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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
Molecular and functional characterization of polymorphisms in the secreted phospholipase A2 group X gene: relevance to coronary artery disease.
Published in:
Journal of Molecular Medicine, 2009, v. 87, n. 7, p. 723, doi. 10.1007/s00109-009-0483-y
By:
- Gora, Sarah;
- Perret, Claire;
- Jemel, Ikram;
- Nicaud, Viviane;
- Lambeau, Gérard;
- Cambien, François;
- Ninio, Ewa;
- Blankenberg, Stefan;
- Tiret, Laurence;
- Karabina, Sonia-Athina
Publication type:
Article
The association of telomere length with paternal history of premature myocardial infarction in the European Atherosclerosis Research Study II.
Published in:
Journal of Molecular Medicine, 2008, v. 86, n. 7, p. 815, doi. 10.1007/s00109-008-0347-x
By:
- Salpea, Klelia D.;
- Nicaud, Viviane;
- Tiret, Laurence;
- Talmud, Philippa J.;
- Humphries, Steve E.
Publication type:
Article
Polymorphisms in 33 inflammatory genes and risk of myocardial infarction—a system genetics approach.
Published in:
Journal of Molecular Medicine, 2007, v. 85, n. 11, p. 1271, doi. 10.1007/s00109-007-0234-x
By:
- Barbaux, Sandrine;
- Tregouet, David-Alexandre;
- Nicaud, Viviane;
- Poirier, Odette;
- Perret, Claire;
- Godefroy, Tiphaine;
- Francomme, Carole;
- Combadiere, Christophe;
- Arveiler, Dominique;
- Luc, Gerald;
- Ruidavets, Jean-Bernard;
- Evans, Alun E.;
- Kee, Frank;
- Morrison, Caroline;
- Tiret, Laurence;
- Brand-Herrmann, Stefan Martin;
- Cambien, François
Publication type:
Article
Lack of association between complement factor H polymorphisms and coronary artery disease or myocardial infarction.
Published in:
Journal of Molecular Medicine, 2007, v. 85, n. 7, p. 771, doi. 10.1007/s00109-007-0185-2
By:
- Nicaud, Viviane;
- Francomme, Carole;
- Ruidavets, Jean-Bernard;
- Luc, Gérald;
- Arveiler, Dominique;
- Kee, Frank;
- Evans, Alun;
- Morrison, Caroline;
- Blankenberg, Stefan;
- Cambien, François;
- Tiret, Laurence
Publication type:
Article
Polymorphisms in the genes encoding platelet-derived growth factor A and α receptor.
Published in:
Journal of Molecular Medicine, 2000, v. 78, n. 5, p. 287, doi. 10.1007/s001090000111
By:
- Herrmann, Stefan-Martin;
- Ricard, Sylvain;
- Nicaud, Viviane;
- Brand, Eva;
- Behague, Isabelle;
- Blanc, Hervé;
- Ruidavets, Jean-Bernard;
- Evans, Alun;
- Arveiler, Dominique;
- Luc, Gérald;
- Poirier, Odette;
- Cambien, François
Publication type:
Article
Identification of two polymorphisms in the early growth response protein-1 gene: possible association with lipid variables.
Published in:
Journal of Molecular Medicine, 2000, v. 78, n. 2, p. 81, doi. 10.1007/s001090000074
By:
- Brand, Eva;
- Herrmann, Stefan-Martin;
- Nicaud, Viviane;
- Evans, Alun;
- Ruidavets, Jean-Bernard;
- Arveiler, Dominique;
- Luc, Gerald;
- Cambien, François;
- Soubrier, Florent
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
Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.
Published in:
European Journal of Human Genetics, 2005, v. 13, n. 11, p. 1213, doi. 10.1038/sj.ejhg.5201489
By:
- Gouas, Laetitia;
- Nicaud, Viviane;
- Berthet, Myriam;
- Forhan, Anne;
- Tiret, Laurence;
- Balkau, Beverley;
- Guicheney, Pascale
Publication type:
Article
Polymorphism R92Q of the tumour necrosis factor receptor 1 gene is associated with myocardial infarction and carotid intima-media thickness - The ECTIM, AXA, EVA and GENIC Studies.
