Works by Proust, Carole

Results: 23

Overlapping upstream ORFs ending at c.125 lead to reduced Endoglin, contributing to Hereditary Hemorrhagic Telangiectasia.

Published in:

Communications Biology, 2025, v. 8, n. 1, p. 1, doi. 10.1038/s42003-025-08461-6

By:

Proust, Carole;
Deiber, Clémence;
Meguerditchian, Caroline;
Tusseau, Maud;
Guilhem, Alexandre;
Mohamed, Shirine;
Goyenvalle, Aurélie;
Jaspard-Vinassa, Béatrice;
Dupuis-Girod, Sophie;
Trégouët, David-Alexandre;
Soukarieh, Omar

Publication type:

Article

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.

Published in:

European Heart Journal, 2011, v. 32, n. 9, p. 1065, doi. 10.1093/eurheartj/ehr105

By:

Villard, Eric;
Perret, Claire;
Gary, Françoise;
Proust, Carole;
Dilanian, Gilles;
Hengstenberg, Christian;
Ruppert, Volker;
Arbustini, Eloisa;
Wichter, Thomas;
Germain, Marine;
Dubourg, Olivier;
Tavazzi, Luigi;
Aumont, Marie-Claude;
DeGroote, Pascal;
Fauchier, Laurent;
Trochu, Jean-Noël;
Gibelin, Pierre;
Aupetit, Jean-François;
Stark, Klaus;
Erdmann, Jeanette

Publication type:

Article

Plasma levels of hsa-miR-152-3p are associated with diabetic nephropathy in patients with type 2 diabetes.

Published in:

Nephrology Dialysis Transplantation, 2018, v. 33, n. 12, p. 2201, doi. 10.1093/ndt/gfx367

By:

Roux, Maguelonne;
Perret, Claire;
Feigerlova, Eva;
Oumoussa, Badreddine Mohand;
Saulnier, Pierre-Jean;
Proust, Carole;
Trégouët, David-Alexandre;
Hadjadj, Samy

Publication type:

Article

DNA‐pools targeted‐sequencing as a robust cost‐effective method to detect rare variants: Application to dilated cardiomyopathy genetic diagnosis.

Published in:

Clinical Genetics, 2024, v. 105, n. 2, p. 185, doi. 10.1111/cge.14427

By:

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

Publication type:

Article

Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM Project.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 12, p. 1512, doi. 10.1038/ejhg.2008.127

By:

Grisoni, Marie-Lise;
Proust, Carole;
Alanne, Mervi;
DeSuremain, Maylis;
Salomaa, Veikko;
Kuulasmaa, Kari;
Cambien, François;
Nicaud, Viviane;
Stegmayr, Birgitta;
Virtamo, Jarmo;
Shields, Denis;
Kee, Frank;
Tiret, Laurence;
Evans, Alun;
Tregouet, David-Alexandre

Publication type:

Article

Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.

Published in:

2020

By:

Esslinger, Ulrike;
Garnier, Sophie;
Korniat, Agathe;
Proust, Carole;
Kararigas, Georgios;
Müller-Nurasyid, Martina;
Empana, Jean-Philippe;
Morley, Michael P.;
Perret, Claire;
Stark, Klaus;
Bick, Alexander G.;
Prasad, Sanjay K.;
Kriebel, Jennifer;
Li, Jin;
Tiret, Laurence;
Strauch, Konstantin;
O'Regan, Declan P.;
Marguiles, Kenneth B.;
Seidman, Jonathan G.;
Boutouyrie, Pierre

Publication type:

Correction Notice

Targeting Pdzrn3 maintains adult blood-brain barrier and central nervous system homeostasis.

Published in:

Journal of Cerebral Blood Flow & Metabolism, 2022, v. 42, n. 4, p. 613, doi. 10.1177/0271678X211048981

By:

Gueniot, Florian;
Rubin, Sebastien;
Bougaran, Pauline;
Abelanet, Alice;
Morel, Jean Luc;
Bontempi, Bruno;
Proust, Carole;
Dufourcq, Pascale;
Couffinhal, Thierry;
Duplàa, Cecile

Publication type:

Article

Integrating Genome-Wide Genetic Variations and Monocyte Expression Data Reveals Trans-Regulated Gene Modules in Humans.

