Alzheimer disease (AD) is a progressive neurodegenerative disorder of later life with a complex etiology and a strong genetic component. Several genomic screens have suggested that a region between chromosome 12p13 and 12q22 contains at least one additional locus underlying the susceptibility of AD. However, localization of this locus has been difficult. We performed a 5 cM microsatellite marker screen across 74 cM on chromosome 12 with 15 markers in 585 multiplex families consisting of 994 affected sibpairs and 213 other affected relative pairs. Analyses across the entire data set did not reveal significant evidence of linkage. However, suggestive linkage was observed in several subsets. In the 91 families where no affected individuals carry an ApoE ε4 allele, an HLOD score of 1.55 was generated at D12S1042. We further examined the linkage data considering the proposed linkages to chromosome 9 (D9S741) and chromosome 10 (α-catenin gene). There was a modest (P = 0.20) increase in the LOD score for D12S368 (MLOD = 1.70) when using the D9S741 LOD scores as a covariate and a highly significant (P
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Liang, X., Schnetz-Boutaud, N., Kenealy, S. J., Jiang, L., Bartlett, J., Lynch, B., … Haines, J. L. (2006). Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus. Molecular Psychiatry, 11(3), 280–285. https://doi.org/10.1038/sj.mp.4001766
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