부산대학교 도서관

Alexander F. Brown; Michael H. Parkinson; Hector Garcia-Moreno; Ese Mudanohwo; Robyn Labrum; Mary Sweeney; Paola Giunti

Frontiers in Neurology, Vol 12 (2021)

Robak, Laurie A.; Jansen, Iris E.; Rooij, Jeroen van; Uitterlinden, André G.; Kraaij, Robert; Jankovic, Joseph; Heutink, Peter; Shulman, Joshua M.; Nalls, Mike A.; Plagnol, Vincent; Hernandez, Dena G.; Sharma, Manu; Sheerin, Una Marie; Saad, Mohamad; Simón-Sánchez, Javier; Schulte, Claudia; Lesage, Suzanne; Sveinbjörnsdóttir, Sigurlaug; Arepalli, Sampath; 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; 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; Dong, Jing; Gardner, Michelle; Gibbs, J. Raphael; Goate, Alison; Gray, Emma; Guerreiro, Rita; Harris, Clare; van Hilten, Jacobus J.; Hofman, Albert; Hollenbeck, Albert; Holton, Janice; Hu, Michele; Huang, Xuemei; Wurster, Isabel; Mätzler, Walter; Hudson, Gavin; Hunt, Sarah E.; Huttenlocher, Johanna; Illig, Thomas; Jónsson, Pálmi V.; Lambert, Jean Charles; Langford, Cordelia; Lees, Andrew; Lichtner, Peter; Limousin, Patricia; Lopez, Grisel; Lorenz, Delia; 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.; Pétursson, Hjörvar; Pollak, Pierre; Post, Bart; Potter, Simon; Ravina, Bernard; Revesz, Tamas; Riess, Olaf; Rivadeneira, Fernando; Rizzu, Patrizia; Ryten, Mina; Sawcer, Stephen; Schapira, Anthony; Scheffer, Hans; Shaw, Karen; Shoulson, Ira; Shulman, Joshua; 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; Tison, François; Trabzuni, Daniah; Traynor, Bryan J.; Velseboer, Daan; Vidailhet, Marie; Walker, Robert; Warrenburg, Bart van de; Wickremaratchi, Mirdhu; Williams, Nigel; Williams-Gray, Caroline H.; Winder-Rhodes, Sophie; Stefánsson, Kári; Martinez, Maria; Wood, Nicholas W.; Hardy, John; Brice, Alexis; Gasser, Thomas; Singleton, Andrew B.

Robak, L A, Jansen, I E, van Rooij, J, Uitterlinden, A G, Kraaij, R, Jankovic, J, Heutink, P, Shulman, J M, International Parkinson’s Disease Genomics Consortium (IPDGC), IPDGC Consortium members & International Parkinson’s Disease Genomics Consortium (IPDGC) 2017, 'Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease', Brain : a journal of neurology, vol. 140, no. 12, pp. 3191-3203. https://doi.org/10.1093/brain/awx285
Brain 140(12), 3191-3203 (2017). doi:10.1093/brain/awx285
Brain, 140, 12, pp. 3191-3203
Brain 140, 3191-3203 (2017)