Published in:

PLoS Genetics, 2011, v. 7, n. 12, p. 1, doi. 10.1371/journal.pgen.1002367

By:

Rotival, Maxime;
Zeller, Tanja;
Wild, Philipp S.;
Maouche, Seraya;
Szymczak, Silke;
Schillert, Arne;
Castagné, Raphaele;
Deiseroth, Arne;
Proust, Carole;
Brocheton, Jessy;
Godefroy, Tiphaine;
Perret, Claire;
Germain, Marine;
Eleftheriadis, Medea;
Sinning, Christoph R.;
Schnabel, Renate B.;
Lubos, Edith;
Lackner, Karl J.;
Rossmann, Heidi;
Münzel, Thomas

Publication type:

Article

Preservation Analysis of Macrophage Gene Coexpression Between Human and Mouse Identifies PARK2 as a Genetically Controlled Master Regulator of Oxidative Phosphorylation in Humans.

Published in:

G3: Genes | Genomes | Genetics, 2016, v. 6, n. 10, p. 3361, doi. 10.1534/g3.116.033894

By:

Codoni, Veronica;
Blum, Yuna;
Civelek, Mete;
Proust, Carole;
Franzén, Oscar;
Björkegren, Johan L. M.;
Le Goff, Wilfried;
Cambien, Francois;
Lusis, Aldons J.;
Trégouët, David-Alexandre

Publication type:

Article

Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.

Published in:

PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0172995

By:

Esslinger, Ulrike;
Garnier, Sophie;
Korniat, Agathe;
Proust, Carole;
Kararigas, Georgios;
Müller-Nurasyid, Martina;
Empana, Jean-Philippe;
Morley, Michael P.;
Perret, Claire;
Stark, Klaus;
Bick, Alexander G.;
Prasad, Sanjay K.;
Kriebel, Jennifer;
Li, Jin;
Tiret, Laurence;
Strauch, Konstantin;
O'Regan, Declan P.;
Marguiles, Kenneth B.;
Seidman, Jonathan G.;
Boutouyrie, Pierre

Publication type:

Article

Removing Batch Effects from Longitudinal Gene Expression - Quantile Normalization Plus ComBat as Best Approach for Microarray Transcriptome Data.

Published in:

PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0156594

By:

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

Publication type:

Article

Role of lipid phosphate phosphatase 3 in human aortic endothelial cell function.

Published in:

Cardiovascular Research, 2016, v. 112, n. 3, p. 702, doi. 10.1093/cvr/cvw217

By:

Touat-Hamici, Zahia;
Weidmann, Henri;
Blum, Yuna;
Proust, Carole;
Durand, Hervé;
Iannacci, Francesca;
Codoni, Veronica;
Gaignard, Pauline;
Thérond, Patrice;
Civelek, Mete;
Karabina, Sonia A.;
Lusis, Aldons J.;
Cambien, François;
Ninio, Ewa

Publication type:

Article

Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.

Published in:

Journal of Molecular Medicine, 2008, v. 86, n. 10, p. 1163, doi. 10.1007/s00109-008-0376-5

By:

Wolfgang Lieb;
Zeller, Tanja;
Mangino, Massimo;
Götz, Anika;
Braund, Peter;
Wenzel, Juergen;
Horn, Christian;
Proust, Carole;
Linsel-Nitschke, Patrick;
Amouyel, Philippe;
Bruse, Petra;
Arveiler, Dominique;
König, Inke;
Ferrières, Jean;
Ziegler, Andreas;
Balmforth, Anthony;
Evans, Alun;
Ducimetière, Pierre;
Cambien, Francois;
Hengstenberg, Christian

Publication type:

Article

uAUG creating variants in the 5'UTR of ENG causing Hereditary Hemorrhagic Telangiectasia.

Published in:

NPJ Genomic Medicine, 2023, v. 8, n. 1, p. 1, doi. 10.1038/s41525-023-00378-5

By:

Soukarieh, Omar;
Tillet, Emmanuelle;
Proust, Carole;
Dupont, Charlène;
Jaspard-Vinassa, Béatrice;
Soubrier, Florent;
Goyenvalle, Aurélie;
Eyries, Mélanie;
Trégouët, David-Alexandre

Publication type:

Article

Common CX3CR1 Alleles Are Associated With a Reduced Risk of Headaches.

Published in:

Headache: The Journal of Head & Face Pain, 2008, v. 48, n. 7, p. 1061, doi. 10.1111/j.1526-4610.2007.01011.x

By:

Combadière, Christophe;
Godin, Ophelia;
Vidal, Cécile;
Cangialosi, Arnaud;
Proust, Carole;
Tzourio, Christophe

Publication type:

Article

Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage.

Published in:

Journal of Neurosurgery, 2020, v. 133, n. 6, p. 1837, doi. 10.3171/2019.9.JNS191305

By:

Pulcrano-Nicolas, Anne-Sophie;
Jacquens, Alice;
Proust, Carole;
Clarençon, Frédéric;
Perret, Claire;
Shotar, Eimad;
Puybasset, Louis;
Le Goff, Wilfried;
Degos, Vincent;
Trégouët, David-Alexandre;
Garnier, Sophie

Publication type:

Article

Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM Project.

