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

المصدر: ADHD Attention Deficit and Hyperactivity Disorders 9(2), 121-127 (2017). doi:10.1007/s12402-017-0219-8

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Attention Deficit Disorder with Hyperactivity: genetics, Genetic Association Studies, Genetic Predisposition to Disease: genetics, Humans, Parkinson Disease: genetics, Polymorphism, Single Nucleotide: genetics

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1866-6116; info:eu-repo/semantics/altIdentifier/issn/1866-6647; info:eu-repo/semantics/altIdentifier/pmid/pmid:28176268; https://pub.dzne.de/record/139288Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-05610%22Test

الإتاحة: https://doi.org/10.1007/s12402-017-0219-8Test
https://pub.dzne.de/record/139288Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-05610%22Test

المؤلفون: Jansen, Iris E, Ye, Hui, Gibbs, J Raphael, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, Lungu, Codrin, Nalls, Mike A, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Escott-Price, Valentina, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Perlmutter, Joel S, Ryten, Mina, Pétursson, Hjörvar, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Sawcer, Stephen, Botia, Juan A, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Shulman, Joshua, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Bettella, Francesco, Vandrovcova, Jana, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Simon Sanchez, Javier, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Wood, Nicholas W, Castillo Lizardo, Melissa Gissel, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K, Heetveld, Sasja, Li, Yarong, Yogi, Puja, Amin, Najaf, van Duijn, Cornelia M, Consortium, International Parkinson’s Disease Genetics, David, Della C, Nollen, Ellen A, Lechler, Marie C, Jain, Shushant, Shulman, Joshua M, Plagnol, Vincent, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Saad, Mohamad, SimónSánchez, Javier, Schulte, Claudia, Michels, Helen, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Arepalli, Sampath, Barker, Roger, Ben-Shlomo, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Seinstra, Renée I, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Majounie, Elisa, Lubbe, Steven, Price, Ryan, Lubbe, Steven J, Nicolas, Aude, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Cooper, J Mark, Corvol, Jean Christophe, Drouet, Valérie, Counsell, Carl, Damier, Philippe, 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, Foltynie, Thomas, Dong, Jing, Gardner, Michelle, Goate, Alison, Gray, Emma, Guerreiro, Rita, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Wurster, Isabel, Mätzler, Walter, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna

المصدر: Genome biology 18(1), 22 (2017). doi:10.1186/s13059-017-1147-9

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Adolescent, Adult, Animals, Genetically Modified, Caenorhabditis elegans: genetics, Case-Control Studies, Cells, Cultured, Child, Disease Models, Animal, Drosophila melanogaster: genetics, Exome, Genetic Predisposition to Disease, High-Throughput Nucleotide Sequencing: methods, Humans, Middle Aged, Parkinson Disease: genetics, RNA Interference, Sequence Analysis, DNA: methods, Young Adult, alpha-Synuclein: genetics, alpha-Synuclein

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1474-760X; info:eu-repo/semantics/altIdentifier/issn/1465-6914; info:eu-repo/semantics/altIdentifier/pmid/pmid:28137300; info:eu-repo/semantics/altIdentifier/issn/1465-6906; info:eu-repo/semantics/altIdentifier/issn/1474-7596; https://pub.dzne.de/record/139064Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-05386%22Test

الإتاحة: https://doi.org/10.1186/s13059-017-1147-9Test
https://pub.dzne.de/record/139064Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-05386%22Test

