Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Margus Putku"'
Autor:
Siim Sõber, Elin Org, Katrin Kepp, Peeter Juhanson, Susana Eyheramendy, Christian Gieger, Peter Lichtner, Norman Klopp, Gudrun Veldre, Margus Viigimaa, Angela Döring, Kooperative Gesundheitsforschung in der Region Augsburg Study, Margus Putku, Piret Kelgo, HYPertension in ESTonia Study, Sue Shaw-Hawkins, Philip Howard, Abiodun Onipinla, Richard J Dobson, Stephen J Newhouse, Morris Brown, Anna Dominiczak, John Connell, Nilesh Samani, Martin Farrall, MRC British Genetics of Hypertension Study, Mark J Caulfield, Patricia B Munroe, Thomas Illig, H-Erich Wichmann, Thomas Meitinger, Maris Laan
Publikováno v:
PLoS ONE, Vol 4, Iss 6, p e6034 (2009)
The outcome of Genome-Wide Association Studies (GWAS) has challenged the field of blood pressure (BP) genetics as previous candidate genes have not been among the top loci in these scans. We used Affymetrix 500K genotyping data of KORA S3 cohort (n =
Externí odkaz:
https://doaj.org/article/ef94bebe2af8403fadc7eb137e315483
Autor:
Katrin Kepp, Pille Hallast, Neeme Tõnisson, Maris Laan, Patricia B. Munroe, Gudrun Veldre, Elza Khusnutdinova, Margus Putku, Peeter Juhanson, David Comas, Margus Viigimaa, Elin Org, Mark J. Caulfield, Siim Sõber, Viktor Kožich, Sue Shaw-Hawkins
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Human Mutation
Human Mutation, Wiley, 2011, 32 (7), pp.806. ⟨10.1002/humu.21508⟩
instname
Human Mutation
Human Mutation, Wiley, 2011, 32 (7), pp.806. ⟨10.1002/humu.21508⟩
9 páginas, 2 figuras, 3 tablas.-- Grupos de trabajo: HYPEST, BRIGHT.-- Putku, Margus et al.
Mutations in WNK1 and WNK4 cause familial hypertension, the Gordon syndrome. WNK1 and WNK4 conserved noncoding regions were targeted to polymorphism scr
Mutations in WNK1 and WNK4 cause familial hypertension, the Gordon syndrome. WNK1 and WNK4 conserved noncoding regions were targeted to polymorphism scr
Autor:
Jacqueline C.M. Witteman, Nicole Probst-Hensch, Gail Davies, Anna Köttgen, Qunyuan Zhang, Pio D'Adamo, Nicholas G. Martin, Silvia Tore, Stephan J. L. Bakker, Gian Andri Thun, Cinzia Sala, Peter P. Pramstaller, Tamara B. Harris, Aaron Isaacs, Sheila Ulivi, Rossella Sorice, Xuan Liu, Andrew A. Hicks, Henry Völzke, Daniela Ruggiero, Arnold von Eckardstein, Yukinori Okada, Andres Metspalu, Jeffrey Metter, Serena Sanna, Jennifer E. Huffman, Philipp S. Wild, Florian Ernst, Eva Albrecht, Mary F. Feitosa, Claudia Schurmann, Kathrin Budde, Veikko Salomaa, Darina Czamara, Elizabeth G. Holliday, Marcel Bruinenberg, Laura Portas, Maris Laan, Alan J. Gow, Caroline Hayward, Tim D. Spector, Ozren Polasek, Ilja M. Nolte, Rodney J. Scott, Massimo Mangino, David S. Siscovick, Nilesh J. Samani, Toomas Haller, Laura Frogheri, A. Jula, Mika Kähönen, Bruce H. R. Wolffenbuttel, Caroline S. Fox, David R. Jacobs, Julia Shi, Yusuke Nakamura, Daniel I. Chasman, Fabian J. Theis, Alan F. Wright, Ayse Demirkan, Francesco Cucca, Paolo Gasparini, Paul M. Ridker, Olli T. Raitakari, Daniela Toniolo, Maristella Steri, Mario Pirastu, Susan Campbell, Maksim Struchalin, So-Youn Shin, Mark J. Caulfield, H.