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    Results: 1 to 50 of 255

    1.

    Identification and functional analyses of molecular haplotypes of the human osteoprotegerin gene promoter.

    Hagedorn C, Telgmann R, Dördelmann C, Schmitz B, Hasenkamp S, Cambien F, Paul M, Brand E, Brand-Herrmann SM.

    Arterioscler Thromb Vasc Biol. 2009 Oct;29(10):1638-43. Epub 2009 Aug 6.PMID: 19661483 [PubMed - indexed for MEDLINE]Related articles

    2.

    Low plasma retinol predicts coronary events in healthy middle-aged men: The PRIME Study.

    Gey KF, Ducimetière P, Evans A, Amouyel P, Arveiler D, Ferrières J, Luc G, Kee F, Bingham A, Yarnell J, Cambien F.

    Atherosclerosis. 2009 Jul 14. [Epub ahead of print]PMID: 19660753 [PubMed - as supplied by publisher]Related articles

    3.

    Molecular and functional characterization of polymorphisms in the secreted phospholipase A2 group X gene: relevance to coronary artery disease.

    Gora S, Perret C, Jemel I, Nicaud V, Lambeau G, Cambien F, Ninio E, Blankenberg S, Tiret L, Karabina SA.

    J Mol Med. 2009 Jul;87(7):723-33. Epub 2009 Jun 3.PMID: 19495570 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

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

    Grisoni ML, Proust C, Alanne M, Desuremain M, Salomaa V, Kuulasmaa K, Cambien F, Nicaud V, Wiklund PG, Virtamo J, Kee F, Tiret L, Evans A, Tregouet DA.

    BMC Med Genet. 2009 May 27;10:44.PMID: 19473509 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population.

    Ghazouani L, Khalifa SB, Abboud N, Perret C, Nicaud V, Khalfallah AB, Alamawi WY, Cambien F, Mahjoub T.

    J Thromb Thrombolysis. 2009 Apr 17. [Epub ahead of print]PMID: 19373437 [PubMed - as supplied by publisher]Related articles

    6.

    Osteopontin gene variation and cardio/cerebrovascular disease phenotypes.

    Schmidt-Petersen K, Brand E, Telgmann R, Nicaud V, Hagedorn C, Labreuche J, Dördelmann C, Elbaz A, Gautier-Bertrand M, Fischer JW, Evans A, Morrison C, Arveiler D, Stoll M, Amarenco P, Cambien F, Paul M, Brand-Herrmann SM.

    Atherosclerosis. 2009 Sep;206(1):209-15. Epub 2009 Feb 21.PMID: 19281985 [PubMed - in process]Related articles

    8.

    New susceptibility locus for coronary artery disease on chromosome 3q22.3.

    Erdmann J, Grosshennig A, Braund PS, König IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Trégouët DA, Cambien F, Bruse P, Aherrahrou Z, Wagner AK, Stark K, Schwartz SM, Salomaa V, Elosua R, Melander O, Voight BF, O'Donnell CJ, Peltonen L, Siscovick DS, Altshuler D, Merlini PA, Peyvandi F, Bernardinelli L, Ardissino D, Schillert A, Blankenberg S, Zeller T, Wild P, Schwarz DF, Tiret L, Perret C, Schreiber S, El Mokhtari NE, Schäfer A, März W, Renner W, Bugert P, Klüter H, Schrezenmeir J, Rubin D, Ball SG, Balmforth AJ, Wichmann HE, Meitinger T, Fischer M, Meisinger C, Baumert J, Peters A, Ouwehand WH; Italian Atherosclerosis, Thrombosis, and Vascular Biology Working Group; Myocardial Infarction Genetics Consortium; Wellcome Trust Case Control Consortium; Cardiogenics Consortium, Deloukas P, Thompson JR, Ziegler A, Samani NJ, Schunkert H.

    Nat Genet. 2009 Mar;41(3):280-2. Epub 2009 Feb 8.PMID: 19198612 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.

    Trégouët DA, König IR, Erdmann J, Munteanu A, Braund PS, Hall AS, Grosshennig A, Linsel-Nitschke P, Perret C, DeSuremain M, Meitinger T, Wright BJ, Preuss M, Balmforth AJ, Ball SG, Meisinger C, Germain C, Evans A, Arveiler D, Luc G, Ruidavets JB, Morrison C, van der Harst P, Schreiber S, Neureuther K, Schäfer A, Bugert P, El Mokhtari NE, Schrezenmeir J, Stark K, Rubin D, Wichmann HE, Hengstenberg C, Ouwehand W; Wellcome Trust Case Control Consortium; Cardiogenics Consortium, Ziegler A, Tiret L, Thompson JR, Cambien F, Schunkert H, Samani NJ.

