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Items where Author is "Humphries, S"

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Number of items: 10.

Article

Seed, M, Roughton, M, Pedersen, K, Nair, D, Wang, T, Neil, A and Humphries, S (2012) Current statin treatment, DNA testing and cascade testing of UK patients with familial hypercholesterolaemia Primary Care Cardiovascular Journal, 5 (4). pp. 181-185.

Humphries, SE, Cranston, T, Allen, M, Middleton-Price, H, Fernandez, MC, Senior, V, Hawe, E, Iversen, A, Wray, R, Crook, MA and Wierzbicki, AS (2006) Mutational analysis in UK patients with a clinical diagnosis of familial hypercholesterolaemia: relationship with plasma lipid traits, heart disease risk and utility in relative tracing Journal of Molecular Medicine-Jmm, 84 (3). pp. 203-214.

Marteau, T, Senior, V, Humphries, SE, Bobrow, M, Cranston, T, Crook, MA, Day, L, Fernandez, M, Horne, R, Iversen, A, Jackson, Z, Lynas, J, Middleton-Price, H, Savine, R, Sikorski, J, Watson, M, Weinman, J, Wierzbicki, AS and Wray, R (2004) Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: A randomized controlled trial American Journal of Medical Genetics Part A, 128A (3). pp. 285-293.

Marteau, TM, Senior, V and Humphries, S (2002) Impact on perceived control and risk-reducing behaviour of genetic testing for familial hypercholesterolaemia (FH): a randomised controlled trial European Journal of Human Genetics, 10. pp. 306-307.

Curran, JM, Fatah-Ardalani, K, Tornvall, P, Humphries, SE and Green, FR (2001) A hypothesis to explain the reported association of the alpha-fibrinogen A312 allele with thromboembolic disease THROMBOSIS AND HAEMOSTASIS, 85 (6). pp. 1122-1123.

Montgomery, H, Clarkson, P, Barnard, M, Bell, J, Brynes, A, Dollery, C, Hajnal, J, Hemingway, H, Mercer, D, Jarman, P, Marshall, R, Prasad, K, Rayson, M, Saeed, N, Talmud, P, Thomas, L, Jubb, M, World, M and Humphries, S (1999) Angiotensin-converting-enzyme gene insertion/deletion polymorphism and response to physical training LANCET, 353 (9152). pp. 541-545.

Curran, JM, Evans, A, Arveiler, D, Luc, G, Ruidavets, JB, Humphries, SE and Green, FR (1998) The alpha fibrinogen T/A312 polymorphism in the ECTIM study THROMBOSIS AND HAEMOSTASIS, 79 (5). pp. 1057-1058.

Thomas, AE, Green, FR and Humphries, SE (1996) Association of genetic variation at the beta-fibrinogen gene locus and plasma fibrinogen levels interaction between allele frequency of the G/A(-455) polymorphism, age and smoking CLINICAL GENETICS, 50 (4). pp. 184-190.

Humphries, S, Temple, A, Lane, A, Green, F, Cooper, J and Miller, G (1996) Low plasma levels of factor VIIc and antigen are more strongly associated with the 10 base pair promoter (-323) insertion than the glutamine 353 variant. Thromb Haemost, 75 (4). pp. 567-572.

Conference or Workshop Item

Curran, JM, Fatah, K, Blomback, M, Humphries, S, Hamsten, A and Green, FR (1997) Alpha fibrinogen genotype is associated with the porosity and density of the fibrin gel matrix in MI patients

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