Auflistung Universitätsbibliographie nach Autor "Sharma, Manu"

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Auflistung Universitätsbibliographie nach Autor "Sharma, Manu"

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  • SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
    Fernandez-Santiago, Ruben; Martin-Flores, Nuria; Antonelli, Francesca; Cerquera, Catalina; Moreno, Veronica; Bandres-Ciga, Sara; Manduchi, Elisabetta; Tolosa, Eduard; Singleton, Andrew B.; Moore, Jason H.; Noyce, Alastair J.; Kaiyrzhanov, Rauan; Middlehurst, Ben; Kia, Demis A.; Tan, Manuela; Houlden, Henry; Morris, Huw R.; Plun-Favreau, Helene; Holmans, Peter; Hardy, John; Trabzuni, Daniah; Bras, Jose; Quinn, John; Mok, Kin Y.; Kinghorn, Kerri J.; Billingsley, Kimberley; Wood, Nicholas W.; Lewis, Patrick; Schreglmann, Sebastian; Guerreiro, Rita; Lovering, Ruth; R'Bibo, Lea; Manzoni, Claudia; Rizig, Mie; Ryten, Mina; Guelfi, Sebastian; Escott-Price, Valentina; Chelban, Viorica; Foltynie, Thomas; Williams, Nigel; Morrison, Karen E.; Clarke, Carl; Brice, Alexis; Danjou, Fabrice; Lesage, Suzanne; Corvol, Jean-Christophe; Martinez, Maria; Schulte, Claudia; Brockmann, Kathrin; Simon-Sanchez, Javier; Heutink, Peter; Rizzu, Patrizia; Sharma, Manu; Gasser, Thomas; Nicolas, Aude; Cookson, Mark R.; Bandres-Ciga, Sara; Blauwendraat, Cornelis; Craig, David W.; Faghri, Faraz; Gibbs, J. Raphael; Hernandez, Dena G.; Van Keuren-Jensen, Kendall; Shulman, Joshua M.; Iwaki, Hirotaka; Leonard, Hampton L.; Nalls, Mike A.; Robak, Laurie; Lubbe, Steven; Finkbeiner, Steven; Mencacci, Niccolo E.; Lungu, Codrin; Singleton, Andrew B.; Scholz, Sonja W.; Reed, Xylena; Alcalay, Roy N.; Gan-Or, Ziv; Rouleau, Guy A.; Krohn, Lynne; van Hilten, Jacobus J.; Marinus, Johan; Adarmes-Gomez, Astrid D.; Aguilar, Iquel; Alvarez, Ignacio; Alvarez, Victoria; Javier Barrero, Francisco; Bergareche Yarza, Jesus Alberto; Bernal-Bernal, Inmaculada; Blazquez, Marta; Bonilla-Toribio, Marta; Botia, Juan A.; Teresa Boungiorno, Maria; Buiza-Rueda, Dolores; Camara, Ana; Carrillo, Fatima; Carrion-Claro, Mario; Cerdan, Debora; Clarimon, Jordi; Compta, Yaroslau; de la Casa, Beatriz; Diez-Fairen, Monica (2019)
  • The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
    Heckman, Michael G.; Elbaz, Alexis; Soto-Ortolaza, Alexandra I.; Serie, Daniel J.; Aasly, Jan O.; Annesi, Grazia; Auburger, Georg; Bacon, Justin A.; Boczarska-Jedynak, Magdalena; Bozi, Maria; Brighina, Laura; Chartier-Harlin, Marie-Christine; Dardiotism, Efthimios; Destee, Alain; Ferrarese, Carlo; Ferraris, Alessandro; Fiske, Brian; Gispert, Suzana; Hadjigeorgioum, Georgios M.; Hattori, Nobutaka; Ioannidis, John P. A.; Jasinska-Myga, Barbara; Jeon, Beom S.; Kim, Yun