Zobrazeno 1 - 10
of 556
pro vyhledávání: '"LEHTIMAKI, T."'
Autor:
Zanoni, P., Khetarpal, S. A., Larach, D. B., Hancock-Cerutti, W. F., Millar, J. S., Cuchel, M., DerOhannessian, S., Kontush, A., Surendran, P., Saleheen, D., Trompet, S., Cooper, R. S., Chowdhury, R., Dedoussis, G., de Faire, U., Feranil, A. B., Sheu, W. H.- H., Ferrucci, L., Freimer, N. B., Gieger, C., Sengupta, S., Grallert, H., Groop, L. C., Gudnason, V., Tanaka, T., Gyllensten, U., Hamsten, A., Erdmann, J., Harris, T. B., Shuldiner, A. R., Hingorani, A., Hirschhorn, J. N., Gravito, M. L., Wilson, J. F., Hofman, A., Hovingh, G. K., Hsiung, C. A., Humphries, S. E., Teslovich, T. M., Hunt, S. C., Hveem, K., Iribarren, C., Siegbahn, A., Groves, C. J., Nordestgaard, B. G., Njolstad, I., Jarvelin, M.-R., Jula, A., Kahonen, M., Kaprio, J., Kesaniemi, A., Kivimaki, M., Thorleifsson, G., Kooner, J. S., Hallmans, G., Koudstaal, P. J., Kuulasmaa, K., Gustafsson, S., Krauss, R. M., Kuh, D., Nielsen, S. F., Kuusisto, J., Kyvik, K. O., Laakso, M., Lakka, T. A., Hartikainen, A.-L., Lind, L., Van den Herik, E. G., Lindgren, C. M., Kanoni, S., Spector, T. D., Martin, N. G., Marz, W., McCarthy, M. I., McKenzie, C. A., Tybjaerg-Hansen, A., Assimes, T. L., Meneton, P., Metspalu, A., Moilanen, L., Morris, A. D., Ganna, A., Voight, B. F., Stefansson, K., Munroe, P. B., van Pelt, L. J., Waite, L. L., Hayward, C., Strachan, D. P., Tayo, B. O., Tremoli, E., Tuomilehto, J., Uusitupa, M., Chen, J., van Duijn, C. M., Vollenweider, P., Wallentin, L., Liu, D. J., Hernandez, D., Vedantam, S., Wareham, N. J., Jukema, J. W., Whitfield, J. B., Wolffenbuttel, B. H. R., Ordovas, J. M., Buchkovich, M. L., Boerwinkle, E., Palmer, C. N. A., Thorsteinsdottir, U., Hicks, A. A., Chasman, D. I., Rotter, J. I., Wainwright, N., Franks, P. W., Perola, M., Wong, A., Riatti, S., Mora, S., Cupples, L. A., Sandhu, M. S., Rauramaa, R., Rich, S. S., Boehnke, M., Deloukas, P., Mohlke, K. L., Wijmenga, C., Ingelsson, E., Gu, D., Roberts, R., Beckmann, J. S., Wu, Y., Peloso, G. M., Blankenberg, S., Watkins, H., Clarke, R., Collins, R., Kim, B.-J., Wild, S. H., McPherson, R., Nieminen, M. S., Barroso, I., Holm, H., O'Donnell, C., Schreiber, S., Zhang, W., Salomaa, V., Zalloua, P. A., Mannisto, S., Amouyel, P., Willemsen, G., Arveiler, D., Hung, Y.-J., Bragg-Gresham, J. L., Ferrieres, J., Muller-Nurasyid, M., Ferrario, M., Kee, F., Absher, D., Willer, C. J., Samani, N., Schunkert, H., Butterworth, A. S., Sattar, N., Wilsgaard, T., Chang, H.