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Kruger, Rejko, Sharma, Manu, Riess, Olaf, Gasser, Thomas, Van Broeckhoven, Christine, Theuns, Jessie, Aasly, Jan, Annesi, Grazia, Bentivoglio, Anna Rita, Brice, Alexis, Djarmati, Ana, Elbaz, Alexis, Farrer, Matthew, Ferrarese, Carlo, Gibson, J. Mark, Hadjigeorgiou, Georgios M., Hattori, Nobutaka, Ioannidis, John P.A., Jasinska-Myga, Barbara, Klein, Christine, Lambert, Jean-Charles, Lesage, Suzanne, Lin, Juei-Jueng, Lynch, Timothy, Mellick, George D., de Nigris, Francesa, Opala, Grzegorz, Prigione, Alessandro, Quattrone, Aldo, Ross, Owen A., Satake, Wataru, Silburn, Peter A., Tan, Eng King, Toda, Tatsushi, Tomiyama, Hiroyuki, Wirdefeldt, Karin, Wszolek, Z., Xiromerisiou, Georgia and Maraganore, Demetrius M. (2011) A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. Neurobiology of Aging, 32 3: 548.e9-548.e18. doi:10.1016/j.neurobiolaging.2009.11.021 169   9 Cited 16 times in Scopus16 0
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 and GEOPD consortium (2012) A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics, 49 11: 721-726. doi:10.1136/jmedgenet-2012-101155 83   22 Cited 21 times in Scopus21 1
Simon-Sanchez, Javier, Kilarski, Laura L., Nalls, Michael A., Martinez, Maria, Schulte, Claudia, Holmans, Peter, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium, Gasser, Thomas, Hardy, John, Singleton, Andrew B., Wood, Nicholas W., Brice, Alexis, Heutink, Peter, Williams, Nigel, Morris, Huw R. and Brown, Matthew (2012) Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's Disease. Plos One, 7 3: e28787.1-e28787.2. doi:10.1371/journal.pone.0028787 45   8 Cited 8 times in Scopus8 1
Sharma, Manu, Ioannidis, John P. A., Aasly, Jan O., Annesi, Grazia, Brice, Alexis, Van Broeckhoven, Christine, Bertram, Lars, Bozi, Maria, Crosiers, David, Clarke, Carl, Facheris, Maurizio, Farrer, Matthew, Garraux, Gaetan, Gispert, Suzana, Auburger, Georg, Vilarino-Gueell, Carles, Hadjigeorgiou, Georgios M., Hicks, Andrew A., Hattori, Nobutaka, Jeon, Beom, Lesage, Suzanne, Lill, Christina M., Lin, Juei-Jueng, Lynch, Timothy, Lichtner, Peter, Lang, Anthony E., Mok, Vincent, Jasinska-Myga, Barbara, Mellick, George D., Morrison, Karen E., 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., Theuns, Jessie, Tan, Eng-King, Toda, Tatsushi, Tomiyama, Hiroyuki, Uitti, Ryan J., Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Yueh, Kuo-Chu, Zhao, Yi, Gasser, Thomas, Maraganore, Demetrius, Krueger, Rejko and On behalf of the GEO-PD Consortium (2012) Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology, 79 7: 659-667. doi:10.1212/WNL.0b013e318264e353 90 1 42 Cited 41 times in Scopus41 5
Sharma, Manu, Maraganore, Demetrius M., Ioannidis, John P. A., Riess, Olaf, Aasly, Jan O., Annesi, Grazia, Abahuni, Nadine, Bentivoglio, Anna Rita, Brice, Alexis, Van Broeckhoven, Christine, Chartier-Harlin, Marie-Christine, Destee, Alain, Djarmati, Ana, Elbaz, Alexis, Farrer, Matthew, Ferrarese, Carlo, Gibson, J. Mark, Gispert, Suzana, Hattori, Nobutaka, Jasinska-Myga, Barbara, Klein, Christine, Lesage, Suzanne, Lynch, Timothy, Lichtner, Peter, Lambert, Jean-Charles, Lang, Anthony E., Mellick, George D., De Nigris, Francesca, Opala, Grzegorz, Quattrone, Aldo, Riva, Chiara, Rogaeva, Ekaterina, Ross, Owen A., Satake, Wataru, Silburn, Peter A., Theuns, Jessie, Toda, Tatsushi, Tomiyama, Hiroyuki, Uitti, Ryan J., Wirdefeldt, Karin, Wszolek, Zbigniew, Gasser, Thomas, Kruger, Rejko and for the Genetic Epidemiology of Parkinson's Disease Consortium (2011) Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Neurobiology of Aging, 32 11: 2108.e1-2108.e5. doi:10.1016/j.neurobiolaging.2011.05.024 68   0 Cited 6 times in Scopus6 0
Maraganore, Demetrius M., Lesnick, Timothy G., Elbaz, Alexis, Chartier-Harlin, Marie-Christine, Gasser, Thomas, Krüger, Rejko, Hattori, Nobutaka, Mellick, George D., Quattrone, Aldo, Satoh, Jun-Ichi, Toda, Taksushi, Wang, Jian, Ioannidis, John P. A., de Andrade, Mariza, Rocca, Walter A., UCHL1 Global Genetics Consortium and Silburn, Peter A. (2004) UCHL1 is a Parkinson's disease susceptibility gene. Annals of Neurology, 55 4: 512-521. doi:10.1002/ana.20017 115   143 Cited 165 times in Scopus165 6
Keller, Margaux F., Saad, Mohamad, Bras, Jose, Bettella, Francesco, Nicolaou, Nayia, Simon-Sanchez, Javier, Mittag, Florian, Buchel, 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., for International Parkinson's Disease Geonomics Consortium (IPDGC), for The Welcome Trust Case Control Consortium 2 (WTCCC2) and Brown, Matthew A. (2012) Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Human Molecular Genetics, 21 22: 4996-5009. doi:10.1093/hmg/dds335 22   30 Cited 28 times in Scopus28 13