PerryGaskellMD

PubMed

• 3 citations
  Longitudinal follow-up of late-onset Alzheimer disease families.
  Regina M. Carney, Michael A. Slifer, Ping-I Lin, P. C. Gaskell, William K. Scott, C.F. Potocky, Christine M. Hulette, Kathleen A. Welsh-Bohmer, Donald E. Schmechel, Je...> ;American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 2008 Jul 5
• 173 citations
  Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.
  Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, Martha Nance, Perry C. Gaskell, Jeffery M. Vance, Allison E. Ashley-Koch, Margaret A. Pericak-Vance> ;American Journal of Human Genetics. 2006 Aug 1
• 21 citations
  A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12
  Stephan Züchner, Melanie E. Kail, Martha Nance, Perry C. Gaskell, Ingrid K. Svenson, Douglas A. Marchuk, Margaret A. Pericak-Vance, Allison E. Ashley-Koch> ;Neurogenetics. 2006 Mar 25
• 39 citations
  A genome-wide linkage analysis of dementia in the Amish†
  Daniel W. Hahs, Jacob L. McCauley, Amy E. Crunk, Lynne L. McFarland, Perry C. Gaskell, Lan Jiang, Susan H. Slifer, Jeffery M. Vance, William K. Scott, Kathleen A. Wels...> ;American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 2006 Mar 5
• 25 citations
  Maternal lineages and Alzheimer disease risk in the Old Order Amish
  Joelle M. van der Walt, William K. Scott, Susan H. Slifer, P. C. Gaskell, Eden R. Martin, Kathleen A. Welsh-Bohmer, Marilyn Creason, Amy E. Crunk, Denise Fuzzell, Lynn...> ;Human Genetics. 2005 Aug 3
• 27 citations
  An autosomal genomic screen for dementia in an extended Amish family.
  Allison E. Ashley-Koch, Yujun Shao, J. B. Rimmler, P. C. Gaskell, Kathleen A. Welsh-Bohmer, Charles E. Jackson, William K. Scott, Jonathan L. Haines, Margaret A. Peric...> ;Neuroscience Letters. 2005 May 13
• 68 citations
  Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.
  Ingrid K. Svenson, Mark T. Kloos, P. Craig Gaskell, Martha Nance, James Y. Garbern, Shin-ichi Hisanaga, Margaret A. Pericak-Vance, Allison E. Ashley-Koch, Douglas A. M...> ;Neurogenetics. 2004 Jul 10
• 2 citations
  Alzheimer's disease genes and genetic testing in clinical practice.
  P. C. Gaskell, Jeffery M. Vance> ;JAAPA. 2004 Mar 1
• 36 citations
  Lewy body pathology is a frequent co-pathology in familial Alzheimer's disease
  Yuri Trembath, Carolyn Rosenberg, John F. Ervin, Donald E. Schmechel, Perry C. Gaskell, Margaret A. Pericak-Vance, Jeffery M. Vance, Christine M. Hulette> ;Acta Neuropathologica. 2003 Feb 11
• 385 citations
  A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10)
  Evan Reid, Mark T. Kloos, Allison E. Ashley-Koch, Lori Hughes, Simon Bevan, Ingrid K. Svenson, Felicia L. Graham, Perry C. Gaskell, A M Dearlove, Margaret A. Pericak-V...> ;American Journal of Human Genetics. 2002 Nov 1
• 6 citations
  Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432.