-Y., Howson, J. M. M., Pedersen, N. L., Di Angelantonio, E., Demirkan, A., Den Hertog, H. M., Do, R., Donnelly, L. A., Ehret, G. B., Illig, T., Esko, T., Feitosa, M. F., Ferreira, T., Been, L. F., Power, C., Fischer, K., Song, C., Fontanillas, P., Fraser, R. M., Freitag, D. F., Jones, M. R., Gurdasani, D., Heikkila, K., Hypponen, E., Isaacs, A., Jackson, A. U., Pramstaller, P. P., Johansson, A., Bolton, J. L., Young, E. H., Johnson, T., Kaleebu, P., Kaakinen, M., Kettunen, J., Kleber, M. E., Li, X., Luan, J., Lyytikainen, L.-P., Price, J. F., Magnusson, P. K. E., Mangino, M., Mihailov, E., Kastelein, J. J. P., Zhao, J. H., Bonnycastle, L. L., Montasser, M. E., Nolte, I. M., OConnell, J. R., Palmer, C. D., Petersen, A.-K., Schmidt, R. F., Sanna, S., Saxena, R., Bandinelli, S., Service, S. K., Shah, S., Adair, L. S., Shungin, D., Brambilla, P., Sidore, C., De Craen, A., Burnett, M. S., Psaty, B. M., Cesana, G., Khaw, K.-T., Dimitriou, M., Doney, A. S. F., Doring, A., Elliott, P., Epstein, S. E., Eyjolfsson, G. I., Gigante, B., Goodarzi, M. O., Quertermous, T., Kim, E., Stitziel, N. O., Volcik, K. A., Klopp, N., Komulainen, P., Kumari, M., Langenberg, C., Ford, I., Lehtimaki, T., Lin, S.-Y., Lindstrom, J., Bennett, F., Danesh, J., Loos, R. J. F., Uitterlinden, A. G., Mach, F., McArdle, W. L., Meisinger, C., Mitchell, B. D., Muller, G., Nagaraja, R., Packard, C., Narisu, N., Kathiresan, S., Nieminen, T. V. M., Bochud, M., Nsubuga, R. N., Olafsson, I., Ong, K. K., Palotie, A., Papamarkou, T., Pomilla, C., Pouta, A., Rader, D. J., Reilly, M. P., Majumder, A. a. S., Ridker, P. M., Sanghera, D. K., Boehm, B. O., Rivadeneira, F., Rudan, I., Ruokonen, A., Scharnagl, H., Seeley, J., Asiki, G., Silander, K., Stancakova, A., Stirrups, K., Swift, A. J., Saramies, J., Alam, D. S., Boomsma, D. I., Tiret, L., Strawbridge, R. J., Abecasis, G., Watson, S., Borecki, I. B., Bornstein, S. R., Bovet, P., Burnier, M., Campbell, H., Schwarz, P. E. H., Chakravarti, A., Chambers, J. C., Chen, Y.-D. I., Collins, F. S., Schmidt, E. M., Surakka, I.
Scavenger receptor BI (SR-BI) is the major receptor for high-density lipoprotein (HDL) cholesterol (HDL-C). In humans, high amounts of HDL-C in plasma are associated with a lower risk of coronary heart disease (CHD). Mice that have depleted Scarb1 (S
Externí odkaz:
http://hdl.handle.net/10150/623258
http://arizona.openrepository.com/arizona/handle/10150/623258
http://arizona.openrepository.com/arizona/handle/10150/623258
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Jr Jacobs DR, Woo JG, Sinaiko AR, Daniels SR, Ikonen J, Juonala M, Kartiosuo N, Lehtimaki T, Magnussen CG, Viikari JSA, Zhang N, Bazzano LA, Burns TL, Prineas RJ, Steinberger J, Urbina EM, Venn AJ, Raitakari OT, Dwyer T
Publikováno v:
Yearbook of Paediatric Endocrinology.
