Now showing items 1-3 of 3

  • Bonham, Luke W.; Karch, Celeste M.; Fan, Chun C.; Tan, Chin; Geier, Ethan G.; Wang, Yunpeng; Wen, Natalie; Broce, Iris J.; Li, Yi; Barkovich, Matthew J.; Ferrari, Raffaele; Hardy, John; Momeni, Parastoo; Höglinger, Günter U.; Müller, Ulrich; Hess, Christopher P.; Sugrue, Leo P.; Dillon, William P.; Schellenberg, Gerard D.; Miller, Bruce L.; Andreassen, Ole Andreas; Dale, Anders; Barkovich, A. James; Yokoyama, Jennifer S.; Desikan, Rahul S. (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2018)
    Neurodegenerative diseases likely share common underlying pathobiology. Although prior work has identified susceptibility loci associated with various dementias, few, if any, studies have systematically evaluated shared ...
  • Broce, Iris J.; Karch, Celeste M.; Wen, Natalie; Fan, Chun C.; Wang, Yunpeng; Hong Tan, Chin; Kouri, Naomi; Ross, Owen A.; Höglinger, Günter U.; Müller, Ulrich; Hardy, John; Momeni, Parastoo; Hess, Christopher P.; Dillon, William P.; Miller, Zachary A.; Bonham, Luke W.; Rabinovici, Gil D.; Rosen, Howard J.; Schellenberg, Gerard D.; Franke, Andre; Karlsen, Tom Hemming; Veldink, Jan H.; Ferrari, Raffaele; Yokoyama, Jennifer S.; Miller, Bruce L.; Andreassen, Ole Andreas; Dale, Anders; Desikan, Rahul S.; Sugrue, Leo P. (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2018)
    Background: Converging evidence suggests that immune-mediated dysfunction plays an important role in the pathogenesis of frontotemporal dementia (FTD). Although genetic studies have shown that immune-associated loci are ...
  • Li, Yi; Barkovich, Matthew J.; Karch, Celeste M.; Nillo, Ryan M.; Fan, Chun-Chieh; Broce, Iris J.; Tan, Chin Hong; Cuneo, Daniel; Hess, Christopher P.; Dillon, William P.; Glenn, Orit A.; Glastonbury, Christine M.; Olney, Nicholas; Yokoyama, Jennifer S.; Bonham, Luke W.; Miller, Bruce; Kao, Aimee; Schmansky, Nicholas; Fischl, Bruce; Andreassen, Ole Andreas; Jernigan, Terry; Dale, Anders; Barkovich, A. James; Desikan, Rahul S.; Sugrue, Leo P. (Journal article / Tidsskriftartikkel / PublishedVersion; Peer reviewed, 2018)
    Tuberous sclerosis complex (TSC), a heritable neurodevelopmental disorder, is caused by mutations in the TSC1 or TSC2 genes. To date, there has been little work to elucidate regional TSC1 and TSC2 gene expression within ...