المؤلفون: Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden P, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin NA, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Spencer, Chris CA, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Pirinen, Matti, Pearson, Richard D, Strange, Amy, Su, Zhan, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Tashakkori-Ghanbaria, Avazeh, Waller, Matthew J, Weston, Paul, Widaa, Sara, Whittaker, Pamela, McCarthy, Mark I

المصدر: Nature Genetics. 45(10)

مصطلحات موضوعية: Mental health, Case-Control Studies, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Polymorphism, Single Nucleotide, Schizophrenia, Sweden, Multicenter Genetic Studies of Schizophrenia Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case Control Consortium 2, Biological Sciences, Medical and Health Sciences, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5m70r4qgTest

المؤلفون: Ripke, Stephan, O'Dushlaine, Colm, Chambert, Kimberly, Moran, Jennifer L, Kähler, Anna K, Akterin, Susanne, Bergen, Sarah E, Collins, Ann L, Crowley, James J, Fromer, Menachem, Kim, Yunjung, Bender, Stephan, Bramon, Elvira, Collier, David, Crespo-Facorro, Benedicto, Hall, Jeremy, Iyegbe, Conrad, McIntosh, Andrew, Murray, Robin M, Lee, Sang Hong, Ophoff, Roel A, Scolnick, Edward, Powell, John, Rujescu, Dan, Van Os, Jim, Walshe, Muriel, Weisbrod, Matthias, Wiersma, Durk, Donnelly, Peter, Barroso, Ines, Blackwell, Jenefer M, Magnusson, Patrik K E, Purcell, Shaun, Brown, Matthew A, Casas, Juan P, Corvin, Aiden P, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, McCarroll, Steven A, Sanchez, Nick, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Spencer, Chris C A, Band, Gavin, Bellenguez, Céline, Sklar, Pamela, Freeman, Colin, Stahl, Eli A, Hellenthal, Garrett, Giannoulatou, Eleni, Pirinen, Matti, Pearson, Richard D, Strange, Amy, Su, Zhan, Vukcevic, Damjan, Hultman, Christina M, Langford, Cordelia, Hunt, Sarah E, Williams, Stephanie, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Sullivan, Patrick F, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T, Wray, Naomi R, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Tashakkori-Ghanbaria, Avazeh, Waller, Matthew J, Borglum, Anders D, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Xia, Kai, Bulik-Sullivan, Brendan K, McCarthy, Mark I, O'Donovan, Michael C, Bettella, Francesco, Stefansson, Kari, Cormican, Paul, Craddock, Nick, Jablensky, Assen, de Leeuw, Christiaan, Durmishi, Naser, Gill, Michael, Golimbet, Vera, Hamshere, Marian L, Holmans, Peter, Hougaard, David M, Kendler, Kenneth S, Lin, Kuang, Morris, Derek W, Kahn, Rene S, Mors, Ole, Mortensen, Preben B, Neale, Benjamin M, O'Neill, Francis A, Owen, Michael J, Milovancevic, Milica Pejovic, Posthuma, Danielle, Richards, Alexander L, Riley, Brien P, Kalaydjieva, Luba, Ruderfer, Douglas, Sigurdsson, Engilbert, Silagadze, Teimuraz, Smit, August B, Stefansson, Hreinn, Steinberg, Stacy, Suvisaari, Jaana, Tosato, Sarah, Verhage, Matthijs, Lawrie, Stephen, Walters, James T, Levinson, Douglas F, Gejman, Pablo V, Laurent, Claudine, Mowry, Bryan J, Pulver, Ann E, Lewis, Cathryn M, Schwab, Sibylle G, Wildenauer, Dieter B, Dudbridge, Frank, Shi, Jianxin, Albus, Margot, Alexander, Madeline, Campion, Dominique, Cohen, David, Dikeos, Dimitris, Duan, Jubao, Eichhammer, Peter, Godard, Stephanie, Hansen, Mark, Lerer, F Bernard, Liang, Kung-Yee, Maier, Wolfgang, Mallet, Jacques, Nertney, Deborah A, Nestadt, Gerald, Linszen, Don H, Norton, Nadine, Papadimitriou, George N, Ribble, Robert, Sanders, Alan R, Silverman, Jeremy M, Walsh, Dermot, Williams, Nigel M, Wormley, Brandon, Arranz, Maria J, Mata, Ignacio, Bakker, Steven