Lesage, Suzanne; Tison, François; Vidailhet, Marie; Corvol, Jean-Christophe; Agid, Yves; Anheim, Mathieu; Bonnet, Anne-Marie; Borg, Michel; Broussolle, Emmanuel; Damier, Philippe; Destée, Alain; Dürr, Alexandra; Durif, Franck; Krack, Paul; Klebe, Stephan; Lohmann, Ebba; Martinez, Maria; Pollak, Pierre; Rascol, Olivier; Tranchant, Christine; Vérin, Marc; Viallet, François; Brice, Alexis; Majounie, Elisa; Corvol, Jean Christophe; Nalls, Michael A.; Hernandez, Dena G.; Gibbs, J. Raphael; Arepalli, Sampath; Barker, Roger A.; Ben-Shlomo, Yoav; Berg, Daniela; Bettella, Francesco; Bhatia, Kailash; de Bie, Rob M.A.; Biffi, Alessandro; Bloem, Bastiaan R.; 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.; Counsell, Carl; Dartigues, Jean-François; Deloukas, Panos; Deuschl, Günther; Dexter, David T.; van Dijk, Karin D.; Dillman, Allissa; Dong, Jing; Durif, Frank; Edkins, Sarah; Escott-Price, Valentina; Evans, Jonathan R.; Foltynie, Thomas; Gao, Jianjun; Gardner, Michelle; Goate, Alison; Gray, Emma; Guerreiro, Rita; Harris, Clare; van Hilten, Jacobus J.; Hofman, Albert; Hollenbeck, Albert; Holmans, Peter; Holton, Janice; Hu, Michèle; Huang, Xuemei; Huber, Heiko; Hudson, Gavin; Hunt, Sarah E.; Huttenlocher, Johanna; Illig, Thomas; Jónsson, Pálmi V.; Kilarski, Laura L.; Jansen, Iris E.; Lambert, Jean-Charles; Langford, Cordelia; Lees, Andrew; Lichtner, Peter; Limousin, Patricia; Lopez, Grisel; Lorenz, Delia; Lubbe, Steven; Lungu, Codrin; Martinez, María; Mätzler, Walter; McNeill, Alisdair; Moorby, Catriona; Moore, Matthew; Morrison, Karen E.; Mudanohwo, Ese; O’Sullivan, Sean S.; Owen, Michael J.; Pearson, Justin; Perlmutter, Joel S.; Pétursson, Hjörvar; Plagnol, Vincent; Post, Bart; Potter, Simon; Ravina, Bernard; Revesz, Tamas; Riess, Olaf; Rivadeneira, Fernando; Rizzu, Patrizia; Ryten, Mina; Saad, Mohamad; Simón-Sánchez, Javier; Sawcer, Stephen; Schapira, Anthony; Scheffer, Hans; Schulte, Claudia; Sharma, Manu; Shaw, Karen; Sheerin, Una-Marie; Shoulson, Ira; 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; 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; Wurster, Isabel; Williams, Nigel; Morris, Huw R.; Heutink, Peter; Hardy, John; Wood, Nicholas W.; Gasser, Thomas; Singleton, Andrew B.; Drouet, Valérie ; Deramecourt, Vincent ; Jacoupy, Maxime ; Nicolas, Aude ; Cormier-Dequaire, Florence ; Hassoun, Sidi Mohamed ; Pujol, Claire ; Ciura, Sorana ; Erpapazoglou, Zoi ; Usenko, Tatiana ; Maurage, Claude-Alain ; Sahbatou, Mourad ; Liebau, Stefan ; Ding, Jinhui ; Bilgic, Basar ; Emre, Murat ; Erginel-Unaltuna, Nihan ; Guven, Gamze ; Leutenegger, Anne-Louise ; Durr, Alexandra ; Deleuze, Jean-François ; Tazir, Meriem ; Kabashi, Edor ; Singleton, Andrew ; Corti, Olga

In The American Journal of Human Genetics 3 March 2016 98(3):500-513

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

Geissler, J M, Schulte, C, Berg, D & International Parkinson Disease Genomics Consortium members 2017, 'No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs', ADHD Attention Deficit and Hyperactivity Disorders, vol. 9, no. 2, pp. 121-127. https://doi.org/10.1007/s12402-017-0219-8
ADHD Attention Deficit and Hyperactivity Disorders 9(2), 121-127 (2017). doi:10.1007/s12402-017-0219-8
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Nat Genet
Berendse, H W, GenePD, NeuroGenetics Research Consortium (NGRC), Hussman Institute of Human Genomics (HIHG), The Ashkenazi Jewish Dataset Investigator, Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE), North American Brain Expression Consortium (NABEC), United Kingdom Brain Expression Consortium (UKBEC), Greek Parkinson’s Disease Consortium, Alzheimer Genetic Analysis Group, International Parkinson’s Disease Genomics Consortium (IPDGC), Parkinson’s Study Group (PSG) Parkinson’s Research: The Organized GENetics Initiative (PROGENI) & 23andMe 2014, 'Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease', Nature Genetics, vol. 46, no. 9, pp. 989-993. https://doi.org/10.1038/ng.3043
Nature genetics 46(9), 989-993 (2014). doi:10.1038/ng.3043
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Nature Genetics
Nature Genetics, vol 46, iss 9

