Parkinsonism Syndrome in Heterozygotes for Niemann Pick C1

Por Kluenemann, Hans H., Nutt, John G., Davis, Marie Y., Bird, Thomas D.
Publicado no J Neurol Sci (2013)

Unusually Long Duration and Delayed Penetrance in a Family With FTD and Mutation in MAPT (V337M)

Por Domoto-Reilly, Kimiko, Davis, Marie Y., Keene, C. Dirk, Bird, Thomas D.
Publicado no Am J Med Genet B Neuropsychiatr Genet (2016)

Novel mutations in ataxia telangiectasia and AOA2 associated with prolonged survival

Por Davis, Marie Y., Keene, C. Dirk, Swanson, Phillip D., Sheehy, Conor, Bird, Thomas D.
Publicado em 2013

Vreteno, a gonad-specific protein, is essential for germline development and primary piRNA biogenesis in Drosophila

Por Zamparini, Andrea L., Davis, Marie Y., Malone, Colin D., Vieira, Eric, Zavadil, Jiri, Sachidanandam, Ravi, Hannon, Gregory J., Lehmann, Ruth
Publicado em 2011

Glucocerebrosidase Deficiency in Drosophila Results in α-Synuclein-Independent Protein Aggregation and Neurodegeneration

Por Davis, Marie Y., Trinh, Kien, Thomas, Ruth E., Yu, Selina, Germanos, Alexandre A., Whitley, Brittany N., Sardi, Sergio Pablo, Montine, Thomas J., Pallanck, Leo J.
Publicado no PLoS Genet (2016)

The Discovery of LRRK2 p.Arg1441Ser, a novel mutation for Parkinson’s disease, Adds to the Complexity of a Mutational Hotspot

Por Mata, Ignacio F., Davis, Marie Y., Lopez, Alexis N., Dorschner, Michael O., Martinez, Erica, Yearout, Dora, Cholerton, Brenna A., Hu, Shu-Ching, Edwards, Karen L., Bird, Thomas D., Zabetian, Cyrus P.
Publicado no Am J Med Genet B Neuropsychiatr Genet (2016)

ADCY5-related dyskinesia: Broader spectrum and genotype–phenotype correlations

Por Chen, Dong-Hui, Méneret, Aurélie, Friedman, Jennifer R., Korvatska, Olena, Gad, Alona, Bonkowski, Emily S., Stessman, Holly A., Doummar, Diane, Mignot, Cyril, Anheim, Mathieu, Bernes, Saunder, Davis, Marie Y., Damon-Perrière, Nathalie, Degos, Bertrand, Grabli, David, Gras, Domitille, Hisama, Fuki M., Mackenzie, Katherine M., Swanson, Phillip D., Tranchant, Christine, Vidailhet, Marie, Winesett, Steven, Trouillard, Oriane, Amendola, Laura M., Dorschner, Michael O., Weiss, Michael, Eichler, Evan E., Torkamani, Ali, Roze, Emmanuel, Bird, Thomas D., Raskind, Wendy H.
Publicado no Neurology (2015)

Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease

Por Davis, Marie Y., Johnson, Catherine O., Leverenz, James B., Weintraub, Daniel, Trojanowski, John Q., Chen-Plotkin, Alice, Van Deerlin, Vivianna M., Quinn, Joseph F., Chung, Kathryn A., Peterson-Hiller, Amie L., Rosenthal, Liana S., Dawson, Ted M., Albert, Marilyn S., Goldman, Jennifer G., Stebbins, Glenn T., Bernard, Bryan, Wszolek, Zbigniew K., Ross, Owen A., Dickson, Dennis W., Eidelberg, David, Mattis, Paul J., Niethammer, Martin, Yearout, Dora, Hu, Shu-Ching, Cholerton, Brenna A., Smith, Megan, Mata, Ignacio F., Montine, Thomas J., Edwards, Karen L., Zabetian, Cyrus P.
Publicado no JAMA Neurol (2016)