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Autor:
Healy, Daniel G., Mario, Falchi, O'Sullivan, Sean S., Bonifati, Vincenzo, Alexandra, Durr, Susan, Bressman, Alexis, Brice, Jan, Aasly, Zabetian, Cyrus P., Stefano, Goldwurm, Ferreira, Joaquim J., Eduardo, Tolosa, Kay, Denise M., Christine, Klein, Williams, David R., Connie, Marras, Lang, Anthony E., Wszolek, Zbigniew K., Jose, Berciano, Schapira, Anthony H. V., Timothy, Lynch, Bhatia, Kailash P., Thomas, Gasser, Lees, Andrew J., Wood, Nicholas W., International Lrrk Consortium, Collaborators, Tazir, M., Ysmail Dahlouk, F., Belarbi, S., Hecham, N., Barbosa, E., Chien, H. F., Rieder, C. R., Jardim, L. B., Rogaeva, E., Lesage, S., Lohmann, E., Vidailhet, M., Bonnet, A. M., Agid, Y., Pollak, P., Tison, F., Durif, F., Broussolle, E., Berg, D., Hagenah, J., Gosal, D., Gibson, M., Vanacore, Nicola, Berardelli, Alfredo, Fabbrini, Giovanni, Fabrizio, E., Meco, Giuseppe, Stocchi, F., Dalla Libera, A., De Mari, M., Lamberti, P., Cossu, G., Pezzoli, G., Zini, M., Tesei, S., Zecchinelli, A., Sironi, F., Antonini, A., Mariani, C., Sacilotto, G., Meucci, N., Canesi, M., Di Fonzo, A., Oostra, B., Correia Guedes, L., Rosa, Mm, Coelho, M., Sampaio, C., Gaig, C., C. S., Lu, Wu Chou, Y. H., Quinn, N. P., Abou Sleiman, P. M., Muqit, M. M., Khan, N. L., Gandhi, S., Vaughan, J., Payami, H., Nutt, J. J., Factor, S. A., Higgins, D. S., Farrer, M. J., Hulihan, M., Brown, L., Mata, I. F., Samii, A., Yearout, D., Griffith, A., Leis, B. C., Roberts, J. W.
Publikováno v:
Lancet Neurology, 7(7), 583-590. Lancet Publishing Group
The Lancet Neurology
The Lancet Neurology, 2008, 7 (7), pp.583-590
The Lancet Neurology, Elsevier, 2008, 7 (7), pp.583-590
The Lancet Neurology
The Lancet Neurology, 2008, 7 (7), pp.583-590
The Lancet Neurology, Elsevier, 2008, 7 (7), pp.583-590
Summary Background Mutations in LRRK2 , the gene that encodes leucine-rich repeat kinase 2, are a cause of Parkinson's disease (PD). The International LRRK2 Consortium was established to answer three key clinical questions: can LRRK2 -associated PD b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86cd088b2dcd94204ede5ac47e6f14f6
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:
Lill, C., Roehr, C., McQueen, M., Kavvoura, F., Bagade, S., Schjeide, B., Schjeide, L., Meissner, E., Zauft, U., Allen, N., Liu, T., Schilling, M., Anderson, K., Beecham, G., Berg, D., Biernacka, J., Brice, A., DeStefano, A., Do, C., Eriksson, N., Factor, S., Farrer, M., Foroud, T., Gasser, T., Hamza, T., Hardy, J., Heutink, P., Hill-Burns, E., Klein, C., Latourelle, J., Maraganore, D., Martin, E., Martinez, M., Myers, R., Nalls, M., Pankratz, N., Payami, H., Satake, W., Scott, W., Sharma, M., Singleton, A., Stefansson, K., Toda, T., Tung, J., Vance, J., Wood, N., Zabetian, C., Young, P., Tanzi, R., Khoury, M., Zipp, F., Lehrach, H., Ioannidis, J., Bertram, L., Parkinson's, G., IPDGC, Consortium, P., WTCCC2
Publikováno v:
PLoS Genetics 8(3), e1002548 (2012). doi:10.1371/journal.pgen.1002548
PLoS Genetics, Vol 8, Iss 3, p e1002548 (2012)