Published in:

BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-44

By:

Grisoni, Marie-Lise;
Proust, Carole;
Alanne, Mervi;
DeSuremain, Maylis;
Salomaa, Veikko;
Kuulasmaa, Kari;
Cambien, François;
Nicaud, Viviane;
Wiklund, Per-Gunnar;
Virtamo, Jarmo;
Kee, Frank;
Tiret, Laurence;
Evans, Alun;
Tregouet, David-Alexandre

Publication type:

Article

A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant.

Published in:

PLoS Genetics, 2021, v. 17, n. 1, p. 1, doi. 10.1371/journal.pgen.1009284

By:

Morange, Pierre-Emmanuel;
Peiretti, Franck;
Gourhant, Lenaick;
Proust, Carole;
Soukarieh, Omar;
Pulcrano-Nicolas, Anne-Sophie;
Saripella, Ganapathi-Varma;
Stefanucci, Luca;
Lacroix, Romaric;
Ibrahim.Kosta, Manal;
Lemarié, Catherine A.;
Frontini, Mattia;
Alessi, Marie-Christine;
Trégouët, David-Alexandre;
Couturaud, Francis

Publication type:

Article

Powerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression.

Published in:

PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0052260

By:

Almlöf, Jonas Carlsson;
Lundmark, Per;
Lundmark, Anders;
Bing Ge;
Maouche, Seraya;
Göring, Harald H. H.;
Liljedahl, Ulrika;
Enström, Camilla;
Brocheton, Jessy;
Proust, Carole;
Godefroy, Tiphaine;
Sambrook, Jennifer G.;
Jolley, Jennifer;
Crisp-Hihn, Abigail;
Foad, Nicola;
Lloyd-Jones, Heather;
Stephens, Jonathan;
Gwilliam, Rhian;
Rice, Catherine M.;
Hengstenberg, Christian

Publication type:

Article

miR-421 and miR-30c Inhibit SERPINE 1 Gene Expression in Human Endothelial Cells.

Published in:

PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0044532

By:

Marchand, Alexandre;
Proust, Carole;
Morange, Pierre-Emmanuel;
Lompré, Anne-Marie;
Trégouët, David-Alexandre;
Chadwick, Brian P.

Publication type:

Article

Genetics and Beyond -- The Transcriptome of Human Monocytes and Disease Susceptibility.

Published in:

PLoS ONE, 2010, v. 5, n. 5, p. 1, doi. 10.1371/journal.pone.0010693

By:

Zeller, Tanja;
Wild, Philipp;
Szymczak, Silke;
Rotival, Maxime;
Schillert, Arne;
Castagne, Raphaele;
Maouche, Seraya;
Germain, Marine;
Lackner, Karl;
Rossmann, Heidi;
Eleftheriadis, Medea;
Sinning, Christoph R.;
Schnabel, Renate B.;
Lubos, Edith;
Mennerich, Detlev;
Rust, Werner;
Perret, Claire;
Proust, Carole;
Nicaud, Viviane;
Loscalzo, Joseph

Publication type:

Article

An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-93390-7

By:

Razzaq, Misbah;
Iglesias, Maria Jesus;
Ibrahim-Kosta, Manal;
Goumidi, Louisa;
Soukarieh, Omar;
Proust, Carole;
Roux, Maguelonne;
Suchon, Pierre;
Boland, Anne;
Daiain, Delphine;
Olaso, Robert;
Havervall, Sebastian;
Thalin, Charlotte;
Butler, Lynn;
Deleuze, Jean-François;
Odeberg, Jacob;
Morange, Pierre-Emmanuel;
Trégouët, David-Alexandre

Publication type:

Article

Association Between a Thyroid Hormone Receptor-α Gene Polymorphism and Blood Pressure but Not With Coronary Heart Disease Risk.

Published in:

American Journal of Hypertension, 2011, v. 24, n. 9, p. 1027, doi. 10.1038/ajh.2011.94

By:

Goumidi, Louisa;
Gauthier, Karine;
Legry, Vanessa;
Mayi, Thérèse Hèrvée;
Houzet, Alexia;
Cottel, Dominique;
Montaye, Michèle;
Proust, Carole;
Kee, Frank;
Ferrières, Jean;
Arveiler, Dominique;
Ducimetière, Pierre;
Staels, Bart;
Dallongeville, Jean;
Chinetti, Giulia;
Flamant, Frédéric;
Amouyel, Philippe;
Meirhaeghe, Aline

Publication type:

Article