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Lema Haddad

Research Profile

Chemicals & Drugs

Physiology

Disorders

Procedures

Phenomena

Polymorphism, Single-Stranded Conformational

Concepts & Ideas

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Publications

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Khalid K Alharbi; Mohammed Aldahmesh; Emmanuel Spanakis; Lema Haddad; Ros A Whittall; Xiao-he Chen; Hamid Rassoulian; Matt J Smith; Julie Sillibourne; Nicola J Ball; Nikki J Graham; Patricia J Briggs; Iain A Simpson; David I W Phillips; Deborah A Lawlor; Shu Ye; Stephen E Humphries; Cyrus Cooper; George Davey Smith; Shah Ebrahim; Diana Eccles; Ian N M Day
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.
Lema Haddad; Ian N M Day; S Hunt; R R Williams; Steve E Humphries; P N Hopkins
Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred.
D J Wilson; M Gahan; Lema Haddad; KE Heath; Ros A Whittall; R R Williams; Steve E Humphries; Ian N M Day
A World Wide Web site for low-density lipoprotein receptor gene mutations in familial hypercholesterolemia: sequence-based, tabular, and direct submission data handling.

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All Publications

2005: Khalid K Alharbi; Mohammed Aldahmesh; Emmanuel Spanakis; Lema Haddad; Ros A Whittall; Xiao-he Chen; Hamid Rassoulian; Matt J Smith; Julie Sillibourne; Nicola J Ball; Nikki J Graham; Patricia J Briggs; Iain A Simpson; David I W Phillips; Deborah A Lawlor; Shu Ye; Stephen E Humphries; Cyrus Cooper; George Davey Smith; Shah Ebrahim; Diana Eccles; Ian N M Day
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.
Genome research 2005;15(7):967-77.
1999: Lema Haddad; Ian N M Day; S Hunt; R R Williams; Steve E Humphries; P N Hopkins
Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindred.
Journal of lipid research 1999;40(6):1113-22.
1998: D J Wilson; M Gahan; Lema Haddad; KE Heath; Ros A Whittall; R R Williams; Steve E Humphries; Ian N M Day
A World Wide Web site for low-density lipoprotein receptor gene mutations in familial hypercholesterolemia: sequence-based, tabular, and direct submission data handling.
The American journal of cardiology 1998;81(12):1509-11.
1997: Lema Haddad; Lorna B Day; J Attwood; Sue Povey; Steve E Humphries; Ian N M Day
Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindreds.
Annals of human genetics 1997;61(Pt 6):497-506.
1997: Ian N M Day; Lema Haddad; SD O'Dell; Lorna B Day; Ros A Whittall; Steve E Humphries
Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394.
Journal of medical genetics 1997;34(2):111-6.
1997: Ian N M Day; Ros A Whittall; SD O'Dell; Lema Haddad; M K Bolla; Vilmundur Gudnason; Steve E Humphries
Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia.
Human mutation 1997;10(2):116-27.
1995: M K Bolla; Lema Haddad; Steve E Humphries; AF Winder; Ian N M Day
High-throughput method for determination of apolipoprotein E genotypes with use of restriction digestion analysis by microplate array diagonal gel electrophoresis.
Clinical chemistry 1995;41(11):1599-604.