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Publications
Konstantoulas C, Hawe E , Saut N, Yudkin JS, di Minno G, Margaglione M, Hamsten A, Humphries SE, Juhan-Vague I, Ireland H, Hifmech Study Group. Common variants in the thrombomodulin gene as a risk for myocardial infarction in the north of Europe (HIFMECH Study) . Thromb Haemost. 2004 Mar;91(3):628-30.
Serrano NC, Casas JP, Díaz LA, Páez C, Mesa CM, Cifuentes R, Monterrosa A, Bautista A, Hawe E , Hingorani AD, Vallance P, López-Jaramillo P. Endothelial NO synthase genotype and risk of preeclampsia: a multicenter case-control study . J Clin Hypertens (Greenwich). 2004;44(5):702-7.
Williams AG, Dhamrait SS, Wootton PT, Day SH, Hawe E , Payne JR, Myerson SG, World M, Budgett R, Humphries SE, Montgomery HE. Bradykinin receptor gene variant and human physical performance . J Appl Physiol. 2004;96(3):938-42.
Elrayess MA, Webb KE, Bellingan GJ, Whittall RA, Kabir J, Hawe E , Syvänne M, Taskinen MR, Frick MH, Nieminen MS, Kesäniemi YA, Pasternack A, Miller GJ, Humphries SE. R643G polymorphism in PECAM-1 influences transendothelial migration of monocytes and is associated with progression of CHD and CHD events . Atherosclerosis. 2004;177(1):105-12.