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356 results

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Page 1
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. Telgmann R, et al. Among authors: cambien f. J Hypertens. 2007 Mar;25(3):557-64. doi: 10.1097/HJH.0b013e3280144779. J Hypertens. 2007. PMID: 17278971
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. Schönfelder J, et al. Among authors: cambien f. Pharmacogenet Genomics. 2007 Aug;17(8):629-37. doi: 10.1097/FPC.0b013e328042bb46. Pharmacogenet Genomics. 2007. PMID: 17622939
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. Vischer P, et al. Among authors: cambien f. Pharmacogenet Genomics. 2008 Nov;18(11):1017-9. doi: 10.1097/FPC.0b013e32830d32ad. Pharmacogenet Genomics. 2008. PMID: 18820595
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. Schmidt-Petersen K, et al. Among authors: cambien f. Atherosclerosis. 2009 Sep;206(1):209-15. doi: 10.1016/j.atherosclerosis.2009.02.015. Epub 2009 Feb 21. Atherosclerosis. 2009. PMID: 19281985 Free article.
Increased monocyte adhesion by endothelial expression of VCAM-1 missense variation in vitro.
Schmitz B, Vischer P, Brand E, Schmidt-Petersen K, Korb-Pap A, Guske K, Nedele J, Schelleckes M, Hillen J, Rötrige A, Simmet T, Paul M, Cambien F, Brand SM. Schmitz B, et al. Among authors: cambien f. Atherosclerosis. 2013 Oct;230(2):185-90. doi: 10.1016/j.atherosclerosis.2013.07.039. Epub 2013 Jul 31. Atherosclerosis. 2013. PMID: 24075742 Free article.
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. Trégouet DA, et al. Among authors: cambien f. Diabetes. 2008 Oct;57(10):2843-50. doi: 10.2337/db08-0073. Epub 2008 Jul 15. Diabetes. 2008. PMID: 18633107 Free PMC article.
A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.
Morange PE, Bezemer I, Saut N, Bare L, Burgos G, Brocheton J, Durand H, Biron-Andreani C, Schved JF, Pernod G, Galan P, Drouet L, Zelenika D, Germain M, Nicaud V, Heath S, Ninio E, Delluc A, Münzel T, Zeller T, Brand-Herrmann SM, Alessi MC, Tiret L, Lathrop M, Cambien F, Blankenberg S, Emmerich J, Trégouët DA, Rosendaal FR. Morange PE, et al. Among authors: cambien f. Am J Hum Genet. 2010 Apr 9;86(4):592-5. doi: 10.1016/j.ajhg.2010.02.011. Epub 2010 Mar 11. Am J Hum Genet. 2010. PMID: 20226436 Free PMC article.
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. Brenner D, et al. Among authors: cambien f. Stroke. 2006 Jul;37(7):1691-6. doi: 10.1161/01.STR.0000226565.76113.6c. Epub 2006 Jun 1. Stroke. 2006. PMID: 16741188
356 results