Auflistung Universitätsbibliographie nach Autor "Sharma, Manu"

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Auflistung Universitätsbibliographie nach Autor "Sharma, Manu"

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  • A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants
    Sharma, Manu; Ioannidis, John P. A.; Aasly, Jan O.; Annesi, Grazia; Brice, Alexis; Bertram, Lars; Bozi, Maria; Barcikowska, Maria; Crosiers, David; Clarke, Carl E.; Facheris, Maurizio F.; Farrer, Matthew; Garraux, Gaetan; Gispert, Suzana; Auburger, Georg; Vilarino-Guell, Carles; Hadjigeorgiou, Georgios M.; Hicks, Andrew A.; Hattori, Nobutaka; Jeon, Beom S.; Jamrozik, Zygmunt; Krygowska-Wajs, Anna; Lesage, Suzanne; Lill, Christina M.; Lin, Juei-Jueng; Lynch, Timothy; Lichtner, Peter; Lang, Anthony E.; Libioulle, Cecile; Murata, Miho; Mok, Vincent; Jasinska-Myga, Barbara; Mellick, George D.; Morrison, Karen E.; Meitnger, Thomas; Zimprich, Alexander; Opala, Grzegorz; Pramstaller, Peter P.; Pichler, Irene; Park, Sung Sup; Quattrone, Aldo; Rogaeva, Ekaterina; Ross, Owen A.; Stefanis, Leonidas; Stockton, Joanne D.; Satake, Wataru; Silburn, Peter A.; Strom, Tim M.; Theuns, Jessie; Tan, Eng-King; Toda, Tatsushi; Tomiyama, Hiroyuki; Uitti, Ryan J.; Van Broeckhoven, Christine; Wirdefeldt, Karin; Wszolek, Zbigniew; Xiromerisiou, Georgia; Yomono, Harumi S.; Yueh, Kuo-Chu; Zhao, Yi; Gasser, Thomas; Maraganore, Demetrius; Krueger, Rejko (2012)
  • A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsons disease
    Holmans, Peter; Moskvina, Valentina; Jones, Lesley; Sharma, Manu; Vedernikov, Alexey; Buchel, Finja; Sadd, Mohamad; Bras, Jose M.; Bettella, Francesco; Nicolaou, Nayia; Simon-Sanchez, Javier; Mittag, Florian; Gibbs, J. Raphael; Schulte, Claudia; Durr, Alexandra; Guerreiro, Rita; Hernandez, Dena; Brice, Alexis; Stefansson, Hreinn; Majamaa, Kari; Gasser, Thomas; Heutink, Peter; Wood, Nicholas W.; Martinez, Maria; Singleton, Andrew B.; Nalls, Michael A.; Hardy, John; Morris, Huw R.; Williams, Nigel M. (2013)
  • Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
    Lubbe, Steven J.; Escott-Price, Valentina; Gibbs, J. Raphael; Nalls, Mike A.; Bras, Jose; Price, T. Ryan; Nicolas, Aude; Jansen, Iris E.; Mok, Kin Y.; Pittman, Alan M.; Tomkins, James E.; Lewis, Patrick A.; Noyce, Alastair J.; Lesage, Suzanne; Sharma, Manu; Schiff, Elena R.; Levine, Adam P.; Brice, Alexis; Gasser, Thomas; Hardy, John; Heutink, Peter; Wood, NicholasW.; Singleton, Andrew B.; Williams, Nigel M.; Morris, Huw R. (2016)
  • Alpha-synuclein gene variants may predict neurostimulation outcome
    Weiss, Daniel; Herrmann, Sonja; Wang, Lisa; Schulte, Claudia; Brockmann, Kathrin; Plewina, Christian; Gasser, Thomas; Sharma, Manu; Gharabaghi, Alireza; Krüger, Rejko (2016)
  • Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk
    Moskvina, Valentina; Harold, Denise; Russo, GianCarlo; Vedemikov, Alexey; Sharma, Manu; Saad, Mohamad; Holmans, Peter; Bras, Jose M.; Bettella, Francesco; Keller, Margaux F.; Nicolaou, Nayia; Simon-Sanchez, Javier; Gibbs, J. Raphael; Schulte, Claudia; Durr, Alexandra; Guerreiro, Rita; Hernandez, Dena; Brice, Alexis; Stefansson, Hreinn; Majamaa, Kari; 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; Morris, Huw R.; Williams, Nigel M. (2013)