المساهمون: Massachusetts Gen Hosp, Analyt & Translat Genet Unit, Boston, MA 02114 USA Broad Inst MIT & Harvard, Stanley Ctr Psychiat Res, Cambridge, MA USA Univ N Carolina, Dept Genet, Chapel Hill, NC 27515 USA Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden Oslo Univ Hosp, Div Mental Hlth & Addict, Oslo, Norway Icahn Sch Med Mt Sinai, Dept Psychiat, Div Psychiat Genom, New York, NY USA Univ Queensland, Queensland Brain Inst, Brisbane, Qld, Australia Univ N Carolina, Dept Psychiat, Chapel Hill, NC USA deCODE Genet, Reykjavik, Iceland Aarhus Univ Hosp, Risskov, Denmark Aarhus Univ, Ctr Integrat Sequencing iSEQ, Aarhus, Denmark Lundbeck Fdn Initiat Integrat Psychiat Res iPSYCH, Aarhus, Denmark Lundbeck Fdn Initiat Integrat Psychiat Res iPSYCH, Copenhagen, Denmark Univ Dublin Trinity Coll, Dept Psychiat, Dublin 2, Ireland Cardiff Univ, Sch Med, Ctr Psychiat Genet & Genom, MRC, Cardiff CF10 3AX, S Glam, Wales Vrije Univ Amsterdam, Ctr Neurogen & Cognit Res, Dept Funct Genom, Amsterdam, Netherlands Vrije Univ Amsterdam Med Ctr, Amsterdam, Netherlands Radboud Univ Nijmegen, Inst Comp & Informat Sci, NL-6525 ED Nijmegen, Netherlands Univ Clin Psychiat, Dept Child & Adolescent Psychiat, Skopje, Macedonia Univ Dublin Trinity Coll, Neuropsychiat Genet Res Grp, Dublin 2, Ireland Russian Acad Med Sci, Mental Hlth Res Ctr, Moscow 109801, Russia Statens Serum Inst, DK-2300 Copenhagen, Denmark Virginia Commonwealth Univ, Dept Psychiat, Richmond, VA USA Virginia Commonwealth Univ, Virginia Inst Psychiat & Behav Genet, Richmond, VA USA Kings Coll London, Inst Psychiat, London, England Aarhus Univ Hosp, Ctr Psychiat Res, Risskov, Denmark Aarhus Univ, Natl Ctr Register Based Res, Aarhus, DenmarkQueens Univ Belfast, Ctr Publ Hlth, Belfast, Antrim, North Ireland Univ Belgrade, Fac Med, Belgrade, Serbia Erasmus Univ, Med Ctr, Dept Child & Adolescent Psychiat, Rotterdam, Netherlands Kings Coll London, Dept Neurosci, London, England Virginia Commonwealth Univ, Dept Human & Mol Genet, Richmond, VA USA Univ Halle, Dept Psychiat, Halle, Germany Univ Munich, Dept Psychiat, D-80539 Munich, Germany Univ Iceland, Dept Psychiat, Reykjavik, Iceland Landspitali University Hospital Reykjavik, Iceland Tbilisi State Univ, Dept Psychiat, GE-380086 Tbilisi, Rep of Georgia Vrije Univ Amsterdam, Ctr Neurogen & Cognit Res, Amsterdam, Netherlands Vrije Univ Amsterdam, Dept Mol & Cellular Neurosci, Amsterdam, Netherlands Natl Inst Hlth & Welf, Mental Hlth & Subst Abuse Serv, Helsinki, Finland Univ Verona, Sect Psychiat, I-37100 Verona, Italy UCL, Inst Cognit Neurosci, London, England UCL, Mental Hlth Sci Unit, London, England Massachusetts Gen Hosp, Psychiat & Neurodev Genet Unit, Boston, MA 02114 USA Harvard Univ, Sch Med, Dept Genet, Boston, MA USA

مصطلحات موضوعية: Case-Control Studies, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Polymorphism, Single Nucleotide, Schizophrenia, Sweden

العلاقة: info:eu-repo/grantAgreement/EC/FP7/223423; http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827979/pdf/nihms512111.pdfTest; http://dx.doi.org/10.1038/ng.2742Test; Nat. Genet. 2013, 45(10):1150-9; http://hdl.handle.net/2336/317149Test; Nature genetics

الإتاحة: https://doi.org/10.1038/ng.2742Test
http://hdl.handle.net/2336/317149Test

