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

von 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.
Veröffentlicht 2006

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

von 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.
Veröffentlicht 2002

Linkage analysis of familial Alzheimer disease, using chromosome 21 markers

von 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.
Veröffentlicht 1991

A genome-wide linkage analysis of dementia in the Amish

von 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.
Veröffentlicht 2006