Philippa J. Talmud

University Street
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 84 publications

Familial hypercholesterolaemia workshop for leveraging point-of-care testing and personalised medicine in association with the Lipid and Atherosclerosis Society of Southern Africa.

Familial hypercholesterolaemia workshop for leveraging point-of-care testing and personalised medicine in association with the Lipid and Atherosclerosis Society of Southern Africa.

Journal: Cardiovascular journal of Africa

Published: August 20, 2019

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

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

Journal: Circulation. Genomic and precision medicine

Published: May 04, 2017

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.

Journal: BioData mining

Published: January 02, 2017

Genetically determined telomeres shortening is associated with carotid atherosclerosis progression and increased incidence of cardiovascular events.

Genetically determined telomeres shortening is associated with carotid atherosclerosis progression and increased incidence of cardiovascular events.

Journal: International journal of cardiology

Published: July 18, 2016

Corrigendum to "APOA5 variants predispose hyperlipidemic patients to atherogenic dyslipidemia and subclinical atherosclerosis" [Atherosclerosis 240/1 (2015) 98-104].

Corrigendum to "APOA5 variants predispose hyperlipidemic patients to atherogenic dyslipidemia and subclinical atherosclerosis" [Atherosclerosis 240/1 (2015) 98-104].

Journal: Atherosclerosis

Published: May 17, 2016

Marginal role for 53 common genetic variants in cardiovascular disease prediction.

Marginal role for 53 common genetic variants in cardiovascular disease prediction.

Journal: Heart (British Cardiac Society)

Published: January 08, 2016

Post-GWAS methodologies for localisation of functional non-coding variants: ANGPTL3.

Post-GWAS methodologies for localisation of functional non-coding variants: ANGPTL3.

Journal: Atherosclerosis

Published: October 21, 2015

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

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

Journal: Arteriosclerosis, thrombosis, and vascular biology

Published: July 20, 2015

D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile.

D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile.

Journal: Nature communications

Published: June 01, 2015

Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.

Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.

Journal: Nature communications

Published: May 13, 2015

Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis.

Plasma urate concentration and risk of coronary heart disease: a Mendelian randomisation analysis.

Journal: The lancet. Diabetes & endocrinology

Published: April 24, 2015

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis.

Journal: International journal of epidemiology

Published: April 15, 2015

Showing 1-12 of 84

Last Updated: 09/26/2026