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711 results

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Page 1
Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease.
Lavedan C, Buchholtz S, Auburger G, Albin RL, Athanassiadou A, Blancato J, Burguera JA, Ferrell RE, Kostic V, Leroy E, Leube B, Mota-Vieira L, Papapetropoulos T, Pericak-Vance MA, Pinkus J, Scott WK, Ulm G, Vasconcelos J, Vilchez JJ, Nussbaum RL, Polymeropoulos MH. Lavedan C, et al. DNA Res. 1998 Dec 31;5(6):401-2. doi: 10.1093/dnares/5.6.401. DNA Res. 1998. PMID: 10048491 Free article. No abstract available.
Genetic analysis of complex diseases.
Scott WK, Pericak-Vance MA, Haines JL. Scott WK, et al. Science. 1997 Feb 28;275(5304):1327; author reply 1329-30. Science. 1997. PMID: 9064788 No abstract available.
The alpha-synuclein gene is not a major risk factor in familial Parkinson disease.
Scott WK, Yamaoka LH, Stajich JM, Scott BL, Vance JM, Roses AD, Pericak-Vance MA, Watts RL, Nance M, Hubble J, Koller W, Stern MB, Colcher A, Allen FH Jr, Hiner BC, Jankovic J, Ondo W, Laing NG, Mastaglia F, Goetz C, Pappert E, Small GW, Masterman D, Haines JL, Davies TL. Scott WK, et al. Neurogenetics. 1999 Sep;2(3):191-2. doi: 10.1007/s100480050083. Neurogenetics. 1999. PMID: 10541595 No abstract available.
Genetic polymorphisms of the N-acetyltransferase genes and risk of Parkinson's disease.
van der Walt JM, Martin ER, Scott WK, Zhang F, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Mastaglia F, Roses AD, Stajich JM, Booze MW, Fujiwara K, Gibson RA, Middleton LT, Scott BL, Pericak-Vance MA, Vance JM. van der Walt JM, et al. Neurology. 2003 Apr 8;60(7):1189-91. doi: 10.1212/01.wnl.0000055929.84668.9a. Neurology. 2003. PMID: 12682333
Presenilin-1 polymorphism and Alzheimer's disease.
Scott WK, Growdon JH, Roses AD, Haines JL, Pericak-Vance MA. Scott WK, et al. Lancet. 1996 Apr 27;347(9009):1186-7. Lancet. 1996. PMID: 8609784 No abstract available.
Complete genomic screen in Parkinson disease: evidence for multiple genes.
Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Masterman D, Mastaglia F, Laing NG, Stajich JM, Slotterbeck B, Booze MW, Ribble RC, Rampersaud E, West SG, Gibson RA, Middleton LT, Roses AD, Haines JL, Scott BL, Vance JM, Pericak-Vance MA. Scott WK, et al. JAMA. 2001 Nov 14;286(18):2239-44. doi: 10.1001/jama.286.18.2239. JAMA. 2001. PMID: 11710888
Life after the screen: making sense of many P-values.
Schmidt S, Shao Y, Hauser ER, Slifer SH, Martin ER, Scott WK, Speer MC, Pericak-Vance MA. Schmidt S, et al. Genet Epidemiol. 2001;21 Suppl 1:S546-51. doi: 10.1002/gepi.2001.21.s1.s546. Genet Epidemiol. 2001. PMID: 11793734
711 results