Molecular Pathology of Myotonic Dystrophy Type 1 in Iceland von Hallgrímsdóttir, E. G., Svansson, H., Stefánsdóttir, V. F., Sveinsson, Ó. Á., Ólafsdóttir, H., Briem, E., Sveinbjörnsdóttir, S., Jónsson, J. J.

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Cerebral microbleeds, retinopathy, and dementia: The AGES-Reykjavik Study von QIU, C, COTCH, M. F, GUDNASON, V, LAUNER, L. J, SIGURDSSON, S, JONSSON, P. V, JONSDOTTIR, M. K, SVEINBJÖRNSDOTTIR, S, EIRIKSDOTTIR, G, KLEIN, R, HARRIS, T. B, VAN BUCHEM, M. A

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Börnin okkar von Sveinbjörnsdóttir, Steingerður

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Familial Aggregation of Parkinson's Disease in Iceland von Sveinbjörnsdóttir, Sigurlaug, Hicks, Andrew A, Jónsson, Thorlákur, Pétursson, Hjörvar, Guðmundsson, Grétar, Frigge, Michael L, Kong, Augustine, Gulcher, Jeffrey R, Stefánsson, Kári

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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease von Nalls, Mike A, Pankratz, Nathan, Lill, Christina M, Do, Chuong B, Hernandez, Dena G, Saad, Mohamad, DeStefano, Anita L, Kara, Eleanna, Bras, Jose, Sharma, Manu, Schulte, Claudia, Keller, Margaux F, Arepalli, Sampath, Letson, Christopher, Edsall, Connor, Stefansson, Hreinn, Liu, Xinmin, Pliner, Hannah, Lee, Joseph H, Cheng, Rong, Ikram, M Arfan, Ioannidis, John P A, Hadjigeorgiou, Georgios M, Bis, Joshua C, Martinez, Maria, Perlmutter, Joel S, Goate, Alison, Marder, Karen, Fiske, Brian, Sutherland, Margaret, Xiromerisiou, Georgia, Myers, Richard H, Clark, Lorraine N, Stefansson, Kari, Hardy, John A, Heutink, Peter, Chen, Honglei, Wood, Nicholas W, Houlden, Henry, Payami, Haydeh, Brice, Alexis, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, Singleton, Andrew B

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Cerebral microbleeds in the population based AGES-Reykjavik study: prevalence and location von Sveinbjornsdottir, S, Sigurdsson, S, Aspelund, T, Kjartansson, O, Eiriksdottir, G, Valtysdottir, B, Lopez, O L, van Buchem, M A, Jonsson, P V, Gudnason, V, Launer, L J

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Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease von Robak, Laurie A, Jansen, Iris E, van Rooij, Jeroen, Uitterlinden, André G, Kraaij, Robert, Jankovic, Joseph, Heutink, Peter, Shulman, Joshua M

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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease von Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.

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Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption von Cornelis, M C, Byrne, E M, Esko, T, Nalls, M A, Paynter, N, Monda, K L, Amin, N, Renstrom, F, Cavadino, A, Nolte, I M, Teumer, A, Yu, K, Manichaikul, A, Wojczynski, M K, Vink, J M, Zhao, J H, Burlutsky, G, Lahti, J, Lemaitre, R N, Eriksson, J, Musani, S K, Tanaka, T, Luan, J, Hui, J, Ho, W-K, Magnusson, P K E, Pedersen, N L, Couper, D, Oostra, B A, Tiemeier, H W, Uitterlinden, A G, Barroso, I, Xue, L, Kaakinen, M, Milani, L, Power, C, Baumeister, S E, Biffar, R, Kutalik, Z, Jacobs, D R, Lind, L, Jensen, M, Luben, R N, Wang, J J, Männistö, S, Lehtimäki, T, Viikari, J, Mozaffarian, D, Mukamal, K, Döring, A, Montgomery, G W, Dahmen, N, Tucker, K L, Ferrucci, L, Treur, J L, Mellström, D, Hottenga, J J, Tönjes, A, Deloukas, P, Kanoni, S, Lorentzon, M, Houston, D K, Liu, Y, Mason, M A, Zonderman, A B, Franke, L, Kristal, B S, Karjalainen, J, Reed, D R, Westra, H-J, Evans, M K, Dedoussis, G, Stumvoll, M, Bandinelli, S, Ordovas, J M, Chan, A T, Ohlsson, C, Gieger, C, Martin, N G, Siscovick, D S, Raitakari, O, Eriksson, J G, Mitchell, P, Hunter, D J, Rimm, E B, Borecki, I B, Vollenweider, P, Grabe, H J, Neuhouser, M L, Wolffenbuttel, B H R, Hyppönen, E, Cupples, L A, Franks, P W, van Duijn, C M, Heiss, G, Metspalu, A, North, K E, Ingelsson, E, Nettleton, J A, van Dam, R M

