المؤلفون: Consortium, International Parkinson's Disease Genomics, 2, Wellcome Trust Case Control Consortium, Schulte, Claudia, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, de Silva, Rohan, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Lesage, Suzanne, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Su, Zhan, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Sveinbjörnsdóttir, Sigurlaug, Uitterlinden, André G, Vandrovcova, Jana, Velseboer, Daan, Vidailhet, Marie, Vukcevic, Damjan, Walker, Robert, van de Warrenburg, Bart, Weale, Michael E, Williams, Nigel, Williams-Gray, Caroline H, Amouyel, Philippe, Wickremaratchi, Mirdhu, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Donnelly, Peter, Singleton, Andrew B, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Arepalli, Sampath, Wood, Nicholas W, Band, Gavin, Barker, Roger A, Bellinguez, Céline, Ben-Shlomo, Yoav, Berendse, Henk W, Plagnol, Vincent, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Nalls, Michael A, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Bras, Jose M, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Dillman, Allissa, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, Evans, Jonathan R, Hernandez, Dena G, Foltynie, Thomas, Freeman, Colin, Gao, Jianjun, Gardner, Michelle, Gibbs, J Raphael, Goate, Alison, Gray, Emma, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, Sharma, Manu, Hellenthal, Garrett, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E, Sheerin, Una-Marie, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Saad, Mohamad, Moorby, Catriona, Moore, Matthew, Morris, Huw, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Pearson, Richard, Perlmutter, Joel S, Pétursson, Hjörvar, Simón-Sánchez, Javier, Pirinen, Matti, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina

المصدر: PLoS Genetics 7(6), e1002142 (2011). doi:10.1371/journal.pgen.1002142

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Brain: metabolism, DNA Methylation, Gene Expression Profiling, Gene Expression Regulation, Genetic Loci: genetics, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Parkinson Disease: genetics, Polymorphism, Single Nucleotide: genetics, Risk Assessment

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:21738488; info:eu-repo/semantics/altIdentifier/issn/1553-7390; info:eu-repo/semantics/altIdentifier/issn/1553-7404; https://pub.dzne.de/record/136256Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-02578%22Test

الإتاحة: https://doi.org/10.1371/journal.pgen.1002142Test
https://pub.dzne.de/record/136256Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-02578%22Test

المؤلفون: Guerreiro, Rita J., Beck, John, Gibbs, J. Raphael, Santana, Isabel, Rossor, Martin N., Schott, Jonathan M., Nalls, Michael A., Ribeiro, Helena, Santiago, Beatriz, Fox, Nick C., Oliveira, Catarina, Collinge, John, Mead, Simon, Singleton, Andrew, Hardy, John

العلاقة: PLoS ONE. 5:3 (2010) e9510; http://hdl.handle.net/10316/12861Test

الإتاحة: https://doi.org/10.1371/journal.pone.0009510Test
http://hdl.handle.net/10316/12861Test

المؤلفون: Nalls, Michael A., Simón-Sánchez, Javier, Gibbs, J. Raphael, Paisan-Ruiz, Coro, Bras, Jose Tomas, Tanaka, Toshiko, Matarin, Mar, Scholz, Sonja, Weitz, Charles, Harris, Tamara B., Ferrucci, Luigi, Hardy, John, Singleton, Andrew B.

وصف الملف: 153274 bytes; application/pdf

العلاقة: htpp://dx.doi.org/10.1371/journal.pgen.1000415; PLoS Genet;5 (3): e1000415; http://hdl.handle.net/10261/16325Test

الإتاحة: https://doi.org/10.1371/journal.pgen.1000415Test
http://hdl.handle.net/10261/16325Test

المؤلفون: Melzer, David, Perry, John R. B., Hernandez, Dena, Corsi, Anna-Maria, Stevens, Kara, Rafferty, Ian, Lauretani, Fulvio, Murray, Anna, Gibbs, J. Raphael, Paolisso, Giuseppe, Rafiq, Sajjad, Simon-Sanchez, Javier, Lango, Hana, Scholz, Sonja, Weedon, Michael N., Arepalli, Sampath, Rice, Neil, Washecka, Nicole, Hurst, Alison, Britton, Angela, Henley, William, van de Leemput, Joyce, Li, Rongling, Newman, Anne B., Tranah, Greg, Harris, Tamara, Panicker, Vijay, Dayan, Colin Mark, Bennett, Amanda, McCarthy, Mark I., Ruokonen, Aimo, Jarvelin, Marjo-Riitta, Guralnik, Jack, Bandinelli, Stefania, Frayling, Timothy M., Singleton, Andrew, Ferrucci, Luigi