المؤلفون: Lesage, Suzanne, Drouet, Valérie, Erpapazoglou, Zoi, Bras, Jose M, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Counsell, Carl, Usenko, Tatiana, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Dillman, Allissa, Dong, Jing, Durif, Frank, Edkins, Sarah, Maurage, Claude-Alain, Escott-Price, Valentina, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Goate, Alison, Gray, Emma, Guerreiro, Rita, Harris, Clare, van Hilten, Jacobus J, Sahbatou, Mourad, Hofman, Albert, Hollenbeck, Albert, Holmans, Peter, Holton, Janice, Hu, Michèle, Huang, Xuemei, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Illig, Thomas, Liebau, Stefan, Jónsson, Pálmi V, Kilarski, Laura L, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, Lubbe, Steven, Ding, Jinhui, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean S, Owen, Michael J, Bilgic, Basar, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Plagnol, Vincent, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Emre, Murat, Rivadeneira, Fernando, Ryten, Mina, Saad, Mohamad, Simón-Sánchez, Javier, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Sheerin, Una-Marie, Shoulson, Ira, Erginel-Unaltuna, Nihan, Shulman, Joshua, Sidransky, Ellen, Spencer, Chris C A, Stefánsson, Hreinn, Stefánsson, Kári, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Guven, Gamze, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Williams, Nigel, Majounie, Elisa, Tison, François, Morris, Huw R, Hardy, John, Wood, Nicholas W, Singleton, Andrew B, Brice, Alexis, Tranchant, Christine, Vidailhet, Marie, Corvol, Jean-Christophe, Krack, Paul, Leutenegger, Anne-Louise, Nalls, Michael A, Hernandez, Dena G, Heutink, Peter, Gibbs, J Raphael, Deramecourt, Vincent, Gasser, Thomas, Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Kabashi, Edor, Singleton, Andrew, Jacoupy, Maxime, Corti, Olga, Study, French Parkinson's Disease Genetics, Consortium, International Parkinson's Disease Genomics, Agid, Yves, Anheim, Mathieu, Nicolas, Aude, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Klebe, Stephan, Martinez, Maria, Cormier-Dequaire, Florence, Rascol, Olivier, Vérin, Marc, Viallet, François, Corvol, Jean Christophe, Hassoun, Sidi Mohamed, Arepalli, Sampath, Barker, Roger A, Bettella, Francesco, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bastiaan R, Bochdanovits, Zoltan, Pujol, Claire, Bonin, Michael, Ciura, Sorana

المصدر: The American journal of human genetics 98(3), 500-513 (2016). doi:10.1016/j.ajhg.2016.01.014

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Adult, Aged, Animals, COS Cells, Case-Control Studies, Consanguinity, Female, Gene Silencing, Genetic Heterogeneity, HEK293 Cells, Heterozygote, Homozygote, Humans, Male, Middle Aged, Mitophagy: genetics, Parkinsonian Disorders: diagnosis, Parkinsonian Disorders: genetics, Pedigree, Phenotype, Protein Kinases: genetics, Protein Kinases: metabolism, Proteins: genetics, Proteins: metabolism, Reproducibility of Results, Turkey, Ubiquitin-Protein Ligases: genetics, Ubiquitin-Protein Ligases: metabolism, Proteins

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1537-6605; info:eu-repo/semantics/altIdentifier/issn/0002-9297; info:eu-repo/semantics/altIdentifier/pmid/pmid:26942284; https://pub.dzne.de/record/138456Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-04778%22Test

الإتاحة: https://doi.org/10.1016/j.ajhg.2016.01.014Test
https://pub.dzne.de/record/138456Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-04778%22Test

المؤلفون: Bramon, Elvira, Pirinen, Matti, Strange, Amy, Lin, Kuang, Freeman, Colin, Bellenguez, Celine, Su, Zhan, Band, Gavin, Pearson, Richard, Vukcevic, Damjan, Langford, Cordelia, Deloukas, Panos, Hunt, Sarah, Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Edkins, Sarah, Bumpstead, Suzannah J., Arranz, Maria J., Bakker, Steven, Bender, Stephan, Bruggeman, Richard, Cahn, Wiepke, Chandler, David, Collier, David A., Crespo-Facorro, Benedicto, Dazzan, Paola, de Haan, Lieuwe, di Forti, Marta, Dragovic, Milan, Giegling, Ina, Hall, Jeremy, Iyegbe, Conrad, Jablensky, Assen, Kahn, Rene S., Kalaydjieva, Luba, Kravariti, Eugenia, Lawrie, Stephen, Lins-Zen, Don H., Mata, Ignacio, McDonald, Colm, McIntosh, Andrew, Myin-Germeys, Inez, Ophoff, Roel A., Pariante, Carmine M., Paunio, Tiina, Picchioni, Marco, Ripke, Stephan, Rujescu, Dan, Sauer, Heinrich, Shaikh, Madiha, Sussmann, Jessika, Suvisaari, Jaana, Tosato, Sarah, Toulopoulou, Timothea, Van Os, Jim, Walshe, Muriel, Weisbrod, Matthias, Whalley, Heather, Wiersma, Durk, Blackwell, Jenefer M., Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz A. Z., Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Wood, Nicholas W., Barroso, Ines, Peltonen, Leena, Lewis, Cathryn M., Murray, Robin M., Donnelly, Peter, Powell, John, Spencer, Chris C. A.

