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Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study

The Lancet (British edition), 2013-04, Vol.381 (9874), p.1293-1301

2013

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Apolipoproteins C-I and C-III Inhibit Lipoprotein Lipase Activity by Displacement of the Enzyme from Lipid Droplets

The Journal of biological chemistry, 2013-11, Vol.288 (47), p.33997-34008

2013

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Deciphering the Causal Role of sPLA2s and Lp-PLA2 in Coronary Heart Disease

Arteriosclerosis, thrombosis, and vascular biology, 2015-11, Vol.35 (11), p.2281-2289

2015

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Oxidation-Specific Biomarkers, Lipoprotein(a), and Risk of Fatal and Nonfatal Coronary Events

Journal of the American College of Cardiology, 2010-09, Vol.56 (12), p.946-955

2010

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Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation

Atherosclerosis, 2010-03, Vol.209 (1), p.42-50

2010

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Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk

PloS one, 2012-03, Vol.7 (3), p.e31930-e31930

2012

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Relationship of IgG and IgM autoantibodies and immune complexes to oxidized LDL with markers of oxidation and inflammation and cardiovascular events: results from the EPIC-Norfolk Study

Journal of lipid research, 2011-10, Vol.52 (10), p.1829-1836

2011

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The genetic architecture of the familial hyperlipidaemia syndromes: rare mutations and common variants in multiple genes

Current opinion in lipidology, 2014-08, Vol.25 (4), p.274-281

2014

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Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart disease

PloS one, 2013-12, Vol.8 (12), p.e83122-e83122

2013

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Insulin stimulates hepatic low density lipoprotein receptor-related protein 1 (LRP1) to increase postprandial lipoprotein clearance

Atherosclerosis, 2009-05, Vol.204 (1), p.105-111

2009

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A common single-nucleotide variant in T is strongly associated with chordoma

Nature genetics, 2012-11, Vol.44 (11), p.1185-1187

2012

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Gene–environment interaction and its impact on coronary heart disease risk

Nutrition, metabolism, and cardiovascular diseases, 2007-02, Vol.17 (2), p.148-152

Talmud, Philippa J

2007

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Chromosome 9p21.3 Coronary Heart Disease Locus Genotype and Prospective Risk of CHD in Healthy Middle-Aged Men

Clinical chemistry (Baltimore, Md.), 2008-03, Vol.54 (3), p.467-474

2008

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Coronary Heart Disease Risk Prediction in the Era of Genome-Wide Association Studies Current Status and What the Future Holds

Circulation (New York, N.Y.), 2010-05, Vol.121 (20), p.2235-2248

2010

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Rare APOA5 mutations : Clinical consequences, metabolic and functional effects An ENID review

Atherosclerosis, 2007-10, Vol.194 (2), p.287-292

TALMUD, Philippa J

2007

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Improving Interpretation of Cardiac Phenotypes and Enhancing Discovery With Expanded Knowledge in the Gene Ontology

Circulation. Genomic and precision medicine, 2018-02, Vol.11 (2), p.e001813-e001813

2018

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Commentary on the paper by Gustavsson et al. entitled ‘Interaction of apolipoprotein E genotype with smoking and physical inactivity on coronary heart disease risk in men and women’

Atherosclerosis, 2012-02, Vol.220 (2), p.323-324

Talmud, Philippa J

2012

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APOA5 variants predispose hyperlipidemic patients to atherogenic dyslipidemia and subclinical atherosclerosis

Atherosclerosis, 2015-05, Vol.240 (1), p.98-104

2015

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Demonstration of the presence of the "deleted" MIR122 gene in HepG2 cells

PloS one, 2015-03, Vol.10 (3), p.e0122471

2015

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Inflammatory biomarkers, physical activity, waist circumference, and risk of future coronary heart disease in healthy men and women

European heart journal, 2011-02, Vol.32 (3), p.336-344

2011

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Relative contribution of variation within the APOC3/A4/A5 gene cluster in determining plasma triglycerides

Human molecular genetics, 2002-11, Vol.11 (24), p.3039-3046

2002

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Marginal role for 53 common genetic variants in cardiovascular disease prediction

Heart (British Cardiac Society), 2016-10, Vol.102 (20), p.1640-1647

2016

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Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium

PloS one, 2013-08, Vol.8 (8), p.e71345-e71345

2013

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Nonfasting apolipoprotein B and triglyceride levels as a useful predictor of coronary heart disease risk in middle-aged UK men

Arteriosclerosis, thrombosis, and vascular biology, 2002-11, Vol.22 (11), p.1918-1923

2002

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Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolaemia: a case-control study

Apolipoproteins C-I and C-III Inhibit Lipoprotein Lipase Activity by Displacement of the Enzyme from Lipid Droplets

Deciphering the Causal Role of sPLA2s and Lp-PLA2 in Coronary Heart Disease

Oxidation-Specific Biomarkers, Lipoprotein(a), and Risk of Fatal and Nonfatal Coronary Events

Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation

Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk

Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries

Relationship of IgG and IgM autoantibodies and immune complexes to oxidized LDL with markers of oxidation and inflammation and cardiovascular events: results from the EPIC-Norfolk Study

The genetic architecture of the familial hyperlipidaemia syndromes: rare mutations and common variants in multiple genes

Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart disease

Insulin stimulates hepatic low density lipoprotein receptor-related protein 1 (LRP1) to increase postprandial lipoprotein clearance

A common single-nucleotide variant in T is strongly associated with chordoma

Gene–environment interaction and its impact on coronary heart disease risk

Chromosome 9p21.3 Coronary Heart Disease Locus Genotype and Prospective Risk of CHD in Healthy Middle-Aged Men

Coronary Heart Disease Risk Prediction in the Era of Genome-Wide Association Studies Current Status and What the Future Holds

Rare APOA5 mutations : Clinical consequences, metabolic and functional effects An ENID review

Improving Interpretation of Cardiac Phenotypes and Enhancing Discovery With Expanded Knowledge in the Gene Ontology

Commentary on the paper by Gustavsson et al. entitled ‘Interaction of apolipoprotein E genotype with smoking and physical inactivity on coronary heart disease risk in men and women’

APOA5 variants predispose hyperlipidemic patients to atherogenic dyslipidemia and subclinical atherosclerosis

Demonstration of the presence of the "deleted" MIR122 gene in HepG2 cells

Inflammatory biomarkers, physical activity, waist circumference, and risk of future coronary heart disease in healthy men and women

Relative contribution of variation within the APOC3/A4/A5 gene cluster in determining plasma triglycerides

Marginal role for 53 common genetic variants in cardiovascular disease prediction

Population genomics of cardiometabolic traits: design of the University College London-London School of Hygiene and Tropical Medicine-Edinburgh-Bristol (UCLEB) Consortium

Nonfasting apolipoprotein B and triglyceride levels as a useful predictor of coronary heart disease risk in middle-aged UK men

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