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Purification and Characterization of Progenitor and Mature Human Astrocytes Reveals Transcriptional and Functional Differences with Mouse

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BET Bromodomain Inhibition Suppresses the Function of Hematopoietic Transcription Factors in Acute Myeloid Leukemia

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Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease

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Partitioning heritability by functional annotation using genome-wide association summary statistics

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An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex

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Polarization of the Effects of Autoimmune and Neurodegenerative Risk Alleles in Leukocytes

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Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics

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Integrated Systems Approach Identifies Genetic Nodes and Networks in Late-Onset Alzheimer’s Disease

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The Rotterdam Study: 2014 objectives and design update

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The transcription factor PU.1 is critical for viability and function of human brain microglia

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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

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GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer’s Disease

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Genome-Wide Haplotype Analysis of Cis Expression Quantitative Trait Loci in Monocytes

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Dynamic epigenetic enhancer signatures reveal key transcription factors associated with monocytic differentiation states

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IL-34 is a tissue-restricted ligand of CSF1R required for the development of Langerhans cells and microglia

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Genome-Wide Association Identifies Nine Common Variants Associated With Fasting Proinsulin Levels and Provides New Insights Into the Pathophysiology of Type 2 Diabetes

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Genome-wide association analysis of age-at-onset in Alzheimer's disease

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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

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HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

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Association of a functional polymorphism in the 3′-untranslated region of SPI1 with systemic lupus erythematosus

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Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease

(2010) Sudha Seshadri   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

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Beta Amyloid in Alzheimer's Disease: Increased Deposition in Brain Is Reflected in Reduced Concentration in Cerebrospinal Fluid

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A neuronal VLDLR variant lacking the third complement-type repeat exhibits high capacity binding of apoE containing lipoproteins

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Safety of Lumbar Puncture Procedures in Patients with Alzheimers Disease

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Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

(2009) Denise Harold et al.   NATURE GENETICS

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

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A Polymorphism in CALHM1 Influences Ca2+ Homeostasis, Aβ Levels, and Alzheimer's Disease Risk

(2008) Ute Dreses-Werringloer et al.   CELL

Cox proportional hazards models have more statistical power than logistic regression models in cross-sectional genetic association studies

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Alzheimer’s disease risk variants show association with cerebrospinal fluid amyloid beta

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