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Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

International Consortium for Blood Pressure Genome-Wide Associat, ; Ehret, GB; Munroe, PB; Rice, KM; Bochud, M; Johnson, AD; Chasman, DI; Smith, AV; Tobin, MD; Verwoert, GC; et al. International Consortium for Blood Pressure Genome-Wide Associat, ; Ehret, GB; Munroe, PB; Rice, KM; Bochud, M; Johnson, AD; Chasman, DI; Smith, AV; Tobin, MD; Verwoert, GC; Hwang, SJ; Pihur, V; Vollenweider, P; O'Reilly, PF; Amin, N; Bragg-Gresham, JL; Teumer, A; Glazer, NL; Launer, L; Zhao, JH; Aulchenko, Y; Heath, S; Sõber, S; Parsa, A; Luan, J; Arora, P; Dehghan, A; Zhang, F; Lucas, G; Hicks, AA; Jackson, AU; Peden, JF; Tanaka, T; Wild, SH; Rudan, I; Igl, W; Milaneschi, Y; Parker, AN; Fava, C; Chambers, JC; Fox, ER; Kumari, M; Go, MJ; van der Harst, P; Kao, WH; Sjögren, M; Vinay, DG; Alexander, M; Tabara, Y; Shaw-Hawkins, S; Whincup, PH; Liu, Y; Shi, G; Kuusisto, J; Tayo, B; Seielstad, M; Sim, X; Nguyen, KD; Lehtimäki, T; Matullo, G; Wu, Y; Gaunt, TR; Onland-Moret, NC; Cooper, MN; Platou, CG; Org, E; Hardy, R; Dahgam, S; Palmen, J; Vitart, V; Braund, PS; Kuznetsova, T; Uiterwaal, CS; Adeyemo, A; Palmas, W; Campbell, H; Ludwig, B; Tomaszewski, M; Tzoulaki, I; Palmer, ND; CARDIoGRAM consortium, ; CKDGen Consortium, ; KidneyGen Consortium, ; EchoGen consortium, ; CHARGE-HF consortium, ; Aspelund, T; Garcia, M; Chang, YP; O'Connell, JR; Steinle, NI; Grobbee, DE; Arking, DE; Kardia, SL; Morrison, AC; Hernandez, D; Najjar, S; McArdle, WL; Hadley, D; Brown, MJ; Connell, JM; Hingorani, AD; Day, IN; Lawlor, DA; Beilby, JP; Lawrence, RW; Clarke, R; Hopewell, JC; Ongen, H; Dreisbach, AW; Li, Y; Young, JH; Bis, JC; Kähönen, M; Viikari, J; Adair, LS; Lee, NR; Chen, MH; Olden, M; Pattaro, C; Bolton, JA; Köttgen, A; Bergmann, S; Mooser, V; Chaturvedi, N; Frayling, TM; Islam, M; Jafar, TH; Erdmann, J; Kulkarni, SR; Bornstein, SR; Grässler, J; Groop, L; Voight, BF; Kettunen, J; Howard, P; Taylor, A; Guarrera, S; Ricceri, F; Emilsson, V; Plump, A; Barroso, I; Khaw, KT; Weder, AB; Hunt, SC; Sun, YV; Bergman, RN; Collins, FS; Bonnycastle, LL; Scott, LJ; Stringham, HM; Peltonen, L; Perola, M; Vartiainen, E; Brand, SM; Staessen, JA; Wang, TJ; Burton, PR; Soler Artigas, M; Dong, Y; Snieder, H; Wang, X; Zhu, H; Lohman, KK; Rudock, ME; Heckbert, SR; Smith, NL; Wiggins, KL; Doumatey, A; Shriner, D; Veldre, G; Viigimaa, M; Kinra, S; Prabhakaran, D; Tripathy, V; Langefeld, CD; Rosengren, A; Thelle, DS; Corsi, AM; Singleton, A; Forrester, T; Hilton, G; McKenzie, CA; Salako, T; Iwai, N; Kita, Y; Ogihara, T; Ohkubo, T; Okamura, T; Ueshima, H; Umemura, S; Eyheramendy, S; Meitinger, T; Wichmann, HE; Cho, YS; Kim, HL; Lee, JY; Scott, J; Sehmi, JS; Zhang, W; Hedblad, B; Nilsson, P; Smith, GD; Wong, A; Narisu, N; Stančáková, A; Raffel, LJ; Yao, J; Kathiresan, S; O'Donnell, CJ; Schwartz, SM; Ikram, MA; Longstreth, WT; Mosley, TH; Seshadri, S; Shrine, NR; Wain, LV; Morken, MA; Swift, AJ; Laitinen, J; Prokopenko, I; Zitting, P; Cooper, JA; Humphries, SE; Danesh, J; Rasheed, A; Goel, A; Hamsten, A; Watkins, H; Bakker, SJ; van