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pro vyhledávání: '"Majmnder, A.A.S."'
Autor:
Surendran, P., Drenos, F., Young, R., Warren, H., Cook, J.P., Manning, A.K., Grarup, N., Sim, X., Barnes, D.R., Witkowska, K., Staley, J.R., Tragante, V., Tukiainen, T., Yaghootkar, H., Masca, N., Freitag, D.F., Ferreira, T., Giannakopoulou, O., Tinker, A., Harakalova, M., Mihailov, E., Liu, C., Kraja, A.T., Nielsen, S.F., Rasheed, A., Samue, M., Zhao, W., Bonnycastle, L.L., Jackson, A.U., Narisu, N., Swift, A.J., Southam, L., Marten, J., Huyghe, J.R., Stancakova, A., Fava, C., Ohlsson, T., Matchan, A., Stirrups, K.E., Bork-Jensen, J., Gjesing, A.P., Kontto, J., Perola, M., Shaw-Hawkins, S., Havulinna, A.S., Zhang, H., Donnelly, L.A., Groves, C.J., Rayner, N.W., Neville, M.J., Robertson, N.R., Yiorkas, A.M., Herzig, K.H., Kajantie, E., Zhang, W., Willems, S.M., Lannfelt, L., Malerba, G., Soranzo, N., Trabetti, E., Verweij, N., Evangelou, E., Moayyeri, A., Vergnaud, A.C., Nelson, C.P., Poveda, A., Varga, T.V., Caslake, M., Craen, A.J.M. de, Trompet, S., Luan, J., Scott, R.A., Harris, S.E., Liewald, D.C.M., Marioni, R., Menni, C., Farmaki, A.E., Hallmans, G., Renstrom, F., Huffman, J.E., Hassinen, M., Burgess, S., Vasan, R.S., Felix, J.F., Uria-Nickelsen, M., Malarstign, A., Reilly, D.F., Hoek, M., Vogt, T.F., Lin, H.H., Lieb, W., Traylor, M., Markus, H.S., Highland, H.M., Justice, A.E., Marouli, E., Lindstrom, J., Uusitupa, M., Komulainen, P., Lakka, T.A., Rauramaa, R., Polasek, O., Rudan, I., Rolandsson, O., Franks, P.W., Dedoussis, G., Spector, T.D., Jousilahti, P., Mannisto, S., Deary, I.J., Starr, J.M., Langenberg, C., Wareham, N.J., Brown, M.J., Dominiczak, A.F., Connell, J.M., Jukema, J.W., Sattar, N., Ford, I., Packard, C.J., Esko, T., Magi, R., Metspalu, A., Boer, R.A. de, Meer, P. van der, Harst, P. van der, Gambaro, G., Ingelsson, E., Lind, L., Bakker, P.I.W. de, Numans, M.E., Brandslund, I., Christensen, C., Petersen, E.R.B., Korpi-Hyovalti, E., Oksa, H., Chambers, J.C., Kooner, J.S., Blakemore, A.I.F., Franks, S., Jarvelin, M.R., Husemoen, L.L., Linneberg, A., Skaaby, T., Thuesen, B., Karpe, F., Tuomilehto, J., Doney, A.S.F., Morris, A.D., Palmer, C.N.A., Holmen, O.L., Hveem, K., Willer, C.J., Tuomi, T., Groop, L., Karajamaki, A., Palotie, A., Ripatti, S., Salomaa, V., Alam, D.S., Majmnder, A.A.S., Angelantonio, E. di, Chowdhury, R., McCarthy, M.I., Poulter, N., Stanton, A.V., Sever, P., Amouyel, P., Arveiler, D., Blankenberg, S., Ferrieres, J., Kee, F., Kuulasmaa, K., Muller-Nurasyid, M., Veronesi, G., Virtamo, J., Deloukas, P., Elliott, P., Zeggini, E., Kathiresan, S., Melander, O., Kuusisto, J., Laakso, M., Padmanabhan, S., Porteous, D.J., Hayward, C., Scotland, G., Collins, F.S., Mohlke, K.L., Hansen, T., Pedersen, O., Boehnke, M., Stringham, H.M., Frossard, P., Newton-Cheh, C., Tobin, M.D., Nordestgaard, B.G., Caulfield, M.J., Mahajan, A., Morris, A.P., Tomaszewski, M., Samani, N.J., Saleheen, D., Asselbergs, F.W., Lindgren, C.M., Danesh, J., Wain, L.V., Butterworth, A.S., Howson, J.M.M., Munroe, P.B., CHARGE Heart Failure Consortiumm, EchoGen Consortiumm, Metastroke Consortiumm, Giant Consortiumm, EPIC-InterAct Consortium, Lifelines Cohort Study, Wellcome Trust Case Control Consor, Understanding Soc Sci Grp, EPIC-CVD Consortium, CHARGE Exome Chip Blood Pressure C, T2D-GENES Consortium, GoT2DGenes Consortium, ExomeBP Consortium, CHD Exome Consortium