-Erich Wichmann, Grant W. Montgomery, Åsa Johansson, Alexander Teumer, Ulf Gyllensten, Robert M. Plenge, Michel Burnier, Michael Schallert, Jan Krumsiek, Jing Hua Zhao, Andres Salumets, Poorva Mudgal, Anke Tönjes, James F. Meschia, Gauti Kjartan Gislason, Perttu Salo, Angela Döring, Afshin Parsa, Vilmundur Gudnason, Patrick F. McArdle, Rita P. S. Middelberg, W. H. Linda Kao, Aldi Kraja, Christopher Oldmeadow, Adrienne Tin, Loic Yengo, Murielle Bochud, Gerjan Navis, Christian Gieger, Toshiko Tanaka, Cornelia M. van Duijn, Samuli Ripatti, Terho Lehtimäki, Claudia Langenberg, Bernhard O. Boehm, Conall M. O'Seaghdha, Eric Boerwinkle, Nicole Soranzo, Tõnu Esko, Susan M. Farrington, Mike A. Nalls, John F. Peden, Hyon K. Choi, Anuj Goel, Andrew D. Johnson, Norman Klopp, Anne Grotevendt, Halit Ongen, Marcus E. Kleber, Myriam Fornage, Malcolm G. Dunlop, Igor Rudan, Federico Murgia, Beverley Balkau, Jorma Viikari, Christopher P. Nelson, Gérard Waeber, Lenore J. Launer, Ivana Persico, Inga Prokopenko, Guo Li, Tatijana Zemunik, Elisabetta Trabetti, Tanja Zeller, Hugh Watkins, Qiong Yang, James F. Wilson, Peter Vollenweider, Veronique Vitart, Markus Perola, Nicola Pirastu, Olivier Devuyst, Irene Mateo Leach, John Attia, Bruce M. Psaty, Nicholas J. Wareham, Susanne Lucae, Josef Coresh, Ingrid B. Borecki, Claudia Hundertmark, Weihua Zhang, Luigi Ferrucci, Jaspal S. Kooner, Stefan Kloiber, Lynda M. Rose, Naoyuki Kamatani, Zoltán Kutalik, Giovanni Malerba, Ian J. Deary, Albert V. Smith, Helena Schmidt, Eva Lattka, Philippe Froguel, Harry Campbell, Medea Imboden, Antonio Lupo, Angelo L. Gaffo, Vasiliki Lagou, Alan R. Shuldiner, John Whitfield, Abbas Dehghan, Winfried März, Elin Org, Albert Hofman, Margus Viigimaa, Konstantin Strauch, Toshihiro Tanaka, Andrew B. Singleton, Stefania Bandinelli, Christian Hengstenberg, Xinzhong Li, Wiek H. van Gilst, Pim van der Harst, Giorgio Pistis, Jerome I. Rotter, Maria Grazia Piras, Gary C. Curhan, Brenda W.J.H. Penninx, Ramaiah Nagaraja, Nabila Bouatia-Naji, Christian Müller, Ronald P. Stolk, Pau Navarro, Lorna M. Lopez, Ruth J. F. Loos, Albert Tenesa, Johannes H. Smit, Peter Kraft, Giovanni Gambaro, Sarah H. Wild, Patricia B. Munroe, André G. Uitterlinden, Ivana Kolcic, Bernhard R. Winkelmann, Pankaj Sharma, John C. Chambers, Nicholas D. Hastie, Matthias Nauck, Harold Snieder, Michael Stumvoll, Reinhold Schmidt, Hans L. Hillege, Kiang Liu, Fernando Rivadeneira, Owen M. Woodward, Morris J. Brown, Margus Putku, Sabine Schipf, Mirna Kirin, Kay-Tee Khaw, Melanie Waldenberger, Evropi Theodoratou, Marina Ciullo, Michiaki Kubo
Publikováno v:
Nature Genetics, 45(2), 145-154. Nature Publishing Group
Nature Genetics
Nature Genetics, 45(2), 145-54. Nature Publishing Group
Kottgen, A, Albrecht, E, Teumer, A, Vitart, V, Krumsiek, J, Hundertmark, C, Pistis, G, Ruggiero, D, O'Seaghdha, C M, Haller, T, Yang, Q, Johnson, A D, Kutalik, Z, Smith, A V, Shi, J L, Struchalin, M, Middelberg, R P S, Brown, M J, Gaffo, A L, Pirastu, N, Li, G, Hayward, C, Zemunik, T, Huffman, J, Yengo, L, Zhao, J H, Demirkan, A, Feitosa, M F, Liu, X, Malerba, G, Lopez, L M, van der Harst, P, Li, X Z, Kleber, M E, Hicks, A A, Nolte, I M, Johansson, A, Murgia, F, Wild, S H, Bakker, S J L, Peden, J F, Dehghan, A, Steri, M, Tenesa, A, Lagou, V, Salo, P, Mangino, M, Rose, L M, Lehtimaki, T, Woodward, O M, Okada, Y, Tin, A, Muller, C, Oldmeadow, C, Putku, M, Czamara, D, Kraft, P, Frogheri, L, Thun, G A, Grotevendt, A, Gislason, G K, Harris, T B, Launer, L J, McArdle, P, Shuldiner, A R, Boerwinkle, E, Coresh, J, Schmidt, H, Schallert, M, Martin, N G, Montgomery, G W, Kubo, M, Nakamura, Y, Tanaka, T, Munroe, P B, Samani, N J, Jacobs, D R, Liu, K, d'Adamo, P, Ulivi, S, Rotter, J I, Psaty, B M, Vollenweider, P, Waeber, G, Campbell, S, Devuyst, O, Navarro, P, Kolcic, I, Hastie, N, Balkau, B, Froguel, P, Esko, T, Salumets, A, Khaw, K T, Langenberg, C, Wareham, N J, Isaacs, A, Kraja, A, Zhang, Q Y, Penninx, B W J H, Smit, J H, Bochud, M & Gieger, C 2013, ' Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ', Nature Genetics, vol. 45, no. 2, pp. 145-154 . https://doi.org/10.1038/ng.2500
