Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity

Septin 4, the Drosophila Ortholog of Human CDCrel-1, Accumulates in parkin Mutant Brains and is Functionally Related to the Nedd4 E3 Ubiquitin Ligase

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Common variants at 12q15 and 12q24 are associated with infant head circumference

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Common variants at 6q22 and 17q21 are associated with intracranial volume

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Common variants at 12q14 and 12q24 are associated with hippocampal volume

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Identification of common variants associated with human hippocampal and intracranial volumes

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F-spondin gene transfer improves memory performance and reduces amyloid-β levels in mice

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Cognitive Dysfunction in Early Multiple Sclerosis: Altered Centrality Derived from Resting-State Functional Connectivity Using Magneto-Encephalography

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High-cost, high-capacity backbone for global brain communication

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Hierarchical Genetic Organization of Human Cortical Surface Area

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The Amyloid Precursor Protein Has a Flexible Transmembrane Domain and Binds Cholesterol

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The Geometric Structure of the Brain Fiber Pathways

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Gene networks associated with conditional fear in mice identified using a systems genetics approach

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Common Alzheimer's Disease Risk Variant Within the CLU Gene Affects White Matter Microstructure in Young Adults

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Genetic Influences on Cost-Efficient Organization of Human Cortical Functional Networks

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Rich-Club Organization of the Human Connectome

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Parietal cortex matters in Alzheimer's disease: An overview of structural, functional and metabolic findings

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A Versatile Gene-Based Test for Genome-wide Association Studies

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Endophenotypes in a Dynamically Connected Brain

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Sequential relationships between grey matter and white matter atrophy and brain metabolic abnormalities in early Alzheimer's disease

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Novel missense mutations in the ubiquitination-related geneUBE2Acause a recognizable X-linked mental retardation syndrome

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A genome-wide scan for common alleles affecting risk for autism

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Variance component model to account for sample structure in genome-wide association studies

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Amyloid-β–induced neuronal dysfunction in Alzheimer's disease: from synapses toward neural networks

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Fractional anisotropy of water diffusion in cerebral white matter across the lifespan

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Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

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Genetic control over the resting brain

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A domain level interaction network of amyloid precursor protein and Aβ of Alzheimer's disease

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Prediction of Individual Brain Maturity Using fMRI

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Cortical Hubs Revealed by Intrinsic Functional Connectivity: Mapping, Assessment of Stability, and Relation to Alzheimer's Disease

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Complex network measures of brain connectivity: Uses and interpretations

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Meeting the Challenges of Neuroimaging Genetics

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A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

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Functional interactions of APP with the apoE receptor family

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

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Tensor-based morphometry as a neuroimaging biomarker for Alzheimer's disease: An MRI study of 676 AD, MCI, and normal subjects

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