Scott WK - Search Results

1

Linkage of the CCR5 Delta 32 mutation with a functional polymorphism of CD45RA.

Liao HX, Montefiori DC, Patel DD, Lee DM, Scott WK, Pericak-Vance M, Haynes BF. Liao HX, et al. Among authors: scott wk. J Immunol. 2000 Jul 1;165(1):148-57. doi: 10.4049/jimmunol.165.1.148. J Immunol. 2000. PMID: 10861047

2

No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease.

Scott WK, Yamaoka LH, Locke PA, Rosi BL, Gaskell PC, Saunders AM, Conneally PM, Small GW, Farrer LA, Growdon JH, Roses AD, Pericak-Vance MA, Haines JL. Scott WK, et al. Genet Epidemiol. 1997;14(3):307-15. doi: 10.1002/(SICI)1098-2272(1997)14:3<307::AID-GEPI8>3.0.CO;2-1. Genet Epidemiol. 1997. PMID: 9181359

3

No association of alpha1-antichymotrypsin flanking region polymorphism and Alzheimer disease risk in early- and late-onset Alzheimer disease patients.

Bass MP, Yamaoka LH, Scott WK, Gaskell PC, Welsh-Bohmer KA, Roses AD, Saunders AM, Haines JL, Pericak-Vance MA. Bass MP, et al. Among authors: scott wk. Neurosci Lett. 1998 Jul 3;250(2):79-82. doi: 10.1016/s0304-3940(98)00398-x. Neurosci Lett. 1998. PMID: 9697923

4

Analysis of association between Alzheimer disease and the K variant of butyrylcholinesterase (BCHE-K).

Grubber JM, Saunders AM, Crane-Gatherum AR, Scott WK, Martin ER, Haynes CS, Conneally PM, Small GW, Roses AD, Haines JL, Pericak-Vance MA. Grubber JM, et al. Among authors: scott wk. Neurosci Lett. 1999 Jul 9;269(2):115-9. doi: 10.1016/s0304-3940(99)00426-7. Neurosci Lett. 1999. PMID: 10430518

5

False positive rates in a genomic screen for complex quantitative traits.

Scott WK, Speer MC, Leal SM, Brzustowicz LM, Haynes CS, Pericak-Vance MA. Scott WK, et al. Genet Epidemiol. 1997;14(6):891-6. doi: 10.1002/(SICI)1098-2272(1997)14:6<891::AID-GEPI55>3.0.CO;2-H. Genet Epidemiol. 1997. PMID: 9433596 Free PMC article. Clinical Trial.

6

An autosomal genomic screen for dementia in an extended Amish family.

Ashley-Koch AE, Shao Y, Rimmler JB, Gaskell PC, Welsh-Bohmer KA, Jackson CE, Scott WK, Haines JL, Pericak-Vance MA. Ashley-Koch AE, et al. Among authors: scott wk. Neurosci Lett. 2005 May 13;379(3):199-204. doi: 10.1016/j.neulet.2004.12.065. Neurosci Lett. 2005. PMID: 15843063

7

Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity.

Scott WK, Grubber JM, Conneally PM, Small GW, Hulette CM, Rosenberg CK, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. Scott WK, et al. Am J Hum Genet. 2000 Mar;66(3):922-32. doi: 10.1086/302828. Am J Hum Genet. 2000. PMID: 10712207 Free PMC article.

8

Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.

Scott WK, Gaskell PC, Lennon F, Wolpert CM, Menold MM, Aylsworth AS, Warner C, Farrell CD, Boustany RM, Albright SG, Boyd E, Kingston HM, Cumming WJ, Vance JM, Pericak-Vance MA. Scott WK, et al. Neurogenetics. 1997 Sep;1(2):95-102. doi: 10.1007/s100480050014. Neurogenetics. 1997. PMID: 10732810

9

Evidence for anticipation in autosomal dominant limb-girdle muscular dystrophy.

Speer MC, Gilchrist JM, Stajich JM, Gaskell PC, Westbrook CA, Horrigan SK, Bartoloni L, Yamaoka LH, Scott WK, Pericak-Vance MA. Speer MC, et al. Among authors: scott wk. J Med Genet. 1998 Apr;35(4):305-8. doi: 10.1136/jmg.35.4.305. J Med Genet. 1998. PMID: 9598725 Free PMC article.

10

Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease.

Scott WK, Saunders AM, Gaskell PC, Locke PA, Growdon JH, Farrer LA, Auerbach SA, Roses AD, Haines JL, Pericak-Vance MA. Scott WK, et al. Ann Neurol. 1997 Sep;42(3):376-8. doi: 10.1002/ana.410420317. Ann Neurol. 1997. PMID: 9307262

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