Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease
Corder, E. H, Saunders, A. M, Risch, N. J, Strittmatter, W. J, Schmechel, D. E, Gaskell, P. C, Rimmler, J. B, Locke, P. A, Conneally, P. M, Schmader, K. E, Small, G. W, Roses, A. D, Haines, J. L, Pericak-Vance, M. A
Published in Nature genetics (01.06.1994)
Published in Nature genetics (01.06.1994)
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Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families
Corder, E. H., Saunders, A. M., Strittmatter, W. J., Schmechel, D. E., Gaskell, P. C., Small, G. W., Roses, A. D., Haines, J. L., Pericak-Vance, M. A.
Published in Science (American Association for the Advancement of Science) (13.08.1993)
Published in Science (American Association for the Advancement of Science) (13.08.1993)
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Linkage studies in familial Alzheimer disease : evidence for chromosome 19 linkage
PERICAK-VANCE, M. A, BEBOUT, J. L, EARL, N. L, HEYMAN, A, CLARK, C. M, ROSES, A. D, GASKELL, P. C, YAMAOKA, L. H, HUNG, W.-Y, ALBERTS, M. J, WALKER, A. P, BARTLETT, R. J, HAYNES, C. A, WELSH, K. A
Published in American journal of human genetics (01.06.1991)
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Published in American journal of human genetics (01.06.1991)
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Myotilin is mutated in limb girdle muscular dystrophy 1A
HAUSER, M. A, HORRIGAN, S. K, STAJICH, J. M, GASKELL, P. C, GILBERT, J. R, VANCE, J. M, PERICAK-VANCE, M. A, CARPEN, O, WESTBROOK, C. A, SPEER, M. C, SALMIKANGAS, P, TORIAN, U. M, VILES, K. D, DANCEL, R, TIM, R. W, TAIVAINEN, A, BARTOLONI, L, GILCHRIST, J. M
Published in Human molecular genetics (01.09.2000)
Published in Human molecular genetics (01.09.2000)
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Maternal lineages and Alzheimer disease risk in the Old Order Amish
VAN DER WALT, Joelle M, SCOTT, William K, KRONER, Charles C, JACKSON, C. E, HAINES, Jonathan L, PERICAK-VANCE, Margaret A, SLIFER, Susan, GASKELL, P. C, MARTIN, Eden R, WELSH-BOHMER, Kathleen, CREASON, Marilyn, CRUNK, Amy, FUZZELL, Denise, MCFARLAND, Lynne
Published in Human genetics (01.11.2005)
Published in Human genetics (01.11.2005)
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Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus
LIANG, X, SCHNETZ-BOUTAUD, N, BRONSON, P, GILBERT, J. R, MARTIN, E. R, PERICAK-VANCE, M. A, HAINES, J. L, KENEALY, S. J, JIANG, L, BARTLETT, J, LYNCH, B, GASKELL, P. C, GWIRTSMAN, H, MCFARLAND, L, BEMBE, M. L
Published in Molecular psychiatry (01.03.2006)
Published in Molecular psychiatry (01.03.2006)
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An autosomal genomic screen for dementia in an extended Amish family
Ashley-Koch, A.E., Shao, Y., Rimmler, J.B., Gaskell, P.C., Welsh-Bohmer, K.A., Jackson, C.E., Scott, W.K., Haines, J.L., Pericak-Vance, M.A.
