Enhanced somatosensory information decreases postural sway in older people

Autor: Qiu, F., Cole, M.H., Davids, K.W., Hennig, E.M., Silburn, P.A., Netscher, H., Kerr, G.K.

Publikováno v: In Gait & Posture April 2012 35(4):630-635

Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson's disease heritability

Autor: Reynolds, R.H., Botia, J., Nalls, M.A., Hardy, J., Taliun, S.A.G., Ryten, M., Noyce, A.J., Nicolas, A., Cookson, M.R., Bandres-Ciga, S., Gibbs, J.R., Hernandez, D.G., Singleton, A.B., Reed, X., Leonard, H., Blauwendraat, C., Faghri, F., Bras, J., Guerreiro, R., Tucci, A., Kia, D.A., Houlden, H., Plun-Favreau, H., Mok, K.Y., Wood, N.W., Lovering, R., R'Bibo, L., Rizig, M., Chelban, V., Trabzuni, D., Tan, M., Morris, H.R., Middlehurst, B., Quinn, J., Billingsley, K., Holmans, P., Kinghorn, K.J., Lewis, P., Escott-Price, V., Williams, N., Foltynie, T., Brice, A., Danjou, F., Lesage, S., Corvol, J.C., Martinez, M., Giri, A., Schulte, C., Brockmann, K., Simon-Sanchez, J., Heutink, P., Gasser, T., Rizzu, P., Sharma, M., Shulman, J.M., Robak, L., Lubbe, S., Mencacci, N.E., Finkbeiner, S., Lungu, C., Scholz, S.W., Gan-Or, Z., Rouleau, G.A., Krohan, L., Hilten, J.J. van, Marinus, J., Adarmes-Gomez, A.D., Bernal-Bernal, I., Bonilla-Toribio, M., Buiza-Rueda, D., Carrillo, F., Carrion-Claro, M., Mir, P., Gomez-Garre, P., Jesus, S., Labrador-Espinosa, M.A., Macias, D., Vargas-Gonzalez, L., Mendez-del-Barrio, C., Perinan-Tocino, T., Tejera-Parrado, C., Diez-Fairen, M., Aguilar, M., Alvarez, I., Boungiorno, M.T., Carcel, M., Pastor, P., Tartari, J.P., Alvarez, V., Gonzalez, M.M., Blazquez, M., Garcia, C., Suarez-Sanmartin, E., Barrero, F.J., Rezola, E.M., Yarza, J.A.B., Pagola, A.G., Arregui, A.L.D., Ruiz-Martinez, J., Cerdan, D., Duarte, J., Clarimon, J., Dols-Icardo, O., Infante, J., Marin, J., Kulisevsky, J., Pagonabarraga, J., Gonzalez-Aramburu, I., Rodriguez, A.S., Sierra, M., Duran, R., Ruz, C., Vives, F., Escamilla-Sevilla, F., Minguez, A., Camara, A., Compta, Y., Ezquerra, M., Marti, M.J., Fernandez, M., Munoz, E., Fernandez-Santiago, R., Tolosa, E., Valldeoriola, F., Garcia-Ruiz, P., Heredia, M.J.G., Errazquin, F.P., Hoenicka, J., Jimenez-Escrig, A., Martinez-Castrillo, J.C., Lopez-Sendon, J.L., Torres, I.M., Tabernero, C., Vela, L., Zimprich, A., Pihlstrom, L., Koks, S., Taba, P., Majamaa, K., Siitonen, A., Okubadejo, N.U., Ojo, O.O., Pitcher, T., Anderson, T., Bentley, S., Fowdar, J., Mellick, G., Dalrymple-Alford, J., Henders, A.K., Kassam, I., Montgomery, G., Sidorenko, J., Zhang, F.T., Xue, A.L., Vallerga, C.L., Wallace, L., Wray, N.R., Yang, J., Visscher, P.M., Gratten, J., Silburn, P.A., Halliday, G., Hickie, I., Kwok, J., Lewis, S., Kennedy, M., Pearson, J., Int Parkinsons Dis Genomics, Syst Genomics Parkinsons Dis

Publikováno v: npj Parkinson's Disease, 5

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::15558a829cd2ccd32d8196e2ff7c4991
https://hdl.handle.net/1887/120798

Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study

Autor: Wang, L. Heckman, M.G. Aasly, J.O. Annesi, G. Bozi, M. Chung, S.J. Clarke, C. Crosiers, D. Eckstein, G. Garraux, G. Hadjigeorgiou, G.M. Hattori, N. Jeon, B. Kim, Y.J. Kubo, M. Lesage, S. Lin, J.J. Lynch, T. Lichtner, P. Mellick, G.D. Mok, V. Morrison, K.E. Quattrone, A. Satake, W. Silburn, P.A. Stefanis, L. Stockton, J.D. Tan, E.K. Toda, T. Brice, A. Van Broeckhoven, C. Uitti, R.J. Wirdefeldt, K. Wszolek, Z. Xiromerisiou, G. Maraganore, D.M. Gasser, T. Krüger, R. Farrer, M.J. Ross, O.A. Sharma, M.

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

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Large-scale assessment of polyglutamine repeat expansions in Parkinson disease

Autor: Wang, L. Aasly, J.O. Annesi, G. Bardien, S. Bozi, M. Brice, A. Carr, J. Chung, S.J. Clarke, C. Crosiers, D. Deutschländer, A. Eckstein, G. Farrer, M.J. Goldwurm, S. Garraux, G. Hadjigeorgiou, G.M. Hicks, A.A. Hattori, N. Klein, C. Jeon, B. Kim, Y.J. Lesage, S. Lin, J.-J. Lynch, T. Lichtner, P. Lang, A.E. Mok, V. Jasinska-Myga, B. Mellick, G.D. Morrison, K.E. Opala, G. PihlstrØm, L. Pramstaller, P.P. Park, S.S. Quattrone, A. Rogaeva, E. Ross, O.A. Stefanis, L. Stockton, J.D. Silburn, P.A. Theuns, J. Tan, E.K. Tomiyama, H. Toft, M. Van Broeckhoven, C. Uitti, R.J. Wirdefeldt, K. Wszolek, Z. Xiromerisiou, G. Yueh, K.-C. Zhao, Y. Gasser, T. Maraganore, D.M. Krüger, R. Sharma, M.

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