    Nat Genet. 2009 Mar;41(3):283-5. Epub 2009 Feb 8.PMID: 19198611 [PubMed - indexed for MEDLINE]Related articles

    10.

    Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

    Myocardial Infarction Genetics Consortium, Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H, Erdmann J, Reilly MP, Rader DJ, Morgan T, Spertus JA, Stoll M, Girelli D, McKeown PP, Patterson CC, Siscovick DS, O'Donnell CJ, Elosua R, Peltonen L, Salomaa V, Schwartz SM, Melander O, Altshuler D, Ardissino D, Merlini PA, Berzuini C, Bernardinelli L, Peyvandi F, Tubaro M, Celli P, Ferrario M, Fetiveau R, Marziliano N, Casari G, Galli M, Ribichini F, Rossi M, Bernardi F, Zonzin P, Piazza A, Mannucci PM, Schwartz SM, Siscovick DS, Yee J, Friedlander Y, Elosua R, Marrugat J, Lucas G, Subirana I, Sala J, Ramos R, Kathiresan S, Meigs JB, Williams G, Nathan DM, MacRae CA, O'Donnell CJ, Salomaa V, Havulinna AS, Peltonen L, Melander O, Berglund G, Voight BF, Kathiresan S, Hirschhorn JN, Asselta R, Duga S, Spreafico M, Musunuru K, Daly MJ, Purcell S, Voight BF, Purcell S, Nemesh J, Korn JM, McCarroll SA, Schwartz SM, Yee J, Kathiresan S, Lucas G, Subirana I, Elosua R, Surti A, Guiducci C, Gianniny L, Mirel D, Parkin M, Burtt N, Gabriel SB, Samani NJ, Thompson JR, Braund PS, Wright BJ, Balmforth AJ, Ball SG, Hall AS; Wellcome Trust Case Control Consortium, Schunkert H, Erdmann J, Linsel-Nitschke P, Lieb W, Ziegler A, König I, Hengstenberg C, Fischer M, Stark K, Grosshennig A, Preuss M, Wichmann HE, Schreiber S, Schunkert H, Samani NJ, Erdmann J, Ouwehand W, Hengstenberg C, Deloukas P, Scholz M, Cambien F, Reilly MP, Li M, Chen Z, Wilensky R, Matthai W, Qasim A, Hakonarson HH, Devaney J, Burnett MS, Pichard AD, Kent KM, Satler L, Lindsay JM, Waksman R, Epstein SE, Rader DJ, Scheffold T, Berger K, Stoll M, Huge A, Girelli D, Martinelli N, Olivieri O, Corrocher R, Morgan T, Spertus JA, McKeown P, Patterson CC, Schunkert H, Erdmann E, Linsel-Nitschke P, Lieb W, Ziegler A, König IR, Hengstenberg C, Fischer M, Stark K, Grosshennig A, Preuss M, Wichmann HE, Schreiber S, Hólm H, Thorleifsson G, Thorsteinsdottir U, Stefansson K, Engert JC, Do R, Xie C, Anand S, Kathiresan S, Ardissino D, Mannucci PM, Siscovick D, O'Donnell CJ, Samani NJ, Melander O, Elosua R, Peltonen L, Salomaa V, Schwartz SM, Altshuler D.

    Nat Genet. 2009 Mar;41(3):334-41. Epub 2009 Feb 8.PMID: 19198609 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Molecular genetic analysis of a human insulin-like growth factor 1 promoter P1 variation.

    Telgmann R, Dördelmann C, Brand E, Nicaud V, Hagedorn C, Pavenstädt H, Cambien F, Tiret L, Paul M, Brand-Herrmann SM.

    FASEB J. 2009 May;23(5):1303-13. Epub 2008 Dec 22.PMID: 19103645 [PubMed - indexed for MEDLINE]Related articles

    12.

    P-selectin gene polymorphisms and risk of coronary heart disease among Tunisians.

    Ghazouani L, Abboud N, Khlifa SB, Perret C, Nicaud V, Cambien F, Almawi WY, Mahjoub T.

    J Thromb Thrombolysis. 2009 Oct;28(3):314-9. Epub 2008 Dec 11.PMID: 19082691 [PubMed - in process]Related articles

    13.

