Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Corticobasal Degeneration[original query] |
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Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.
Nature communications 2015 6 7247. Kouri Naomi, Ross Owen A, Dombroski Beth, Younkin Curtis S, Serie Daniel J, Soto-Ortolaza Alexandra, Baker Matthew, Finch Ni Cole A, Yoon Hyejin, Kim Jungsu, Fujioka Shinsuke, McLean Catriona A, Ghetti Bernardino, Spina Salvatore, Cantwell Laura B, Farlow Martin R, Grafman Jordan, Huey Edward D, Ryung Han Mi, Beecher Sherry, Geller Evan T, Kretzschmar Hans A, Roeber Sigrun, Gearing Marla, Juncos Jorge L, Vonsattel Jean Paul G, Van Deerlin Vivianna M, Grossman Murray, Hurtig Howard I, Gross Rachel G, Arnold Steven E, Trojanowski John Q, Lee Virginia M, Wenning Gregor K, White Charles L, Höglinger Günter U, Müller Ulrich, Devlin Bernie, Golbe Lawrence I, Crook Julia, Parisi Joseph E, Boeve Bradley F, Josephs Keith A, Wszolek Zbigniew K, Uitti Ryan J, Graff-Radford Neill R, Litvan Irene, Younkin Steven G, Wang Li-San, Ertekin-Taner Nilüfer, Rademakers Rosa, Hakonarsen Hakon, Schellenberg Gerard D, Dickson Dennis |
Genome-wide association study identifies MAPT locus influencing human plasma tau levels.
Neurology 2017 Jan . Chen Jason, Yu Jin-Tai, Wojta Kevin, Wang Hui-Fu, Zetterberg Henrik, Blennow Kaj, Yokoyama Jennifer S, Weiner Michael W, Kramer Joel H, Rosen Howard, Miller Bruce L, Coppola Giovanni, Boxer Adam L, |
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