Autor:
Schillemans, T., Tragante, V., Maitusong, B., Gigante, B., Cresci, S., Laguzzi, F., Vikstrom, M., Richards, M., Pilbrow, A., Cameron, V., Foco, L., Doughty, R.N., Kuukasjarvi, P., Allayee, H., Hartiala, J.A., Tang, W.H.W., Lyytikainen, L.P., Nikus, K., Laurikka, J.O., Srinivasan, S., Mordi, I.R., Trompet, S., Kraaijeveld, A., Setten, J. van, Gijsberts, C.M., Maitland-van der Zee, A.H., Saely, C.H., Gong, Y., Johnson, J.A., Cooper-DeHoff, R.M., Pepine, C.J., Casu, G., Leiherer, A., Drexel, H., Horne, B.D., Laan, S.W. van der, Marziliano, N., Hazen, S.L., Sinisalo, J., Kahonen, M., Lehtimaki, T., Lang, C.C., Burkhardt, R., Scholz, M., Jukema, J.W., Eriksson, N., Akerblom, A., James, S., Held, C., Hagstrom, E., Spertus, J.A., Algra, A., Faire, U. de, Akesson, A., Asselbergs, F.W., Patel, R.S., Leander, K.
Publikováno v:
Frontiers in Physiology, 13
Frontiers in Physiology, 13. FRONTIERS MEDIA SA
Frontiers in physiology, 13:909870. Frontiers Media S.A.
Frontiers in Physiology, 13. FRONTIERS MEDIA SA
Frontiers in physiology, 13:909870. Frontiers Media S.A.
Contains fulltext : 283506.pdf (Publisher’s version ) (Open Access) Background: The knowledge of factors influencing disease progression in patients with established coronary heart disease (CHD) is still relatively limited. One potential pathway is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3b41ac3f7ec707ef5e8eea7f48704a37
http://hdl.handle.net/10138/347156
http://hdl.handle.net/10138/347156
Autor:
Hautakangas, H., Winsvold, B.S., Ruotsalainen, S.E., Bjornsdottir, G., Harder, A.V.E., Kogelman, L.J.A., Thomas, L.F., Noordam, R., Benner, C., Gormley, P., Artto, V., Banasik, K., Bjornsdottir, A., Boomsma, D.I., Brumpton, B., Burgdorf, K.S., Buring, J.E., Chalmer, M.A., Boer, I. de, Dichgans, M., Erikstrup, C., Farkkila, M., Garbrielsen, M.E., Ghanbari, M., Hagen, K., Happola, P., Hottenga, J.J., Hrafnsdottir, M.G., Hveem, K., Johnsen, M.B., Kahonen, M., Kristoffersen, E.S., Kurth, T., Lehtimaki, T., Lighart, L., Magnusson, S.H., Malik, R., Pedersen, O.B., Pelzer, N., Penninx, B.W.J.H., Ran, C., Ridker, P.M., Rosendaal, F.R., Sigurdardottir, G.R., Skogholt, A.H., Sveinsson, O.A., Thorgeirsson, T.E., Ullum, H., Vijfhuizen, L.S., Widen, E., Dijk, K.W. van, Aromaa, A., Belin, A.C., Freilinger, T., Ikram, M.A., Jarvelin, M.R., Raitakari, O.T., Terwindt, G.M., Kallela, M., Wessman, M., Olesen, J., Chasman, D.I., Nyholt, D.R., Stefansson, H., Stefansson, K., Maagdenberg, A.M.J.M. van den, Hansen, T.F., Ripatti, S., Zwart, J.A., Palotie, A., Pirinen, M., Int Headache Genetics Consortium, HUNT All-in Headache, Danish Blood Donor Study Genomic C
Publikováno v:
Nature genetics, 54(2), 152-160. Nature Publishing Group
Nature Genetics
International Headache Genetics Consortium, HUNT All-in Headache & Danish Blood Donor Study Genomic Cohort 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Nature Genetics, 54, 152-160. NATURE PORTFOLIO