    The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.

    Karvanen J, Silander K, Kee F, Tiret L, Salomaa V, Kuulasmaa K, Wiklund PG, Virtamo J, Saarela O, Perret C, Perola M, Peltonen L, Cambien F, Erdmann J, Samani NJ, Schunkert H, Evans A; MORGAM Project.

    Genet Epidemiol. 2009 Apr;33(3):237-46.PMID: 18979498 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Molecular investigation of the functional relevance of missense variants of ICAM-1.

    Vischer P, Telgmann R, Schmitz B, Hasenkamp S, Schmidt-Petersen K, Beining K, Huge A, Paul M, Amarenco P, Cambien F, Brand E, Brand-Herrmann SM.

    Pharmacogenet Genomics. 2008 Nov;18(11):1017-9.PMID: 18820595 [PubMed - indexed for MEDLINE]Related articles

    15.

    G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes.

    Trégouet DA, Groop PH, McGinn S, Forsblom C, Hadjadj S, Marre M, Parving HH, Tarnow L, Telgmann R, Godefroy T, Nicaud V, Rousseau R, Parkkonen M, Hoverfält A, Gut I, Heath S, Matsuda F, Cox R, Kazeem G, Farrall M, Gauguier D, Brand-Herrmann SM, Cambien F, Lathrop M, Vionnet N; EURAGEDIC Consortium.

    Diabetes. 2008 Oct;57(10):2843-50. Epub 2008 Jul 15.PMID: 18633107 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

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

    Grisoni ML, Proust C, Alanne M, DeSuremain M, Salomaa V, Kuulasmaa K, Cambien F, Nicaud V, Stegmayr B, Virtamo J, Shields D, Kee F, Tiret L, Evans A, Tregouet DA; MORGAM Project.

    Eur J Hum Genet. 2008 Dec;16(12):1512-20. Epub 2008 Jul 16.PMID: 18628791 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Cholesterol gene polymorphisms and cardiovascular events.

    Tiret L, Tregouet DA, Cambien F.

    N Engl J Med. 2008 Jul 3;359(1):92-3; author reply 93. No abstract available. PMID: 18609752 [PubMed - indexed for MEDLINE]Related articles

    18.

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

    Lieb W, Zeller T, Mangino M, Götz A, Braund P, Wenzel JJ, Horn C, Proust C, Linsel-Nitschke P, Amouyel P, Bruse P, Arveiler D, König IR, Ferrières J, Ziegler A, Balmforth AJ, Evans A, Ducimetière P, Cambien F, Hengstenberg C, Stark K, Hall AS, Schunkert H, Blankenberg S, Samani NJ, Erdmann J, Tiret L.

    J Mol Med. 2008 Oct;86(10):1163-70. Epub 2008 Jul 1.PMID: 18592168 [PubMed - indexed for MEDLINE]Related articles

    19.

    Performance comparison of two microarray platforms to assess differential gene expression in human monocyte and macrophage cells.

    Maouche S, Poirier O, Godefroy T, Olaso R, Gut I, Collet JP, Montalescot G, Cambien F.

    BMC Genomics. 2008 Jun 25;9:302.PMID: 18578872 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    The renin-angiotensin-aldosterone system in cerebral small vessel disease.

    Brenner D, Labreuche J, Pico F, Scheltens P, Poirier O, Cambien F, Amarenco P; GENIC Investigators.

    J Neurol. 2008 Jul;255(7):993-1000. Epub 2008 May 2.PMID: 18446309 [PubMed - indexed for MEDLINE]Related articles

    21.

    Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

    Schunkert H, Götz A, Braund P, McGinnis R, Tregouet DA, Mangino M, Linsel-Nitschke P, Cambien F, Hengstenberg C, Stark K, Blankenberg S, Tiret L, Ducimetiere P, Keniry A, Ghori MJ, Schreiber S, El Mokhtari NE, Hall AS, Dixon RJ, Goodall AH, Liptau H, Pollard H, Schwarz DF, Hothorn LA, Wichmann HE, König IR, Fischer M, Meisinger C, Ouwehand W, Deloukas P, Thompson JR, Erdmann J, Ziegler A, Samani NJ; Cardiogenics Consortium.

    Circulation. 2008 Apr 1;117(13):1675-84. Epub 2008 Mar 24.PMID: 18362232 [PubMed - indexed for MEDLINE]Related articlesFree article

    22.

    APOE genotype, ethnicity, and the risk of cerebral hemorrhage.

