المؤلفون: Holmans, Peter, Moskvina, Valentina, Jones, Lesley, Sharma, Manu, The International Parkinson's Disease Genomics Consortium (IPDGC), Vedernikov, Alexey, Buchel, Finja, Sadd, Mohamad, Bras, Jose M., Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Morris, Huw R., Williams, Nigel M., Arepalli, Sampath, Barker, Roger, Barrett, Jeffrey, Ben-Shlomo, Yoav, Berendse, Henk W., Berg, Daniela, Bhatia, Kailash, de Bie, Rob M.A., Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Brockmann, Kathrin, Brooks, Janet, Burn, David J., Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F., Chong, Sean, Clarke, Carl E., Cookson, Mark R., Cooper, Jonathan M., Corvol, Jen-Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean Francois, Deloukas, Panagiotis, Deuschl, Günther, Dexter, David T., van Dijk, Karin D., Dillman, Allissa, Durif, Frank, Edkins, Sarah, Evans, Jonathan R., Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Goate, Alison, Gray, Emma, Gústafsson, Ómar, Harris, Clare, Hernandez, Dena G., van Hilten, Jacobus J., Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E., Huttenlocher, Johanna, Illig, Thomas, Langford, Cordelia, Lees, Andrew, Lesage, Suzanne, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw, Morrison, Karen E., Mudanohwo, Ese, Pearson, Justin, Perlmutter, Joel S., Pétursson, Hjörvar, Plagnol, Vincent, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Saad, Mohamad, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Sheerin, Una-Marie, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Stefánsson, Kári, Steinberg, Stacy, Stockton, Joanna D., Sveinbjornsdottir, Sigurlaug, Talbot, Kevin, Tanner, Carlie M., Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J., Uitterlinden, AndréG., Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Wood, Nicholas

مصطلحات موضوعية: ASSOCIATION STUDIES ARTICLES

وصف الملف: text/html

العلاقة: http://hmg.oxfordjournals.org/cgi/content/short/22/5/1039Test; http://dx.doi.org/10.1093/hmg/dds492Test

الإتاحة: https://doi.org/10.1093/hmg/dds492Test
http://hmg.oxfordjournals.org/cgi/content/short/22/5/1039Test

المؤلفون: Holmans, Peter, Moskvina, Valentina, Jones, Lesley, Sharma, Manu, The International Parkinson's Disease Genomics Consortium (IPDGC), Vedernikov, Alexey, Buchel, Finja, Sadd, Mohamad, Bras, Jose M., Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Morris, Huw R., Williams, Nigel M., Arepalli, Sampath, Barker, Roger, Barrett, Jeffrey, Ben-Shlomo, Yoav, Berendse, Henk W., Berg, Daniela, Bhatia, Kailash, de Bie, Rob M.A., Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Brockmann, Kathrin, Brooks, Janet, Burn, David J., Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F., Chong, Sean, Clarke, Carl E., Cookson, Mark R., Cooper, Jonathan M., Corvol, Jen-Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean Francois, Deloukas, Panagiotis, Deuschl, Günther, Dexter, David T., van Dijk, Karin D., Dillman, Allissa, Durif, Frank, Edkins, Sarah, Evans, Jonathan R., Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Goate, Alison, Gray, Emma, Gústafsson, Ómar, Harris, Clare, Hernandez, Dena G., van Hilten, Jacobus J., Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E., Huttenlocher, Johanna, Illig, Thomas, Langford, Cordelia, Lees, Andrew, Lesage, Suzanne, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw, Morrison, Karen E., Mudanohwo, Ese, Pearson, Justin, Perlmutter, Joel S., Pétursson, Hjörvar, Plagnol, Vincent, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Saad, Mohamad, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Sheerin, Una-Marie, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Stefánsson, Kári, Steinberg, Stacy, Stockton, Joanna D., Sveinbjornsdottir, Sigurlaug, Talbot, Kevin, Tanner, Carlie M., Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J., Uitterlinden, AndréG., Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Wood, Nicholas

