12 papers found
Genetic architecture of subcortical brain structures in 38,851 individuals
A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease
Novel genetic loci associated with hippocampal volume
Rare coding variants in PLCG2, ABI3 and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression
Novel genetic loci underlying human intracranial volume identified through genome-wide association
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease
Association of Alzheimer’s related genotypes with cognitive decline in multiple domains: results from the Three-City Dijon study
A novel Alzheimer disease locus located near the gene encoding tau protein.
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.
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