    Tzourio C, Arima H, Harrap S, Anderson C, Godin O, Woodward M, Neal B, Bousser MG, Chalmers J, Cambien F, MacMahon S.

    Neurology. 2008 Apr 15;70(16):1322-8. Epub 2008 Feb 6.PMID: 18256366 [PubMed - indexed for MEDLINE]Related articles

    23.

    Thrombomodulin gene polymorphisms in brain infarction and mortality after stroke.

    Olivot JM, Labreuche J, De Broucker T, Poirier O, Cambien F, Aiach M, Amarenco P; GENIC Investigators.

    J Neurol. 2008 Apr;255(4):514-9. Epub 2008 Jan 23.PMID: 18204921 [PubMed - indexed for MEDLINE]Related articles

    24.

    Genetics of cardiovascular diseases: from single mutations to the whole genome.

    Cambien F, Tiret L.

    Circulation. 2007 Oct 9;116(15):1714-24. Review. No abstract available. PMID: 17923582 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy.

    Tarnow L, Groop PH, Hadjadj S, Kazeem G, Cambien F, Marre M, Forsblom C, Parving HH, Trégouët D, Thévard A, Farrall M, Gut I, Gauguier D, Cox R, Matsuda F, Lathrop M, Vionnet N; EURAGEDIC Consortium.

    Nephrol Dial Transplant. 2008 Jan;23(1):161-8. Epub 2007 Aug 17.PMID: 17704113 [PubMed - indexed for MEDLINE]Related articles

    26.

    Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach.

    Barbaux S, Tregouet DA, Nicaud V, Poirier O, Perret C, Godefroy T, Francomme C, Combadiere C, Arveiler D, Luc G, Ruidavets JB, Evans AE, Kee F, Morrison C, Tiret L, Brand-Herrmann SM, Cambien F.

    J Mol Med. 2007 Nov;85(11):1271-80. Epub 2007 Jul 19.PMID: 17634906 [PubMed - indexed for MEDLINE]Related articles

    27.

    Genomewide association analysis of coronary artery disease.

    Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, König IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H; WTCCC and the Cardiogenics Consortium.

    N Engl J Med. 2007 Aug 2;357(5):443-53. Epub 2007 Jul 18.PMID: 17634449 [PubMed - indexed for MEDLINE]Related articlesFree article

    28.

    Neutrophil elastase gene variation and coronary heart disease.

    Schönfelder J, Telgmann R, Nicaud V, Brand E, Dördelmann C, Rüssmann C, Beining K, Schmidt-Petersen K, Evans A, Kee F, Morrison C, Arveiler D, Cambien F, Paul M, Brand-Herrmann SM.

    Pharmacogenet Genomics. 2007 Aug;17(8):629-37.PMID: 17622939 [PubMed - indexed for MEDLINE]Related articles

    29.

    SNPs of PSMA6 gene--investigation of possible association with myocardial infarction and type 2 diabetes mellitus.

    Sjakste T, Poudziunas I, Ninio E, Perret C, Pirags V, Nicaud V, Lazdins M, Evanss A, Morrison C, Cambien F, Sjakste N.

    Genetika. 2007 Apr;43(4):553-9.PMID: 17555133 [PubMed - indexed for MEDLINE]Related articles

    30.

    Coronary heart disease aetiology: associations and causality.

    Ducimetière P, Cambien F.

    C R Biol. 2007 Apr;330(4):299-305. Epub 2007 Mar 23. Review.PMID: 17502286 [PubMed - indexed for MEDLINE]Related articles

    31.

    Differential haplotypic expression of the interleukin-18 gene.

    Barbaux S, Poirier O, Godefroy T, Kleinert H, Blankenberg S, Cambien F, Tiret L.

    Eur J Hum Genet. 2007 Aug;15(8):856-63. Epub 2007 May 9.PMID: 17487222 [PubMed - indexed for MEDLINE]Related articlesFree article

    32.

    Lack of association between complement factor H polymorphisms and coronary artery disease or myocardial infarction.

    Nicaud V, Francomme C, Ruidavets JB, Luc G, Arveiler D, Kee F, Evans A, Morrison C, Blankenberg S, Cambien F, Tiret L.

    J Mol Med. 2007 Jul;85(7):771-5. Epub 2007 Mar 30.PMID: 17396242 [PubMed - indexed for MEDLINE]Related articles

    33.

    Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations.