Joong; Klein, Christine; Kruger, Rejko; Kyratzi, Elli; Lin, Chin-Hsien; Lohmann, Katja; Loriot, Marie-Anne; Lynch, Timothy; Mellick, George D.; Mutez, Eugenie; Opala, Grzegorz; Park, Sung Sup; Petrucci, Simona; Quattrone, Aldo; Sharma, Manu; Silburn, Peter A.; Sohn, Young Ho; Stefanis, Leonidas; Tadic, Vera; Tomiyama, Hiroyuki; Uitti, Ryan J.; Valente, Enza Maria; Vassilatis, Demetrios K.; Vilarino-Guell, Carles; White, Linda R.; Wirdefeldt, Karin; Wszolek, Zbigniew K.; Wu, Ruey-Meei; Xiromerisiou, Georgia; Maraganore, Demetrius M.; Farrer, Matthew J.; Ross, Owen A. (2014)
  • TREM2 R47H variant and risk of essential tremor: A cross-sectional international multicenter study
    Ortega-Cubero, Sara; Lorenzo-Betancor, Oswaldo; Lorenzo, Elena; Agundez, Jose A. G.; Jimenez-Jimenez, Felix J.; Ross, Owen A.; Wurster, Isabel; Mielke, Carina; Lin, Juei-Jueng; Coria, Francisco; Clarimon, Jordi; Ezquerra, Mario; Brighina, Laura; Annesi, Grazia; Alonso-Navarro, Hortensia; Garcia-Martin, Elena; Gironell, Alex; Marti, Maria J.; Yueh, Kuo-Chu; Wszolek, Zbigniew K.; Sharma, Manu; Berg, Daniela; Krueger, Rejko; Pastor, Maria A.; Pastor, Pau (2015)
  • Understanding the missing heritability of Parkinson disease
    Sharma, Manu (2021)
  • Understanding the role of genetic variability in LRRK2 in Indian population
    Kishore, Asha; Sreelatha, Ashwin Ashok Kumar; Sturm, Marc; von-Zweydorf, Felix; Pihlstrom, Lasse; Raimondi, Francesco; Russell, Rob; Lichtner, Peter; Banerjee, Moinak; Krishnan, Syam; Rajan, Roopa; Puthenveedu, Divya Kalikavil; Chung, Sun Ju; Bauer, Peter; Riess, Olaf; Gloeckner, Christian Johannes; Kruger, Rejko; Gasser, Thomas; Sharma, Manu (2019)
  • Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities
    Mittag, Florian; Buechel, Finja; Saad, Mohamad; Jahn, Andreas; Schulte, Claudia; Bochdanovits, Zoltan; Simon-Sanchez, Javier; Nalls, Mike A.; Keller, Margaux; Hernandez, Dena G.; Gibbs, J. Raphael; Lesage, Suzanne; Brice, Alexis; Heutink, Peter; Martinez, Maria; Wood, Nicholas W.; Hardy, John; Singleton, Andrew B.; Zell, Andreas; Gasser, Thomas; Sharma, Manu (2012)
  • Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
    Keller, Margaux F.; Saad, Mohamad; Bras, Jose; Bettella, Francesco; Nicolaou, Nayia; Simon-Sanchez, Javier; Mittag, Florian; Buechel, Finja; Sharma, Manu; Gibbs, J. Raphael; Schulte, Claudia; Moskvina, Valentina; Durr, Alexandra; Holmans, Peter; Kilarski, Laura L.; Guerreiro, Rita; Hernandez, Dena G.; Brice, Alexis; Ylikotila, Pauli; Stefansson, Hreinn; Majamaa, Kari; Morris, Huw R.; Williams, Nigel; Gasser, Thomas; Heutink, Peter; Wood, Nicholas W.; Hardy, John; Martinez, Maria; Singleton, Andrew B.; Nalls, Michael A. (2012)
  • What have we learned from genome-wide association studies (GWAS) in Parkinson's disease?
    Fernandez-Santiago, Ruben; Sharma, Manu (2022)