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Year Number of Results
2009 2
2010 3
2011 8
2012 5
2013 3
2014 3
2015 3
2024 0

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21 results

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Page 1
Interleukin 18 and coronary heart disease: prospective study and systematic review.
Jefferis BJ, Papacosta O, Owen CG, Wannamethee SG, Humphries SE, Woodward M, Lennon LT, Thomson A, Welsh P, Rumley A, Lowe GD, Whincup PH. Jefferis BJ, et al. Atherosclerosis. 2011 Jul;217(1):227-33. doi: 10.1016/j.atherosclerosis.2011.03.015. Epub 2011 Mar 24. Atherosclerosis. 2011. PMID: 21481392 Free PMC article. Review.
Genetic variation in complement factor H and risk of coronary heart disease: eight new studies and a meta-analysis of around 48,000 individuals.
Sofat R, Casas JP, Kumari M, Talmud PJ, Ireland H, Kivimaki M, Marmot M, Hughes AD, Thom S, Ebrahim S, Whittaker JC, Smeeth L, Lawlor DA, Humphries SE, Hingorani AD. Sofat R, et al. Atherosclerosis. 2010 Nov;213(1):184-90. doi: 10.1016/j.atherosclerosis.2010.07.021. Epub 2010 Jul 29. Atherosclerosis. 2010. PMID: 20708732
Causal relevance of blood lipid fractions in the development of carotid atherosclerosis: Mendelian randomization analysis.
Shah S, Casas JP, Drenos F, Whittaker J, Deanfield J, Swerdlow DI, Holmes MV, Kivimaki M, Langenberg C, Wareham N, Gertow K, Sennblad B, Strawbridge RJ, Baldassarre D, Veglia F, Tremoli E, Gigante B, de Faire U, Kumari M, Talmud PJ, Hamsten A, Humphries SE, Hingorani AD. Shah S, et al. Circ Cardiovasc Genet. 2013 Feb;6(1):63-72. doi: 10.1161/CIRCGENETICS.112.963140. Epub 2012 Dec 28. Circ Cardiovasc Genet. 2013. PMID: 23275344
Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD; ASCOT investigators; NORDIL investigators; BRIGHT Consortium. Talmud PJ, et al. Am J Hum Genet. 2009 Nov;85(5):628-42. doi: 10.1016/j.ajhg.2009.10.014. Am J Hum Genet. 2009. PMID: 19913121 Free PMC article.
A genetic instrument for Mendelian randomization of fibrinogen.
Ken-Dror G, Humphries SE, Kumari M, Kivimaki M, Drenos F. Ken-Dror G, et al. Eur J Epidemiol. 2012 Apr;27(4):267-79. doi: 10.1007/s10654-012-9666-x. Epub 2012 Mar 3. Eur J Epidemiol. 2012. PMID: 22388766 Free PMC article.
IRS1 gene variants, dysglycaemic metabolic changes and type-2 diabetes risk.
Yiannakouris N, Cooper JA, Shah S, Drenos F, Ireland HA, Stephens JW, Li KW, Elkeles R, Godsland IF, Kivimaki M, Hingorani AD, Kumari M, Talmud PJ, Humphries SE. Yiannakouris N, et al. Nutr Metab Cardiovasc Dis. 2012 Dec;22(12):1024-30. doi: 10.1016/j.numecd.2011.05.009. Epub 2011 Sep 14. Nutr Metab Cardiovasc Dis. 2012. PMID: 21917432 Free PMC article.
Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip.
Zabaneh D, Gaunt TR, Kumari M, Drenos F, Shah S, Berry D, Power C, Hypponen E, Shah T, Palmen J, Pallas J, Talmud PJ, Casas JP, Sofat R, Lowe G, Rumley A, Morris RW, Whincup PH, Rodriguez S, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Kivimaki M, Whittaker J, Hingorani AD, Day IN, Humphries SE. Zabaneh D, et al. Ann Hum Genet. 2011 Jul;75(4):456-67. doi: 10.1111/j.1469-1809.2011.00654.x. Epub 2011 Apr 28. Ann Hum Genet. 2011. PMID: 21534939
21 results