Publikováno v:
Nature Genetics, 48(10), 1151-1161. Nature Publishing Group
Nature Genetics, 48(10), 1151-1161
Nature Genetics, 48(10), 1151. Nature Publishing Group
NATURE GENETICS
Nature genetics
CHARGE-Heart Failure Consortium, EchoGen Consortium, METASTROKE Consortium, GIANT Consortium, EPIC-InterAct Consortium, Lifelines Cohort Study, Wellcome Trust Case Control Consortium, Understanding Society Scientific Group, Generation Scotland, EPIC-CVD Consortium, CHARGE+ Exome Chip Blood Pressure Consortium, T2D-GENES Consortium, GoT2DGenes Consortium, ExomeBP Consortium & CHD Exome+ Consortium 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics, vol. 48, no. 10, pp. 1151-1161 . https://doi.org/10.1038/ng.3654
Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J P, Manning, A K, Grarup, N, Sim, X, Barnes, D R, Witkowska, K, Staley, J R, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D F, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A T, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L L, Jackson, A U, Narisu, N, Swift, A J, Southam, L, Marten, J, Huyghe, J R, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K E, Bork-Jensen, J, Gjesing, A P, Kontto, J, Perola, M, Shaw-Hawkins, S, Havulinna, A S, Zhang, H, Donnelly, L A, Groves, C J, Rayner, N W, Neville, M J, Robertson, N R, Yiorkas, A M, Herzig, K H, Kajantie, E, Zhang, W, Willems, S M, Lannfelt, L, Malerba, G, Soranzo, N, Trabetti, E, Verweij, N, Evangelou, E, Moayyeri, A, Vergnaud, A C, Nelson, C P, Poveda, A, Varga, T V, Caslake, M, De Craen, A J M, Trompet, S, Luan, JA, Scott, R A, Harris, S E, Liewald, D C M, Marioni, R, Menni, C, Farmaki, A E, Hallmans, G, Renström, F, Huffman, J E, Hassinen, M, Burgess, S, Vasan, R S, Felix, J F, Uria-Nickelsen, M, Malarstig, A, Reilly, D F, Hoek, M, Vogt, T F, Lin, H, Lieb, W, Traylor, M, Markus, H S, Highland, H M, Justice, A E, Marouli, E, Lindström, J, Uusitupa, M, Komulainen, P, Lakka, T A, Rauramaa, R, Polasek, O, Rudan, I, Rolandsson, O, Franks, P W, Dedoussis, G, Spector, T D, Jousilahti, P, Männistö, S, Deary, I J, Starr, J M, Langenberg, C, Wareham, N J, Brown, M J, Dominiczak, A F, Connell, J M, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Esko, T, Mägi, R, Metspalu, A, De Boer, R A, Van Der Meer, P, Van Der Harst, P, Gambaro, G, Ingelsson, E, Lind, L, De Bakker, P I W, Numans, M E, Brandslund, I, Christensen, C, Petersen, E R B, Korpi-Hyövälti, E, Oksa, H, Chambers, J C, Kooner, J S, Blakemore, A I F, Franks, S, Jarvelin, M R, Husemoen, L L, Linneberg, A, Skaaby, T, Thuesen, B, Karpe, F, Tuomilehto, J, Doney, A S F, Morris, A D, Palmer, C