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A recent study MacLeod et al. has shown that an interaction between variants at the LRRK2 and PARK16 loci influences risk of development of Parkinson's disease (PD). Our study examines the proposed interaction between LRRK2 and PARK16 variants in mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::50052c4c033bfba5f15d999a8ea1216b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2998435
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2998435
Publikováno v:
Lancet. 10/27/2001, Vol. 358 Issue 9291, p1410. 7p. 1 Diagram, 1 Chart, 2 Graphs.
Objectives: We aim to clarify the pathogenic role of intermediate size repeat expansions of SCA2, SCA3, SCA6, and SCA17 as risk factors for idiopathic Parkinson disease (PD). Methods: We invited researchers from the Genetic Epidemiology of Parkinson'
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d4a28ec88f720f71e062f5341fce4917
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3109868
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3109868
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
Background Two recent studies identified a mutation (p.Asp620Asn) in the vacuolar protein sorting 35 gene as a cause for an autosomal dominant form of Parkinson disease. Although additional missense variants were described, their pathogenic role yet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e3f3da5990a5e396ddee46c5f6e0f6c9
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3089247
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3089247
Objective: Eleven genetic loci have reached genome-wide significance in a recent meta-analysis of genome-wide association studies in Parkinson disease (PD) based on populations of Caucasian descent. The extent to which these genetic effects are consi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6ddef51a352a47d17923c42a009f9340
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3111046
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3111046
Autor:
Plagnol, V., Nalls, M.A., Bras, J.M., Hernandez, D., Sharma, M., Sheerin, U.M., Saad, M., Simon-Sanchez, J., Schulte, C., Lesage, S., Sveinbjornsdottir, S., Amouyel, P., Arepalli, S., Band, G., Barker, R.A., Bellinguez, C., Ben-Shlomo, Y., Berendse, H.W., Berg, D., Bhatia, K.P., Bie, R.M. de, Biffi, A., Bloem, B.R., Bochdanovits, Z., Bonin, M., Brockmann, K., Brooks, J., Burn, D.J., Charlesworth, G., Chen, H., Chinnery, P.F., Chong, S., Clarke, C.E., Cookson, M.R., Cooper, J.M., Corvol, J.C., Counsell, J., Damier, P., Dartigues, J.F., Deloukas, P., Deuschl, G., Dexter, D.T., Dijk, K.D. van, Dillman, A., Durif, F., Durr, A., Edkins, S., Evans, J.R., Foltynie, T., Freeman, C., Gao, J., Gardner, M., Gibbs, J.R., Goate, A., Gray, E., Guerreiro, R., Gustafsson, O., Harris, C., Hellenthal, G., Hilten, J.J. van, Hofman, A., Hollenbeck, A., Holton, J.L., Hu, M., Huang, X., Huber, H, Hudson, G., Hunt, S.E., Huttenlocher, J., Illig, T., Jonsson, P.V., Langford, C., Lees, A.J., Lichtner, P., Limousin, P., Lopez, G., McNeill, A., Moorby, C., Moore, M., Morris, H.A., Morrison, K.E., Mudanohwo, E., O'Sullivan, S.S, Pearson, J., Pearson, R., Perlmutter, J., Petursson, H., Pirinen, M., Polnak, P., Post, B., Potter, S.C., Ravina, B., Revesz, T., Riess, O., Rivadeneira, F., Rizzu, P., Ryten, M., Sawcer, S.J., Schapira, A., Scheffer, H., Shaw, K., Shoulson, I., Sidransky, E., Silva, R. de, Smith, C., Spencer, C.C., Stefansson, H., Steinberg, S., Stockton, J.D., Strange, A., Su, Z., Talbot, K., Tanner, C.M., Tashakkori-Ghanbaria, A., Tison, F., Trabzuni, D., Traynor, B.J., Uitterlinden, A.G., Vandrovcova, J., Velseboer, D., Vidailhet, M., Vukcevic, D., Walker, R., Warrenburg, B.P.C. van de, Weale, M.E., Wickremaratchi, M., Williams, N., Williams-Gray, C.H., Winder-Rhodes, S., Stefansson, K., Martinez, M., Donnelly, P., Singleton, A.B., Hardy, J., Heutink, P., Brice, A., Gasser, T., Wood, N.W.
Publikováno v:
Plos Genetics, 7, e1002142-e1002142
Plos Genetics, 7, 6, pp. e1002142-e1002142
Plos Genetics, 7, 6, pp. e1002142-e1002142
Contains fulltext : 97597.pdf (Publisher’s version ) (Open Access) A previous genome-wide association (GWA) meta-analysis of 12,386 PD cases and 21,026 controls conducted by the International Parkinson's Disease Genomics Consortium (IPDGC) discover
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f6650ffcea1af9ca28b2f6b8d836a80f
http://hdl.handle.net/2066/97597
http://hdl.handle.net/2066/97597
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