Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Sara Hӓgg"'
Autor:
Momoko Horikoshi, Reedik Mӓgi, Martijn van de Bunt, Ida Surakka, Antti-Pekka Sarin, Anubha Mahajan, Letizia Marullo, Gudmar Thorleifsson, Sara Hӓgg, Jouke-Jan Hottenga, Claes Ladenvall, Janina S Ried, Thomas W Winkler, Sara M Willems, Natalia Pervjakova, Tõnu Esko, Marian Beekman, Christopher P Nelson, Christina Willenborg, Steven Wiltshire, Teresa Ferreira, Juan Fernandez, Kyle J Gaulton, Valgerdur Steinthorsdottir, Anders Hamsten, Patrik K E Magnusson, Gonneke Willemsen, Yuri Milaneschi, Neil R Robertson, Christopher J Groves, Amanda J Bennett, Terho Lehtimӓki, Jorma S Viikari, Johan Rung, Valeriya Lyssenko, Markus Perola, Iris M Heid, Christian Herder, Harald Grallert, Martina Müller-Nurasyid, Michael Roden, Elina Hypponen, Aaron Isaacs, Elisabeth M van Leeuwen, Lennart C Karssen, Evelin Mihailov, Jeanine J Houwing-Duistermaat, Anton J M de Craen, Joris Deelen, Aki S Havulinna, Matthew Blades, Christian Hengstenberg, Jeanette Erdmann, Heribert Schunkert, Jaakko Kaprio, Martin D Tobin, Nilesh J Samani, Lars Lind, Veikko Salomaa, Cecilia M Lindgren, P Eline Slagboom, Andres Metspalu, Cornelia M van Duijn, Johan G Eriksson, Annette Peters, Christian Gieger, Antti Jula, Leif Groop, Olli T Raitakari, Chris Power, Brenda W J H Penninx, Eco de Geus, Johannes H Smit, Dorret I Boomsma, Nancy L Pedersen, Erik Ingelsson, Unnur Thorsteinsdottir, Kari Stefansson, Samuli Ripatti, Inga Prokopenko, Mark I McCarthy, Andrew P Morris, ENGAGE Consortium
Publikováno v:
PLoS Genetics, Vol 11, Iss 7, p e1005230 (2015)
Reference panels from the 1000 Genomes (1000G) Project Consortium provide near complete coverage of common and low-frequency genetic variation with minor allele frequency ≥0.5% across European ancestry populations. Within the European Network for G
Externí odkaz:
https://doaj.org/article/4951b009b4df434e8a71bfb9ab373a22
Autor:
Letizia Marullo, Jouke-Jan Hottenga, Kari Stefansson, Antti Jula, Johan Rung, Kyle J. Gaulton, Claes Ladenvall, Marian Beekman, Jeanine J. Houwing-Duistermaat, Anton J. M. de Craen, Nancy L. Pedersen, Teresa Ferreira, Jeanette Erdmann, Terho Lehtimӓki, Valgerdur Steinthorsdottir, Antti-Pekka Sarin, Christopher J. Groves, Anders Hamsten, Cecilia M. Lindgren, Veikko Salomaa, Unnur Thorsteinsdottir, Lennart C. Karssen, Valeriya Lyssenko, Cornelia M. van Duijn, Samuli Ripatti, Patrik K. E. Magnusson, Anubha Mahajan, Evelin Mihailov, Eco J. C. de Geus, P. Eline Slagboom, Martijn van de Bunt, Tõnu Esko, Andrew P. Morris, Aaron Isaacs, Sara Hӓgg, Jaakko Kaprio, Aki S. Havulinna, S Wiltshire, Sara M. Willems, Neil R. Robertson, Juan Fernandez, Momoko Horikoshi, Heribert Schunkert, Lars Lind, Erik Ingelsson, Yuri Milaneschi, Dorret I. Boomsma, Harald Grallert, Martina Müller-Nurasyid, Janina S. Ried, Gudmar Thorleifsson, Ida Surakka, Leif Groop, Joris Deelen, Martin D. Tobin, Jorma Viikari, Christian Gieger, Christian Herder, Natalia Pervjakova, Amanda J. Bennett, Matthew Blades, Annette Peters, Johannes H. Smit, Gonneke Willemsen, Markus Perola, Christina Willenborg, Thomas W. Winkler, Reedik Mӓgi, Iris M. Heid, Brenda W.J.H. Penninx, Michael Roden, Chris Power, Inga Prokopenko, Christopher P. Nelson, Elisabeth M. van Leeuwen, Mark I. McCarthy, Nilesh J. Samani, Johan G. Eriksson, Andres Metspalu, Olli T. Raitakari, Elina Hyppönen, Christian Hengstenberg
Publikováno v:
PLoS genetics, vol 11, iss 7
PLoS Genet. 11:e1005230 (2015)
