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Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14.
Alpha-2 macroglobulin is genetically associated with Alzheimer disease.
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease.
Association of a haplotype for tumor necrosis factor in siblings with late-onset Alzheimer disease: the NIMH Alzheimer Disease Genetics Initiative.
Huntington disease: no evidence for locus heterogeneity.
Follow-up mapping supports the evidence for linkage in the candidate region at 9q22 in the NIMH Alzheimer's disease Genetics Initiative cohort.
Studies of a DNA marker (G8) genetically linked to Huntington disease in British families.
ApoE-4 and age at onset of Alzheimer's disease: the NIMH genetics initiative.
Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21.
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Molecular genetics of Alzheimer's disease and the amyloid beta peptide precursor gene.
Apolipoprotein E4 allele and Alzheimer disease: examination of allelic association and effect on age at onset in both early- and late-onset cases.
Genetic linkage map of human chromosome 21.
Search for the familial Alzheimer's disease gene.
ISOLATION AND CHARACTERIZATION OF THE FAD GENE ON CHR14