Published in:
European Journal of Human Genetics, 2004, v. 12, n. 3, p. 213, doi. 10.1038/sj.ejhg.5201143
By:
- Poirier, Odette;
- Nicaud, Viviane;
- Gariépy, Jérôme;
- Courbon, Dominique;
- Elbaz, Alexis;
- Morrison, Caroline;
- Kee, Franck;
- Evans, Alun;
- Arveiler, Dominique;
- Ducimetière, Pierre;
- Amarenco, Pierre;
- Cambien, François
Publication type:
Article
Polymorphisms of genes of the cardiac calcineurin pathway and cardiac hypertrophy.
Published in:
European Journal of Human Genetics, 2003, v. 11, n. 9, p. 659, doi. 10.1038/sj.ejhg.5201023
By:
- Poirier, Odette;
- Nicaud, Viviane;
- McDonagh, Theresa;
- Dargie, Henry J;
- Desnos, Michel;
- Dorent, Richard;
- Gerard Roiz&ebreve;s;
- Schwartz, Ketty;
- Tiret, Laurence;
- Komajda, Michel;
- Cambien, François
Publication type:
Article
Contribution of SELP and PSGL-1 genotypes and haplotypes to the presence of coronary heart disease in Tunisians.
Published in:
Molecular Biology Reports, 2011, v. 38, n. 1, p. 495, doi. 10.1007/s11033-010-0133-z
By:
- Ghazouani, Lakhdar;
- Abboud, Nesrine;
- Khalifa, Sonia Ben Hadj;
- Perret, Claire;
- Nicaud, Viviane;
- Almawi, Wassim Youssef;
- Cambien, François;
- Mahjoub, Touhami
Publication type:
Article
Molecular genetic analysis of a human insulin-like growth factor 1 promoter P1 variation.
Published in:
FASEB Journal, 2009, v. 23, n. 5, p. 1303, doi. 10.1096/fj.08-116863
By:
- Telgmann, Ralph;
- Dördelmann, Corinna;
- Brand, Eva;
- Nicaud, Viviane;
- Hagedorn, Claudia;
- Pavenstädt, Hermann;
- Cambien, Francois;
- Tiret, Laurence;
- Paul, Martin;
- Brand-Herrmann, Stefan-Martin
Publication type:
Article
G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes.
Published in:
Diabetes, 2008, v. 57, n. 10, p. 2843, doi. 10.2337/db08-0073
By:
- Trégouet, David-Alexandre;
- Groop, Per-Henrik;
- McGinn, Steven;
- Forsblom, Carol;
- Hadjadj, Samy;
- Marre, Michel;
- Parving, Hans-Henrik;
- Tarnow, Lise;
- Telgmann, Ralph;
- Godefroy, Tiphaine;
- Nicaud, Viviane;
- Rousseau, Rachel;
- Parkkonen, Maikki;
- Hoverfält, Anna;
- Gut, Ivo;
- Heath, Simon;
- Matsuda, Fumihiko;
- Cox, Roger;
- Kazeem, Gbenga;
- Farrall, Martin
Publication type:
Article
Combined effects of genetic and environmental factors on insulin resistance associated with reduced fetal growth.
Published in:
2002
By:
- Jaquet D;
- Trégouët DA;
- Godefroy T;
- Nicaud V;
- Chevenne D;
- Tiret L;
- Czernichow P;
- Lévy-Marchal C;
- Jaquet, Delphine;
- Trégouët, David A;
- Godefroy, Thierry;
- Nicaud, Viviane;
- Chevenne, Didi;
- Tiret, Laurence;
- Czernichow, Paul;
- Lévy-Marchal, Claire
Publication type:
journal article
Combines Effects of Genetic and Environmental Factors on Insulin Resistance Associated With Reduced Fetal Growth.
Published in:
Diabetes, 2002, v. 51, n. 12, p. 3473, doi. 10.2337/diabetes.51.12.3473
By:
- Jaquet, Delphine;
- Trégouët, David A.;
- Godefroy, Thierry;
- Nicaud, Viviane;
- Chevenne, Didi;
- Tiret, Laurence;
- Czernichow, Paul;
- LÉvy-Marchal, Claire
Publication type:
Article
Polymorphism Screening of Four Genes Encoding Advanced Glycation End-Product Putative Receptors: Association Study With Nephropathy in Type 1 Diabetic Patients.
