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Probabilistic diagnosis in linkage analysis of bipolar disorder: putting weights on the fringe.
Alpha-2 macroglobulin is genetically associated with Alzheimer disease.
Family-based tests of association in the presence of linkage.
Neuregulin-1 polymorphism in late onset Alzheimer's disease families with psychoses.
Variance calculations for identity-by-descent estimation.
Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease.
The importance of watching our weights: how the choice of weights for non-independent sib pairs can dramatically alter results.
Genetic association of Alzheimer's disease with multiple polymorphisms in alpha-2-macroglobulin.
Systematic meta-analyses of Alzheimer disease genetic association studies: the AlzGene database.
Results of a high-resolution genome screen of 437 Alzheimer's disease families.
Family-based association between Alzheimer's disease and variants in UBQLN1.
ACAT1 is not associated with Alzheimer's disease in two independent family-based samples.
Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13.
No evidence for genetic association or linkage of the cathepsin D (CTSD) exon 2 polymorphism and Alzheimer disease.
Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q.
Unipolar relatives in bipolar pedigrees: a search for elusive indicators of underlying bipolarity.
ApoE-4 and age at onset of Alzheimer's disease: the NIMH genetics initiative.
A QTL genome scan of the metabolic syndrome and its component traits.
Evidence for genetic linkage of Alzheimer's disease to chromosome 10q.
No association between marker D10S1423 and Alzheimer's disease.
A genomic scan for age at onset of Alzheimer's disease in 437 families from the NIMH Genetic Initiative.
GENETIC KNOWLEDGE AND ATTITUDES IN ALZHEIMER'S DISEASE