Köttgen, A, Albrecht, E, Teumer, A, Vitart, V, Krumsiek, J, Hundertmark, C, Pistis, G, Ruggiero, D, O'Seaghdha, C M, Haller, T, Yang, Q, Tanaka, T, Johnson, A D, Kutalik, Z, Smith, A V, Shi, J, Struchalin, M, Middelberg, R P S, Brown, M J, Gaffo, A L, Pirastu, N, Li, G, Hayward, C, Zemunik, T, Huffman, J, Yengo, L, Zhao, J H, Demirkan, A, Feitosa, M F, Liu, X, Malerba, G, Lopez, L M, van der Harst, P, Li, X, Kleber, M E, Wild, S H, Tenesa, A, Navarro, P, Hastie, N, Davies, G, Gow, A J, Wilson, J F, Farrington, S M, Theodoratou, E, Polasek, O, Campbell, H, Rudan, I, Deary, I J & Wright, A F & Dunlop, M G 2013, ' Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ', Nature Genetics, vol. 45, no. 2, pp. 145-154 . https://doi.org/10.1038/ng.2500
Nature genetics
(2013). doi:10.1038/ng.2500
info:cnr-pdr/source/autori:Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T, Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM, Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A, Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtimäki T, Woodward OM, Okada Y, Tin A, Müller C, Oldmeadow C, Putku M, Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK, Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M, Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR Jr, Liu K, D'Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G, Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B, Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ, Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E, Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R, Döring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann HE, Davies G, Gow AJ, Bruinenberg M; LifeLines Cohort Study, Stolk RP, Kooner JS, Zhang W, Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G, Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Mateo Leach I, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F, Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R, Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM, Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa V, Shin SY, Spector TD, Sala C, Ridker PM, Kähönen M, Viikari J, Hengstenberg C, Nelson CP; CARDIoGRAM Consortium; DIAGRAM Consortium; ICBP Consortium; MAGIC Consortium, Meschia JF, Nalls MA, Sharma P, Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M, Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S, Probst-Hensch NM, Völzke H, Gudnason V, Parsa A, Schmidt R, Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Pola?ek O, Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH, Chambers JC, März W, Pramstaller PP, Snieder H, Gyllensten U, Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S, Dunlop MG, Tönjes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI, Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M, Gieger C./titolo:Genome-wide association analyses identify 18 new loci associated with serum urate concentrations/doi:10.1038%2Fng.2500/rivista:Nature genetics (Print)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
Nature Genetics; Vol 45
Nature Genetics, vol. 45, no. 2, pp. 145-154
Human Genetics, 45(2):145, 154-11. Springer-Verlag
Nature Genetics
Nature Genetics, 45(2), 145-54. Nature Publishing Group