Published in:
Diabetes, 2001, v. 50, n. 5, p. 1214, doi. 10.2337/diabetes.50.5.1214
By:
- Poirier, Odette;
- Nicaud, Viviane;
- Vionnet, Nathalie;
- Raoux, Ségolène;
- Tarnow, Lise;
- Vlassara, Helen;
- Parving, Hans-Henrik;
- Cambien, François
Publication type:
Article
P-selectin gene polymorphisms and risk of coronary heart disease among Tunisians.
Published in:
Journal of Thrombosis & Thrombolysis, 2009, v. 28, n. 3, p. 314, doi. 10.1007/s11239-008-0297-8
By:
- Ghazouani, Lakhdar;
- Abboud, Nesrine;
- Khlifa, Sonia;
- Perret, Claire;
- Nicaud, Viviane;
- Cambien, François;
- Almawi, Wassim;
- Mahjoub, Touhami
Publication type:
Article
Variation in USF1 shows haplotype effects, gene : gene and gene : environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II.
Published in:
Human Molecular Genetics, 2004, v. 13, n. 15, p. 1587, doi. 10.1093/hmg/ddh168
By:
- Putt, Wendy;
- Palmen, Jutta;
- Nicaud, Viviane;
- Tregouet, David-Alexandre;
- Tahri-Daizadeh, Nadia;
- Flavell, David M.;
- Humphries, Steve E.;
- Talmud, Philippa J.
Publication type:
Article
Heterogeneity of linkage disequilibriumin human genes has implications for association studies of commondiseases.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 4, p. 419, doi. 10.1093/hmg/11.4.419
By:
- Tiret, Laurence;
- Poirier, Odette;
- Nicaud, Viviane;
- Barbaux, Sandrine;
- Herrmann, Stefan-Martin;
- Perret, Claire;
- Raoux, Ségolène;
- Francomme, Carole;
- Lebard, Géraud;
- Trégouët, David;
- Cambien, François
Publication type:
Article
Angiotensin II type 2 receptor gene polymorphism and cardiovascular phenotypes: the GLAECO and GLAOLD studies
Published in:
2002
By:
- Herrmann, Stefan-Martin;
- Nicaud, Viviane;
- Schmidt-Petersen, Klaus;
- Pfeifer, Jacqueline;
- Erdmann, Jeanette;
- McDonagh, Theresa;
- Dargie, Henry J.;
- Paul, Martin;
- Regitz-Zagrosek, Vera
Publication type:
journal article
Segregation analysis of fat mass and fat-free mass with age- and sex-dependent effects: The Stanislas family study.
Published in:
Genetic Epidemiology, 1997, v. 14, n. 1, p. 51, doi. 10.1002/(SICI)1098-2272(1997)14:1<51::AID-GEPI4>3.0.CO;2-8
By:
- Lecomte, Edith;
- Herbeth, Bernard;
- Nicaud, Viviane;
- Rakotovao, Roger;
- Artur, Yves;
- Tiret, Laurence
Publication type:
Article
Polymorphisms of the endothelin-A and -B receptor genes in relation to blood pressure and myocardial infarction<sup>*</sup>.
Published in:
American Journal of Hypertension, 1999, v. 12, n. 3, p. 304, doi. 10.1016/S0895-7061(98)00255-6
By:
- Nicaud, Viviane;
- Poirier, Odette;
- Behague, Isabelle;
- Herrmann, Stefan-Martin;
- Mallet, Christine;
- Troesch, Alain;
- Bouyer, Jérôme;
- Evans, Alun;
- Luc, Gérald;
- Ruidavets, Jean-Bernard;
- Arveiler, Dominique;
- Bingham, Annie;
- Tiret, Laurence;
- Cambien, François
Publication type:
Article
The P-selectin gene is highly polymorphic: reduced frequency of the Pro715 allele carriers in patients with myocardial infarction.
Published in:
Human Molecular Genetics, 1998, v. 7, n. 8, p. 1277, doi. 10.1093/hmg/7.8.1277
By:
- Herrmann, Stefan‐Martin;
- Ricard, Sylvain;
- Nicaud, Viviane;
- Mallet, Christine;
- Evans, Alun;
- Ruidavets, Jean‐Bernard;
- Arveiler, Dominique;
- Luc, Gerald;
- Cambien, François
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

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