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

Human molecular genetics 23(3), 831-841 (2013). doi:10.1093/hmg/ddt465
Human Molecular Genetics, 23, 3, pp. 831-41

Klebe, Stephan; Golmard, Jean-Louis; Charfi, Rim; Edkins, Sarah; Evans, Jonathan R; Foltynie, Thomas; Freeman, Colin; Gao, Jianjun; Gardner, Michelle; Gibbs, Raphael; Goate, Alison; Gray, Emma; Guerreiro, Rita; Klein, Christine; Gústafsson, Omar; Harris, Clare; Hellenthal, Garrett; van Hilten, Jacobus J; Hofman, Albert; Hollenbeck, Albert; Holton, Janice; Hu, Michele; Huang, Xuemei; Huber, Heiko; Hagenah, Johann; Hudson, Gavin; Hunt, Sarah E; Huttenlocher, Johanna; Illig, Thomas; Jónsson, Pálmi V; Langford, Cordelia; Lees, Andrew; Lichtner, Peter; Limousin, Patricia; Lopez, Grisel; Gasser, Thomas; Lorenz, Delia; McNeill, Alisdair; Moorby, Catriona; Morris, Huw; Morrison, Karen E; Mudanohwo, Ese; O'Sullivan, Sean S; Pearson, Justin; Pearson, Richard; Perlmutter, Joel S; Wurster, Isabel; Pétursson, Hjörvar; Pirinen, Matti; Pollak, Pierre; Post, Bart; Potter, Simon; Ravina, Bernard; Revesz, Tamas; Riess, Olaf; Rivadeneira, Fernando; Rizzu, Patrizia; Lesage, Suzanne; Ryten, Mina; Sawcer, Stephen; Schapira, Anthony; Scheffer, Hans; Shaw, Karen; Shoulson, Ira; Sidransky, Ellen; de Silva, Rohan; Smith, Colin; Spencer, Chris Ca; Stefánsson, Hreinn; Steinberg, Stacy; Stockton, Joanna D; Strange, Amy; Su, Zhan; Talbot, Kevin; Tanner, Carlie M; Tashakkori-Ghanbaria, Avazeh; Tison, François; Trabzuni, Daniah; Deuschl, Günther; Traynor, Bryan J; Uitterlinden, G.; Vandrovcova, Jana; Velseboer, Daan; Vidailhet, Marie; Vukcevic, Damjan; Walker, Robert; van de Warrenburg, Bart; Weale, Michael E; Wickremaratchi, Mirdhu; Durif, Franck; Williams, Nigel; Williams-Gray, Caroline H; Winder-Rhodes, Sophie; Martinez, Maria; Donnelly, Peter; Hardy, John; Heutink, Peter; Brice, Alexis; Wood, Nicholas W; Singleton, Andrew B; Nalls, Michael A; Damier, Philippe; Durr, Alexandra; Amouyel, Philippe; Lambert, Jean-Charles; Tzourio, Christophe; Maubaret, Cécilia; Charbonnier-Beaupel, Fanny; Tahiri, Khadija; Saad, Mohamad; Corvol, Jean-Christophe; Group, French Parkinson's Disease Genetics Study; Consortium, International Parkinson's Disease Genomics; Agid, Y.; Anheim, M.; Bonnet, A-M; Borg, M.; Brice, A.; Broussolle, E.; Corvol, J-C; Damier, Ph; Destée, A.; Durr, A.; Durif, F.; Klebe, S.; Lohmann, E.; Martinez, M.; Penet, C.; Bras, Jose M; Pollak, P.; Krack, P.; Rascol, O.; Tison, F.; Tranchant, C.; Vérin, M.; Viallet, F.; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; Sheerin, Una-Marie; Simón-Sánchez, Javier; Schulte, Claudia; Sveinbjörnsdóttir, Sigurlaug; Arepalli, Sampath; Band, Gavin; Simon-Sanchez, Javier; Barker, Roger A; Bellinguez, Céline; Ben-Shlomo, Yoav; Berendse, Henk W; Berg, Daniela; Bhatia, Kailash; de Bie, Rob Ma; 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; Kuhlenbäumer, Gregor; Cooper, J Mark; Corvol, Jean Christophe; Counsell, Carl; Dartigues, Jean-François; Deloukas, Panos; Dexter, David T; van Dijk, Karin D; Dillman, Allissa; Durif, Frank

