Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk
Humphries, S E, Whittall, R A, Hubbart, C S, Maplebeck, S, Cooper, J A, Soutar, A K, Naoumova, R, Thompson, G R, Seed, M, Durrington, P N, Miller, J P, Betteridge, D J B, Neil, H A W
Published in Journal of medical genetics (01.12.2006)
Published in Journal of medical genetics (01.12.2006)
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Development of a high-resolution melting method for mutation detection in familial hypercholesterolaemia patients
Whittall, R A, Scartezini, M, Li, Kawah, Hubbart, C, Reiner, Z, Abraha, A, Neil, H A W, Dedoussis, G, Humphries, S E
Published in Annals of clinical biochemistry (01.01.2010)
Published in Annals of clinical biochemistry (01.01.2010)
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Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia
Day, INM, Whittall, RA, O'Dell, SD, Haddad, L, Bolla, MK, Gudnason, V, Humphries, SE
Published in Human mutation (1997)
Published in Human mutation (1997)
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Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394
Day, I N, Haddad, L, O'Dell, S D, Day, L B, Whittall, R A, Humphries, S E
Published in Journal of medical genetics (01.02.1997)
Published in Journal of medical genetics (01.02.1997)
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A World Wide Web Site for Low-Density Lipoprotein Receptor Gene Mutations in Familial Hypercholesterolemia: Sequence-Based, Tabular, and Direct Submission Data Handling
Wilson, Darren J., Gahan, Mike, Haddad, Lema, Heath, Karen, Whittall, Ros A., Williams, Roger R., Humphries, Steve E., Day, Ian N.M.
Published in The American journal of cardiology (15.06.1998)
Published in The American journal of cardiology (15.06.1998)
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Health of juvenile delinquents
Weindling, A M, Bamford, F N, Whittall, R A
Published in British Medical Journal (Clinical research ed.) (15.02.1986)
Published in British Medical Journal (Clinical research ed.) (15.02.1986)
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R643G polymorphism in PECAM-1 influences transendothelial migration of monocytes and is associated with progression of CHD and CHD events
Elrayess, Mohamed A., Webb, Karen E., Bellingan, Geoff J., Whittall, Ros A., Kabir, Jahangir, Hawe, Emma, Syvänne, Mikko, Taskinen, Marja-Riitta, Frick, M. Heikki, Nieminen, Markku S., Kesäniemi, Y. Antero, Pasternack, Amos, Miller, George J., Humphries, Steve E.
Published in Atherosclerosis (01.11.2004)
Published in Atherosclerosis (01.11.2004)
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Serum homocysteine concentrations, gemfibrozil treatment, and progression of coronary atherosclerosis
Syvänne, Mikko, Whittall, Roslyn A., Turpeinen, Ursula, Nieminen, Markku S., Frick, M.Heikki, Kesäniemi, Y.Antero, Pasternack, Amos, Humphries, Steve E., Taskinen, Marja-Riitta
Published in Atherosclerosis (01.02.2004)
Published in Atherosclerosis (01.02.2004)
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Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the general population
Alharbi, Khalid K, Aldahmesh, Mohammed A, Spanakis, Emmanuel, Haddad, Lema, Whittall, Roslyn A, Chen, Xiao-he, Rassoulian, Hamid, Smith, Matt J, Sillibourne, Julie, Ball, Nicola J, Graham, Nikki J, Briggs, Patricia J, Simpson, Iain A, Phillips, David I W, Lawlor, Deborah A, Ye, Shu, Humphries, Stephen E, Cooper, Cyrus, Smith, George Davey, Ebrahim, Shah, Eccles, Diana M, Day, Ian N M
Published in Genome research (01.07.2005)
Published in Genome research (01.07.2005)
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