  Marcy C. Speer, Felicia L. Graham, Erin Bonner, Keva Collier, Jeffrey M. Stajich, Perry C. Gaskell, Margaret A. Pericak-Vance, Jeffery M. Vance> ;Neurogenetics. 2002 Oct 1
• 242 citations
  Age at onset in two common neurodegenerative diseases is genetically controlled
  Yi-Ju Li, William K. Scott, Dale J. Hedges, Fengyu Zhang, P. Craig Gaskell, Martha Nance, Ray L. Watts, Jean P. Hubble, William C. Koller, Rajesh Pahwa, Matthew B. Ste...> ;American Journal of Human Genetics. 2002 Apr 1
• 121 citations
  Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia
  Ingrid K. Svenson, Allison E. Ashley-Koch, P. Craig Gaskell, Travis J. Riney, W. J.Ken Cumming, Helen Kingston, Edward L. Hogan, Rose-Mary Boustany, Jeffery M. Vance, ...> ;American Journal of Human Genetics. 2001 May 1
• 10 citations
  Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
  Allison E. Ashley-Koch, Erin Bonner, P. Craig Gaskell, Sandra G. West, Richard W. Tim, Chantelle M. Wolpert, Rodney Jones, Carolyn Farrell, Martha Nance, Ingrid K. Sve...> ;Neurogenetics. 2001 Jan 30
• 205 citations
  Myotilin is mutated in limb girdle muscular dystrophy 1A
  Michael A. Hauser, Stephen K. Horrigan, Paula Salmikangas, Udana Torian, Kristi D. Viles, Ria Dancel, Richard W. Tim, Anu Taivainen, Luria Bartoloni, James M. Gilchris...> ;Human Molecular Genetics. 2000 Sep 1
• 58 citations
  Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutation
  Carlyn K. Rosenberg, Margaret A. Pericak-Vance, Ann M. Saunders, John R. Gilbert, P. C. Gaskell, Christine M. Hulette> ;Acta Neuropathologica. 2000 Aug 1
• 40 citations
  Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684.
  Christine M. Hulette, Margaret A. Pericak-Vance, A. D. Roses, Donald E. Schmechel, Larry H. Yamaoka, P. C. Gaskell, Kathleen A. Welsh-Bohmer, R. A. Crowther, M. G. Spi...> ;Journal of Neuropathology and Experimental Neurology. 1999 Aug 1
• 2 citations
  No association of α1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients
  Meredyth P. Bass, Larry H. Yamaoka, William K. Scott, P. Craig Gaskell, Kathleen A. Welsh-Bohmer, Allen D. Roses, Ann M. Saunders, Jonathan L. Haines, Margaret A. Peri...> ;Neuroscience Letters. 1998 Jun 19
• 11 citations
  Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.
  Marcy C. Speer, James M. Gilchrist, Jeffrey M. Stajich, P. C. Gaskell, Carol A. Westbrook, Stephen K. Horrigan, Lucia Bartoloni, Larry H. Yamaoka, William K. Scott, Ma...> ;Journal of Medical Genetics. 1998 Apr 1
• 34 citations
  No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease.
  William K. Scott, Larry H. Yamaoka, Meredyth P. Bass, P. Craig Gaskell, P. Michael Conneally, Gary W. Small, Lindsay A. Farrer, S. A. Auerbach, Ann M. Saunders, Allen ...> ;Neurogenetics. 1998 Mar 1
• 287 citations
  Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12.
  Margaret A. Pericak-Vance, Meredyth P. Bass, Larry H. Yamaoka, Perry C. Gaskell, William K. Scott, Henry Terwedow, M. M. Menold, P. Michael Conneally, Gary W. Small, J...> ;JAMA. 1997 Oct 15
• 7 citations
  Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation
  Jeffrey M. Stajich, James M. Gilchrist, Felicia Lennon, Arnold Lee, Larry H. Yamaoka, B.L. Rosi, Perry C. Gaskell, Meredyth L. Pritchard, Lauren Donald, Allen D. Roses...> ;Neuromuscular Disorders. 1997 Oct 1
• 18 citations
  Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
  William K. Scott, P. C. Gaskell, Felicia Lennon, Chantelle M. Wolpert, M. M. Menold, Arthur S. Aylsworth, C. Warner, Carolyn Farrell, Rose-Mary Boustany, S.G. Albright...> ;Neurogenetics. 1997 Sep 1
• 11 citations
  Apolipoprotein E ε2 does not increase risk of early-onset sporadic Alzheimer's disease
  William K. Scott, Ann M. Saunders, P. C. Gaskell, P. A. Locke, John H. Growdon, Lindsay A. Farrer, S. A. Auerbach, A. D. Roses, Jonathan L. Haines, Margaret A. Pericak...> ;Annals of Neurology. 1997 Sep 1
• 26 citations
  No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease.
  William K. Scott, Larry H. Yamaoka, P. A. Locke, B.L. Rosi, P. C. Gaskell, Ann M. Saunders, P. M. Conneally, Gary W. Small, Lindsay A. Farrer, John H. Growdon, A. D. R...> ;Genetic Epidemiology. 1997 Jan 1
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