  • Analysis of shared heritability in common disorders of the brain
    Anttila, Verneri; Bulik-Sullivan, Brendan; Finucane, Hilary K.; Walters, Raymond K.; Bras, Jose; Duncan, Laramie; Escott-Price, Valentina; Falcone, Guido J.; Gormley, Padhraig; Malik, Rainer; Patsopoulos, Nikolaos A.; Ripke, Stephan; Wei, Zhi; Yu, Dongmei; Lee, Phil H.; Turley, Patrick; Grenier-Boley, Benjamin; Chouraki, Vincent; Kamatani, Yoichiro; Berr, Claudine; Letenneur, Luc; Hannequin, Didier; Amouyel, Philippe; Boland, Anne; Deleuze, Jean-Francois; Duron, Emmanuelle; Vardarajan, Badri N.; Reitz, Christiane; Goate, Alison M.; Huentelman, Matthew J.; Kamboh, M. Ilyas; Larson, Eric B.; Rogaeva, Ekaterina; St George-Hyslop, Peter; Hakonarson, Hakon; Kukull, Walter A.; Farrer, Lindsay A.; Barnes, Lisa L.; Beach, Thomas G.; Demirci, F. Yesim; Head, Elizabeth; Hulette, Christine M.; Jicha, Gregory A.; Kauwe, John S. K.; Kaye, Jeffrey A.; Leverenz, James B.; Levey, Allan I.; Lieberman, Andrew P.; Pankratz, Vernon S.; Poon, Wayne W.; Quinn, Joseph F.; Saykin, Andrew J.; Schneider, Lon S.; Smith, Amanda G.; Sonnen, Joshua A.; Stern, Robert A.; Van Deerlin, Vivianna M.; Van Eldik, Linda J.; Harold, Denise; Russo, Giancarlo; Rubinsztein, David C.; Bayer, Anthony; Tsolaki, Magda; Proitsi, Petra; Fox, Nick C.; Hampel, Harald; Owen, Michael J.; Mead, Simon; Passmore, Peter; Morgan, Kevin; Noethen, Markus M.; Rossor, Martin; Lupton, Michelle K.; Hoffmann, Per; Kornhuber, Johannes; Lawlor, Brian; McQuillin, Andrew; Al-Chalabi, Ammar; Bis, Joshua C.; Ruiz, Agustin; Boada, Merce; Seshadri, Sudha; Beiser, Alexa; Rice, Kenneth; van der Lee, Sven J.; De Jager, Philip L.; Geschwind, Daniel H.; Riemenschneider, Matthias; Riedel-Heller, Steffi; Rotter, Jerome I.; Ransmayr, Gerhard; Hyman, Bradley T.; Cruchaga, Carlos; Alegret, Montserrat; Winsvold, Bendik; Palta, Priit; Farh, Kai-How; Cuenca-Leon, Ester; Furlotte, Nicholas; Kurth, Tobias; Ligthart, Lannie (2018)
  • Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database
    Lill, Christina M.; Roehr, Johannes T.; McQueen, Matthew B.; Kavvoura, Fotini K.; Bagade, Sachin; Schjeide, Brit-Maren M.; Schjeide, Leif M.; Meissner, Esther; Zauft, Ute; Allen, Nicole C.; Liu, Tian; Schilling, Marcel; Anderson, Kari J.; Beecham, Gary; Berg, Daniela; Biernacka, Joanna M.; Brice, Alexis; DeStefano, Anita L.; Do, Chuong B.; Eriksson, Nicholas; Factor, Stewart A.; Farrer, Matthew J.; Foroud, Tatiana; Gasser, Thomas; Hamza, Taye; Hardy, John A.; Heutink, Peter; Hill-Burns, Erin M.; Klein, Christine; Latourelle, Jeanne C.; Maraganore, Demetrius M.; Martin, Eden R.; Martinez, Maria; Myers, Richard H.; Nalls, Michael A.; Pankratz, Nathan; Payami, Haydeh; Satake, Wataru; Scott, William K.; Sharma, Manu; Singleton, Andrew B.; Stefansson, Kari; Toda, Tatsushi; Tung, Joyce Y.; Vance, Jeffery; Wood, Nick W.; Zabetian, Cyrus P.; Young, Peter; Tanzi, Rudolph E.; Khoury, Muin J.; Zipp, Frauke; Lehrach, Hans; Ioannidis, John P. A.; Bertram, Lars (2012)
  • Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study