المصدر: Bramon , E , Pirinen , M , Strange , A , Lin , K , Freeman , C , Bellenguez , C , Su , Z , Band , G , Pearson , R , Vukcevic , D , Langford , C , Deloukas , P , Hunt , S , Gray , E , Dronov , S , Potter , S C , Tashakkori-Ghanbaria , A , Edkins , S , Bumpstead , S J , Arranz , M J , Bakker , S , Bender , S , Bruggeman , R , Cahn , W , ....

مصطلحات موضوعية: Bipolar disorder, genome-wide association, meta-analysis, polygenic score analysis, psychosis, schizophrenia

الإتاحة: https://doi.org/10.1016/j.biopsych.2013.03.033Test
https://cris.maastrichtuniversity.nl/en/publications/9bb6e977-e91c-4ddd-9c2e-ee8254455a83Test

المؤلفون: Nalls, Mike A, Pankratz, Nathan, Schulte, Claudia, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, Evans, Jonathan R, Foltynie, Thomas, Dong, Jing, Gardner, Michelle, Gibbs, J Raphael, Goate, Alison, Gray, Emma, Keller, Margaux F, Guerreiro, Rita, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Wurster, Isabel, Mätzler, Walter, Arepalli, Sampath, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Letson, Christopher, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Edsall, Connor, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Stefansson, Hreinn, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Liu, Xinmin, Bettella, Francesco, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Pliner, Hannah, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Lee, Joseph H, Wood, Nicholas W, Hardy, John, Brice, Alexis, Singleton, Andrew B, Factor, S., Higgins, D., Evans, S., Shill, H., Stacy, M., Danielson, J., Cheng, Rong, Marlor, L., Williamson, K., Jankovic, J., Hunter, C., Simon, D., Ryan, P., Scollins, L., Saunders-Pullman, R., Boyar, K., Costan-Toth, C., Lill, Christina M, Consortium, International Parkinson's Disease Genomics, Ohmann, E., Sudarsky, L., Joubert, C., Friedman, J., Chou, K., Fernandez, H., Lannon, M., Galvez-Jimenez, N., Podichetty, A., Thompson, K., Group, Parkinson's Study, Lewitt, P., DeAngelis, M., O'Brien, C., Seeberger, L., Dingmann, C., Judd, D., Marder, K., Fraser, J., Harris, J., Bertoni, J., 23andMe, Peterson, C., Rezak, M., Medalle, G., Chouinard, S., Panisset, M., Hall, J., Poiffaut, H., Calabrese, V., Roberge, P., Wojcieszek, J., GenePD, Belden, J., Jennings, D., Marek, K., Mendick, S., Reich, S., Dunlop, B., Jog, M., Horn, C., Uitti, R., Turk, M., Consortium, NeuroGenetics Research, Ajax, T., Mannetter, J., Sethi, K., Carpenter, J., Dill, B., Hatch, L., Ligon, K., Narayan, S., Blindauer, K., Abou-Samra, K., Genomics, Hussman Institute of Human, Petit, J., Elmer, L., Aiken, E., Davis, K., Schell, C., Wilson, S., Velickovic, M., Koller, W., Phipps, S., Feigin, A., Investigator, Ashkenazi Jewish Dataset, Gordon, M., Hamann, J., Licari, E., Marotta-Kollarus, M., Shannon, B., Winnick, R., Simuni, T., Videnovic, A., Kaczmarek, A., Williams, K., Epidemiology, Cohorts for Health and Aging Research in Genetic, Wolff, M., Rao, J., Cook, M., Fernandez, M., Kostyk, S., Hubble, J., Campbell, A., Reider, C., Seward, A., Camicioli, R., Consortium, North American Brain Expression, Carter, J., Nutt, J., Andrews, P., Morehouse, S., Stone, C., Mendis, T., Grimes, D., Alcorn-Costa, C., Gray, P., Haas, K., Consortium, United Kingdom Brain Expression, Vendette, J., Sutton, J., Hutchinson, B., Young, J., Rajput, A., Klassen, L., Shirley, T., Manyam, B., Simpson, P., Whetteckey, J., Do, Chuong B, Consortium, Greek Parkinson's Disease, Wulbrecht, B., Truong, D., Pathak, M., Frei, K., Luong, N., Tra, T., Tran, A., Vo, J., Lang, A., Kleiner- Fisman, G., Group, Alzheimer