Kottgen, A, Albrecht, E, Teumer, A, Vitart, V, Krumsiek, J, Hundertmark, C, Pistis, G, Ruggiero, D, O'Seaghdha, C M, Haller, T, Yang, Q, Johnson, A D, Kutalik, Z, Smith, A V, Shi, J L, Struchalin, M, Middelberg, R P S, Brown, M J, Gaffo, A L, Pirastu, N, Li, G, Hayward, C, Zemunik, T, Huffman, J, Yengo, L, Zhao, J H, Demirkan, A, Feitosa, M F, Liu, X, Malerba, G, Lopez, L M, van der Harst, P, Li, X Z, Kleber, M E, Hicks, A A, Nolte, I M, Johansson, A, Murgia, F, Wild, S H, Bakker, S J L, Peden, J F, Dehghan, A, Steri, M, Tenesa, A, Lagou, V, Salo, P, Mangino, M, Rose, L M, Lehtimaki, T, Woodward, O M, Okada, Y, Tin, A, Muller, C, Oldmeadow, C, Putku, M, Czamara, D, Kraft, P, Frogheri, L, Thun, G A, Grotevendt, A, Gislason, G K, Harris, T B, Launer, L J, McArdle, P, Shuldiner, A R, Boerwinkle, E, Coresh, J, Schmidt, H, Schallert, M, Martin, N G, Montgomery, G W, Kubo, M, Nakamura, Y, Tanaka, T, Munroe, P B, Samani, N J, Jacobs, D R, Liu, K, d'Adamo, P, Ulivi, S, Rotter, J I, Psaty, B M, Vollenweider, P, Waeber, G, Campbell, S, Devuyst, O, Navarro, P, Kolcic, I, Hastie, N, Balkau, B, Froguel, P, Esko, T, Salumets, A, Khaw, K T, Langenberg, C, Wareham, N J, Isaacs, A, Kraja, A, Zhang, Q Y, Penninx, B W J H, Smit, J H, Bochud, M & Gieger, C 2013, ' Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ', Nature Genetics, vol. 45, no. 2, pp. 145-154 . https://doi.org/10.1038/ng.2500
Köttgen, A, Albrecht, E, Teumer, A, Vitart, V, Krumsiek, J, Hundertmark, C, Pistis, G, Ruggiero, D, O'Seaghdha, C M, Haller, T, Yang, Q, Tanaka, T, Johnson, A D, Kutalik, Z, Smith, A V, Shi, J, Struchalin, M, Middelberg, R P S, Brown, M J, Gaffo, A L, Pirastu, N, Li, G, Hayward, C, Zemunik, T, Huffman, J, Yengo, L, Zhao, J H, Demirkan, A, Feitosa, M F, Liu, X, Malerba, G, Lopez, L M, van der Harst, P, Li, X, Kleber, M E, Wild, S H, Tenesa, A, Navarro, P, Hastie, N, Davies, G, Gow, A J, Wilson, J F, Farrington, S M, Theodoratou, E, Polasek, O, Campbell, H, Rudan, I, Deary, I J & Wright, A F & Dunlop, M G 2013, ' Genome-wide association analyses identify 18 new loci associated with serum urate concentrations ', Nature Genetics, vol. 45, no. 2, pp. 145-154 . https://doi.org/10.1038/ng.2500
Nature genetics
(2013). doi:10.1038/ng.2500
info:cnr-pdr/source/autori:Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T, Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM, Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A, Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtimäki T, Woodward OM, Okada Y, Tin A, Müller C, Oldmeadow C, Putku M, Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK, Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M, Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR Jr, Liu K, D'Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G, Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B, Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ, Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E, Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R, Döring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann HE, Davies G, Gow AJ, Bruinenberg M; LifeLines Cohort Study, Stolk RP, Kooner JS, Zhang W, Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G, Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Mateo Leach I, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F, Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R, Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM, Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa V, Shin SY, Spector TD, Sala C, Ridker PM, Kähönen M, Viikari J, Hengstenberg C, Nelson CP; CARDIoGRAM Consortium; DIAGRAM Consortium; ICBP Consortium; MAGIC Consortium, Meschia JF, Nalls MA, Sharma P, Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M, Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S, Probst-Hensch NM, Völzke H, Gudnason V, Parsa A, Schmidt R, Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Pola?ek O, Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH, Chambers JC, März W, Pramstaller PP, Snieder H, Gyllensten U, Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S, Dunlop MG, Tönjes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI, Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M, Gieger C./titolo:Genome-wide association analyses identify 18 new loci associated with serum urate concentrations/doi:10.1038%2Fng.2500/rivista:Nature genetics (Print)/anno:2013/pagina_da:/pagina_a:/intervallo_pagine:/volume
Nature Genetics; Vol 45
Nature Genetics, vol. 45, no. 2, pp. 145-154
Human Genetics, 45(2):145, 154-11. Springer-Verlag
Elevated serum urate concentrations can cause gout, a prevalent and painful inflammatory arthritis. By combining data from >140,000 individuals of European ancestry within the Global Urate Genetics Consortium (GUGC), we identified and replicated 28 g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc47fb35390519f51b5ff7c2f271262b
https://www.bib.irb.hr/639277
https://www.bib.irb.hr/639277
Autor:
Meena Kumari, Claire E. Hastie, Jonathan Stephens, Patricia B. Munroe, Christopher P. Nelson, John M. C. Connell, Martin D. Tobin, Hani Neuvrith, Jean Tichet, Paul Burton, Gudrun Veldre, Daniele Cusi, Anna Levinsson, Paul Elliott, Elin Org, Erika Salvi, Tina Shah, Nabila Devos, Harm-Jan Westra, Juan-Pablo Casas, Olle Melander, Jan A. Staessen, Nilesh J. Samani, Jackie A. Cooper, Peter S. Braund, Neil R Poulter, Alive V. Stanton, Abiodun Onipinla, Marcel G. M. Wolfs, Steve E. Humphries, Philippa J. Talmud, Rebecca Hardy, Fotios Drenos, Maris Laan, Mark J. Caulfield, Richard Dobson, Willem H. Ouwehand, Yun Zhang, Li Chen, SG Wannamethee, Sue Shaw-Hawkins, Christopher Newton-Cheh, Eoin O'Brien, Simon A. McG. Thom, Maria Grazia Franzosi, Charles A. Mein, Mika Kivimäki, Tom R. Gaunt, Jennifer G. Sambrook, Andrea Stucchi, Annika Rosengren, Sonia Shah, Thomas Hedner, George A. Wells, Dag S. Thelle, Debbie A Lawlor, Pierre-François Plouin, Fredrik Nyberg, Richard W Morris, Ian N M Day, Vesela Gateva, Lude Franke, Peter S. Sever, Morris J. Brown, Margus Putku, Sandosh Padmanabhan, John F. Peden, Pim van der Harst, Jutta Palmen, Ioanna Tzoulaki, Alexandre F.R. Stewart, Andrew Wong, Peeter Juhanson, Marciej Tomaszewski, Alison H. Goodall, Martin Farrall, Wai K. Lee, Nicola Glorioso, Hugh Watkins, Xavier Jeunemaitre, Anders Hamsten, Robert Clarke, Anna F. Dominiczak, Mark Lathrop, Stephen Newhouse, Margus Viigimaa, George Davey Smith, Robert Roberts, John C. Whittaker, Michael V. Holmes, Toby Johnson, F. Gerald R. Fowkes, Aroon D. Hingorani, Udo Seedorf, Siim Sõber, Denis C. Shields, Diana Kuh, Chris Wallace, Philip Howard, Peter H. Whincup, Gonçalo R. Abecasis, Anuj Goel, Christian Delles, Björn Wahlstrand
Publikováno v:
American Journal of Human Genetics, 89(6), 688-700. CELL PRESS
American journal of human genetics, vol. 89, no. 6, pp. 688-700
The American Journal of Human Genetics; Vol 89
Johnson, T, Gaunt, T R, Newhouse, S J, Padmanabhan, S, Tomaszewski, M, Kumari, M, Morris, R W, Tzoulaki, I, O'Brien, E T, Poulter, N R, Sever, P, Shields, D C, Thom, S, Wannamethee, S G, Whincup, P H, Brown, M J, Connell, J M, Dobson, R J, Howard, P J, Mein, C A, Onipinla, A, Shaw-Hawkins, S, Zhang, Y, Smith, G D, Day, I N M, Lawlor, D A, Goodall, A H, Fowkes, F G, Abecasis, G R, Elliott, P, Gateva, V, Braund, P S, Burton, P R, Nelson, C P, Tobin, M D, van der Harst, P, Glorioso, N, Neuvrith, H, Salvi, E, Staessen, J A, Stucchi, A, Devos, N, Jeunemaitre, X, Plouin, P-F, Tichet, J, Juhanson, P, Org, E, Putku, M, Sober, S, Veldre, G 2011, ' Blood Pressure Loci Identified with a Gene-Centric Array ', American Journal of Human Genetics, vol. 89, no. 6, pp. 688-700 . https://doi.org/10.1016/j.ajhg.2011.10.013