    Domenighetti, Cloe; Sugier, Pierre-Emmanuel; Sreelatha, Ashwin Ashok Kumar; Schulte, Claudia; Grover, Sandeep; Mohamed, Oceane; Portugal, Berta; May, Patrick; Bobbili, Dheeraj R.; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Singleton, Andrew B.; Hernandez, Dena G.; Edsall, Connor; Mellick, George D.; Zimprich, Alexander; Pirker, Walter; Rogaeva, Ekaterina; Lang, Anthony E.; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Chartier-Harlin, Marie-Christine; Mutez, Eugenie; Brockmann, Kathrin; Deutschlaender, Angela B.; Hadjigeorgiou, Georges M.; Dardiotis, Efthimos; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Duga, Stefano; Straniero, Letizia; Zecchinelli, Anna; Pezzoli, Gianni; Brighina, Laura; Ferrarese, Carlo; Annesi, Grazia; Quattrone, Andrea; Gagliardi, Monica; Matsuo, Hirotaka; Kawamura, Yusuke; Hattori, Nobutaka; Nishioka, Kenya; Chung, Sun Ju; Kim, Yun Joong; Kolber, Pierre; van de Warrenburg, Bart P. C.; Bloem, Bastiaan R.; Aasly, Jan; Toft, Mathias; Pihlstrom, Lasse; Guedes, Leonor Correia; Ferreira, Joaquim J.; Bardien, Soraya; Carr, Jonathan; Tolosa, Eduardo; Ezquerra, Mario; Pastor, Pau; Diez-Fairen, Monica; Wirdefeldt, Karin; Pedersen, Nancy L.; Ran, Caroline; Belin, Andrea C.; Puschmann, Andreas; Hellberg, Clara; Clarke, Carl E.; Morrison, Karen E.; Tan, Manuela; Krainc, Dimitri; Burbulla, Lena F.; Farrer, Matt J.; Kruger, Rejko; Gasser, Thomas; Sharma, Manu; Elbaz, Alexis (2022)
  • Establishing the role of rare coding variants in known Parkinson's disease risk loci
    Jansen, Iris E.; Gibbs, J. Raphael; Nalls, Mike A.; Price, T. Ryan; Lubbe, Steven; van Rooij, Jeroen; Uitterlinden, Andre G.; Kraaij, Robert; Williams, Nigel M.; Brice, Alexis; Hardy, John; Wood, Nicholas W.; Morris, Huw R.; Gasser, Thomas; Singleton, Andrew B.; Heutink, Peter; Sharma, Manu (2017)
  • Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study
    Wang, Lisa; Heckman, Michael G.; Aasly, Jan O.; Annesi, Grazia; Bozi, Maria; Chung, Sun Ju; Clarke, Carl; Crosiers, David; Eckstein, Gertrud; Garraux, Gaetan; Hadjigeorgiou, Georgios M.; Hattori, Nobu; Jeon, Beom; Kim, Yun J.; Kubo, Masato; Lesage, Suzanne; Lin, Juei Jueng; Lynch, Timothy; Lichtner, Peter; Mellick, George D.; Mok, Vincent; Morrison, Karin E.; Quattrone, Aldo; Satake, Wataru; Silburn, Peter A.; Stefanis, Leonidas; Stockton, Joanne D.; Tan, Eng King; Toda, Tatsushi; Brice, Alexis; Van Broeckhoven, Christine; Uitti, Ryan J.; Wirdefeldt, Karin; Wszolek, Zbigniew; Xiromerisiou, Georgia; Maraganore, Demetrius M.; Gasser, Thomas; Krueger, Rejko; Farrer, Matthew J.; Ross, Owen A.; Sharma, Manu (2017)
  • Fine mapping of the HLA locus in Parkinson's disease in Europeans
    Yu, Eric; Ambati, Aditya; Andersen, Maren Stolp; Krohn, Lynne; Estiar, Mehrdad A.; Saini, Prabhjyot; Senkevich, Konstantin; Sosero, Yuri L.; Sreelatha, Ashwin Ashok Kumar; Ruskey, Jennifer A.; Asayesh, Farnaz; Spiegelman, Dan; Toft, Mathias; Viken, Marte K.; Sharma, Manu; Blauwendraat, Cornelis; Pihlstrom, Lasse; Mignot, Emmanuel; Gan-Or, Ziv (2021)
  • Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated LRRK2 Locus