    Hadjadj S, Tarnow L, Forsblom C, Kazeem G, Marre M, Groop PH, Parving HH, Cambien F, Tregouet DA, Gut IG, Théva A, Gauguier D, Farrall M, Cox R, Matsuda F, Lathrop M, Hager-Vionnet N; EURAGEDIC (European Rational Approach for Genetics of Diabetic Complications) Study Group.

    J Am Soc Nephrol. 2007 Apr;18(4):1284-91. Epub 2007 Mar 21.PMID: 17376814 [PubMed - indexed for MEDLINE]Related articlesFree article

    34.

    Association of eNOS Glu298Asp gene polymorphism with circadian blood pressure rhythm.

    Ormezzano O, Amar J, Mounier Vehier C, Cambien F, Poirier O, Chamontin B, François P, Mallion JM, Baguet JP.

    J Hum Hypertens. 2007 Jun;21(6):501-3. Epub 2007 Mar 1.PMID: 17330057 [PubMed - indexed for MEDLINE]Related articles

    35.

    SAH gene variants are associated with obesity-related hypertension in Caucasians: the PEGASE Study.

    Telgmann R, Brand E, Nicaud V, Hagedorn C, Beining K, Schönfelder J, Brink-Spalink V, Schmidt-Petersen K, Matanis T, Vischer P, Nofer JR, Hasenkamp S, Plouin PF, Drouet L, Cambien F, Paul M, Tiret L, Brand-Herrmann SM.

    J Hypertens. 2007 Mar;25(3):557-64.PMID: 17278971 [PubMed - indexed for MEDLINE]Related articles

    36.

    Further evidence that the UGT1A1*28 allele is not associated with coronary heart disease: The ECTIM Study.

    Gajdos V, Petit FM, Perret C, Mollet-Boudjemline A, Colin P, Capel L, Nicaud V, Evans A, Arveiler D, Parisot F, Francoual J, Genin E, Cambien F, Labrune P.

    Clin Chem. 2006 Dec;52(12):2313-4. No abstract available. PMID: 17138857 [PubMed - indexed for MEDLINE]Related articlesFree article

    37.

    Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin gene.

    Vionnet N, Tregouët D, Kazeem G, Gut I, Groop PH, Tarnow L, Parving HH, Hadjadj S, Forsblom C, Farrall M, Gauguier D, Cox R, Matsuda F, Heath S, Thévard A, Rousseau R, Cambien F, Marre M, Lathrop M.

    Diabetes. 2006 Nov;55(11):3166-74.PMID: 17065357 [PubMed - indexed for MEDLINE]Related articlesFree article

    38.

    Haemostatic factors and the risk of cardiovascular death in patients with coronary artery disease: the AtheroGene study.

    Morange PE, Bickel C, Nicaud V, Schnabel R, Rupprecht HJ, Peetz D, Lackner KJ, Cambien F, Blankenberg S, Tiret L; AtheroGene Investigators.

    Arterioscler Thromb Vasc Biol. 2006 Dec;26(12):2793-9. Epub 2006 Oct 5.PMID: 17023678 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    Gene polymorphisms of the renin-angiotensin system and early development of hypertension.

    Barbalić M, Skarić-Jurić T, Cambien F, Barbaux S, Poirier O, Turek S, Vrhovski-Hebrang D, Cubrilo-Turek M, Rudan I, Rudan P, Narancić NS.

    Am J Hypertens. 2006 Aug;19(8):837-42.PMID: 16876684 [PubMed - indexed for MEDLINE]Related articles

    40.

    Comparative impact of multiple biomarkers and N-Terminal pro-brain natriuretic peptide in the context of conventional risk factors for the prediction of recurrent cardiovascular events in the Heart Outcomes Prevention Evaluation (HOPE) Study.

    Blankenberg S, McQueen MJ, Smieja M, Pogue J, Balion C, Lonn E, Rupprecht HJ, Bickel C, Tiret L, Cambien F, Gerstein H, Münzel T, Yusuf S; HOPE Study Investigators.

    Circulation. 2006 Jul 18;114(3):201-8. Epub 2006 Jul 10.PMID: 16831981 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

    Haplotypes of the caspase-1 gene, plasma caspase-1 levels, and cardiovascular risk.

    Blankenberg S, Godefroy T, Poirier O, Rupprecht HJ, Barbaux S, Bickel C, Nicaud V, Schnabel R, Kee F, Morrison C, Evans A, Lackner KJ, Cambien F, Münzel T, Tiret L; AtheroGene Investigators.

