Zobrazeno 1 - 10
of 153
pro vyhledávání: '"Day, I N"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Pedagogische Studien; 2023, Vol. 100 Issue 2, p137-146, 10p
Autor:
Nüesch, Eveline, Dale, Caroline, Palmer, Tom M., White, Jon, Keating, Brendan J., van Iperen, Erik P A, Goel, Anuj, Padmanabhan, Sandosh, Asselbergs, F. W., Verschuren, W. M., Wijmenga, C., Van der Schouw, Y. T., Onland-Moret, N. C., Lange, Leslie A., Hovingh, G. K., Sivapalaratnam, Suthesh, Morris, Richard W., Whincup, Peter H., Wannamethe, Goya S., Gaunt, Tom R., Ebrahim, Shah, Steel, Laura, Nair, Nikhil, Reiner, Alexander P., Kooperberg, Charles, Wilson, James F., Bolton, Jennifer L., McLachlan, Stela, Price, Jacqueline F., Strachan, Mark W J, Robertson, Christine M., Kleber, Marcus E., Delgado, Graciela, März, Winfried, Melander, Olle, Dominiczak, Anna F., Farrall, Martin, Watkins, Hugh, Leusink, Maarten, Maitland-van der Zee, Anke H., de Groot, Mark C H, Dudbridge, Frank, Hingorani, Aroon, Ben-Shlomo, Yoav, Lawlor, Debbie A., Amuzu, A., Caufield, M., Cavadino, A., Cooper, J., Davies, T. L., Day, I. N., Drenos, F., Engmann, J., Finan, C., Giambartolomei, C., Hardy, R., Humphries, S. E., Hypponen, E., Kivimaki, M., Kuh, D., Kumari, M., Ong, K., Plagnol, V., Power, C., Richards, M., Shah, S., Shah, T., Sofat, R., Talmud, P. J., Wareham, N., Warren, H., Whittaker, J. C., Wong, A., Zabaneh, D., Smith, George Davey, Wells, Jonathan C., Leon, David A., Holmes, Michael V., Casas, Juan P.
Publikováno v:
International Journal of Epidemiology, 45(6), 1927. Oxford University Press
© The Author 2015; all rights reserved. Background: We investigated causal effect of completed growth, measured by adult height, on coronary heart disease (CHD), stroke and cardiovascular traits, using instrumental variable (IV) Mendelian randomizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2f0112c7e185d039dfc19dd0c6244ba0
https://dspace.library.uu.nl/handle/1874/332756
https://dspace.library.uu.nl/handle/1874/332756
Autor:
Shihab, H. A., Rogers, M. F., Gough, J., Mort, Matthew, Cooper, David Neil, Day, I. N. M., Gaunt, T. R., Campbell, C.
Motivation: Technological advances have enabled the identification of an increasingly large spectrum of single nucleotide variants within the human genome, many of which may be associated with monogenic disease or complex traits. Here, we propose an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::f5e6f855a00a1786446f5924485356c4
https://orca.cardiff.ac.uk/id/eprint/84066/1/Bioinformatics-2015-Shihab-1536-43.pdf
https://orca.cardiff.ac.uk/id/eprint/84066/1/Bioinformatics-2015-Shihab-1536-43.pdf
Autor:
Guo, Y., Lanktree, M. B., Taylor, K. C., Hakonarson, H., Lange, L. A., Keating, B. J., Fairfax, B. P., Elbers, C. C., Barnard, J., Farrall, M., Padmanabhan, S., Baumert, J., Castillo, B. A., Gaunt, T. R., Gong, Y., Rajagopalan, R., Romaine, S. P., Kumari, M., Rafelt, S., Smith, E. N., Li, Y. R., Sivapalaratnam, S., van Iperen, E. P., Speliotes, E. K., Toskala, E., Zhang, L., Ochs-Balcom, H. M., Bhangale, T. R., Chandrupatla, H. R., Drenos, F., Gieger, C., Gupta, J., Johnson, T., Kleber, M. E., Makino, S., Mangino, M., Meng, Y., Nelson, C. P., Pankow, J. S., Pankratz, N., Price, T. S., Shaffer, J., Shen, H., Tischfield, S., Tomaszewski, M., Atwood, L. D., Bailey, K. M., Balasubramanyam, A., Baldwin, C. T., Basart, H., Bauer, F., Behr, E. R., Beitelshees, A. L., Berenson, G. S., Beresford, S. A., Bezzina, C. R., Bhatt, D. L., Boer, J. M., Braund, P. S., Burke, G. L., Burkley, B., Carty, C., Chen, W., Clarke, R., Cooper-DeHoff, R. M., Curtis, S. P., de Bakker, P. I., de Jong, J. S., Delles, C., Dominiczak, A. F., Duggan, D., Feldman, H. I., Furlong, C. E., Gorski, M. M., Gums, J. G., Hardwick, R., Hastie, C., Heid, I. M., Huang, G.