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Journal of Molecular Medicine (Berlin, Germany)|September 21, 2004
Cytokine gene polymorphisms in ischaemic heart disease: investigation using family-based tests of associationPaul G McGlinchey, Mark S Spence, Chris C Patterson, et al.
Open Heart|May 15, 2021
Exercise prescription improves exercise tolerance in young children with CHD: a randomised clinical trialSinead Callaghan, Margaret Louise Morrison, Pascal P McKeown, et al.
Atherosclerosis|November 6, 2002
Family-based investigation of the C677T polymorphism of the methylenetetrahydrofolate reductase gene in ischaemic heart diseaseMark S Spence, Paul G McGlinchey, Chris C Patterson, et al.
Plos One|August 22, 2022
Association of TGFB1 rs1800469 and BCMO1 rs6564851 with coronary heart disease and IL1B rs16944 with all-cause mortality in men from the Northern Ireland PRIME studyRachel E Mooney, Gerry J Linden, Lewis Winning, et al.
Metabolites|October 2, 2019
Application of <sup>1</sup>H-NMR Metabolomics for the Discovery of Blood Plasma Biomarkers of a Mediterranean DietShirin Macias, Joseph Kirma, Ali Yilmaz, et al.
Journal of Nutritional Science|July 16, 2026
Identification of blood biomarkers of a healthy dietary pattern as facilitated by cluster analysis in patients from the MEDDINI study: a pilot randomised trialShirin Macias, Ali Yilmaz, Joseph Kirma, et al.
American Heart Journal|November 4, 2004
Endothelial nitric oxide synthase gene polymorphism and ischemic heart diseaseMark S Spence, Paul G McGlinchey, Chris C Patterson, et al.
JACC. Heart Failure|June 23, 2014
The effect of multiple micronutrient supplementation on left ventricular ejection fraction in patients with chronic stable heart failure: a randomized, placebo-controlled trialNicholas A McKeag, Michelle C McKinley, Mark T Harbinson, et al.
Experimental Gerontology|March 31, 2004
Paraoxonase polymorphisms PON1 192 and 55 and longevity in Italian centenarians and Irish nonagenarians. A pooled analysisIrene M Rea, Pascal P McKeown, Dorothy McMaster, et al.
BMC Medical Genetics|July 29, 2006
Lack of MEF2A Delta7aa mutation in Irish families with early onset ischaemic heart disease, a family based studyPaul G Horan, Adrian R Allen, Anne E Hughes, et al.
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