Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.
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DOI:
10.1038/ng.305
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发表时间:
2009-02
期刊:
影响因子:
30.8
通讯作者:
Younkin, Steven G.
中科院分区:
文献类型:
--
作者:
Carrasquillo, Minerva M.;Zou, Fanggeng;Pankratz, V. Shane;Wilcox, Samantha L.;Ma, Li;Walker, Louise P.;Younkin, Samuel G.;Younkin, Curtis S.;Younkin, Linda H.;Bisceglio, Gina D.;Ertekin-Taner, Nilufer;Crook, Julia E.;Dickson, Dennis W.;Petersen, Ronald C.;Graff-Radford, Neill R.;Younkin, Steven G.
By analyzing late onset Alzheimer's disease (LOAD) in a genome wide association study (313,504 SNPs, 3 series, 844 cases/1,255 controls) and evaluating the 25 SNPs with most significant allelic association in 4 additional series (1,547 cases/1,209 controls), we identified a SNP (rs5984894) on Xq21.3 in PCDH11X that is strongly associated with LOAD in American Caucasians. Analysis of rs5984894 by multivariable logistic regression adjusted for sex gave global P values of 5.7×10-5 in stage I, 4.8×10-6 in stage II, and 3.9×10-12 in the combined data. Odds ratios were 1.75 (95% CI 1.42-2.16) for female homozygotes (P=2.0×10-7) and 1.26 (95% CI 1.05-1.51) for female heterozygotes (P=0.01) compared to female non-carriers. For male hemizygotes (P=0.07) compared to male non-carriers the odds ratio was 1.18 (95% CI 0.99-1.41).
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DOI:
10.1002/ajmg.b.30229
发表时间:
2006-01-05
影响因子:
2.8
作者:
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通讯作者:
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影响因子:
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作者:
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通讯作者:
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