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Replication of BIN1 Association with Alzheimer's Disease and Evaluation of Genetic Interactions.
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- Journal of Alzheimer's Disease, 2011, v. 24, n. 4, p. 751, doi. 10.3233/JAD-2011-101932
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- Article
NOVEL CANDIDATE AD-RISK LOCI IDENTIFIED THROUGH WHOLE EXOME SEQUENCING IN AFRICAN-AMERICANS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P971, doi. 10.1016/j.jalz.2017.06.1306
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- Article
ANALYSIS OF WILD TYPE AND R47H MUTANT TREM2 EXPRESSION IN ALZHEIMER'S DISEASE BRAINS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P659, doi. 10.1016/j.jalz.2016.06.1495
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- Article
Neurox associations with Alzheimer's disease in african americans.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P361, doi. 10.1016/j.jalz.2015.06.257
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- Article
Evaluation of memory endophenotypes for association with CLU, CR1, and PICALM variants in black and white subjects.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, n. 2, p. 205, doi. 10.1016/j.jalz.2013.01.016
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Genetic association of progressive supranuclear palsy (PSP) risk loci variants with brain gene expression and neuropathology endophenotypes
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- 2012
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- Abstract
The genetics of cognitively healthy aging
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- 2012
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Investigation of established Alzheimer's disease–risk SNPs for association with Alzheimer's disease in an African-American case control series
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- 2012
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Genetic association of variants with late-onset Alzheimer's disease risk and brain gene expression
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- 2012
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Identification of human disease-associated variants in a brain expression genome-wide association study (eGWAS)
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- 2012
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Replication of LOAD GWAS Associations
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- 2011
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Evaluation of known Alzheimer's genes for SNPs that influence their brain expression (eSNPs)
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- 2011
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Characterization of brain region- and disease-specific IDE expression in Alzheimer patients and controls
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- 2010
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Association of glyceraldehyde-3-phosphate dehydrogenase locus variant with late-onset Alzheimer's disease
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- 2010
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eSNPs within VAMP1 show genetic association with late onset Alzheimer's disease
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- 2010
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Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease
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- 2009
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P4-167: Investigation of mitochondrial DNA damage in late-onset Alzheimer's disease
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- 2008
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P3-276: BRI2 (ITM2B) shows genetic association with late-onset Alzheimer's disease
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- 2008
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- Abstract
P3-275: Genome-wide association study for Braak neurofibrillary tangle (NFT) staging
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- 2008
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- Abstract
P3-216: Identification of CIS variants associating with expression levels of 12 late-onset Alzheimer's disease (LOAD) candidate genes in a Genome-Wide Association Study (GWAS)
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- 2008
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- Abstract
P3-208: Genetic variation in PCDH11X associates with Alzheimer's disease in a two-stage GWAS study
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- 2008
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P1-370: Reduction of interference in sandwich ELISAs measuring the amyloid β protein in human plasma
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- 2008
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- Abstract
O2-06-04: Identification of late-onset Alzheimer's disease (LOAD) susceptibility alleles in the PAI-1 gene
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- 2008
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- Abstract
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.
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- Nature Genetics, 2009, v. 41, n. 2, p. 192, doi. 10.1038/ng.305
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- Article
Multiplication of the α-synuclein gene is not a common disease mechanism in Lewy body disease.
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- Journal of Molecular Neuroscience, 2004, v. 24, n. 3, p. 337, doi. 10.1385/JMN:24:3:337
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- Article
Linking Protective <i>GAB2</i> Variants, Increased Cortical <i>GAB2</i> Expression and Decreased Alzheimer’s Disease Pathology
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- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064802
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- Article
Multiple Insulin Degrading Enzyme Variants Alter In Vitro Reporter Gene Expression.
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- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021429
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- Article
Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease.
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- Human Genetics, 2011, v. 129, n. 3, p. 273, doi. 10.1007/s00439-010-0924-2
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- Article
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members.
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- Brain: A Journal of Neurology, 2009, v. 132, n. 3, p. 583, doi. 10.1093/brain/awn352
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- Article
Association of MAPT haplotypes with Alzheimer's disease risk and MAPT brain gene expression levels.
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- Alzheimer's Research & Therapy, 2014, v. 6, n. 4, p. 1, doi. 10.1186/alzrt268
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- Article
Genetically-controlled Vesicle-Associated Membrane Protein 1 expression may contribute to Alzheimer's pathophysiology and susceptibility.
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- Molecular Neurodegeneration, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13024-015-0015-x
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- Article
Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants.
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- PLoS Genetics, 2012, v. 8, n. 6, p. 1, doi. 10.1371/journal.pgen.1002707
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- Article
Parkinsonism, FXTAS, and FMR1 premutations.
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- Movement Disorders, 2005, v. 20, n. 2, p. 230, doi. 10.1002/mds.20297
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Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations.
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- Movement Disorders, 2004, v. 19, n. 6, p. 677, doi. 10.1002/mds.10703
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- Article
ABCA7 Deficiency Accelerates Amyloid-β Generation and Alzheimer's Neuronal Pathology.
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- Journal of Neuroscience, 2016, v. 36, n. 13, p. 3848, doi. 10.1523/JNEUROSCI.3757-15.2016
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- Article