Hautakangas, H, Winsvold, B S, Ruotsalainen, S E, Bjornsdottir, G, Harder, A V E, Kogelman, L J A, Thomas, L F, Noordam, R, Benner, C, Gormley, P, Artto, V, Banasik, K, Bjornsdottir, A, Boomsma, D I, Brumpton, B M, Burgdorf, K S, Buring, J E, Chalmer, M A, de Boer, I, Dichgans, M, Erikstrup, C, Farkkila, M, Garbrielsen, M E, Ghanbari, M, Hagen, K, Happola, P, Hottenga, J-J, Hrafnsdottir, M G, Hveem, K, Johnsen, M B, Kahonen, M, Kristoffersen, E S, Kurth, T, Lehtimaki, T, Lighart, L, Magnusson, S H, Malik, R, Pedersen, O B, Pelzer, N, Penninx, B W J H, Ran, C, Ridker, P M, Rosendaal, F R, Sigurdardottir, G R, Skogholt, A H, Sveinsson, O A, Thorgeirsson, T E, Ullum, H, Vijfhuizen, L S, Widen, E, van Dijk, K W, Aromaa, A, Belin, A C, Freilinger, T, Ikram, M A, Jarvelin, M-R, Raitakari, O T, Terwindt, G M, Kallela, M, Wessman, M, Olesen, J, Chasman, D I, Nyholt, D R, Stefansson, H, Stefansson, K, van den Maagdenberg, A M J M, Hansen, T F, Ripatti, S, Zwart, J-A, Palotie, A & Pirinen, M 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Hautakangas, H, Winsvold, B S, Ruotsalainen, S E, Bjornsdottir, G, Harder, A V E, Kogelman, L J A, Thomas, L F, Noordam, R, Benner, C, Gormley, P, Artto, V, Banasik, K, Bjornsdottir, A, Boomsma, D I, Brumpton, B M, Burgdorf, K S, Buring, J E, Chalmer, M A, de Boer, I, Dichgans, M, Erikstrup, C, Färkkilä, M, Garbrielsen, M E, Ghanbari, M, Hagen, K, Häppölä, P, Hottenga, J J, Hrafnsdottir, M G, Hveem, K, Johnsen, M B, Kähönen, M, Kristoffersen, E S, Kurth, T, Lehtimäki, T, Lighart, L, Magnusson, S H, Malik, R, Pedersen, O B, Pelzer, N, Penninx, B W J H, Ran, C, Ridker, P M, Rosendaal, F R, Sigurdardottir, G R, Skogholt, A H, Sveinsson, O A, Thorgeirsson, T E, Ullum, H, Vijfhuizen, L S, Widen, E, van Dijk, K W, International Headache Genetics Consortium, HUNT All-in Headache, Danish Blood Donor Study Genomic Cohort, Aromaa, A, Belin, A C, Freilinger, T, Ikram, M A, Järvelin, M-R, Raitakari, O T, Terwindt, G M, Kallela, M, Wessman, M, Olesen, J, Chasman, D I, Nyholt, D R, Stefansson, H, Stefansson, K, van den Maagdenberg, A M J M, Hansen, T F, Ripatti, S, Zwart, J-A, Palotie, A & Pirinen, M 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Nature Genetics, 54(2), 152-160. Nature Publishing Group
Hautakangas, H, Winsvold, B S, Boomsma, D I, Hottenga, J-J, Ligthart, L, Penninx, B W J H, Palotie, A, Pirinen, M & International Headache Genetics Consortium 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Nature Genetics
International Headache Genetics Consortium, HUNT All-in Headache & Danish Blood Donor Study Genomic Cohort 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Nature Genetics, 54, 152-160. NATURE PORTFOLIO
Hautakangas, H, Winsvold, B S, Ruotsalainen, S E, Bjornsdottir, G, Harder, A V E, Kogelman, L J A, Thomas, L F, Noordam, R, Benner, C, Gormley, P, Artto, V, Banasik, K, Bjornsdottir, A, Boomsma, D I, Brumpton, B M, Burgdorf, K S, Buring, J E, Chalmer, M A, de Boer, I, Dichgans, M, Erikstrup, C, Farkkila, M, Garbrielsen, M E, Ghanbari, M, Hagen, K, Happola, P, Hottenga, J-J, Hrafnsdottir, M G, Hveem, K, Johnsen, M B, Kahonen, M, Kristoffersen, E S, Kurth, T, Lehtimaki, T, Lighart, L, Magnusson, S H, Malik, R, Pedersen, O B, Pelzer, N, Penninx, B W J H, Ran, C, Ridker, P M, Rosendaal, F R, Sigurdardottir, G