مصطلحات موضوعية: QH426 Genetics, R Medicine (General)

وصف الملف: application/pdf

العلاقة: https://orca.cardiff.ac.uk/id/eprint/28700/1/Melzer%202008.pdfTest; Melzer, David, Perry, John R. B., Hernandez, Dena, Corsi, Anna-Maria, Stevens, Kara, Rafferty, Ian, Lauretani, Fulvio, Murray, Anna, Gibbs, J. Raphael, Paolisso, Giuseppe, Rafiq, Sajjad, Simon-Sanchez, Javier, Lango, Hana, Scholz, Sonja, Weedon, Michael N., Arepalli, Sampath, Rice, Neil, Washecka, Nicole, Hurst, Alison, Britton, Angela, Henley, William, van de Leemput, Joyce, Li, Rongling, Newman, Anne B., Tranah, Greg, Harris, Tamara, Panicker, Vijay, Dayan, Colin Mark https://orca.cardiff.ac.uk/view/cardiffauthors/A192115G.htmlTest orcid:0000-0002-6557-3462 orcid:0000-0002-6557-3462, Bennett, Amanda, McCarthy, Mark I., Ruokonen, Aimo, Jarvelin, Marjo-Riitta, Guralnik, Jack, Bandinelli, Stefania, Frayling, Timothy M., Singleton, Andrew and Ferrucci, Luigi 2008. A genome-wide association study identifies protein quantitative trait loci (pQTLs). PLoS Genetics 4 (5) , e1000072. 10.1371/journal.pgen.1000072 https://doi.org/10.1371/journal.pgen.1000072Test file https://orca.cardiff.ac.uk/id/eprint/28700/1/Melzer%202008.pdfTest

الإتاحة: https://doi.org/10.1371/journal.pgen.1000072Test
https://orca.cardiff.ac.uk/id/eprint/28700Test/
https://orca.cardiff.ac.uk/id/eprint/28700/1/Melzer%202008.pdfTest

المؤلفون: Guven, Gamze, Lohmann, Ebba, Bras, Jose, Gibbs, J. Raphael, Gurvit, Hakan, Bilgic, Basar, Hanagasi, Hasmet, Rizzu, Patrizia, Heutink, Peter, Emre, Murat, Erginel-Unaltuna, Nihan, Just, Walter, Hardy, John, Singleton, Andrew, Guerreiro, Rita

المصدر: PLoS ONE; 9/15/2016, Vol. 11 Issue 9, p1-16, 16p

مصطلحات موضوعية: FRONTOTEMPORAL dementia, GENETIC mutation, MICROTUBULE-associated proteins, C9ORF72 gene, EXOMES, GENETICS

المؤلفون: Wood, Andrew R., Perry, John R. B., Tanaka, Toshiko, Hernandez, Dena G., Zheng, Hou-Feng, Melzer, David, Gibbs, J. Raphael, Nalls, Michael A., Weedon, Michael N., Spector, Tim D., Richards, J. Brent, Bandinelli, Stefania, Ferrucci, Luigi, Singleton, Andrew B., Frayling, Timothy M.

المصدر: PLoS ONE; May2013, Vol. 8 Issue 5, p1-13, 13p

مصطلحات موضوعية: GENETIC polymorphisms, PHENOTYPES, POPULATION genetics, HUMAN genetics, GLOBULINS, HAPLOTYPES, TRYPSIN inhibitors

المؤلفون: Gibbs, J. Raphael^1,2, van der Brug, Marcel P.^1,3, Hernandez, Dena G.^1,2, Traynor, Bryan J.¹, Nalls, Michael A.¹, Shiao-Lin Lai^1,2, Arepalli, Sampath¹, Dillman, Allissa¹, Rafferty, Ian P.¹, Troncoso, Juan⁴, Johnson, Robert⁵, Zielke, H. Ronald⁵, Ferrucci, Luigi⁶, Longo, Dan L.⁷, Cookson, Mark R.¹ cookson@mail.nih.gov, Singleton, Andrew B.¹ singleta@mail.nih.gov

المصدر: PLoS Genetics. May2010, Vol. 6 Issue 5, p1-13. 13p. 4 Charts, 5 Graphs.

مصطلحات موضوعية: *GENOMES, *METHYLATION, *GENETIC regulation, *BRAIN, *GENE expression

المؤلفون: Gibbs, J. Raphael¹, Singleton, Andrew² singleta@mail.nih.gov

المصدر: PLoS Genetics. Oct2006, Vol. 3 Issue 4, p1511-1517. 7p.

مصطلحات موضوعية: *GENOMES, *NUCLEOTIDES, *GENETIC polymorphisms, *HUMAN genetic variation, *GENE mapping