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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies von Nalls, Michael A, Plagnol, Vincent, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Saad, Mohamad, Simón-Sánchez, J, Schulte, Claudia, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Stefánsson, Kári, Martinez, Maria, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W

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Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing von Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa, Gibbs, J Raphael, Nalls, Mike A, Ryten, Mina, Botia, Juan A, Vandrovcova, Jana, Simon-Sanchez, Javier, Castillo-Lizardo, Melissa, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K, Li, Yarong, Yogi, Puja, Amin, Najaf, van Duijn, Cornelia M, Morris, Huw R, Brice, Alexis, Singleton, Andrew B, David, Della C, Nollen, Ellen A, Jain, Shushant, Shulman, Joshua M, Heutink, Peter

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A two-stage meta-analysis identifies several new loci for Parkinson's disease

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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease von KELLER, Margaux F, SAAD, Mohamad, SCHULTE, Claudia, MOSKVINA, Valentina, DURR, Alexandra, HOLMANS, Peter, KILARSKI, Laura L, GUERREIRO, Rita, HERNANDEZ, Dena G, BRICE, Alexis, YLIKOTILA, Pauli, STEFANSSON, Hreinn, BRAS, Jose, MAJAMAA, Kari, MORRIS, Huw R, WILLIAMS, Nigel, GASSER, Thomas, HEUTINK, Peter, WOOD, Nicholas W, HARDY, John, MARTINEZ, Maria, SINGLETON, Andrew B, NALLS, Michael A, BETTELLA, Francesco, NICOLAOU, Nayia, SIMON-SANCHEZ, Javier, MITTAG, Florian, BÜCHEL, Finja, SHARMA, Manu, RAPHAEL GIBBS, J

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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases von Nalls, Mike A, Bras, Jose, Hernandez, Dena G, Keller, Margaux F, Majounie, Elisa, Renton, Alan E, Saad, Mohamad, Jansen, Iris, Guerreiro, Rita, Lubbe, Steven, Plagnol, Vincent, Gibbs, J. Raphael, Schulte, Claudia, Pankratz, Nathan, Sutherland, Margaret, Bertram, Lars, Lill, Christina M, DeStefano, Anita L, Faroud, Tatiana, Eriksson, Nicholas, Tung, Joyce Y, Edsall, Connor, Nichols, Noah, Brooks, Janet, Arepalli, Sampath, Pliner, Hannah, Letson, Chris, Heutink, Peter, Martinez, Maria, Gasser, Thomas, Traynor, Bryan J, Wood, Nick, Hardy, John, Singleton, Andrew B

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Genetic comorbidities in Parkinson's disease von Nalls, Mike A, Saad, Mohamad, Noyce, Alastair J, Keller, Margaux F, Schrag, Anette, Bestwick, Jonathan P, Traynor, Bryan J, Gibbs, J Raphael, Hernandez, Dena G, Cookson, Mark R, Morris, Huw R, Williams, Nigel, Gasser, Thomas, Heutink, Peter, Wood, Nick, Hardy, John, Martinez, Maria, Singleton, Andrew B

