Haemostatic Factors and the Risk of Cardiovascular Death in Patients With Coronary Artery Disease: The AtheroGene Study von Morange, P E, Bickel, C, Nicaud, V, Schnabel, R, Rupprecht, H J, Peetz, D, Lackner, K J, Cambien, F, Blankenberg, S, Tiret, L

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Association between migraine and endothelin type A receptor (ETA -231 A/G) gene polymorphism von TZOURIO, C, EL AMRANI, M, POIRIER, O, NICAUD, V, BOUSSER, M.-G, ALPEROVITCH, A

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Increased Body Mass Index After Kidney Transplantation in Activating Transcription Factor 6 Single Polymorphism Gene Carriers von Fougeray, S, Loriot, M.-A, Nicaud, V, Legendre, C, Thervet, E, Pallet, N

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Activated thrombin activatable fibrinolysis inhibitor levels are associated with the risk of cardiovascular death in patients with coronary artery disease: the AtheroGene study von TREGOUET, D. A., SCHNABEL, R., ALESSI, M. C., GODEFROY, T., DECLERCK, P. J., NICAUD, V., MUNZEL, T., BICKEL, C., RUPPRECHT, H. J., LUBOS, E., ZELLER, T., JUHAN‐VAGUE, I., BLANKENBERG, S., TIRET, L., MORANGE, P. E.

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Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects von GOUAS, L, NICAUD, V, CHAOUCH, S, BERTHET, M, FORHAN, A, TICHET, J, TIRET, L, BALKAU, B, GUICHENEY, P

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Prognostic value of plasma tissue factor and tissue factor pathway inhibitor for cardiovascular death in patients with coronary artery disease: the AtheroGene study von MORANGE, P. E., BLANKENBERG, S., ALESSI, M. C., BICKEL, C., RUPPRECHT, H. J., SCHNABEL, R., LUBOS, E., MÜNZEL, T., PEETZ, D., NICAUD, V., JUHAN‐VAGUE, I., TIRET, L.

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Polymorphisms of the tumour necrosis factor-α gene, coronary heart disease and obesity von HERRMANN, S.-M, RICARD, S, POIRIER, O, CAMBIEN, F, NICAUD, V, MALLET, C, ARVEILER, D, EVANS, A, RUIDAVETS, J.-B, LUC, G, BARA, L, PARRA, H.-J

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Deletion polymorphism in angiotensin-converting enzyme gene associated with parental history of myocardial infarction von Tiret, L., Nicaud, V., Kee, F., Evans, A., Cambou, J.P., Arveiler, D., Luc, G., Amouyel, P., Poirier, O., Lecerf, L., Cambien, F.

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Cholesteryl ester transfer protein gene effect on CETP activity and plasma high‐density lipoprotein in European populations von Gudnason, V., Kakko, S., Nicaud, V., Savolainen, M. J., Kesäniemi, Y. A., Tahvanainen, E., Humphries, S., On Behalf Of The EARS group

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Polymorphisms of the endothelial nitric oxide synthase gene - no consistent association with myocardial infarction in the ECTIM study von POIRIER, O, MAO, C, SOUBRIER, F, CAMBIEN, F, MALLET, C, NICAUD, V, HERRMANN, S. M, EVANS, A, RUIDAVETS, J. B, ARVEILER, D, LUC, G, TIRET, L

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Polymorphisms of the P-selectin gene and risk of myocardial infarction in men and women in the ECTIM extension study von Kee, F, Morrison, C, Evans, A E, McCrum, E, McMaster, D, Dallongeville, J, Nicaud, V, Poirier, O, Cambien, F

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New polymorphisms in the interleukin-10 gene - relationships to myocardial infarction von Donger, C., Georges, J-L., Nicaud, V., Morrison, C., Evans, A., Kee, F., Arveiler, D., Tiret, L., Cambien, F.

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The TNFα/G-308A polymorphism influences insulin sensitivity in offspring of patients with coronary heart disease: The European Atherosclerosis Research Study II von Nicaud, V, Raoux, S, Poirier, O, Cambien, F, O'Reilly, D.St.J, Tiret, L

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Reliability of reported family history of myocardial infarction von Kee, F, Tiret, L, Robo, J Y, Nicaud, V, McCrum, E, Evans, A, Cambien, F

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Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene von Charron, Ph, Tesson, F, Poirier, O, Nicaud, V, Peuchmaurd, M, Tiret, L, Cambien, F, Amouyel, P, Dubourg, O, Bouhour, J.-B, Millaire, A, Juilliere, Y, Bareiss, P, André-Fouët, X, Pouillart, F, Arveiler, D, Ferrières, J, Dorent, R, Roizès, G, Schwartz, K, Desnos, M, Komajda, M

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Association studies between haemochromatosis gene mutations and the risk of cardiovascular diseases von Hetet, G., Elbaz, A., Gariepy, J., Nicaud, V., Arveiler, D., Morrison, C., Kee, F., Evans, A., Simon, A., Amarenco, P., Cambien, F., Grandchamp, B.

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Polymorphisms of the endothelin-A and -B receptor genes in relation to blood pressure and myocardial infarction: The etude cas-témoins sur l’infarctus du myocarde (ECTIM) study von 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

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Ala147Thr and C+1542G Polymorphisms in the TAFI Gene Are not Asssociated with a Higher Risk of Venous Thrombosis in FV Leiden Carriers von Morange, P. E., Aillaud, M. F., Nicaud, V., Henry, M., Juhan-Vague, I.

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The concomitant occurrence of multiple epidermal cysts, osteomas and thyroid gland nodules is not diagnostic for Gardner syndrome in the absence of intestinal polyposis: a clinical... von Herrmann, S.‐M., Adler, Y.D., Schmidt‐Petersen, K., Nicaud, V., Morrison, C., Paul, M., Zouboulis, Ch.C.

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Factor VII Arg/Gln353 polymorphism determines factor VII coagulant activity in patients with myocardial infarction (MI) and control subjects in Belfast and in France but is not a s... von LANE, A, GREEN, F, CAMBIEN, F, SCARABIN, P. Y, NICAUD, V, BARA, L, HUMPHRIES, S, EVANS, A, LUC, G, CAMBOU, J. P, ARVEILER, D

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