N A, Holmen, O L, Hveem, K, Willer, C J, Tuomi, T, Groop, L, Käräjämäki, A, Palotie, A, Ripatti, S, Salomaa, V, Alam, D S, Majumder, A A S, Di Angelantonio, E, Chowdhury, R, McCarthy, M I, Poulter, N, Stanton, A V, Sever, P, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, Deloukas, P, Elliott, P, Zeggini, E, Kathiresan, S, Melander, O, Kuusisto, J, Laakso, M, Padmanabhan, S, Porteous, D J, Hayward, C, Scotland, G, Collins, F S, Mohlke, K L, Hansen, T, Pedersen, O, Boehnke, M, Stringham, H M, Frossard, P, Newton-Cheh, C, Tobin, M D, Nordestgaard, B G, Caulfield, M J, Mahajan, A, Morris, A P, Tomaszewski, M, Samani, N J, Saleheen, D, Asselbergs, F W, Lindgren, C M, Danesh, J, Wain, L V, Butterworth, A S, Howson, J M M & Munroe, P B 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics, vol. 48, no. 10, pp. 1151-1161 . https://doi.org/10.1038/ng.3654
Nature Genetics
Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J P, Manning, A K, Grarup, N, Sim, X, Barnes, D R, Witkowska, K, Staley, J R, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D F, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A T, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L L, Jackson, A U, Narisu, N, Swift, A J, Southam, L, Marten, J, Huyghe, J R, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K E, Bork-Jensen, J, Harris, S E, Liewald, D C M, Marioni, R, Polasek, O, Rudan, I, Deary, I J, Starr, J M, Morris, A D & Porteous, D J & Hayward, C 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics . https://doi.org/10.1038/ng.3654
Nature Genetics, 48(10), 1151-1161
Nature Genetics, 48(10), 1151. Nature Publishing Group
NATURE GENETICS
Nature genetics
CHARGE-Heart Failure Consortium, EchoGen Consortium, METASTROKE Consortium, GIANT Consortium, EPIC-InterAct Consortium, Lifelines Cohort Study, Wellcome Trust Case Control Consortium, Understanding Society Scientific Group, Generation Scotland, EPIC-CVD Consortium, CHARGE+ Exome Chip Blood Pressure Consortium, T2D-GENES Consortium, GoT2DGenes Consortium, ExomeBP Consortium & CHD Exome+ Consortium 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics, vol. 48, no. 10, pp. 1151-1161 . https://doi.org/10.1038/ng.3654
Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J P, Manning, A K, Grarup, N, Sim, X, Barnes, D R, Witkowska, K, Staley, J R, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D F, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A T, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L L, Jackson, A U, Narisu, N, Swift, A J, Southam, L, Marten, J, Huyghe, J R, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K E, Bork-Jensen, J, Gjesing, A P, Kontto, J, Perola, M, Shaw-Hawkins, S, Havulinna, A S, Zhang, H, Donnelly, L A, Groves, C J, Rayner, N W, Neville, M J, Robertson, N R, Yiorkas, A M, Herzig, K H, Kajantie, E, Zhang, W, Willems, S M, Lannfelt, L, Malerba, G, Soranzo, N, Trabetti, E, Verweij, N, Evangelou, E, Moayyeri, A, Vergnaud, A C, Nelson, C P, Poveda, A, Varga, T V, Caslake, M, De Craen, A