    Trabzuni, Daniah; Ryten, Mina; Emmett, Warren; Ramasamy, Adaikalavan; Lackner, Karl J.; Zeller, Tanja; Walker, Robert; Smith, Colin; Lewis, Patrick A.; Mamais, Adamantios; de Silva, Rohan; Vandrovcova, Jana; Hernandez, Dena; Nalls, Michael A.; Sharma, Manu; Garnier, Sophie; Lesage, Suzanne; Simon-Sanchez, Javier; Gasser, Thomas; Heutink, Peter; Brice, Alexis; Singleton, Andrew; Cai, Huaibin; Schadt, Eric; Wood, Nicholas W.; Bandopadhyay, Rina; Weale, Michael E.; Hardy, John; Plagnol, Vincent (2013)
  • Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
    Blauwendraat, Cornelis; Reed, Xylena; Krohn, Lynne; Heilbron, Karl; Bandres-Ciga, Sara; Tan, Manuela; Gibbs, J. Raphael; Hernandez, Dena G.; Kumaran, Ravindran; Langston, Rebekah; Bonet-Ponce, Luis; Alcalay, Roy N.; Hassin-Baer, Sharon; Greenbaum, Lior; Iwaki, Hirotaka; Leonard, Hampton L.; Grenn, Francis P.; Ruskey, Jennifer A.; Sabir, Marya; Ahmed, Sarah; Makarious, Mary B.; Pihlstrom, Lasse; Toft, Mathias; van Hilten, Jacobus J.; Marinus, Johan; Schulte, Claudia; Brockmann, Kathrin; Sharma, Manu; Siitonen, Ari; Majamaa, Kari; Eerola-Rautio, Johanna; Tienari, Pentti J.; Pantelyat, Alexander; Hillis, Argye E.; Dawson, Ted M.; Rosenthal, Liana S.; Albert, Marilyn S.; Resnick, Susan M.; Ferrucci, Luigi; Morris, Christopher M.; Pletnikova, Olga; Troncoso, Juan; Grosset, Donald; Lesage, Suzanne; Corvol, Jean-Christophe; Brice, Alexis; Noyce, Alastair J.; Masliah, Eliezer; Wood, Nick; Hardy, John; Shulman, Lisa M.; Jankovic, Joseph; Shulman, Joshua M.; Heutink, Peter; Gasser, Thomas; Cannon, Paul; Scholz, Sonja W.; Morris, Huw; Cookson, Mark R.; Nalls, Mike A.; Gan-Or, Ziv; Singleton, Andrew B. (2020)
  • Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus
    Desikan, R. S.; Schork, A. J.; Wang, Y.; Witoelar, A.; Sharma, M.; McEvoy, L. K.; Holland, D.; Brewer, J. B.; Chen, C-H; Thompson, W. K.; Harold, D.; Williams, J.; Owen, M. J.; O'Donovan, M. C.; Pericak-Vance, M. A.; Mayeux, R.; Haines, J. L.; Farrer, L. A.; Schellenberg, G. D.; Heutink, P.; Singleton, A. B.; Brice, A.; Wood, N. W.; Hardy, J.; Martinez, M.; Choi, S. H.; DeStefano, A.; Ikram, M. A.; Bis, J. C.; Smith, A.; Fitzpatrick, A. L.; Launer, L.; van Duijn, C.; Seshadri, S.; Ulstein, I. D.; Aarsland, D.; Fladby, T.; Djurovic, S.; Hyman, B. T.; Snaedal, J.; Stefansson, H.; Stefansson, K.; Gasser, T.; Andreassen, O. A.; Dale, A. M. (2015)
  • Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci
    Smeland, Olav B.; Shadrin, Alexey; Bahrami, Shahram; Broce, Iris; Tesli, Martin; Frei, Oleksandr; Wirgenes, Katrine, V; O'Connell, Kevin S.; Krull, Florian; Bettella, Francesco; Steen, Nils Eiel; Sugrue, Leo; Wang, Yunpeng; Svenningsson, Per; Sharma, Manu; Pihlstrom, Lasse; Toft, Mathias; O'Donovan, Michael; Djurovic, Srdjan; Desikan, Rahul; Dale, Anders M.; Andreassen, Ole A. (2021)
  • Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium
    Grover, Sandeep; Kumar Sreelatha, Ashwin Ashok; Pihlstrom, Lasse; Domenighetti, Cloe; Schulte, Claudia; Sugier, Pierre-Emmanuel; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Mohamed, Oceane; Portugal, Berta; Landoulsi, Zied; May, Patrick; Bobbili, Dheeraj; Edsall, Connor; Bartusch, Felix; Hanussek, Maximilian; Krueger, Jens; Hernandez, Dena G.; Blauwendraat, Cornelis; Mellick, George