-H., Huggins, G. S., Humphries, S. E., Kirkland, S. A., Kivimaki, M., Klein, R., Klein, B. E., Knowler, W. C., Kottke-Marchant, K., LaCroix, A. Z., Langaee, T. Y., Li, M., Lyon, H. N., Maiwald, S., Marshall, J. K., Mehta, A., Meijs, M. F., Melander, O., Meyer, N., Mitra, N., Molony, C. M., Morrow, D. A., Murugesan, G., Newhouse, S. J., Nieto, J. F., Onland-Moret, N. C., Ouwehand, W. H., Palmen, J., Pepine, C. J., Ranchalis, J., Rosas, S. E., Rosenthal, E. A., Scharnagl, H., Schork, N. J., Schreiner, P. J., Shah, T., Shashaty, M., Shimbo, D., Srinivasan, S. R., Thomas, F., Tobin, M. D., Tsai, M. Y., Verschuren, W. M. M., Wagenknecht, L. E., Winkelmann, B. R., Young, T., Yusuf, S., Zafarmand, M. H., Zmuda, J. M., Zwinderman, A. H., Anand, S. S., Balmforth, A. J., Boehm, B. O., Boerwinkle, E., Burton, P. R., Cappola, T. P., Casas, J. P., Caulfield, M. J., Christiani, D. C., Christie, J., Cruickshanks, K. J., Davey-Smith, G., Davidson, K. W., Day, I. N., Doevendans, P. A., Dorn, G. W., FitzGerald, G. A., Hall, A. S., Hingorani, A. D., Hirschhorn, J. N., Hofker, M. H., Hovingh, K. G., Illig, T., Jamshidi, Y., Jarvik, G. P., Johnson, J. A., Kanetsky, P. A., Kastelein, J. J., Koenig, W., Lawlor, D. A., Marz, W., McCaffery, J., Mega, J. L., Mitchell, B. D., Murray, S. S., O'Connell, J. R., Patel, S. R., Peters, A., Pettinger, M., Rader, D. J., Redline, S., Reilly, M. P., Sabatine, M. S., Schadt, E. E., Shuldiner, A. R., Silverstein, R. L., Spector, T. D., Taylor, H. A., Thorand, B., Trip, M. D., Watkins, H., Wichmann, H.- E., Fox, C. S., Grant, S. F., Peter, I., Talmud, P. J., Munroe, P. B., Wilson, J. G., Knight, J. C., Samani, N. J., Hegele, R. A., Asselbergs, F. W., Monda, K. L., van der Schouw, Y. T., Demerath, E. W., Wijmenga, C., Timpson, N. J., Reiner, A. P., North, K. E., Papanicolaou, G. J., Lange , L. A., Keating , B. J.
Publikováno v:
Human molecular genetics, 22(1), 184-201. Oxford University Press
Human Molecular Genetics
Hum. Mol. Genet. 22, 184-201 (2013)
Human Molecular Genetics; Vol 22
Human Molecular Genetics
Hum. Mol. Genet. 22, 184-201 (2013)
Human Molecular Genetics; Vol 22
Recent genetic association studies have made progress in uncovering components of the genetic architecture of the body mass index (BMI). We used the ITMAT-Broad-Candidate Gene Association Resource (CARe) (IBC) array comprising up to 49 320 single nuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0166578e352d396224c5a804613eb43e
https://pure.amc.nl/en/publications/genecentric-metaanalyses-of-108-912-individuals-confirm-known-body-mass-index-loci-and-reveal-three-novel-signals(cfdf63d4-bd63-48df-a043-b47d1a307f9f).html
https://pure.amc.nl/en/publications/genecentric-metaanalyses-of-108-912-individuals-confirm-known-body-mass-index-loci-and-reveal-three-novel-signals(cfdf63d4-bd63-48df-a043-b47d1a307f9f).html
Autor:
Lips, M. A., Syddall, H. E., Tom Gaunt, Rodriguez, S., Day, I. N. M., Cooper, C., Dennison, E. M.
Publikováno v:
Scopus-Elsevier
OBJECTIVE: We sought evidence of interaction between single-nucleotide polymorphisms (SNP) in the calcium-sensing receptor (CASR) gene and early life in determination of bone mineral density (BMD) among individuals from the Hertfordshire Cohort Study
Autor:
Fawcett, K. A., Barroso, I., Wareham, N. J., Luan, J., Syddall, H., Cooper, C., O'Rahilly, S., Day, I. N. M., Sandhu, M. S.
Publikováno v:
Diabetologia. 49(11)
AIMS/HYPOTHESIS: PARL, the gene encoding presenilins-associated rhomboid-like protein, maps to chromosome 3q27 within a quantitative trait locus that influences components of the metabolic syndrome. Recently, an amino acid substitution (Leu262Val, rs
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.