R, Skogholt, A H, Sveinsson, O A, Thorgeirsson, T E, Ullum, H, Vijfhuizen, L S, Widen, E, van Dijk, K W, Aromaa, A, Belin, A C, Freilinger, T, Ikram, M A, Jarvelin, M-R, Raitakari, O T, Terwindt, G M, Kallela, M, Wessman, M, Olesen, J, Chasman, D I, Nyholt, D R, Stefansson, H, Stefansson, K, van den Maagdenberg, A M J M, Hansen, T F, Ripatti, S, Zwart, J-A, Palotie, A & Pirinen, M 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Hautakangas, H, Winsvold, B S, Ruotsalainen, S E, Bjornsdottir, G, Harder, A V E, Kogelman, L J A, Thomas, L F, Noordam, R, Benner, C, Gormley, P, Artto, V, Banasik, K, Bjornsdottir, A, Boomsma, D I, Brumpton, B M, Burgdorf, K S, Buring, J E, Chalmer, M A, de Boer, I, Dichgans, M, Erikstrup, C, Färkkilä, M, Garbrielsen, M E, Ghanbari, M, Hagen, K, Häppölä, P, Hottenga, J J, Hrafnsdottir, M G, Hveem, K, Johnsen, M B, Kähönen, M, Kristoffersen, E S, Kurth, T, Lehtimäki, T, Lighart, L, Magnusson, S H, Malik, R, Pedersen, O B, Pelzer, N, Penninx, B W J H, Ran, C, Ridker, P M, Rosendaal, F R, Sigurdardottir, G R, Skogholt, A H, Sveinsson, O A, Thorgeirsson, T E, Ullum, H, Vijfhuizen, L S, Widen, E, van Dijk, K W, International Headache Genetics Consortium, HUNT All-in Headache, Danish Blood Donor Study Genomic Cohort, Aromaa, A, Belin, A C, Freilinger, T, Ikram, M A, Järvelin, M-R, Raitakari, O T, Terwindt, G M, Kallela, M, Wessman, M, Olesen, J, Chasman, D I, Nyholt, D R, Stefansson, H, Stefansson, K, van den Maagdenberg, A M J M, Hansen, T F, Ripatti, S, Zwart, J-A, Palotie, A & Pirinen, M 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature Genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Nature Genetics, 54(2), 152-160. Nature Publishing Group
Hautakangas, H, Winsvold, B S, Boomsma, D I, Hottenga, J-J, Ligthart, L, Penninx, B W J H, Palotie, A, Pirinen, M & International Headache Genetics Consortium 2022, ' Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles ', Nature genetics, vol. 54, no. 2, pp. 152-160 . https://doi.org/10.1038/s41588-021-00990-0
Genome-wide association analyses identify 123 susceptibility loci for migraine and implicate neurovascular mechanisms in its pathophysiology. Subtype analyses highlight risk loci specific for migraine with or without aura in addition to shared risk v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::271e89f31a913a67875ee7088a9a1e7c
https://research.vu.nl/en/publications/dad00511-8fd1-468a-a806-7f8306e18447
https://research.vu.nl/en/publications/dad00511-8fd1-468a-a806-7f8306e18447
Autor:
J. M., Fu, Satterstrom, F. K., Peng, M., Brand, H., Collins, R. L., Dong, S., Wamsley, B., Klei, L., Wang, L., Hao, S. P., Stevens, C. R., Cusick, C., Babadi, M., Banks, E., Collins, B., Dodge, S., Gabriel, S. B., Gauthier, L., Lee, S. K., Liang, L., Ljungdahl, A., Mahjani, B., Sloofman, L., Smirnov, A. N., Barbosa, M., Betancur, C., Brusco, A., Chung, B. H. Y., Cook, E. H., Cuccaro, M. L., Domenici, E., Ferrero, G. B., Gargus, J. J., Herman, G. E., Hertz-Picciotto, I., Maciel, P., Manoach, D. S., Passos-Bueno, M. R., Persico, A., Renieri, A., Sutcliffe, J. S., Tassone, F., Trabetti, E., Campos