Genetic Analysis, Nieves, A., Johnston, L., So, J., Podskalny, G., Giffin, L., Atchison, P., Allen, C., Martin, W., Wieler, M., Suchowersky, O., Ikram, M Arfan, Furtado, S., Klimek, M., Hermanowicz, N., Niswonger, S., Shults, C., Fontaine, D., Aminoff, M., Christine, C., Diminno, M., Hevezi, J., Ioannidis, John P A, Dalvi, A., Kang, U., Richman, J., Uy, S., Sahay, A., Gartner, M., Schwieterman, D., Hall, D., Hadjigeorgiou, Georgios M, Leehey, M., Culver, S., Derian, T., Demarcaida, T., Thurlow, S., Rodnitzky, R., Dobson, J., Lyons, K., Pahwa, R., Gales, T., Bis, Joshua C, Thomas, S., Shulman, L., Weiner, W., Dustin, K., Singer, C., Zelaya, L., Tuite, P., Hagen, V., Rolandelli, S., Schacherer, R., Kosowicz, J., Gordon, P., Werner, J., Serrano, C., Roque, S., Kurlan, R., Berry, D., Gardiner, I., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Price, K., Rodriguez, P., Wolfrath, S., Pfeiffer, R., Davis, L., Pfeiffer, B., Dewey, R., Hayward, B., Johnson, A., Meacham, M., Estes, B., Walker, F., Hunt, V., O'Neill, C., Marder, Karen, Racette, B., Swisher, L., Dijamco, Cheri, Conley, Emily Drabant, Dorfman, Elizabeth, Tung, Joyce Y, Hinds, David A, Mountain, Joanna L, Wojcicki, Anne, Lew, M., Hernandez, Dena G, Fiske, Brian, Klein, C., Golbe, L., Growdon, J., Wooten, G. F., Watts, R., Guttman, M., Sutherland, Margaret, Goldwurm, S., Saint-Hilaire, M. H., Baker, K., Litvan, I., Nicholson, G., Nance, M., Drasby, E., Isaacson, S., Burn, D., Xiromerisiou, Georgia, Pramstaller, P., Al-hinti, J., Moller, A., Sherman, S., Roxburgh, R., Slevin, J., Perlmutter, J., Mark, M. H., Huggins, N., Pezzoli, G., Myers, Richard H, Massood, T., Itin, I., Corbett, A., Chinnery, P., Ostergaard, K., Snow, B., Cambi, F., Kay, D., Samii, A., Clark, Lorraine N, Agarwal, P., Roberts, J. W., Higgins, D. S., Molho, Eric, Rosen, Ami, Montimurro, J., Martinez, E., Griffith, A., Kusel, V., Yearout, D., Stefansson, Kari, Zabetian, C., Clark, L. N., Liu, X., Lee, J. H., Taub, R Cheng, Louis, E. D., Cote, L. J., Waters, C., Hardy, John A, Ford, B., Fahn, S., Vance, Jeffery M, Beecham, Gary W, Martin, Eden R, Nuytemans, Karen, Pericak-Vance, Margaret A, Haines, Jonathan L, DeStefano, Anita, Seshadri, Sudha, Heutink, Peter, Choi, Seung Hoan, Frank, Samuel, Psaty, Bruce M, Rice, Kenneth, Longstreth, W. T., Ton, Thanh G N, Jain, Samay, van Duijn, Cornelia M, Chen, Honglei, Verlinden, Vincent J, Koudstaal, Peter J, Singleton, Andrew, Cookson, Mark, Hernandez, Dena, Dillman, Allissa, Nalls, Michael, Zonderman, Alan, Ferrucci, Luigi, Johnson, Robert, Longo, Dan, O'Brien, Richard, Traynor, Bryan, Troncoso, Juan, van der Brug, Marcel, Zielke, Ronald, Saad, Mohamad, Houlden, Henry, Weale, Michael, Ramasamy, Adaikalavan, Kara, Eleanna, Dardiotis, Efthimios, Payami, Haydeh, Tsimourtou, Vana, Spanaki, Cleanthe, Plaitakis, Andreas, Bozi, Maria, Stefanis, Leonidas, Vassilatis, Dimitris, Koutsis, Georgios, Panas, Marios, Lunnon, Katie, Lupton, Michelle, Powell, John, Parkkinen, Laura, Ansorge, Olaf, Scott, William K, Gasser, Thomas, Bertram, Lars, Eriksson, Nicholas, Foroud, Tatiana, DeStefano, Anita L, Plagnol, Vincent, Sharma, Manu, Sheerin, Una-Marie, Simón-Sánchez, Javier, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Barker, Roger, Ben-Shlomo, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chinnery, Patrick F, Chong, Sean, Clarke, Carl E, Cookson, Mark R, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, van Dijk, Karin D

