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513 results

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Page 1
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.
Surendran P, Drenos F, Young R, Warren H, Cook JP, Manning AK, Grarup N, Sim X, Barnes DR, Witkowska K, Staley JR, Tragante V, Tukiainen T, Yaghootkar H, Masca N, Freitag DF, Ferreira T, Giannakopoulou O, Tinker A, Harakalova M, Mihailov E, Liu C, Kraja AT, Fallgaard Nielsen S, Rasheed A, Samuel M, Zhao W, Bonnycastle LL, Jackson AU, Narisu N, Swift AJ, Southam L, Marten J, Huyghe JR, Stančáková A, Fava C, Ohlsson T, Matchan A, Stirrups KE, Bork-Jensen J, Gjesing AP, Kontto J, Perola M, Shaw-Hawkins S, Havulinna AS, Zhang H, Donnelly LA, Groves CJ, Rayner NW, Neville MJ, Robertson NR, Yiorkas AM, Herzig KH, Kajantie E, Zhang W, Willems SM, Lannfelt L, Malerba G, Soranzo N, Trabetti E, Verweij N, Evangelou E, Moayyeri A, Vergnaud AC, Nelson CP, Poveda A, Varga TV, Caslake M, de Craen AJ, Trompet S, Luan J, Scott RA, Harris SE, Liewald DC, Marioni R, Menni C, Farmaki AE, Hallmans G, Renström F, Huffman JE, Hassinen M, Burgess S, Vasan RS, Felix JF; CHARGE-Heart Failure Consortium; Uria-Nickelsen M, Malarstig A, Reily DF, Hoek M, Vogt T, Lin H, Lieb W; EchoGen Consortium; Traylor M, Markus HF; METASTROKE Consortium; Highland HM, Justice AE, Marouli E; GIANT Consortium; Lindström J, U… See abstract for full author list ➔ Surendran P, et al. Among authors: kee f. Nat Genet. 2016 Oct;48(10):1151-1161. doi: 10.1038/ng.3654. Epub 2016 Sep 12. Nat Genet. 2016. PMID: 27618447 Free PMC article.
Characterization of polymorphic structure of cathepsin G gene: role in cardiovascular and cerebrovascular diseases.
Herrmann SM, Funke-Kaiser H, Schmidt-Petersen K, Nicaud V, Gautier-Bertrand M, Evans A, Kee F, Arveiler D, Morrison C, Orzechowski HD, Elbaz A, Amarenco P, Cambien F, Paul M. Herrmann SM, et al. Among authors: kee f. Arterioscler Thromb Vasc Biol. 2001 Sep;21(9):1538-43. doi: 10.1161/hq0901.095555. Arterioscler Thromb Vasc Biol. 2001. PMID: 11557685
Homocysteine and coronary heart disease risk in the PRIME study.
Troughton JA, Woodside JV, Young IS, Arveiler D, Amouyel P, Ferrières J, Ducimetière P, Patterson CC, Kee F, Yarnell JW, Evans A; PRIME Study Group. Troughton JA, et al. Among authors: kee f. Atherosclerosis. 2007 Mar;191(1):90-7. doi: 10.1016/j.atherosclerosis.2006.05.014. Epub 2006 Jun 13. Atherosclerosis. 2007. PMID: 16774755
Neutrophil elastase gene variation and coronary heart disease.
Schönfelder J, Telgmann R, Nicaud V, Brand E, Dördelmann C, Rüssmann C, Beining K, Schmidt-Petersen K, Evans A, Kee F, Morrison C, Arveiler D, Cambien F, Paul M, Brand-Herrmann SM. Schönfelder J, et al. Among authors: kee f. Pharmacogenet Genomics. 2007 Aug;17(8):629-37. doi: 10.1097/FPC.0b013e328042bb46. Pharmacogenet Genomics. 2007. PMID: 17622939
Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach.
Barbaux S, Tregouet DA, Nicaud V, Poirier O, Perret C, Godefroy T, Francomme C, Combadiere C, Arveiler D, Luc G, Ruidavets JB, Evans AE, Kee F, Morrison C, Tiret L, Brand-Herrmann SM, Cambien F. Barbaux S, et al. Among authors: kee f. J Mol Med (Berl). 2007 Nov;85(11):1271-80. doi: 10.1007/s00109-007-0234-x. Epub 2007 Jul 19. J Mol Med (Berl). 2007. PMID: 17634906
513 results