D.; Zimprich, Alexander; Pirker, Walter; Tan, Manuela; Rogaeva, Ekaterina; Lang, Anthony; Koks, Sulev; Taba, Pille; Lesage, Suzanne; Brice, Alexis; Corvol, Jean-Christophe; Chartier-Harlin, Marie-Christine; Mutez, Eugenie; Brockmann, Kathrin; Deutschlaender, Angela B.; Hadjigeorgiou, Georges M.; Dardiotis, Efthimos; Stefanis, Leonidas; Simitsi, Athina Maria; Valente, Enza Maria; Petrucci, Simona; Straniero, Letizia; Zecchinelli, Anna; Pezzoli, Gianni; Brighina, Laura; Ferrarese, Carlo; Annesi, Grazia; Quattrone, Andrea; Gagliardi, Monica; Burbulla, Lena F.; Matsuo, Hirotaka; Kawamura, Yusuke; Hattori, Nobutaka; Nishioka, Kenya; Chung, Sun Ju; Kim, Yun Joong; Pavelka, Lukas; van de Warrenburg, Bart P. C.; Bloem, Bastiaan R.; Singleton, Andrew B.; Aasly, Jan; Toft, Mathias; Guedes, Leonor Correia; Ferreira, Joaquim J.; Bardien, Soraya; Carr, Jonathan; Tolosa, Eduardo; Ezquerra, Mario; Pastor, Pau; Diez-Fairen, Monica; Wirdefeldt, Karin; Pedersen, Nancy L.; Ran, Caroline; Belin, Andrea C.; Puschmann, Andreas; Hellberg, Clara; Clarke, Carl E.; Morrison, Karen E.; Krainc, Dimitri; Farrer, Matt J.; Kruger, Rejko; Elbaz, Alexis; Gasser, Thomas; Sharma, Manu (2022)
  • Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases
    Witoelar, Aree; Jansen, Iris E.; Wang, Yunpeng; Desikan, Rahul S.; Gibbs, J. Raphael; Blauwendraat, Cornelis; Thompson, Wesley K.; Hernandez, Dena G.; Djurovic, Srdjan; Schork, Andrew J.; Bettella, Francesco; Ellinghaus, David; Franke, Andre; Lie, Benedicte A.; McEvoy, Linda K.; Karlsen, Tomh.; Lesage, Suzanne; Morris, Huw R.; Brice, Alexis; Wood, Nicholas W.; Heutink, Peter; Hardy, John; Singleton, Andrew B.; Dale, Anders M.; Gasser, Thomas; Andreassen, Ole A.; Sharma, Manu (2017)
  • Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
    Nalls, Mike A.; Blauwendraat, Cornelis; Vallerga, Costanza L.; Heilbron, Karl; Bandres-Ciga, Sara; Chang, Diana; Tan, Manuela; Kia, Demis A.; Noyce, Alastair J.; Xue, Angli; Bras, Jose; Young, Emily; von Coelln, Rainer; Simon-Sanchez, Javier; Schulte, Claudia; Sharma, Manu; Krohn, Lynne; Pihlstrom, Lasse; Siitonen, Ari; Iwaki, Hirotaka; Leonard, Hampton; Faghri, Faraz; Gibbs, J. Raphael; Hernandez, Dena G.; Scholz, Sonja W.; Botia, Juan A.; Martinez, Maria; Corvol, Jean-Christophe; Lesage, Suzanne; Jankovic, Joseph; Shulman, Lisa M.; Sutherland, Margaret; Tienari, Pentti; Majamaa, Kari; Toft, Mathias; Andreassen, Ole A.; Bangale, Tushar; Brice, Alexis; Yang, Jian; Gan-Or, Ziv; Gasser, Thomas; Heutink, Peter; Shulman, Joshua M.; Wood, Nicholas W.; Hinds, David A.; Hardy, John A.; Morris, Huw R.; Gratten, Jacob; Visscher, Peter M.; Graham, Robert R.; Singleton, Andrew B. (2019)
  • Integrative Pathway-Based Approach for Genome-Wide Association Studies: Identification of New Pathways for Rheumatoid Arthritis and Type 1 Diabetes
    Buechel, Finja; Mittag, Florian; Wrzodek, Clemens; Zell, Andreas; Gasser, Thomas; Sharma, Manu (2013)
  • Intronic enhancers of the human SNCA gene predominantly regulate its expression in brain in vivo
    Cheng, Fubo; Zheng, Wenxu; Liu, Chang; Barbuti, Peter Antony; Yu-Taeger, Libo; Casadei, Nicolas; Huebener-Schmid, Jeannette; Admard, Jakob; Boldt, Karsten; Junger, Katrin; Ueffing, Marius; Houlden, Henry; Sharma, Manu; Kruger, Rejko; Grundmann-Hauser, Kathrin; Ott, Thomas; Riess, Olaf (2022)