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