Related references
Note: Only part of the references are listed.Common Variant in GRN Is a Genetic Risk Factor for Hippocampal Sclerosis in the Elderly
Dennis W. Dickson et al.
NEURODEGENERATIVE DISEASES (2010)
Hardy-Weinberg Equilibrium Testing of Biological Ascertainment for Mendelian Randomization Studies
Santiago Rodriguez et al.
AMERICAN JOURNAL OF EPIDEMIOLOGY (2009)
Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models
Sandra Pereson et al.
JOURNAL OF PATHOLOGY (2009)
Variation at GRN 3′-UTR rs5848 Is Not Associated with a Risk of Frontotemporal Lobar Degeneration in Dutch Population
Javier Simon-Sanchez et al.
PLOS ONE (2009)
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
Rosa Rademakers et al.
HUMAN MOLECULAR GENETICS (2008)
Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease
N. Brouwers et al.
NEUROLOGY (2008)
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Matt Baker et al.
NATURE (2006)
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
Marc Cruts et al.
NATURE (2006)
Haploview: analysis and visualization of LD and haplotype maps
JC Barrett et al.
BIOINFORMATICS (2005)
Power and sample size calculations for case-control genetic association tests when errors are present: Application to single nucleotide polymorphisms
D Gordon et al.
HUMAN HEREDITY (2002)
Share Paper