, G., Cardaropoli, S., Carli, D., Chan, M. C. Y., Fallerini, C., Giorgio, E., Girardi, A. C., Hansen-Kiss, E., Lee, S. L., Lintas, C., Ludena, Y., Nguyen, R., Pavinato, L., Pericak-Vance, M., Pessah, I. N., Schmidt, R. J., Smith, M., Costa, C. I. S., Trajkova, S., Wang, J. Y. T., M. H. C., Yu, Aleksic, B., Artomov, M., Benetti, E., Biscaldi-Schafer, M., Borglum, A. D., Carracedo, A., Chiocchetti, A. G., Coon, H., Doan, R. N., Fernandez-Prieto, M., Freitag, C. M., Gerges, S., Guter, S., Hougaard, D. M., Hultman, C. M., Jacob, S., Kaartinen, M., Kolevzon, A., Kushima, I., Lehtimaki, T., Rizzo, C. L., Maltman, N., Manara, M., Meiri, G., Menashe, I., Miller, J., Minshew, N., Mosconi, M., Ozaki, N., Palotie, A., Parellada, M., Puura, K., Reichenberg, A., Sandin, S., Scherer, S. W., Schlitt, S., Schmitt, L., Schneider-Momm, K., Siper, P. M., Suren, P., Sweeney, J. A., Teufel, K., del Pilar Trelles, M., Weiss, L. A., Yuen, R., Cutler, D. J., De Rubeis, S., Buxbaum, J. D., Daly, M. J., Devlin, B., Roeder, K., Sanders, S. J., Talkowski, M. E.
Publikováno v:
Nature genetics, vol 54, iss 9
Nature Genetics
Nature Genetics, 2022, 54 (9), pp.1320-1331. ⟨10.1038/s41588-022-01104-0⟩
Nat Genet
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Nature Genetics
Nature Genetics, 2022, 54 (9), pp.1320-1331. ⟨10.1038/s41588-022-01104-0⟩
Nat Genet
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
International audience; Some individuals with autism spectrum disorder (ASD) carry functional mutations rarely observed in the general population. We explored the genes disrupted by these variants from joint analysis of protein-truncating variants (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e272fcce2991b63297b66fd9e9849ad8
http://hdl.handle.net/11562/1073647
http://hdl.handle.net/11562/1073647
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Ahluwalia, T.S., Prins, B.P., Abdollahi, M., Armstrong, N.J., Aslibekyan, S., Bain, L., Jefferis, B., Baumert, J., Beekman, M., Ben-Shlomo, Y., Bis, J.C., Mitchell, B.D., Geus, E. de, Delgado, G.E., Marek, D., Eriksson, J., Kajantie, E., Kanoni, S., Kemp, J.P., Lu, C., Marioni, R.E., McLachlan, S., Milaneschi, Y., Nolte, I.M., Petrelis, A.M., Porcu, E., Sabater-Lleal, M., Naderi, E., Seppala, I., Shah, T., Singhal, G., Standl, M., Teumer, A., Thalamuthu, A., Thiering, E., Trompet, S., Ballantyne, C.M., Benjamin, E.J., Casas, J.P., Toben, C., Dedoussis, G., Deelen, J., Durda, P., Engmann, J., Feitosa, M.F., Grallert, H., Hammarstedt, A., Harris, S.E., Homuth, G., Hottenga, J.J., Jalkanen, S., Jamshidi, Y., Jawahar, M.C., Jess, T., Kivimaki, M., Kleber, M.E., Lahti, J., Liu, Y., Marques-Vidal, P., Mellstrom, D., Mooijaart, S.P., Muller-Nurasyid, M., Penninx, B., Revez, J.A., Rossing, P., Raikkonen, K., Sattar, N., Scharnagl, H., Sennblad, B., Silveira, A., St