, Claude, Olivier, Roux, Maguelonne, Skelly, Dan, Masurkar, Nihar, Mougenot, Nathalie, Nadaud, Sophie, Blanc, Catherine, Delacroix, Clément, Chardonnet, Solenne, Pionneau, Cédric, Perret, Claire, Yaniz-Galende, Elisa, Rosenthal, Nadia, Trégouët, David-Alexandre, Marazzi, Giovanna, Silvestre, Jean-Sébastien, Sassoon, David, Hulot, Jean-Sébastien
Published in Scientific reports (09.07.2020)
Published in Scientific reports (09.07.2020)
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Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project
Oudot-Mellakh, Tiphaine, Cohen, William, Germain, Marine, Saut, Noémie, Kallel, Choumous, Zelenika, Diana, Lathrop, Mark, Trégouët, David-Alexandre, Morange, Pierre-Emmanuel
Published in British journal of haematology (01.04.2012)
Published in British journal of haematology (01.04.2012)
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Addressing unmeasured confounders in cohort studies: Instrumental variable method for a time‐fixed exposure on an outcome trajectory
Le Bourdonnec, Kateline, Samieri, Cécilia, Tzourio, Christophe, Mura, Thibault, Mishra, Aniket, Trégouët, David‐Alexandre, Proust‐Lima, Cécile
Published in Biometrical journal (01.01.2024)
Published in Biometrical journal (01.01.2024)
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Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score
Bocher, Ozvan, Ludwig, Thomas E, Oglobinsky, Marie-Sophie, Marenne, Gaëlle, Deleuze, Jean-François, Suryakant, Suryakant, Odeberg, Jacob, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre, Perdry, Hervé, Génin, Emmanuelle
Published in PLoS genetics (16.09.2022)
Published in PLoS genetics (16.09.2022)
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A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process
Thibord, Florian, Hardy, Lise, Ibrahim‐Kosta, Manal, Saut, Noémie, Pulcrano‐Nicolas, Anne‐Sophie, Goumidi, Louisa, Civelek, Mete, Eriksson, Per, Deleuze, Jean‐François, Le Goff, Wilfried, Trégouët, David‐Alexandre, Morange, Pierre‐Emmanuel
Published in Journal of thrombosis and haemostasis (01.11.2019)
Published in Journal of thrombosis and haemostasis (01.11.2019)
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Fibrogenic Potential of PW1/Peg3 Expressing Cardiac Stem Cells
Yaniz-Galende, Elisa, Roux, Maguelonne, Nadaud, Sophie, Mougenot, Nathalie, Bouvet, Marion, Claude, Olivier, Lebreton, Guillaume, Blanc, Catherine, Pinet, Florence, Atassi, Fabrice, Perret, Claire, Dierick, France, Dussaud, Sébastien, Leprince, Pascal, Trégouët, David-Alexandre, Marazzi, Giovanna, Sassoon, David, Hulot, Jean-Sébastien
Published in Journal of the American College of Cardiology (08.08.2017)
Published in Journal of the American College of Cardiology (08.08.2017)
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EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension
Eyries, Mélanie, Montani, David, Girerd, Barbara, Perret, Claire, Leroy, Anne, Lonjou, Christine, Chelghoum, Nadjim, Coulet, Florence, Bonnet, Damien, Dorfmüller, Peter, Fadel, Elie, Sitbon, Olivier, Simonneau, Gérald, Tregouët, David-Alexandre, Humbert, Marc, Soubrier, Florent
Published in Nature genetics (01.01.2014)
Published in Nature genetics (01.01.2014)
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Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis
Germain, Marine, Saut, Noémie, Oudot-Mellakh, Tiphaine, Letenneur, Luc, Dupuy, Anne-Marie, Bertrand, Marion, Alessi, Marie-Christine, Lambert, Jean-Charles, Zelenika, Diana, Emmerich, Joseph, Tiret, Laurence, Cambien, Francois, Lathrop, Mark, Amouyel, Philippe, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre
Published in PloS one (04.06.2012)
Published in PloS one (04.06.2012)
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Targeted panel sequencing in adult patients with left ventricular non‐compaction reveals a large genetic heterogeneity
Richard, Pascale, Ader, Flavie, Roux, Maguelonne, Donal, Erwan, Eicher, Jean‐Christophe, Aoutil, Nadia, Huttin, Olivier, Selton‐Suty, Christine, Coisne, Damien, Jondeau, Guillaume, Damy, Thibaud, Mansencal, Nicolas, Casalta, Anne‐Claire, Michel, Nicolas, Haentjens, Julie, Faivre, Laurence, Lavoute, Cecile, Nguyen, Karine, Tregouët, David‐Alexandre, Habib, Gilbert, Charron, Philippe
Published in Clinical genetics (01.03.2019)
Published in Clinical genetics (01.03.2019)
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Maximizing the Power of Principal-Component Analysis of Correlated Phenotypes in Genome-wide Association Studies
Aschard, Hugues, Vilhjálmsson, Bjarni J., Greliche, Nicolas, Morange, Pierre-Emmanuel, Trégouët, David-Alexandre, Kraft, Peter
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
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Genetics of Venous Thrombosis: update in 2015
Morange, Pierre-Emmanuel, Suchon, Pierre, Trégouët, David-Alexandre
Published in Thrombosis and haemostasis (01.11.2015)
Published in Thrombosis and haemostasis (01.11.2015)
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DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis
Perret, Claire, Proust, Carole, Esslinger, Ulrike, Ader, Flavie, Haas, Jan, Pruny, Jean-François, Isnard, Richard, Richard, Pascale, Trégouët, David-Alexandre, Charron, Philippe, Cambien, François, Villard, Eric
Published in Clinical genetics (01.02.2024)
Published in Clinical genetics (01.02.2024)
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Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data
Müller, Christian, Schillert, Arne, Röthemeier, Caroline, Trégouët, David-Alexandre, Proust, Carole, Binder, Harald, Pfeiffer, Norbert, Beutel, Manfred, Lackner, Karl J, Schnabel, Renate B, Tiret, Laurence, Wild, Philipp S, Blankenberg, Stefan, Zeller, Tanja, Ziegler, Andreas
Published in PloS one (07.06.2016)
Published in PloS one (07.06.2016)
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