المصدر: Nature genetics 46(9), 989-993 (2014). doi:10.1038/ng.3043

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Case-Control Studies, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study: methods, Genotype, Humans, Parkinson Disease: genetics, Polymorphism, Single Nucleotide, Risk Factors

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:25064009; info:eu-repo/semantics/altIdentifier/issn/1546-1718; info:eu-repo/semantics/altIdentifier/issn/1061-4036; https://pub.dzne.de/record/137538Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-03860%22Test

الإتاحة: https://doi.org/10.1038/ng.3043Test
https://pub.dzne.de/record/137538Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-03860%22Test

المؤلفون: Nalls, Mike A, Saad, Mohamad, Morris, Huw R, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Williams, Nigel, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Sidransky, Ellen, Gasser, Thomas, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Steinberg, Stacy, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Tison, François, Heutink, Peter, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams-Gray, Caroline H, Wood, Nick, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Hardy, John, Brice, Alexis, Singleton, Andrew B, Wood, Nicholas W, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Pirinen, Matti, Pearson, Richard, Su, Zhan, Vukcevic, Damjan, Consortium, International Parkinson's Disease Genomics, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, 2, Wellcome Trust Case Control Consortium, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Noyce, Alastair J, Consortium, North American Brain Expression, McCarthy, Mark I, Cookson, Mark R, Consortium, United Kingdom Brain Expression, Gibbs, J Raphael, Hernandez, Dena G, Dillman, Allissa, Nalls, Michael A, Zonderman, Alan B, Arepalli, Sampath, Ferrucci, Luigi, Johnson, Robert, Longo, Dan L, O'Brien, Richard, Nalls, Mike, Traynor, Bryan, Troncoso, Juan, van der Brug, Marcel, Zielke, Ronald H, Weale, Michael E, Ramasamy, Adaikalavan, Plagnol, Vincent, Walker, Rober, Sharma, Manu, Sheerin, Una-Marie, Simón-Sánchez, Javier, Schulte, Claudia, Keller, Margaux F, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Barker, Roger, Ben-Shlomo, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Biffi, Alessandro, Schrag, Anette, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Charlesworth, Gavin, Chen, Honglei, Chinnery, Patrick F, Bestwick, Jonathan P, Chong, Sean, Clarke, Carl E, Cooper, J Mark, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deuschl, Günther, Dexter, David T, van Dijk, Karin D, Durif, Frank, Dürr, Alexandra, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Goate, Alison, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Huber, Heiko, Hudson, Gavin, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Lees, Andrew, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morrison, Karen E