Published in Neuroscience letters (13.05.2005)
Published in Neuroscience letters (13.05.2005)
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Apolipoprotein E, survival in Alzheimer's disease patients, and the competing risks of death and Alzheimer's disease
Corder, E H, Saunders, A M, Strittmatter, W J, Schmechel, D E, Gaskell, Jr, P C, Rimmler, J B, Locke, P A, Conneally, P M, Schmader, K E, Tanzi, R E
Published in Neurology (01.07.1995)
Published in Neurology (01.07.1995)
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Specificity, sensitivity, and predictive value of apolipoprotein-E genotyping for sporadic Alzheimer's disease
Saunders, AM, Hulette, C, Welsh-Bohmer, KA, Schmechel, DE, Crain, B, Burke, JR, Alberts, MJ, Strittmatter, WJ, Breitner, JCS, Rosenberg, C, Scott, SV, Gaskell, PC, Pericak-Vance, MA, Roses, AD
Published in The Lancet (British edition) (13.07.1996)
Published in The Lancet (British edition) (13.07.1996)
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Longitudinal follow-up of late-onset Alzheimer disease families
Carney, R.M., Slifer, M.A., Lin, P.I., Gaskell, P.C., Scott, W.K., Potocky, C.F., Hulette, C.M., Welsh-Bohmer, K.A., Schmechel, D.E., Vance, J.M., Pericak-Vance, M.A.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2008)
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Neuropathological Features of Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17q21–22 (FTDP-17): Duke Family 1684
Hulette, C M, Pericak-Vance, M A, Roses, A D, Schmechel, D E, Yamaoka, L H, Gaskell, P C, Welsh-Bohmer, K A, Crowther, R A, Spillantini, M G
Published in Journal of neuropathology and experimental neurology (01.08.1999)
Published in Journal of neuropathology and experimental neurology (01.08.1999)
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Linkage of frontotemporal dementia to chromosome 17 : Clinical and neuropathological characterization of phenotype
YAMAOKA, L. H, WELSH-BOHMER, K. A, PERICAK-VANCE, M. A, HULETTE, C. M, GASKELL, P. C, MURRAY, M, RIMMLER, J. L, ROSI HELMS, B, GUERRA, M, ROSES, A. D, SCHMECHEL, D. E
Published in American journal of human genetics (01.12.1996)
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Published in American journal of human genetics (01.12.1996)
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Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease
Pericak-Vance, M.A, Bass, M.L, Yamaoka, L.H, Gaskell, P.C, Scott, W.K, Terwedow, H.A, Menold, M.M, Conneally, P.M, Small, G.W, Saunders, A.M, Roses, A.D, Haines, J.L
Published in Neurobiology of Aging (1998)
Published in Neurobiology of Aging (1998)
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Conference Proceeding
The apolipoprotein E E4 allele and sex-specific risk of Alzheimer's disease
Corder, E H, Saunders, A M, Strittmatter, W J, Schmechel, D E, Gaskell, Jr, P C, Roses, A D, Pericak-Vance, M A, Small, G W, Haines, J L
Published in JAMA : the journal of the American Medical Association (01.02.1995)
Published in JAMA : the journal of the American Medical Association (01.02.1995)
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Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity
Othmane, Kamel Ben, Middleton, Lefkos T., Loprest, Lorraine J., Wilkinson, Kenneth M., Lennon, Felicia, Rozear, Marvin P., Stajich, Jeffrey U., Gaskell, Perry C., Roses, Allen D., Pericak-Vance, Margaret A., Vance, Jeffery M.
Published in Genomics (San Diego, Calif.) (01.08.1993)
Published in Genomics (San Diego, Calif.) (01.08.1993)
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Age at Onset in Two Common Neurodegenerative Diseases Is Genetically Controlled
Li, Yi-Ju, Scott, William K., Hedges, Dale J., Zhang, Fengyu, Gaskell, P. Craig, Nance, Martha A., Watts, Ray L., Hubble, Jean P., Koller, William C., Pahwa, Rajesh, Stern, Matthew B., Hiner, Bradley C., Jankovic, Joseph, Allen, Fred H., Goetz, Christopher G., Mastaglia, Frank, Stajich, Jeffrey M., Gibson, Rachel A., Middleton, Lefkos T., Saunders, Ann M., Scott, Burton L., Small, Gary W., Nicodemus, Kristin K., Reed, Allison D., Schmechel, Donald E., Welsh-Bohmer, Kathleen A., Conneally, P. Michael, Roses, Allen D., Gilbert, John R., Vance, Jeffery M., Haines, Jonathan L., Pericak-Vance, Margaret A.
Published in American journal of human genetics (01.04.2002)
Published in American journal of human genetics (01.04.2002)
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Hereditary motor and sensory neuropathy, X-linked: a half century follow-up
Rozear, M P, Pericak-Vance, M A, Fischbeck, K, Stajich, J M, Gaskell, Jr, P C, Krendel, D A, Graham, D G, Dawson, D V, Roses, A D
Published in Neurology (01.09.1987)
Published in Neurology (01.09.1987)
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No association between very low density lipoprotein receptor (VLDL-R) and Alzheimer disease in American Caucasians
Pritchard, M.L., Saunders, A.M., Gaskell, P.C., Small, G.W., Conneally, P.M., Rosi, B., Yamaoka, L.H., Roses, A.D., Haines, J.L., Pericak-Vance, M.A.
Published in Neuroscience letters (10.05.1996)
Published in Neuroscience letters (10.05.1996)
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