American journal of human genetics, vol. 89, no. 6, pp. 688-700
The American Journal of Human Genetics; Vol 89
Johnson, T, Gaunt, T R, Newhouse, S J, Padmanabhan, S, Tomaszewski, M, Kumari, M, Morris, R W, Tzoulaki, I, O'Brien, E T, Poulter, N R, Sever, P, Shields, D C, Thom, S, Wannamethee, S G, Whincup, P H, Brown, M J, Connell, J M, Dobson, R J, Howard, P J, Mein, C A, Onipinla, A, Shaw-Hawkins, S, Zhang, Y, Smith, G D, Day, I N M, Lawlor, D A, Goodall, A H, Fowkes, F G, Abecasis, G R, Elliott, P, Gateva, V, Braund, P S, Burton, P R, Nelson, C P, Tobin, M D, van der Harst, P, Glorioso, N, Neuvrith, H, Salvi, E, Staessen, J A, Stucchi, A, Devos, N, Jeunemaitre, X, Plouin, P-F, Tichet, J, Juhanson, P, Org, E, Putku, M, Sober, S, Veldre, G 2011, ' Blood Pressure Loci Identified with a Gene-Centric Array ', American Journal of Human Genetics, vol. 89, no. 6, pp. 688-700 . https://doi.org/10.1016/j.ajhg.2011.10.013
Raised blood pressure (BP) is a major risk factor for cardiovascular disease. Previous studies have identified 47 distinct genetic variants robustly associated with BP, but collectively these explain only a few percent of the heritability for BP phen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a055dcda09bbb36bdfdb963307732402
https://lirias.kuleuven.be/handle/123456789/341626
https://lirias.kuleuven.be/handle/123456789/341626
Autor:
Kärt Tomberg, Maris Laan, Elin Org, Mai Rosenberg, Margus Putku, Tiina Uuetoa, Gudrun Veldre, Peeter Juhanson, Margus Viigimaa
Publikováno v:
BMC Cardiovascular Disorders, Vol 11, Iss 1, p 55 (2011)
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders
Background More than one third of adult population in Estonia has problems with elevated blood pressure (BP). The Hypertension in Estonia (HYPEST) study represents the country's first hypertension-targeted sample collection aiming to examine the epid
Autor:
Neeme Tõnisson, Piret Kelgo, Viktor Kožich, Margus Putku, Peeter Juhanson, Andreas Kindmark, Katrin Kepp, Elin Org, Maris Laan, Siim Sõber, Gudrun Veldre, Margus Viigimaa
Publikováno v:
BMC Medical Genetics, Vol 11, Iss 1, p 15 (2010)
BMC Medical Genetics
BMC Medical Genetics
Background Conserved non-coding regions (CNR) have been shown to harbor gene expression regulatory elements. Genetic variations in these regions may potentially contribute to complex disease susceptibility. Methods We targeted CNRs of cardiovascular
Autor:
Pille Hallast, Piret Kelgo, Katrin Kepp, Siim Sõber, Gudrun Veldre, Margus Viigimaa, Elza Khusnutdinova, Margus Putku, Maris Laan, Elin Org, Peeter Juhanson, V Kozich, Neeme Tõnisson, David Comas
Publikováno v:
Journal of Hypertension. 28:e347-e348
Publikováno v:
Placenta
Introduction Given the physiological role of placental growth hormone (PGH) during intrauterine development and growth, genetic variation in the coding Growth hormone 2 ( GH2) gene may modulate developmental programming of adult stature. Two major GH
CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs
Autor:
Viktor Kožich, Maris Laan, Silva Kasela, Elin Org, Margus Putku, Mart Kals, Lili Milani, Rain Inno
Publikováno v:
Human Genetics
CDH13 encodes T-cadherin, a receptor for high molecular weight (HMW) adiponectin and low-density lipoprotein, promoting proliferation and migration of endothelial cells. Genome-wide association studies have mapped multiple variants in CDH13 associate