المصدر: Human molecular genetics 23(3), 831-841 (2013). doi:10.1093/hmg/ddt465

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Comorbidity, CpG Islands, Crohn Disease: epidemiology, Crohn Disease: genetics, DNA Methylation, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Parkinson Disease: epidemiology, Parkinson Disease: genetics, Polymorphism, Single Nucleotide, Risk Factors, Schizophrenia: epidemiology, Schizophrenia: genetics

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0964-6906; info:eu-repo/semantics/altIdentifier/pmid/pmid:24057672; info:eu-repo/semantics/altIdentifier/issn/1460-2083; https://pub.dzne.de/record/137253Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-03575%22Test

الإتاحة: https://doi.org/10.1093/hmg/ddt465Test
https://pub.dzne.de/record/137253Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-03575%22Test

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

المؤلفون: Ang, Yeng, Su, Zhan, Gay, Laura J, Strange, Amy, Palles, Claire, Band, Gavin, Whiteman, David C, Lescai, Francesco, Langford, Cordelia, Nanji, Manoj, Edkins, Sarah, Winkel, Anouk van der, Levine, David, Sasieni, Peter, Bellenguez, Céline, Howarth, Kimberley, Freeman, Colin, Trudgill, Nigel, Tucker, Art T, Pirinen, Matti, Peppelenbosch, Maikel P, Laan, Luc JW van der, Kuipers, Ernst J, Drenth, Joost PH, Peters, Wilbert H, Reynolds, John V, Kelleher, Dermot P, McManus, Ross, Grabsch, Heike, Prenen, Hans, Bisschops, Raf, Krishnadath, Kausila, Siersema, Peter D, Baal, Jantine WPM van, Middleton, Mark, Petty, Russell, Gillies, Richard, Burch, Nicola, Bhandari, Pradeep, Paterson, Stuart, Edwards, Cathryn, Penman, Ian, Vaidya, Kishor, Murray, Iain, Patel, Praful, Ye, Weimin, Mullins, Paul, Wu, Anna H, Bird, Nigel C, Dallal, Helen, Shaheen, Nicholas J, Murray, Liam J, Koss, Konrad, Bernstein, Leslie, Romero, Yvonne, Hardie, Laura J, Zhang, Rui, Winter, Helen, Corley, Douglas A, Panter, Simon, Risch, Harvey A, Reid, Brian J, Sargeant, Ian, Gammon, Marilie D, Smart, Howard, Dhar, Anjan, McMurtry, Hugh, Ali, Haythem, Liu, Geoffrey, Casson, Alan G, Chow, Wong-Ho, Rutter, Matt, Tawil, Ashref, Morris, Danielle, Nwokolo, Chuka, Isaacs, Peter, Rodgers, Colin, Ragunath, Krish, MacDonald, Chris, Haigh, Chris, Monk, David, Davies, Gareth, Wajed, Saj, Johnston, David, Gibbons, Michael, Cullen, Sue, Church, Nicholas, Langley, Ruth, Griffin, Michael, Alderson, Derek, Deloukas, Panos, Hunt, Sarah E, Gray, Emma, Dronov, Serge, Potter, Simon C, Tashakkori-Ghanbaria, Avazeh, Anderson, Mark, Brooks, Claire, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin NA, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas, Trynka, Gosia, Wijmenga, Cisca, Cazier, Jean-Baptiste, Atherfold, Paul, Nicholson, Anna M, Gellatly, Nichola L, Glancy, Deborah, Cooper, Sheldon C, Cunningham, David, Lind, Tore, Hapeshi, Julie, Ferry, David, Rathbone, Barrie, Brown, Julia, Love, Sharon, Attwood, Stephen, MacGregor, Stuart, Watson, Peter, Sanders, Scott, Ek, Weronica, Harrison, Rebecca F, Moayyedi, Paul, Caestecker, John de, Barr, Hugh, Stupka, Elia, Vaughan, Thomas L, Peltonen, Leena, Spencer, Chris CA, Tomlinson, Ian, Donnelly, Peter, Jankowski, Janusz AZ

المصدر: Ang , Y , Su , Z , Gay , L J , Strange , A , Palles , C , Band , G , Whiteman , D C , Lescai , F , Langford , C , Nanji , M , Edkins , S , Winkel , A V D , Levine , D , Sasieni , P , Bellenguez , C , Howarth , K , Freeman , C , Trudgill , N , Tucker , A T , Pirinen , M , Peppelenbosch , M P , Laan , L JW V D , Kuipers , ....