المؤلفون: Robak, Laurie A, Jansen, Iris E, Plagnol, Vincent, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Hernandez, Dena G, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Bettella, Francesco, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Sharma, Manu, Tison, François, Trabzuni, Daniah, Traynor, Bryan J, Uitterlinden, André G, Velseboer, Daan, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Sheerin, Una-Marie, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Wood, Nicholas W, Hardy, John, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Saad, Mohamad, Simón-Sánchez, Javier, Schulte, Claudia, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Arepalli, Sampath, van Rooij, Jeroen, Barker, Roger, Ben-, Yoav, Berendse, Henk W, 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, Majounie, Elisa, Charlesworth, Gavin, Lungu, Codrin, Chen, Honglei, Chinnery, Patrick F, Chong, Sean, Kraaij, Robert, Clarke, Carl E, Cookson, Mark R, Mark Cooper, J., Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Deuschl, Günther, Dexter, David T, Jankovic, Joseph, van Dijk, Karin D, Dillman, Allissa, Durif, Frank, Dürr, Alexandra, Edkins, Sarah, Evans, Jonathan R, Foltynie, Thomas, Dong, Jing, Gardner, Michelle, Raphael Gibbs, J., Consortium, International Parkinson’s Disease Genomics, Goate, Alison, Gray, Emma, Guerreiro, Rita, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Heutink, Peter, Wurster, Isabel, Mätzler, Walter, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Shulman, Joshua M, Lichtner, Peter, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Nalls, Mike A, Escott-Price, Valentina, Mudanohwo, Ese, O'Sullivan, Sean S, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Post, Bart, Potter, Simon, Ravina, Bernard

المصدر: Brain 140(12), 3191-3203 (2017). doi:10.1093/brain/awx285

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Acid Ceramidase: genetics, Adult, Aged, 80 and over, Case-Control Studies, Cathepsin D: genetics, Cohort Studies, Exome, Female, Genetic Predisposition to Disease, Genotype, Glucosylceramidase: genetics, Humans, Lysosomal Storage Diseases: genetics, Male, Middle Aged, Mutation, Organic Anion Transporters: genetics, Parkinson Disease: genetics, Sphingomyelin Phosphodiesterase: genetics, Symporters: genetics, Organic Anion Transporters, Symporters, sialic acid transport proteins, Sphingomyelin Phosphodiesterase, sphingomyelin phosphodiesterase 1, human, Glucosylceramidase, CTSD protein

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:29140481; info:eu-repo/semantics/altIdentifier/issn/0006-8950; info:eu-repo/semantics/altIdentifier/issn/1460-2156; https://pub.dzne.de/record/139657Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-05979%22Test

الإتاحة: https://doi.org/10.1093/brain/awx285Test
https://pub.dzne.de/record/139657Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-05979%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: 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, 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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: Mittag, Florian, Büchel, Finja, Gibbs, J Raphael, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Potter, Simon, Ravina, Bernard, Revesz, Tamas, Riess, Olaf, Rivadeneira, Fernando, Rizzu, Patrizia, Lesage, Suzanne, Ryten, Mina, Sawcer, Stephen, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Steinberg, Stacy, Brice, Alexis, 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, Heutink, Peter, Vidailhet, Marie, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Stefánsson, Kári, Martinez, Maria, Hardy, John, Singleton, Andrew B, Wood, Nicholas W, Zell, Andreas, Gasser, Thomas, Saad, Mohamad, Sharma, Manu, Consortium, International Parkinson’s Disease Genomics, Nalls, Michael A, Plagnol, Vincent, Sheerin, Una-Marie, Simón-Sánchez, Javier, Sveinbjörnsdóttir, Sigurlaug, Arepalli, Sampath, Jahn, Andreas, 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, Schulte, Claudia, 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, Evans, Jonathan R, Foltynie, Thomas, Gao, Jianjun, Gardner, Michelle, Goate, Alison, Gray, Emma, Nalls, Mike A, Guerreiro, Rita, Gústafsson, Ómar, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Hershey, Milton S, Keller, Margaux, Huber, Heiko, Hudson, Gavin, Hunt, Sarah E, Huttenlocher, Johanna, Illig, Thomas, Jónsson, Pálmi V, Lambert, Jean-Charles, Langford, Cordelia, Lees, Andrew, Lichtner, Peter, Hernandez, Dena G, München, Helmholtz Zentrum, Limousin, Patricia, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, O'Sullivan, Sean S

المصدر: Human mutation 33(12), 1708-1718 (2012). doi:10.1002/humu.22161

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Area Under Curve, Bipolar Disorder: diagnosis, Bipolar Disorder: genetics, Case-Control Studies, Computer Simulation, Diabetes Mellitus, Type 1: diagnosis, Type 1: genetics, Type 2: diagnosis, Type 2: genetics, Genetic Predisposition to Disease, Genome-Wide Association Study: methods, Humans, Models, Genetic, Parkinson Disease: diagnosis, Parkinson Disease: genetics, Polymorphism, Single Nucleotide, ROC Curve, Risk, Software, Support Vector Machine

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/pmid:22777693; info:eu-repo/semantics/altIdentifier/issn/1098-1004; info:eu-repo/semantics/altIdentifier/issn/1059-7794; https://pub.dzne.de/record/136686Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-03008%22Test

الإتاحة: https://doi.org/10.1002/humu.22161Test
https://pub.dzne.de/record/136686Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-03008%22Test