Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31

Por Züchner, Stephan, Wang, Gaofeng, Tran-Viet, Khanh-Nhat, Nance, Martha A., Gaskell, Perry C., Vance, Jeffery M., Ashley-Koch, Allison E., Pericak-Vance, Margaret A.
Publicado em 2006

A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)

Por Reid, Evan, Kloos, Mark, Ashley-Koch, Allison, Hughes, Lori, Bevan, Simon, Svenson, Ingrid K., Graham, Felicia Lennon, Gaskell, Perry C., Dearlove, Andrew, Pericak-Vance, Margaret A., Rubinsztein, David C., Marchuk, Douglas A.
Publicado em 2002

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers

Por Schellenberg, Gerard D., Pericak-Vance, Margaret A., Wijsman, Ellen M., Moore, Deborah K., Gaskell, Perry C., Yamaoka, Larry A., Bebout, Jacqueline L., Anderson, Leojean, Welsh, Kathleen A., Clark, Christopher M., Martin, George M., Roses, Allen D., Bird, Thomas D.
Publicado em 1991

A genome-wide linkage analysis of dementia in the Amish

Por Hahs, Daniel W., McCauley, Jacob L., Crunk, Amy E., McFarland, Lynne L., Gaskell, Perry C., Jiang, Lan, Slifer, Susan H., Vance, Jeffery M., Scott, William K., Welsh-Bohmer, Kathleen A., Johnson, Stephanie R., Jackson, Charles E., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado em 2006