الإتاحة: https://research.manchester.ac.uk/en/publications/77f62545-81b1-4572-9b22-257cc0b6136dTest

المؤلفون: The Esophageal Adenocarcinoma Genetics Consortium, The Wellcome Trust Case Control Consortium 2, Su, Zhan, Gay, Laura J, Strange, Amy, Palles, Claire, Band, Gavin, Whiteman, David C, Lescai, Francesco, Langford, Cordelia, Nanji, Manoj, Koss, Konrad, Bernstein, Leslie, Romero, Yvonne, Hardie, Laura J, Zhang, Ruixin, Winter, Helen, Corley, Douglas A, Panter, Simon, Risch, Harvey A, Reid, Brian J, Blackwell, Jenefer M, Sargeant, Ian, Gammon, Marilie D, Smart, Howard, Dhar, Anjan, McMurtry, Hugh, Ali, Haythem, Liu, Geoffrey, Casson, Alan G, Chow, Wong-Ho, Rutter, Matt, Bramon, Elvira, Tawil, Ashref, Morris, Danielle, Nwokolo, Chuka, Isaacs, Peter, Rodgers, Colin, Ragunath, Krish, Macdonald, Chris, Haigh, Chris, Monk, David, Davies, Gareth, Brown, Matthew A, Wajed, Saj, Johnston, David, Gibbons, Michael, Cullen, Sue, Church, Nicholas, Langley, Ruth, Griffin, Michael, Alderson, Derek, Deloukas, Panos, Hunt, Sarah E, Casas, Juan P, Gray, Emma, Dronov, Serge, Potter, Simon C, Tashakkori-Ghanbaria, Avazeh, Anderson, Mark, Brooks, Claire, Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Edkins, Sarah, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas, Trynka, Gosia, Wijmenga, Cisca, Cazier, Jean-Baptiste, Atherfold, Paul, Nicholson, Anna M, van der Winkel, Anouk, Gellatly, Nichola L, Glancy, Deborah, Cooper, Sheldon C, Cunningham, David, Lind, Tore, Hapeshi, Julie, Ferry, David, Rathbone, Barrie, Brown, Julia, Love, Sharon, Levine, David, Attwood, Stephen, Macgregor, Stuart, Watson, Peter, Sanders, Scott, Ek, Weronica, Harrison, Rebecca F, Moayyedi, Paul, de Caestecker, John, Barr, Hugh, Stupka, Elia, Sasieni, Peter, Vaughan, Thomas L, Peltonen, Leena, Spencer, Chris C A, Tomlinson, Ian, Donnelly, Peter, Jankowski, Janusz A Z, Bellenguez, Céline, Howarth, Kimberley, Freeman, Colin, Trudgill, Nigel, Tucker, Art T, Pirinen, Matti, Peppelenbosch, Maikel P, van der Laan, Luc J W, Kuipers, Ernst J, Drenth, Joost P H, Peters, Wilbert H, Reynolds, John V, Kelleher, Dermot P, McManus, Ross, Grabsch, Heike, Prenen, Hans, Bisschops, Raf, Krishnadath, Kausila, Siersema, Peter D, van Baal, Jantine W P M, Middleton, Mark, Petty, Russell, Gillies, Richard, Burch, Nicola, Bhandari, Pradeep, Paterson, Stuart, Edwards, Cathryn, Penman, Ian, Vaidya, Kishor, Ang, Yeng, Murray, Iain, Patel, Praful, Ye, Weimin, Mullins, Paul, Wu, Anna H, Bird, Nigel C, Dallal, Helen, Shaheen, Nicholas J, Murray, Liam J

العلاقة: Nature Genetics vol:44 issue:10 pages:1131-1136; https://lirias.kuleuven.be/handle/123456789/366755Test; http://dx.doi.org/10.1038/ng.2408Test

الإتاحة: https://doi.org/10.1038/ng.2408Test
https://lirias.kuleuven.be/handle/123456789/366755Test