مصطلحات موضوعية: Article

وصف الملف: text/html

العلاقة: http://hmg.oxfordjournals.org/cgi/content/short/dds492v2Test; http://dx.doi.org/10.1093/hmg/dds492Test

الإتاحة: https://doi.org/10.1093/hmg/dds492Test
http://hmg.oxfordjournals.org/cgi/content/short/dds492v2Test

المؤلفون: Moskvina, Valentina, Harold, Denise, Nicolaou, Nayia, Simón-Sánchez, Javier, Gibbs, J Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Russo, GianCarlo, Gasser, Thomas, Heutink, Peter, Wood, Nick, Martinez, Maria, Singleton, Andrew B, Nalls, Michael A, Hardy, John, Owen, Michael J, O'Donovan, Michael C, Williams, Julie, Vedernikov, Alexey, Morris, Huw R, Williams, Nigel M, Investigators, IPDGC and GERAD, Dillman, Allissa, Brooks, Janet, Chong, Sean, Cookson, Mark R, Moore, Matthew, Keller, Margaux F, Sharma, Manu, Traynor, Bryan J, Arepalli, Sampath, Charlesworth, Gavin, Plagnol, Vincent, Ryten, Mina, Trabzuni, Daniah, Bras, Jose M, Saad, Mohamed, Sheerin, Una-Marie, Bhatia, Kailash, Saad, Mohamad, Bochdanovits, Zoltan, Rizzu, Patrizia, Vidailhet, Marie, Holmans, Peter, Corvol, Jen-Christophe, Curie, Pierre et Marie, Barker, Roger, Hunt, Sarah E, Gray, Emma, Edkins, Sarah, Tashakkori-Ghanbaria, Avazeh, Barrett, Jeffrey, Deloukasm, Panagiotis, Potter, Simon, Ben-Shlomo, Yoav, van Dijk, Karin D, Berendse, Henk W, Velseboer, Daan, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, van deWarrenburg, Bart, Post, Bart, Bettella, Francesco, Riess, Olaf, Bonin, Michael, Burn, David J

المساهمون: Human genetics, NCA - neurodegeneration, Graduate School, ANS - Amsterdam Neuroscience, Neurology

المصدر: JAMA Neurology, 70(10), 1268-1276. American Medical Association
Moskvina, V, Harold, D, Russo, G, Vedernikov, A, Sharma, M, Saad, M, Holmans, P, Bras, J M, Bettella, F, Keller, M F, Nicolaou, N, Simon-Sanchez, J, Gibbs, J R, Schulte, C, Durr, A, Guerreiro, R, Hernandez, D, Brice, A, Stefansson, H, Majamaa, K, Gasser, T, Heutink, P, Wood, N, Martinez, M, Singleton, A B, Nalls, M A, Hardy, J, Owen, M J, O'Donovan, M C, Williams, J, Morris, H R & Williams, N M 2013, ' Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk ', JAMA Neurology, vol. 70, no. 10, pp. 1268-1276 . https://doi.org/10.1001/jamaneurol.2013.448Test
JAMA neurology 70(10), 1268-1276 (2013). doi:10.1001/jamaneurol.2013.448

مصطلحات موضوعية: Adult, Male, statistics & numerical data [Databases, Factual], Databases, Factual, Genotype, genetics [Alzheimer Disease], Single-nucleotide polymorphism, Genome-wide association study, Disease, In Vitro Techniques, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Article, Gene Frequency, genetics [Parkinson Disease], Alzheimer Disease, Risk Factors, medicine, Humans, Dementia, Genetic Predisposition to Disease, ddc:610, genetics [Genetic Predisposition to Disease], Allele, Allele frequency, Aged, Genetic association, Aged, 80 and over, Genetics, Parkinson Disease, Middle Aged, medicine.disease, United States, Europe, Meta-analysis, genetics [Polymorphism, Single Nucleotide], Female, Neurology (clinical), Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dedc2a3d6c48522c8900ec88aa7d326Test
https://doi.org/10.1001/jamaneurol.2013.448Test