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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 76   19 Cited 18 times in Scopus18 1
Samani, Nilesh J., Erdmann, Jeanette, Hall, Alistair S., Hengstenberg, Christian, Mangino, Mangino, Mayer, Bjoern, Dixon, Richard J., Meitinger, Thomas, Braund, Peter, Wichmann, H. Erich, Barrett, Jennifer H., Konig, Inke R., Stevens, Suzanne E., Szymczak, Silke, Tregouet, David-Alexandre, Iles, Mark M., Pahlke, Friedrich, Pollard, Helen, Lieb, Wolfgang, Cambien, Francois, Fischer, Marcus, Ouwehand, Willem, Blankenberg, Stefan, Balmforth, Anthony J., Baessler, Andrea, Ball, Steven G., Strom, Tim M., Braenne, Ingrid, Gieger, Christian, Deloukas, Panos, Tobin, Martin D., Ziegler, Andreas, Thompson, John R., Schunkert, Heribert, for the WTCCC and the Cardiogenics Consortium, Bradbury, Linda A. and Brown, Matthew A. (2007) Genomewide association analysis of coronary artery disease. The New England Journal of Medicine, 357 5: 443-453. doi:10.1056/NEJMoa072366 155   977 Cited 1016 times in Scopus1016 3