المؤلفون: Su, Zhan, Gay, Laura J., Strange, Amy, Palles, Claire, Band, Gavin, Whiteman, David C., Lescai, Francesco, Langford, Cordelia, Nanji, Manoj, Edkins, Sarah, Van Der Winkel, Anouk, Levine, David, Sasieni, Peter, Bellenguez, Celine, Howarth, Kimberley, Freeman, Colin, Trudgill, Nigel, Tucker, Art T., Pirinen, Matti, Peppelenbosch, Maikel P., Van Der Laan, Luc J.W., Kuipers, Ernst J., Drenth, Joost P.H., Peters, Wilbert H., Reynolds, John V., Kelleher, Dermot P., McManus, Ross, Grabsch, Heike, Prenen, Hans, Bisschops, Raf, Krishnadath, Kausila, Siersema, Peter D., Van Baal, Jantine W.P.M., Middleton, Mark, Petty, Russell, Gillies, Richard, Burch, Nicola, Bhandari, Pradeep, Paterson, Stuart, Edwards, Cathryn, Penman, Ian, Vaidya, Kishor, Ang, Yeng, Murray, Iain, Patel, Praful, Ye, Weimin, Mullins, Paul, Wu, Anna H., Bird, Nigel C., Dallal, Helen, Shaheen, Nicholas J., Murray, Liam J., Koss, Konrad, Bernstein, Leslie, Romero, Yvonne, Hardie, Laura J., Zhang, Rui, Winter, Helen, Corley, Douglas .A., Panter, Simon, Risch, Harvey A., Reid, Brian J., Sargeant, Ian, Gammon, Marilie D., Smart, Howard, Dhar, Anjan, McMurtry, Hugh, Ali, Haythem, Liu, Geoffrey, Casson, Allan G., Chow, Wong-Ho, Rutter, Matt, Tawil, Ashref, Morris, Danielle, Nwokolo, Chuka, Isaacs, Peter, Rodgers, Colin, Ragunath, Krish, MacDonald, Chris, Haigh, Chris, Monk, David, Davies, Gareth, Wajed, Saj, Johnston, David, Gibbons, Michael, Cullen, Sue, Church, Nicholas, Langley, Ruth, Griffin, Michael, Alderson, Derek, Deloukas, Panos, Hunt, Sarah E., Gray, Emma, Dronov, Serge, Potter, Simon C., Tashakkori-Ghanbaria, Avazeh, Anderson, Mark, Brooks, Claire, Blackwell, Jenefer M., Bramon, Elvira, Brown, Mathew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N.A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas, Trynka, Gosia, Wijmenga, Cisca, Cazier, Jean-Baptiste, Atherfold, Paul, Nicholson, Anna M., Gellatly, Nichola L., Glancy, Deborah, Cooper, Sheldon C., Cunningham, David, Lind, Tore, Hapeshi, Julie, Ferry, David, Rathbone, Barrie, Brown, Julia, Love, Sharon, Attwood, Stephen, MacGregor, Stuart, Watson, Peter, Sanders, Scott, Ek, Weronica, Harrison, Rebecca F., Moayyedi, Paul, De Caestecker, John, Barr, Hugh, Stupka, Elia, Vaughan, Thomas L., Peltonen, Leena, Spencer, Chris C.A., Tomlinson, Ian, Donnelly, Peter, Jankowski, Janus A.Z.

المصدر: Su , Z , Gay , L J , Strange , A , Palles , C , Band , G , Whiteman , D C , Lescai , F , Langford , C , Nanji , M , Edkins , S , Van Der Winkel , A , Levine , D , Sasieni , P , Bellenguez , C , Howarth , K , Freeman , C , Trudgill , N , Tucker , A T , Pirinen , M , Peppelenbosch , M P , Van Der Laan , L J W , Kuipers , E J , ....

العلاقة: https://discovery.dundee.ac.uk/en/publications/cefa9a5a-6b3d-4c82-a5d4-5d1f090abb34Test

الإتاحة: https://doi.org/10.1038/ng.2408Test
https://discovery.dundee.ac.uk/en/publications/cefa9a5a-6b3d-4c82-a5d4-5d1f090abb34Test