Pourcain, B., Timpson, N.J., Trollor, J., Dongen, J. van, Heemst, D. van, Visvikis-Siest, S., Vollenweider, P., Volker, U., Waldenberger, M., Willemsen, G., Zabaneh, D., Morris, R.W., Arnett, D.K., Baune, B.T., Boomsma, D.I., Chang, Y.P.C., Deary, I.J., Deloukas, P., Eriksson, J.G., Evans, D.M., Ferreira, M.A., Gaunt, T., Gudnason, V., Hamsten, A., Heinrich, J., Hingorani, A., Humphries, S.E., Jukema, J.W., Koenig, W., Kumari, M., Kutalik, Z., Lawlor, D.A., Lehtimaki, T., Marz, W., Mather, K.A., Naitza, S., Nauck, M., Ohlsson, C., Price, J.F., Raitakari, O., Rice, K., Sachdev, P.S., Slagboom, E., Sorensen, T.I.A., Spector, T., Stacey, D., Stathopoulou, M.G., Tanaka, T., Wannamethee, S.G., Whincup, P., Rotter, J.I., Dehghan, A., Boerwinkle, E., Psaty, B.M., Snieder, H., Alizadeh, B.Z., CHARGE Inflammation Working Grp
Interleukin 6 (IL-6) is a multifunctional cytokine with both pro- and anti-inflammatory properties with a heritability estimate of up to 61%. The circulating levels of IL-6 in blood have been associated with an increased risk of complex disease patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10693::419097ac80cd2bb6100b73d0f2eefc60
https://hdl.handle.net/1887/3214139
https://hdl.handle.net/1887/3214139
Autor:
Ahluwalia, TS, Prins, BP, Abdollahi, M, Armstrong, NJ, Aslibekyan, S, Bain, L, Jefferis, B, Baumert, J, Beekman, M, Ben-Shlomo, Y, Bis, JC, Mitchell, BD, de Geus, E, Delgado, GE, Marek, D, Eriksson, J, Kajantie, E, Kanoni, S, Kemp, JP, Lu, C, Marioni, RE, McLachlan, S, Milaneschi, Y, Nolte, IM, Petrelis, AM, Porcu, E, Sabater-Lleal, M, Naderi, E, Seppala, I, Shah, T, Singhal, G, Standl, M, Teumer, A, Thalamuthu, A, Thiering, E, Trompet, S, Ballantyne, CM, Benjamin, EJ, Casas, JP, Toben, C, Dedoussis, G, Deelen, J, Durda, P, Engmann, J, Feitosa, MF, Grallert, H, Hammarstedt, A, Harris, SE, Homuth, G, Hottenga, JJ, Jalkanen, S, Jamshidi, Y, Jawahar, MC, Jess, T, Kivimaki, M, Kleber, ME, Lahti, J, Liu, Y, Marques-Vidal, P, Mellstrom, D, Mooijaart, SP, Muller-Nurasyid, M, Penninx, B, Revez, JA, Rossing, P, Raikkonen, K, Sattar, N, Scharnagl, H, Sennblad, B, Silveira, A, St Pourcain, B, Timpson, NJ, Trollor, J, van Dongen, J, Van Heemst, D, Visvikis-Siest, S, Vollenweider, P, Volker, U, Waldenberger, M, Willemsen, G, Zabaneh, D, Morris, RW, Arnett, DK, Baune, BT, Boomsma, DI, Chang, YPC, Deary, IJ, Deloukas, P, Eriksson, JG, Evans, DM, Ferreira, MA, Gaunt, T, Gudnason, V, Hamsten, A, Heinrich, J, Hingorani, A, Humphries, SE, Jukema, JW, Koenig, W, Kumari, M, Kutalik, Z, Lawlor, DA, Lehtimaki, T, Marz, W, Mather, KA, Naitza, S, Nauck, M, Ohlsson, C, Price, JF, Raitakari, O, Rice, K, Sachdev, PS, Slagboom, E, Sorensen, TIA, Spector, T, Stacey, D, Stathopoulou, MG, Tanaka, T, Wannamethee, SG, Whincup, P, Rotter, JI, Dehghan, A, Boerwinkle, E, Psaty, BM, Snieder, H, Alizadeh, BZ, CHARGE Inflammation Working Grp
Publikováno v:
HUMAN MOLECULAR GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Interleukin 6 (IL-6) is a multifunctional cytokine with both pro- and anti-inflammatory properties with a heritability estimate of up to 61%. The circulating levels of IL-6 in blood have been associated with an increased risk of complex disease patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::d63cd86945e51f83827ae953c4d3d47a
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4913
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=4913