J Neurol Neurosurg Psychiatry
Klebe, S, Golmard, J L, Nalls, M A, Saad, M, Singleton, A B, Bras, J M, Hardy, J, Simon Sanchez, J, Heutink, P, Kuhlenbäumer, G, Charfi, R, Klein, C, Hagenah, J, Gasser, T, Wurster, I, Lesage, S, Lorenz, D, Deuschl, G, Durif, F, Pollak, P, Damier, P, Tison, F, Durr, A, Amouyel, P, Lambert, J C, Tzourio, C, Maubaret, C, Charbonnier-Beaupel, F, Tahiri, K, Vidailhet, M, Martinez, M, Brice, A & Corvol, J C 2013, 'The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism.', Journal of Neurology, Neurosurgery and Psychiatry, vol. 84, no. 6, pp. 666-673. https://doi.org/10.1136/jnnp-2012-304475
Journal of neurology, neurosurgery, and psychiatry 84(6), 666-673 (2013). doi:10.1136/jnnp-2012-304475
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Journal of Neurology, Neurosurgery, and Psychiatry, Vol. 84, No 6 (2013) pp. 666-73

Pitceathly, Robert D S; Murphy, Sinéad M; Cottenie, Ellen; Chalasani, Annapurna; Sweeney, Mary G; Woodward, Cathy; Mudanohwo, Ese E; Hargreaves, Iain; Heales, Simon; Land, John; Holton, Janice L; Houlden, Henry; Blake, Julian; Champion, Michael; Flinter, Frances; Robb, Stephanie A; Page, Rupert; Rose, Michael; Palace, Jacqueline; Crowe, Carol; Longman, Cheryl; Lunn, Michael P; Rahman, Shamima; Reilly, Mary M; Hanna, Michael G

Neurology. 79:1145-1154

Xi, Zhengrui; Zhang, Ming; Bruni, Amalia C.; Maletta, Raffaele G.; Colao, Rosanna; Fratta, Pietro; Polke, James M.; Sweeney, Mary G.; Mudanohwo, Ese; Nacmias, Benedetta; Sorbi, Sandro; Tartaglia, Maria Carmela; Rainero, Innocenzo; Rubino, Elisa; Pinessi, Lorenzo; Galimberti, Daniela; Surace, Ezequiel I.; McGoldrick, Philip; McKeever, Paul; Moreno, Danielle; Sato, Christine; Liang, Yan; Keith, Julia; Zinman, Lorne; Robertson, Janice; Rogaeva, Ekaterina

Acta Neuropathologica. May, 2015, Vol. 129 Issue 5, p715, 13 p.