Gilst, WH; Janipalli, CS; Mani, KR; Yajnik, CS; Hofman, A; Mattace-Raso, FU; Oostra, BA; Demirkan, A; Isaacs, A; Rivadeneira, F; Lakatta, EG; Orru, M; Scuteri, A; Ala-Korpela, M; Kangas, AJ; Lyytikäinen, LP; Soininen, P; Tukiainen, T; Würtz, P; Ong, RT; Dörr, M; Kroemer, HK; Völker, U; Völzke, H; Galan, P; Hercberg, S; Lathrop, M; Zelenika, D; Deloukas, P; Mangino, M; Spector, TD; Zhai, G; Meschia, JF; Nalls, MA; Sharma, P; Terzic, J; Kumar, MV; Denniff, M; Zukowska-Szczechowska, E; Wagenknecht, LE; Fowkes, FG; Charchar, FJ; Schwarz, PE; Hayward, C; Guo, X; Rotimi, C; Bots, ML; Brand, E; Samani, NJ; Polasek, O; Talmud, PJ; Nyberg, F; Kuh, D; Laan, M; Hveem, K; Palmer, LJ; van der Schouw, YT; Casas, JP; Mohlke, KL; Vineis, P; Raitakari, O; Ganesh, SK; Wong, TY; Tai, ES; Cooper, RS; Laakso, M; Rao, DC; Harris, TB; Morris, RW; Dominiczak, AF; Kivimaki, M; Marmot, MG; Miki, T; Saleheen, D; Chandak, GR; Coresh, J; Navis, G; Salomaa, V; Han, BG; Zhu, X; Kooner, JS; Melander, O; Ridker, PM; Bandinelli, S; Gyllensten, UB; Wright, AF; Wilson, JF; Ferrucci, L; Farrall, M; Tuomilehto, J; Pramstaller, PP; Elosua, R; Soranzo, N; Sijbrands, EJ; Altshuler, D; Loos, RJ; Shuldiner, AR; Gieger, C; Meneton, P; Uitterlinden, AG; Wareham, NJ; Gudnason, V; Rotter, JI; Rettig, R; Uda, M; Strachan, DP; Witteman, JC; Hartikainen, AL; Beckmann, JS; Boerwinkle, E; Vasan, RS; Boehnke, M; Larson, MG; Järvelin, MR; Psaty, BM; Abecasis, GR; Chakravarti, A; Elliott, P; van Duijn, CM; Newton-Cheh, C; Levy, D; Caulfield, MJ; Johnson, T (2011) Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. NATURE, 478 (7367). 103 - 109 (7). ISSN 0028-0836 https://doi.org/10.1038/nature10405
SGUL Authors: Strachan, David Peter Whincup, Peter Hynes

Item Type: Article
Additional Information: PubMed ID: 21909115
Keywords: Africa, Asia, Blood Pressure, Cardiovascular Diseases, Coronary Artery Disease, Europe, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Hypertension, Kidney Diseases, Polymorphism, Single Nucleotide, Stroke, Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, GENOME-WIDE ASSOCIATION, COMMON VARIANTS, HYPERTENSION, METAANALYSIS, LOCI, POPULATION, RELEVANCE, RECEPTOR, CLONING, HEALTH
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: NATURE
ISSN: 0028-0836
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Dates:
DateEvent
6 October 2011Published
Web of Science ID: WOS:000295575400043
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URI: http://openaccess.sgul.ac.uk/id/eprint/99986
Publisher's version: https://doi.org/10.1038/nature10405

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