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The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism von Golmard, Jean-Louis, Hardy, John, Simon-Sanchez, Javier, Klein, Christine, Hagenah, Johann, Gasser, Thomas, Lesage, Suzanne, Deuschl, Günther, Tzourio, Christophe, Charbonnier-Beaupel, Fanny, Tahiri, Khadija, Martinez, Maria, Brice, Alexis, Agid, Y, Anheim, M, Brice, A., Broussolle, E, Durif, F, Klebe, S, Lohmann, E, Martinez, M, Penet, C, Pollak, P, Krack, P, Rascol, O, Tranchant, C, Bras, Jose M, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Simón-Sánchez, Javier, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Arepalli, Sampath, Band, Gavin, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob MA, Biffi, Alessandro, Bochdanovits, Zoltan, Bonin, Michael, Brooks, Janet, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cooper, J Mark, Corvol, Jean Christophe, Damier, Philippe, Dexter, David T, Dillman, Allissa, Foltynie, Thomas, Gao, Jianjun, Goate, Alison, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, Hellenthal, Garrett, van Hilten, Jacobus J, Hollenbeck, Albert, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Huttenlocher, Johanna, Langford, Cordelia, Lees, Andrew, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, Moorby, Catriona, Morrison, Karen E, Pearson, Justin, Perlmutter, Joel S, Pollak, Pierre, Post, Bart, Rizzu, Patrizia, Ryten, Mina, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, de Silva, Rohan, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Velseboer, Daan, Vukcevic, Damjan, Wickremaratchi, Mirdhu, Williams, Nigel, Winder-Rhodes, Sophie, Heutink, Peter, Brice, Alexis, Wood, Nicholas W, Singleton, Andrew B

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Susceptibility loci for pigmentation and melanoma in relation to Parkinson's disease von Dong, Jing, Gao, Jianjun, Nalls, Michael, Gao, Xiang, Huang, Xuemei, Han, Jiali, Singleton, Andrew B, Chen, Honglei

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Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities von Mittag, Florian, Büchel, Finja, Saad, Mohamad, Jahn, Andreas, Schulte, Claudia, Bochdanovits, Zoltan, Simón-Sánchez, Javier, Nalls, Mike A., Keller, Margaux, Hernandez, Dena G., Gibbs, J. Raphael, Lesage, Suzanne, Brice, Alexis, Heutink, Peter, Martinez, Maria, Wood, Nicholas W, Hardy, John, Singleton, Andrew B., Zell, Andreas, Gasser, Thomas, Sharma, Manu

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A susceptibility gene for late-onset idiopathic Parkinson's disease von Hicks, Andrew A., Pétursson, Hjörvar, Jónsson, Thorlákur, Stefánsson, Hreinn, Jóhannsdóttir, Hrefna S., Sainz, Jesus, Frigge, Michael L., Kong, Augustine, Gulcher, Jeffrey R., Stefánsson, Kári, Sveinbjörnsdóttir, Sigurlaug

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The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism von Klebe, S, Heutink, P, Charfi, R, Gao, J, Gardner, M, Goate, A, Guerreiro, R, Gústafsson, O, Hellenthal, G, Klein, C, Hofman, A, Holton, J, Huang, X, Hudson, G, Hunt, SE, Huttenlocher, J, Langford, C, Lichtner, P, Limousin, P, Moore, M, Morris, H, Gasser, T, Mudanohwo, E, O'Sullivan, SS, Pearson, J, Pearson, R, Perlmutter, JS, Pétursson, H, Pirinen, M, Post, B, Ravina, B, Revesz, T, Rivadeneira, F, Rizzu, P, Ryten, M, Sawcer, S, Scheffer, H, Shaw, K, Shoulson, I, Smith, C, Spencer, CCA, Stefánsson, H, Steinberg, S, Strange, A, Talbot, K, Lorenz, D, Tanner, CM, Tashakkori-Ghanbaria, A, Trabzuni, D, Uitterlinden, AG, Velseboer, D, Marie, V, Walker, R, Deuschl, G, Wickremaratchi, M, Williams-Gray, CH, Stefánsson, K, Durif, F, Pollak, P, Damier, P, Tison, F, Amouyel, P, Maubaret, C, Vidailhet, M, Corvol, JC, Borg, M, Broussolle, E, Corvol, J-C, Lohmann, E, Penet, C, Krack, P, Rascol, O, Tranchant, C, Vérin, M, Viallet, F, Hernandez, DG, Schulte, C, Arepalli, S, Vukcevic, D, Barker, RA, Bellinguez, C, Ben-Shlomo, Y, Berendse, HW, Berg, D, De Bie, RMA, Bloem, B, Bochdanovits, Z, Bonin, M, Brockmann, K, Burn, DJ, Charlesworth, G, Chinnery, PF, Cookson, MR, Dartigues, JF, Dexter, DT, Dillman, A, Edkins, S, Evans, JR, Foltynie, T, Freeman, C

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