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pro vyhledávání: '"Elbaz, Ales"'
Autor:
Sugier, Pierre-Emmanuel, Lucotte, Elise A., Domenighetti, Cloé, Law, Matthew H., Iles, Mark M., Brown, Kevin, Amos, Christopher, McKay, James D., Hung, Rayjean J., Karimi, Mojgan, Bacq-Daian, Delphine, Boland-Augé, Anne, Olaso, Robert, Deleuze, Jean-François, Lesueur, Fabienne, Ostroumova, Evgenia, Kesminiene, Ausrele, de Vathaire, Florent, Guénel, Pascal, consortium, The Epithyr, Sreelatha, Ashwin Ashok Kumar, Schulte, Claudia, Grover, Sandeep, May, Patrick, Bobbili, Dheeraj Reddy, Radivojkov-Blagojevic, Milena, Lichtner, Peter, Singleton, Andrew B., Hernandez, Dena G., Edsall, Connor, Mellick, George D., Zimprich, Alexander, Pirker, Walter, Rogaeva, Ekaterina, Lang, Anthony E., Koks, Sulev, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugénie, Brockmann, Kathrin, Deutschländer, Angela B., Hadjigeorgiou, Georges M., Dardiotis, Efthimios, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Straniero, Letizia, Zecchinelli, Anna, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Matsuo, Hirotaka, Nakayama, Akiyoshi, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Kolber, Pierre, van de Warrenburg, Bart P. C., Bloem, Bastiaan R., Aasly, Jan, Toft, Mathias, Pihlstrøm, Lasse, Guedes, Leonor Correia, Ferreira, Joaquim J., Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy, Ran, Caroline, Belin, Andrea C., Puschmann, Andreas, Rödström, Emil Ygland, Clarke, Carl E., Morrison, Karen E., Tan, Manuela, Krainc, Dimitri, Burbulla, Lena F., Farrer, Matt J., Krüger, Rejko, Gasser, Thomas, Sharma, Manu, Landoulsi, Zied, consortium, Courage-PD, Truong, Thérèse, Elbaz, Ales
Publikováno v:
Movement Disorders, 38, 4, pp. 604-615
the EPITHYR consortium, the Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease (Courage-PD) consortium, Sugier, PE, Lucotte, E A, Domenighetti, C, Law, M H, Iles, M M, Brown, K, Amos, C, McKay, J D, Hung, R J, Karimi, M, Bacq-Daian, D, Boland-Augé, A, Olaso, R, Deleuze, J, Lesueur, F, Ostroumova, E, Kesminiene, A, de Vathaire, F, Guénel, P, Sreelatha, A A K, Schulte, C, Grover, S, May, P, Bobbili, D R, Radivojkov-Blagojevic, M, Lichtner, P, Singleton, A B, Hernandez, D G, Edsall, C, Mellick, G D, Zimprich, A, Pirker, W, Rogaeva, E, Lang, A E, Koks, S, Taba, P, Lesage, S, Brice, A, Corvol, JC, Chartier-Harlin, MC, Mutez, E, Brockmann, K, Deutschländer, A B, Hadjigeorgiou, G M, Dardiotis, E, Stefanis, L, Simitsi, A M, Valente, E M, Petrucci, S & Morrison, K E 2023, ' Investigation of shared genetic risk factors between Parkinson's disease and cancers ', Movement Disorders . https://doi.org/10.1002/mds.29337
Movement disorders 38(4), 604-615 (2023). doi:10.1002/mds.29337
the EPITHYR consortium, the Comprehensive Unbiased Risk Factor Assessment for Genetics and Environment in Parkinson's Disease (Courage-PD) consortium, Sugier, PE, Lucotte, E A, Domenighetti, C, Law, M H, Iles, M M, Brown, K, Amos, C, McKay, J D, Hung, R J, Karimi, M, Bacq-Daian, D, Boland-Augé, A, Olaso, R, Deleuze, J, Lesueur, F, Ostroumova, E, Kesminiene, A, de Vathaire, F, Guénel, P, Sreelatha, A A K, Schulte, C, Grover, S, May, P, Bobbili, D R, Radivojkov-Blagojevic, M, Lichtner, P, Singleton, A B, Hernandez, D G, Edsall, C, Mellick, G D, Zimprich, A, Pirker, W, Rogaeva, E, Lang, A E, Koks, S, Taba, P, Lesage, S, Brice, A, Corvol, JC, Chartier-Harlin, MC, Mutez, E, Brockmann, K, Deutschländer, A B, Hadjigeorgiou, G M, Dardiotis, E, Stefanis, L, Simitsi, A M, Valente, E M, Petrucci, S & Morrison, K E 2023, ' Investigation of shared genetic risk factors between Parkinson's disease and cancers ', Movement Disorders . https://doi.org/10.1002/mds.29337
Movement disorders 38(4), 604-615 (2023). doi:10.1002/mds.29337
BackgroundEpidemiological studies that examined the association between Parkinson's disease (PD) and cancers led to inconsistent results, but they face a number of methodological difficulties.ObjectiveWe used results from genome-wide association stud