Zobrazeno 1 - 10
of 307
pro vyhledávání: '"WEALE, M"'
Autor:
Sefton, J. A., Weale, M. R.
Publikováno v:
The Review of Economic Studies, 2006 Jan 01. 73(1), 219-249.
Externí odkaz:
https://www.jstor.org/stable/3700623
Publikováno v:
Journal of Applied Econometrics, 2001 Sep 01. 16(5), 599-617.
Externí odkaz:
https://www.jstor.org/stable/2678596
Akademický článek
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Autor:
Gandhi, S., Abou-Sleiman, P. M., Healy, D. G., Weale, M., Gilks, W., Ahmadi, K., Goldstein, D. B., Wood, N. W.
Publikováno v:
Philosophical Transactions: Biological Sciences, 2005 Aug . 360(1460), 1573-1578.
Externí odkaz:
https://www.jstor.org/stable/30040917
This paper uses a nationally representative data set to examine the extent to which family migration history helps explains inter-ethnic variations in mental health in the UK. We confirm that there is significant variation in mental health across eth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::6b37bc358c36725c7226cdfd179223fc
https://doi.org/10.1002/psp.2195
https://doi.org/10.1002/psp.2195
Akademický článek
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This paper argues that a wealth target is an important feature of an economic policy package. A real exchange rate target can be used as an intermediate target to steer national wealth towards its desired value. Such a policy requires that fiscal pol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::617851f63e7d6bd87e44ff0a5f38d7f6
https://ora.ox.ac.uk/objects/uuid:52c817b0-3228-477b-8a9a-173d3ec8271f
https://ora.ox.ac.uk/objects/uuid:52c817b0-3228-477b-8a9a-173d3ec8271f
Akademický článek
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We conducted a meta-analysis of Parkinson's disease genome-wide association studies using a common set of 7,893,274 variants across 13,708 cases and 95,282 controls. Twenty-six loci were identified as having genome-wide significant association; these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::85bd7b207542e068b2cea882da7a6cc6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3087558
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3087558
Autor:
Guerreiro, R, Wojtas, A, Bras, J, Carrasquillo, M, Rogaeva, E, Majounie, E, Cruchaga, C, Sassi, C, Kauwe, Js, Lupton, Mk, Ryten, M, Brown, K, Lowe, J, Ridge, Pg, Hammer, Mb, Wakutani, Y, Hazrati, L, Proitsi, P, Newhouse, S, Lohmann, E, Erginel Unaltuna, N, Medway, C, Hanagasi, H, Troakes, C, Gurvit, H, Bilgic, B, Al Sarraj, S, Benitez, B, Cooper, B, Carrell, D, Emre, M, Zou, F, Ma, L, Murray, M, Dickson, D, Younkin, S, Petersen, Rc, Corcoran, Cd, Cai, Y, Oliveira, C, Ribeiro, Mh, Santana, I, Tschanz, Jt, Gibbs, J, Norton, Mc, Kloszewska, I, Mecocci, Patrizia, Soininen, H, Tsolaki, M, Vellas, B, Munger, Rg, Mann, Dm, Pickering Brown, S, Lovestone, S, Beck, J, Mead, S, Collinge, J, Parsons, L, Pocock, J, Morris, Jc, Revesz, T, Lashley, T, Fox, Nc, Rossor, Mn, Grenier Boley, B, Bellenguez, C, Moskvina, V, Sims, R, Harold, D, Williams, J, Lambert, Jc, Amouyel, P, Graff Radford, N, Goate, A, Rademakers, R, Morgan, K, Powell, J, St George Hyslop, P, Singleton, A, Hardy, J, Gerrish, A, Chapman, J, Abraham, R, Hollingworth, P, Hamshere, M, Pahwa, Js, Dowzell, K, Williams, A, Jones, N, Thomas, C, Stretton, A, Morgan, A, Williams, K, Thomas, S, Brayne, C, Rubinsztein, Dc, Gill, M, Lawlor, B, Lynch, A, Passmore, P, Craig, D, Mcguinness, B, Johnston, Ja, Todd, S, Holmes, C, Smith, A, Love, S, Kehoe, Pg, Maier, W, Jessen, F, Heun, R, Kölsch, H, Schürmann, B, Ramirez, A, van den Bussche, H, Heuser, I, Kornhuber, J, Wiltfang, J, Dichgans, M, Frölich, L, Hampel, H, Hüll, M, Rujescu, D, Nowotny, P, Mayo, K, Livingston, G, Bass, Nj, Gurling, H, Mcquillin, A, Gwilliam, R, Deloukas, P, Nöthen, Mm, Holmans, P, O'Donovan, M, Owen, Mj, Zelenika, D, Epelbaum, J, Dartigues, Jf, Tzourio, C, Berr, C, Boland, A, Campion, D, Alpérovitch, A, Lathrop, M, Smith, C, Trabzuni, D, Walker, R, Weale, M.
Publikováno v:
The New England journal of medicine
BACKGROUND Homozygous loss-of-function mutations in TREM2, encoding the triggering receptor expressed on myeloid cells 2 protein, have previously been associated with an autosomal recessive form of early-onset dementia. METHODS We used genome, exome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa6c8092ff8f294daa5201834bda07de
https://www.ncbi.nlm.nih.gov/pubmed/23150934
https://www.ncbi.nlm.nih.gov/pubmed/23150934