    Circ Res. 2006 Jul 7;99(1):102-8. Epub 2006 Jun 15.PMID: 16778130 [PubMed - indexed for MEDLINE]Related articlesFree article

    42.

    Cytokine polymorphisms associated with carotid intima-media thickness in stroke patients.

    Brenner D, Labreuche J, Touboul PJ, Schmidt-Petersen K, Poirier O, Perret C, Schönfelder J, Combadière C, Lathrop M, Cambien F, Brand-Herrmann SM, Amarenco P; GENIC Investigators.

    Stroke. 2006 Jul;37(7):1691-6. Epub 2006 Jun 1.PMID: 16741188 [PubMed - indexed for MEDLINE]Related articlesFree article

    43.

    B-type natriuretic peptide and the risk of cardiovascular events and death in patients with stable angina: results from the AtheroGene study.

    Schnabel R, Lubos E, Rupprecht HJ, Espinola-Klein C, Bickel C, Lackner KJ, Cambien F, Tiret L, Münzel T, Blankenberg S.

    J Am Coll Cardiol. 2006 Feb 7;47(3):552-8. Epub 2006 Jan 18.PMID: 16458135 [PubMed - indexed for MEDLINE]Related articles

    44.

    Prognostic value of tissue inhibitor of metalloproteinase-1 for cardiovascular death among patients with cardiovascular disease: results from the AtheroGene study.

    Lubos E, Schnabel R, Rupprecht HJ, Bickel C, Messow CM, Prigge S, Cambien F, Tiret L, Münzel T, Blankenberg S.

    Eur Heart J. 2006 Jan;27(2):150-6. Epub 2005 Oct 17.PMID: 16230310 [PubMed - indexed for MEDLINE]Related articlesFree article

    45.

    A polymorphism in the endothelin-A receptor gene is linked to baroreflex sensitivity.

    Ormezzano O, Poirier O, Mallion JM, Nicaud V, Amar J, Chamontin B, Mounier-Véhier C, François P, Cambien F, Baguet JP.

    J Hypertens. 2005 Nov;23(11):2019-26.PMID: 16208144 [PubMed - indexed for MEDLINE]Related articles

    46.

    Asymmetric dimethylarginine and the risk of cardiovascular events and death in patients with coronary artery disease: results from the AtheroGene Study.

    Schnabel R, Blankenberg S, Lubos E, Lackner KJ, Rupprecht HJ, Espinola-Klein C, Jachmann N, Post F, Peetz D, Bickel C, Cambien F, Tiret L, Münzel T.

    Circ Res. 2005 Sep 2;97(5):e53-9. Epub 2005 Aug 11.PMID: 16100045 [PubMed - indexed for MEDLINE]Related articlesFree article

    47.

    Atherosclerosis: from genetic polymorphisms to system genetics.

    Cambien F, Tiret L.

    Cardiovasc Toxicol. 2005;5(2):143-52. Review.PMID: 16046790 [PubMed - indexed for MEDLINE]Related articles

    48.

    Genetic analysis of the interleukin-18 system highlights the role of the interleukin-18 gene in cardiovascular disease.

    Tiret L, Godefroy T, Lubos E, Nicaud V, Tregouet DA, Barbaux S, Schnabel R, Bickel C, Espinola-Klein C, Poirier O, Perret C, Münzel T, Rupprecht HJ, Lackner K, Cambien F, Blankenberg S; AtheroGene Investigators.

    Circulation. 2005 Aug 2;112(5):643-50. Epub 2005 Jul 25.PMID: 16043644 [PubMed - indexed for MEDLINE]Related articlesFree article

    49.

    Renin-angiotensin-aldosterone system in brain infarction and vascular death.

    Brenner D, Labreuche J, Poirier O, Cambien F, Amarenco P; GENIC Investigators.

    Ann Neurol. 2005 Jul;58(1):131-8.PMID: 15984009 [PubMed - indexed for MEDLINE]Related articles

    50.

    TAFI gene haplotypes, TAFI plasma levels and future risk of coronary heart disease: the PRIME Study.

    Morange PE, Tregouet DA, Frere C, Luc G, Arveiler D, Ferrieres J, Amouyel P, Evans A, Ducimetiere P, Cambien F, Tiret L, Juhan-Vague I; Prime Study Group.

    J Thromb Haemost. 2005 Jul;3(7):1503-10.PMID: 15978108 [PubMed - indexed for MEDLINE]Related articles

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