Lill, C M, Roehr, J T, McQueen, M B, Kavvoura, F K, Bagade, S, Schjeide, B M M, Schjeide, L M, Meissner, E, Zauft, U, Allen, N C, Liu, T, Schilling, M, Anderson, K J, Beecham, G, Berg, D, Biernacka, J M, Brice, A, DeStefano, A L, Do, C B, Eriksson, N, Factor, S A, Farrer, M J, Foroud, T, Gasser, T, Hamza, T, Hardy, J A, Heutink, P, Hill-Burns, E M, Klein, C, Latourelle, J C, Maraganore, D M, Martin, E R, Martinez, M, Myers, R H, Nalls, M A, Pankratz, N, Payami, H, Satake, W, Scott, W K, Sharma, M, Singleton, A B, Stefansson, K, Toda, T, Tung, J Y, Vance, J, Wood, N W, Zabetian, C P, Young, P, Tanzi, R E, Khoury, M J, Zipp, F, Lehrach, H, Ioannidis, J P A & Bertram, L 2012, ' Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database ', PLoS Genetics, vol. 8, no. 3, e1002548 . https://doi.org/10.1371/journal.pgen.1002548
PLoS Genetics
PLoS Genetics, 8(3):e1002548. Public Library of Science
PLoS Genetics, Vol 8, Iss 3, p e1002548 (2012)
Lill, C M, Roehr, J T, McQueen, M B, Kavvoura, F K, Bagade, S, Schjeide, B M M, Schjeide, L M, Meissner, E, Zauft, U, Allen, N C, Liu, T, Schilling, M, Anderson, K J, Beecham, G, Berg, D, Biernacka, J M, Brice, A, DeStefano, A L, Do, C B, Eriksson, N, Factor, S A, Farrer, M J, Foroud, T, Gasser, T, Hamza, T, Hardy, J A, Heutink, P, Hill-Burns, E M, Klein, C, Latourelle, J C, Maraganore, D M, Martin, E R, Martinez, M, Myers, R H, Nalls, M A, Pankratz, N, Payami, H, Satake, W, Scott, W K, Sharma, M, Singleton, A B, Stefansson, K, Toda, T, Tung, J Y, Vance, J, Wood, N W, Zabetian, C P, Young, P, Tanzi, R E, Khoury, M J, Zipp, F, Lehrach, H, Ioannidis, J P A & Bertram, L 2012, ' Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database ', PLoS Genetics, vol. 8, no. 3, e1002548 . https://doi.org/10.1371/journal.pgen.1002548
PLoS Genetics
PLoS Genetics, 8(3):e1002548. Public Library of Science
More than 800 published genetic association studies have implicated dozens of potential risk loci in Parkinson's disease (PD). To facilitate the interpretation of these findings, we have created a dedicated online resource, PDGene, that comprehensive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::226e22909c64cab8276862e4ab0e99e8
https://pub.dzne.de/record/136471
https://pub.dzne.de/record/136471
Autor:
Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Kruger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van
Publikováno v:
Lancet neurology
5 (2006): 917–923.
info:cnr-pdr/source/autori:Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Kruger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van/titolo:Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study/doi:/rivista:Lancet neurology (Print)/anno:2006/pagina_da:917/pagina_a:923/intervallo_pagine:917–923/volume:5
5 (2006): 917–923.
info:cnr-pdr/source/autori:Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Kruger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van/titolo:Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study/doi:/rivista:Lancet neurology (Print)/anno:2006/pagina_da:917/pagina_a:923/intervallo_pagine:917–923/volume:5
BACKGROUND: A genome-wide association study identified 13 single-nucleotide polymorphisms (SNPs) significantly associated with Parkinson's disease. Small-scale replication studies were largely non-confirmatory, but a meta-analysis that included data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::ecc2957335a9b6d6a476d3d6a15b43e0
https://publications.cnr.it/doc/49998
https://publications.cnr.it/doc/49998
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Akademický článek
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