J M, Trompet, S, Luan, JA, Scott, R A, Harris, S E, Liewald, D C M, Marioni, R, Menni, C, Farmaki, A E, Hallmans, G, Renström, F, Huffman, J E, Hassinen, M, Burgess, S, Vasan, R S, Felix, J F, Uria-Nickelsen, M, Malarstig, A, Reilly, D F, Hoek, M, Vogt, T F, Lin, H, Lieb, W, Traylor, M, Markus, H S, Highland, H M, Justice, A E, Marouli, E, Lindström, J, Uusitupa, M, Komulainen, P, Lakka, T A, Rauramaa, R, Polasek, O, Rudan, I, Rolandsson, O, Franks, P W, Dedoussis, G, Spector, T D, Jousilahti, P, Männistö, S, Deary, I J, Starr, J M, Langenberg, C, Wareham, N J, Brown, M J, Dominiczak, A F, Connell, J M, Jukema, J W, Sattar, N, Ford, I, Packard, C J, Esko, T, Mägi, R, Metspalu, A, De Boer, R A, Van Der Meer, P, Van Der Harst, P, Gambaro, G, Ingelsson, E, Lind, L, De Bakker, P I W, Numans, M E, Brandslund, I, Christensen, C, Petersen, E R B, Korpi-Hyövälti, E, Oksa, H, Chambers, J C, Kooner, J S, Blakemore, A I F, Franks, S, Jarvelin, M R, Husemoen, L L, Linneberg, A, Skaaby, T, Thuesen, B, Karpe, F, Tuomilehto, J, Doney, A S F, Morris, A D, Palmer, C N A, Holmen, O L, Hveem, K, Willer, C J, Tuomi, T, Groop, L, Käräjämäki, A, Palotie, A, Ripatti, S, Salomaa, V, Alam, D S, Majumder, A A S, Di Angelantonio, E, Chowdhury, R, McCarthy, M I, Poulter, N, Stanton, A V, Sever, P, Amouyel, P, Arveiler, D, Blankenberg, S, Ferrières, J, Kee, F, Kuulasmaa, K, Müller-Nurasyid, M, Veronesi, G, Virtamo, J, Deloukas, P, Elliott, P, Zeggini, E, Kathiresan, S, Melander, O, Kuusisto, J, Laakso, M, Padmanabhan, S, Porteous, D J, Hayward, C, Scotland, G, Collins, F S, Mohlke, K L, Hansen, T, Pedersen, O, Boehnke, M, Stringham, H M, Frossard, P, Newton-Cheh, C, Tobin, M D, Nordestgaard, B G, Caulfield, M J, Mahajan, A, Morris, A P, Tomaszewski, M, Samani, N J, Saleheen, D, Asselbergs, F W, Lindgren, C M, Danesh, J, Wain, L V, Butterworth, A S, Howson, J M M & Munroe, P B 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics, vol. 48, no. 10, pp. 1151-1161 . https://doi.org/10.1038/ng.3654
Nature Genetics
Surendran, P, Drenos, F, Young, R, Warren, H, Cook, J P, Manning, A K, Grarup, N, Sim, X, Barnes, D R, Witkowska, K, Staley, J R, Tragante, V, Tukiainen, T, Yaghootkar, H, Masca, N, Freitag, D F, Ferreira, T, Giannakopoulou, O, Tinker, A, Harakalova, M, Mihailov, E, Liu, C, Kraja, A T, Nielsen, S F, Rasheed, A, Samuel, M, Zhao, W, Bonnycastle, L L, Jackson, A U, Narisu, N, Swift, A J, Southam, L, Marten, J, Huyghe, J R, Stančáková, A, Fava, C, Ohlsson, T, Matchan, A, Stirrups, K E, Bork-Jensen, J, Harris, S E, Liewald, D C M, Marioni, R, Polasek, O, Rudan, I, Deary, I J, Starr, J M, Morris, A D & Porteous, D J & Hayward, C 2016, ' Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension ', Nature Genetics . https://doi.org/10.1038/ng.3654
High blood pressure is a major risk factor for cardiovascular disease and premature death. However, there is limited knowledge on specific causal genes and pathways. To better understand the genetics of blood pressure, we genotyped 242,296 rare, low-