PLoS Genetics, 11(7):e1005230. Public Library of Science
Plos Genetics, 11(7):e1005230. Public Library of Science
PLoS Genetics, Vol 11, Iss 7, p e1005230 (2015)
PLoS Genetics, 11(7)
PLoS Genetics (print), 11(7). Public Library of Science
PLoS Genetics, 11(7):e1005230
Horikoshi, M, Mägi, R, van de Bunt, M, Surakka, I, Sarin, A-P, Mahajan, A, Marullo, L, Thorleifsson, G, Hägg, S, Hottenga, J J, Ladenvall, C, Ried, J S, Winkler, T W, Willems, S M, Pervjakova, N, Esko, T, Beekman, M, Nelson, C P, Willenborg, C, Wiltshire, S, Ferreira, T, Fernandez, J, Gaulton, K J, Steinthorsdottir, V, Hamsten, A, Magnusson, P K E, Willemsen, G, Milaneschi, Y, Robertson, N R, Groves, C J, Bennett, A J, Lehtimäki, T, Viikari, J S, Rung, J, Lyssenko, V, Perola, M, Heid, I M, Herder, C, Grallert, H, Müller-Nurasyid, M, Roden, M, Hypponen, E, Isaacs, A, van Leeuwen, E M, Karssen, L C, Mihailov, E, Houwing-Duistermaat, J J, de Craen, A J, Deelen, J, Havulinna, A S, Blades, M, Hengstenberg, C, Erdmann, J, Schunkert, H, Kaprio, J, Tobin, M D, Samani, N J, Lind, L, Salomaa, V, Lindgren, C M, Slagboom, P E, Metspalu, A, van Duijn, C M, Eriksson, J G, Peters, A, Gieger, C, Jula, A, Groop, L, Raitakari, O T, Power, C, Penninx, B W J H, de Geus, E J C, Smit, J H, Boomsma, D I, Pedersen, N L, Ingelsson, E, Thorsteinsdottir, U, Stefansson, K, Ripatti, S, Prokopenko, I, McCarthy, M I & Morris, A P 2015, ' Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation ', PLoS Genetics, vol. 11, no. 7, e1005230 . https://doi.org/10.1371/journal.pgen.1005230
PLoS Genetics
PLoS Genetics; 11(7), no e1005230 (2015)
PLoS Genet
PLoS Genet. 11:e1005230 (2015)
PLoS Genetics, 11(7):e1005230. Public Library of Science
Plos Genetics, 11(7):e1005230. Public Library of Science
PLoS Genetics, Vol 11, Iss 7, p e1005230 (2015)
PLoS Genetics, 11(7)
PLoS Genetics (print), 11(7). Public Library of Science
PLoS Genetics, 11(7):e1005230
Horikoshi, M, Mägi, R, van de Bunt, M, Surakka, I, Sarin, A-P, Mahajan, A, Marullo, L, Thorleifsson, G, Hägg, S, Hottenga, J J, Ladenvall, C, Ried, J S, Winkler, T W, Willems, S M, Pervjakova, N, Esko, T, Beekman, M, Nelson, C P, Willenborg, C, Wiltshire, S, Ferreira, T, Fernandez, J, Gaulton, K J, Steinthorsdottir, V, Hamsten, A, Magnusson, P K E, Willemsen, G, Milaneschi, Y, Robertson, N R, Groves, C J, Bennett, A J, Lehtimäki, T, Viikari, J S, Rung, J, Lyssenko, V, Perola, M, Heid, I M, Herder, C, Grallert, H, Müller-Nurasyid, M, Roden, M, Hypponen, E, Isaacs, A, van Leeuwen, E M, Karssen, L C, Mihailov, E, Houwing-Duistermaat, J J, de Craen, A J, Deelen, J, Havulinna, A S, Blades, M, Hengstenberg, C, Erdmann, J, Schunkert, H, Kaprio, J, Tobin, M D, Samani, N J, Lind, L, Salomaa, V, Lindgren, C M, Slagboom, P E, Metspalu, A, van Duijn, C M, Eriksson, J G, Peters, A, Gieger, C, Jula, A, Groop, L, Raitakari, O T, Power, C, Penninx, B W J H, de Geus, E J C, Smit, J H, Boomsma, D I, Pedersen, N L, Ingelsson, E, Thorsteinsdottir, U, Stefansson, K, Ripatti, S, Prokopenko, I, McCarthy, M I & Morris, A P 2015, ' Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation ', PLoS Genetics, vol. 11, no. 7, e1005230 . https://doi.org/10.1371/journal.pgen.1005230
PLoS Genetics
PLoS Genetics; 11(7), no e1005230 (2015)
PLoS Genet
Reference panels from the 1000 Genomes (1000G) Project Consortium provide near complete coverage of common and low-frequency genetic variation with minor allele frequency ≥0.5% across European ancestry populations. Within the European Network for G