Clinical Correlates of Depressive Symptoms in Familial Parkinson's Disease

Por Pankratz, Nathan, Marder, Karen S., Halter, Cheryl A., Rudolph, Alice, Shults, Cliff W., Nichols, William C., Foroud, Tatiana
Publicado em 2008

Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations

Por Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana
Publicado em 2002

Significant Linkage of Parkinson Disease to Chromosome 2q36-37

Por Pankratz, Nathan, Nichols, William C., Uniacke, Sean K., Halter, Cheryl, Rudolph, Alice, Shults, Cliff, Conneally, P. Michael, Foroud, Tatiana
Publicado em 2003

Novel recruitment strategy to enrich for LRRK2 mutation carriers

Por Foroud, Tatiana, Smith, Danielle, Jackson, Jacqueline, Verbrugge, Jennifer, Halter, Cheryl, Wetherill, Leah, Sims, Katherine, Xin, Winnie, Arnedo, Vanessa, Lasch, Shirley, Marek, Kenneth
Publicado no Mol Genet Genomic Med (2015)

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

Por Simon, David K, Pankratz, Nathan, Kissell, Diane K, Pauciulo, Michael W, Halter, Cheryl A, Rudolph, Alice, Pfeiffer, Ronald F, Nichols, William C, Foroud, Tatiana
Publicado em 2010

Alpha-Synuclein and Familial Parkinson’s Disease

Por Pankratz, Nathan, Nichols, William C., Elsaesser, Veronika E., Pauciulo, Michael W., Marek, Diane K., Halter, Cheryl A., Wojcieszek, Joanne, Rudolph, Alice, Pfeiffer, Ronald F., Foroud, Tatiana
Publicado em 2009

Genomewide linkage study of modifiers of LRRK2-related Parkinson’s disease

Por LATOURELLE, JEANNE C., HENDRICKS, AUDREY E., PANKRATZ, NATHAN, WILK, JEMMA B., HALTER, CHERYL, NICHOLS, WILLIAM C., GUSELLA, JAMES F., DESTEFANO, ANITA L., MYERS, RICHARD H., FOROUD, TATIANA
Publicado em 2011

Mutations in DJ-1 are rare in familial Parkinson disease

Por Pankratz, Nathan, Pauciulo, Michael W., Elsaesser, Veronika E., Marek, Diane K., Halter, Cheryl A., Wojcieszek, Joanne, Rudolph, Alice, Shults, Clifford W., Foroud, Tatiana, Nichols Ph.D., William C.
Publicado em 2006

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Por Pankratz, Nathan, Wilk, Jemma B., Latourelle, Jeanne C., DeStefano, Anita L., Halter, Cheryl, Pugh, Elizabeth W., Doheny, Kimberly F., Gusella, James F., Nichols, William C., Foroud, Tatiana, Myers, Richard H.
Publicado em 2008

Genomewide association study for onset age in Parkinson disease

Por Latourelle, Jeanne C, Pankratz, Nathan, Dumitriu, Alexandra, Wilk, Jemma B, Goldwurm, Stefano, Pezzoli, Gianni, Mariani, Claudio B, DeStefano, Anita L, Halter, Cheryl, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana
Publicado em 2009

Copy Number Variation in Familial Parkinson Disease

Por Pankratz, Nathan, Dumitriu, Alexandra, Hetrick, Kurt N., Sun, Mei, Latourelle, Jeanne C., Wilk, Jemma B., Halter, Cheryl, Doheny, Kimberly F., Gusella, James F., Nichols, William C., Myers, Richard H., Foroud, Tatiana, DeStefano, Anita L.
Publicado em 2011

Michael J. Fox Foundation Consortium: Geographical Differences in Returning Genetic Research Data to Study Participants

Por Alcalay, Roy N., Aasly, Jan, Berg, Daniela, Bressman, Susan, Brice, Alexis, Brockmann, Kathrin, Chan, Piu, Clark, Lorraine, Corvol, Jean-Christophe, Durr, Alexandra, Farrer, Matthew, Foroud, Tatiana M., Gasser, Thomas, Giladi, Nir, Halter, Cheryl, Hentati, Fayçal, Lang, Anthony, Langston, J. William, Marder, Karen, Marras, Connie, Marti-Masso, Jose-Felix, Martinez, Javier Ruiz, Mejia-Santana, Helen, Mirelman, Anat, Pont, Claustre, Orr-Urtreger, Avi, Raymond, Deborah, Saunders-Pullman, Rachel, Schüle, Birgitt, Tanner, Caroline, Tolosa, Eduardo, Vilas, Dolores, Wise, Adina, Facheris, Maurizio
Publicado no Genet Med (2014)