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Maria Grazia Spillantini et al.
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Ole A. Andreassen et al.
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Yadong Huang et al.
CELL (2012)
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Daniah Trabzuni et al.
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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimers diseases
Giovanni Coppola et al.
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A mutation in APP protects against Alzheimer's disease and age-related cognitive decline
Thorlakur Jonsson et al.
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Tau acts as an independent genetic risk factor in pathologically proven PD
Gavin Charlesworth et al.
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Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants
Fanggeng Zou et al.
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Amyloid-β Associated Volume Loss Occurs Only in the Presence of Phospho-Tau
Rahul S. Desikan et al.
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Michael A. Nalls et al.
LANCET (2011)
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
Adam C. Naj et al.
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Ellen M. Wijsman et al.
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METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
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Sudha Seshadri et al.
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Genetic Control of Human Brain Transcript Expression in Alzheimer Disease
Jennifer A. Webster et al.
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An Association Study of Common Variation at the MAPT Locus With Late-Onset Alzheimer's Disease
Richard Abraham et al.
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H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers
Elisa Canu et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2009)
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
Jean-Charles Lambert et al.
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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Denise Harold et al.
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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Wataru Satake et al.
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Genome-wide association study reveals genetic risk underlying Parkinson's disease
Javier Simon-Sanchez et al.
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Evidence for a common pathway linking neurodegenerative diseases
Joshua M. Shulman et al.
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CSF tau/Aβ42 ratio for increased risk of mild cognitive impairment -: A follow-up study
G. Li et al.
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Tree-structured gatekeeping tests in clinical trials with hierarchically ordered multiple objectives
Alex Dmitrienko et al.
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Anne M. Fagan et al.
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Amanda J. Myers et al.
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Haplotype-based association analysis of the MAPT locus in late onset Alzheimer's disease
Odity Mukherjee et al.
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Untangling the tau gene association with neurodegenerative disorders
Alan M. Pittman et al.
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Lewy bodies in progressive supranuclear palsy represent an independent disease process
Hirotake Uchikado et al.
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The H1c haplotype at the MAPT locus is associated with Alzheimer's disease
AJ Myers et al.
HUMAN MOLECULAR GENETICS (2005)
Genomic medicine: Alzheimer's disease and Parkinson's disease
RL Nussbaum et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)