Publication date
2017 Mar
Authors
Warren, HR Evangelou, E Cabrera, CP Gao, H Ren, MX Mifsud, B Ntalla, I Surendran, P Liu, CY Cook, JP Kraja, AT Drenos, F Loh, M Verweij, N Marten, J Karaman, I Lepe, MPS O'Reilly, PF Knight, J Snieder, H Kato, N He, J Tai, ES Said, MA Porteous, D Alver, M Poulter, N Farrall, M Gansevoort, RT Padmanabhan, S Magi, R Stanton, A Connell, J Bakker, SJL Metspalu, A Shields, DC Thom, S Brown, M Sever, P Esko, T Hayward, C van der Harst, P Saleheen, D Chowdhury, R Chambers, JC Chasman, DI Chakravarti, A Newton-Cheh, C Lindgren, CM Levy, D Kooner, JS Keavney, B Tomaszewski, M Samani, NJ Howson, JMM Tobin, MD Munroe, PB Ehret, GB Wain, LV Barnes, MR Tzoulaki, J Caulfield, MJ Elliott, P Wain, LV Vaez, A Jansen, R Joehanes, R van der Most, PJ Erzurumluoglu, AM O'Reilly, P Cabrera, CP Warren, HR Rose, LM Verwoert, GC Hottenga, JJ Strawbridge, RJ Esko, T Arking, DE Hwang, SJ Guo, XQ Kutalik, Z Trompet, S Shrine, N Teumer, A Ried, JS Bis, JC Smith, AV Amin, N Nolte, IM Lyytikainen, LP Mahajan, A Wareham, NJ Hofer, E Joshi, PK Kristiansson, K Traglia, M Havulinna, AS Goel, A Nalls, MA Sober, S Vuckovic, D Luan, JA Del Greco, F Ayers, KL Marrugat, J Ruggiero, D Lopez, LM Niiranen, T Enroth, S Jackson, AU Nelson, CP Huffman, JE Zhang, WH Marten, J Gandin, I Harris, SE Zemonik, T Lu, YC Evangelou, E Shah, N de Borst, MH Mangino, M Prins, BP Campbell, A Li-Gao, RF Chauhan, G Oldmeadow, C Abecasis, G Abedi, M Barbieri, CM Barnes, MR Batini, C Blake, T Boehnke, M Bottinger, EP Braund, PS Brown, M Brumat, M Campbell, H Chambers, JC Cocca, M Collins, F Connell, J Cordell, HJ Damman, JJ Davies, G de Geus, EJ de Mutsert, R Deelen, J Demirkale, Y Doney, ASF Dorr, M Farrall, M Ferreira, T Franberg, M Gao, H Giedraitis, V Gieger, C Giulianini, F Gow, AJ Hamsten, A Harris, TB Hofman, A Holliday, EG Jarvelin, MR Johansson, A Johnson, AD Jousilahti, P Jula, A Kahonen, M Kathiresan, S Khaw, KT Kolcic, I Koskinen, S Langenberg, C Larson, M Launer, LJ Lehne, B Liewald, DCM Lin, L Lind, L Mach, F Mamasoula, C Menni, C Mifsud, B Milaneschi, Y Morgan, A Morris, AD Morrison, AC Munson, PJ Nandakumar, P Nguyen, QT Nutile, T Oldehinkel, AJ Oostra, BA Org, E Padmanabhan, S Palotie, A Pare, G Pattie, A Penninx, BWJH Poulter, N Pramstaller, PP Raitakari, OT Ren, MX Rice, K Ridker, PM Riese, H Ripatti, S Robino, A Rotter, JI Rudan, I Saba, Y Saint Pierre, A Sala, CF Sarin, AP Schmidt, R Scott, R Seelen, MA Shields, DC Siscovick, D Sorice, R Stanton, A Stott, DJ Sundstrom, J Swertz, M Taylor, KD Thom, S Tzoulaki, I Tzourio, C Uitterlinden, AG Volker, U Vollenweider, P Wild, S Willemsen, G Wright, AF Yao, J Theriault, S Conen, D John, A Sever, P Debette, S Mook-Kanamori, DO Zeggini, E Spector, TD van der Harst, P Palmer, CNA Vergnaud, AC Loos, RJF Polasek, O Starr, JM Girotto, G Hayward, C Kooner, JS Lindgren, CM Vitart, V Samani, NJ Tuomilehto, J Gyllensten, U Knekt, P Deary, IJ Ciullo, M Elosua, R Keavney, BD Hicks, AA Scott, RA Gasparini, P Laan, M Liu, YM Watkins, H Hartman, CA Salomaa, V Toniolo, D Perola, M Wilson, JF Schmidt, H Zhao, JH Lehtimaki, T van Duijn, CM Gudnason, V Psaty, BM Peters, A Rettig, R James, A Jukema, JW Strachan, DP Palmas, W Metspalu, A Ingelsson, E Boomsma, DI Franco, OH Bochud, M Newton-Cheh, C Munroe, PB Elliott, P Chasman, DI Chakravarti, A Knight, J Morris, AP Levy, D Tobin, MD Snieder, H Caulfield, MJ Ehret, GB
Group authors
Int Consortium Blood Pressure ICBP CHD Exome Consortium ExomeBP Consortium T2D-GENES Consortium GoT2D Genes Consortium CHARGE BP Exome Consortium iGEN-BP Consortium UK Biobank CardioMetab Consortium BIOS Consortium Lifelines Cohort Study Understanding Soc Sci Grp
Author KI Usernames
Hamsten, A|andham Strawbridge, RJ|ronstr
Pubmed ID
28135244
Journal
Nature genetics
Doctype
Article
KI Connection
Låg
Mesh SV
Blodtryck Europas ursprungsbefolkning Genetiska loci Genetiska sjukdomsanlag Genome-Wide Association Study Högt blodtryck Kardiovaskulära sjukdomar Kvinnlig Manlig Medelålders personer Människa Polymorfism, enkelnukleotid Riskfaktorer Vuxna
Mesh EN
Blood Pressure Cardiovascular Diseases Genetic Loci Genetic Predisposition to Disease Genome-Wide Association Study Hypertension Polymorphism, Single Nucleotide Risk Factors White People
First date
2017-03-26T10:55:32.944Z