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

Nalls, M A, Plagnol, V, Hernandez, D G, Sharma, M, Sheerin, U M, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Arepalli, S, Barker, R, Ben-Shlomo, Y, Berendse, H W, Berg, D, Bhatia, K, de Bie, R M A, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Bras, J M, Brockmann, K, Brooks, J, Burn, D J, Charlesworth, G, Chen, H L, Chinnery, P F, Chong, S, Clarke, C E, Cookson, M R, Cooper, J M, Corvol, J C, Counsell, C, Damier, P, Dartigues, J F, Deloukas, P, Deuschl, G, Dexter, D T, van Dijk, K D, Dillman, A, Durif, F, Durr, A, Edkins, S, Evans, J R, Foltynie, T, Gao, J J, Gardner, M, Gibbs, J R, Goate, A, Gray, E, Guerreiro, R, Gustafsson, O, Harris, C, van Hilten, J J, Hofman, A, Hollenbeck, A, Holton, J, Hu, M, Huang, X M, Huber, H, Hudson, G, Hunt, S E, Huttenlocher, J, Illig, T, Jonsson, P V, Lambert, J C, Langford, C, Lees, A, Lichtner, P, Limousin, P, Lopez, G, Lorenz, D, McNeill, A, Moorby, C, Moore, M, Morris, H R, Morrison, K E, Mudanohwo, E, O'Sullivan, S S, Pearson, J, Perlmutter, J S, Petursson, H, Pollak, P, Post, B, Potter, S, Ravina, B, Revesz, T, Riess, O, Rivadeneira, F, Rizzu, P, Ryten, M, Sawcer, S, Schapira, A, Scheffer, H, Shaw, K, Shoulson, I, Sidransky, E, Smith, C, Heutink, P, Singleton, A B & Wood, N W 2011, 'Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies', Lancet, vol. 377, no. 9766, pp. 641-649. https://doi.org/10.1016/S0140-6736(10)62345-8
The lancet 377(9766), 641-649 (2011). doi:10.1016/S0140-6736(10)62345-8
The Lancet (London), 377, 9766, pp. 641-9
The Lancet, Vol. 377, No 9766 (2011) pp. 641-9
Nalls, M A, Plagnol, V, Hernandez, D G, Sharma, M, Sheerin, U-M, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Arepalli, S, Barker, R, Ben-Shlomo, Y, Berendse, H W, Berg, D, Bhatia, K, de Bie, R M A, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Bras, J M, Brockmann, K, Brooks, J, Burn, D J, Charlesworth, G, Chen, H, Chinnery, P F, Chong, S, Clarke, C E, Cookson, M R, Cooper, J M, Corvol, J C, Counsell, C, Damier, P, Dartigues, J-F, Deloukas, P, Deuschl, G, Dexter, D T, van Dijk, K D, Dillman, A, Durif, F, Duerr, A, Edkins, S, Evans, J R, Foltynie, T, Gao, J, Gardner, M & Gibbs, J R & Smith, C 2011, ' Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies ', The Lancet, vol. 377, no. 9766, pp. 641-649 . https://doi.org/10.1016/S0140-6736(10)62345-8

Gami, Priya; Murray, Christina; Schottlaender, Lucia; Bettencourt, Conceição; De Pablo Fernandez, Eduardo; Mudanohwo, Ese; Mizielinska, Sarah; Polke, James M.; Holton, Janice L.; Isaacs, Adrian M.; Houlden, Henry; Revesz, Tamas; Lashley, Tammaryn

Acta Neuropathologica. October, 2015, Vol. 130 Issue 4, p599, 3 p.

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

Genome Biol
Jansen, I E, Ye, H, Heetveld, S, Lechler, M C, Michels, H, Seinstra, R I, Lubbe, S, Drouet, V, Lesage, S, Majounie, E, Gibbs, J R, Nalls, M A, Ryten, M, Botia, J A, Vandrovcova, J, Simon-Sanchez, J, Castillo-Lizardo, M, Rizzu, P, Blauwendraat, C, Chouhan, A K, Li, Y, Yogi, P, Amin, N, van Duijn, C M, Morris, H R, Brice, A, Singleton, A B, David, D C, Nollen, E A, Jain, S, Shulman, J M, Heutink, P & International Parkinson's Disease Genetics Consortium (IPGDC) 2017, 'Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing', Genome Biology, vol. 18, no. 1, 22. https://doi.org/10.1186/s13059-017-1147-9
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