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Mediating role of Interleukin-6 in the predictive association of diabetes with Hippocampus atrophy, Amyloid, Tau, and Neurofilament pathology at pre-clinical stages of diabetes-related cognitive impairment.

Multi-population Genome-Wide Association Study Identifies Multiple Novel Loci associated with Asymptomatic Intracranial Large Artery Stenosis.

Interpretable MRI-Based Deep Learning for Alzheimer's Risk and Progression.

D3MI: an efficient and powerful federated imputation method for bias reduction in the analysis of distributed incomplete data by accounting for within-site correlation and between-site heterogeneity.

Alzheimer disease is (sometimes) highly heritable: Drivers of variation in heritability estimates for binary traits, a systematic review.

Mediating effect of pro-inflammatory cytokines in the association between depression, anxiety, and cardiometabolic disorders in an ethnically diverse community-dwelling middle-aged and older US population.

Mediating effect of pro-inflammatory cytokines in the association between depression, anxiety, and cardiometabolic disorders in an ethnically diverse middle-aged and older population.

Chronic emotional stress and mediating role of Interleukine-6 in the association with cardiometabolic disorders in a multiethnic middle-aged and older US-population.

Vision Transformer Autoencoders for Unsupervised Representation Learning: Capturing Local and Non-Local Features in Brain Imaging to Reveal Genetic Associations.

Bayesian inference of genetic pleiotropy identifies drug targets and repurposable medicines for human complex diseases.

Objective Sleep Quality in Diverse Older Adults: the Importance of Race and Ethnicity and Sex.

Leveraging multimodal neuroimaging and GWAS for identifying modality-level causal pathways to Alzheimer's disease.

SingleBrain: A Meta-Analysis of Single-Nucleus eQTLs Linking Genetic Risk to Brain Disorders.

A Novel Method to Disentangle Tightly Linked Risk and Resilience Genes for Brain Disorders: Application to Alzheimer's Disease.

Genetic Regulation of the Metabolome Differs by Sex, Alzheimer's Disease Stage, and Plasma Biomarker Status.

Somatic and Stem Cell Bank to Study the Contribution of African Ancestry to Dementia: African iPSC Initiative.

GWAS links APOE to neuropsychiatric symptoms in mild cognitive impairment and dementia.

Multi-Omics Analysis for Identifying Cell-Type-Specific Druggable Targets in Alzheimer's Disease.

The Dynamics of Cognitive Decline towards Alzheimer's Disease Progression: Results from ADSP-PHC's Harmonized Cognitive Composites.

Efficient multi-phenotype genome-wide analysis identifies genetic associations for unsupervised deep-learning-derived high-dimensional brain imaging phenotypes.

Leveraging functional annotations to map rare variants associated with Alzheimer's disease with gruyere.

Alzheimer's Disease Sequencing Project Release 4 Whole Genome Sequencing Dataset.

Long Sleep Duration, Cognitive Performance, and the Moderating Role of Depression: A Cross-Sectional Analysis in the Framingham Heart Study.

Distinct medical and substance use histories associate with cognitive decline in Alzheimer's Disease.

Mapping rare protein-coding variants on multi-organ imaging traits.

Biobank-scale characterization of Alzheimer's disease and related dementias identifies potential disease-causing variants, risk factors, and genetic modifiers across diverse ancestries.

Genetic Contributions to Alzheimer's Disease and Frontotemporal Dementia in Admixed Latin American Populations.

Cross-Linguistic Analysis of Speech Markers: Insights from English, Chinese, and Italian Speakers.

NIAGADS: A Comprehensive National Data Repository for Alzheimer's Disease and Related Dementia Genetics and Genomics Research.

Genome-wide scan of Flortaucipir PET levels finds JARID2 associated with cerebral tau deposition.

Language Modeling Screens Parkinson's Disease with Self-reported Questionnaires.

LD-informed deep learning for Alzheimer's gene loci detection using WGS data.

Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries.

Rethinking the residual approach: Leveraging machine learning to operationalize cognitive resilience in Alzheimer's disease.

Structural variants linked to Alzheimer's Disease and other common age-related clinical and neuropathologic traits.

Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication.

The Interaction Effects of Sex, Age, APOE and Common Health Risk Factors on Human Brain Functions.

Country Level Incidence of Alzheimer Disease and Related Dementias is Associated with Increased Omega6 PUFA Consumption.

Connecting intermediate phenotypes to disease using multi-omics in heart failure.

A Specialized Reference Panel with Structural Variants Integration for Improving Genotype Imputation in Alzheimer's Disease and Related Dementias (ADRD).

AD plasma biomarkers are stable for an extended period at -20 degrees C: implications for resource-constrained environments.

Ancestry specific distribution of LPA Kringle IV-Type-2 genetic variants highlight associations to apo(a) copy number, glucose, and hypertension.

A Comprehensive Head-to-Head Comparison of Key Plasma Phosphorylated Tau 217 Biomarker Tests.

Benchmarking of a multi-biomarker low-volume panel for Alzheimer's Disease and related dementia research.

The Role of Genomic-Informed Risk Assessments in Predicting Dementia Outcomes.

The Role of X Chromosome in Alzheimer's Disease Genetics.

CWAS-Plus: Estimating category-wide association of rare noncoding variation from whole-genome sequencing data with cell-type-specific functional data.

Comparative gene regulatory networks modulating APOE expression in microglia and astrocytes.

Generalizability of Tau and Amyloid Plasma Biomarkers in Alzheimer's Disease Cohorts of Diverse Genetic Ancestries.

Gene specific effects on brain volume and cognition of TMEM106B in frontotemporal lobar degeneration.

Integration of transcriptomics and long-read genomics prioritizes structural variants in rare disease.

CSF proteomic profiling with amyloid/tau positivity identifies distinctive sex-different alteration of multiple proteins involved in Alzheimer's disease.

Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variation.

Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes.

Individual bioenergetic capacity as a potential source of resilience to Alzheimer's disease.

Region-based analysis with functional annotation identifies genes associated with cognitive function in South Asians from India.

Psychotic symptoms are associated with elevated tau PET signal in the amygdala independent of Alzheimer's disease clinical severity and amyloid burden.

Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literature.

A One-Shot Lossless Algorithm for Cross-Cohort Learning in Mixed-Outcomes Analysis.

Five dominant dimensions of brain aging are identified via deep learning: associations with clinical, lifestyle, and genetic measures.

Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy.

Missense and Loss of Function Variants at GWAS Loci in Familial Alzheimer's Disease.

Genetic analysis of cognitive preservation in the midwestern Amish reveals a novel locus on chromosome 2.

BrainAGE Estimation: Influence of Field Strength, Voxel Size, Race, and Ethnicity.

Traumatic brain injury and Alzheimer's Disease biomarkers: A systematic review of findings from amyloid and tau positron emission tomography (PET).

Long-read RNA-seq atlas of novel microglia isoforms elucidates disease-associated genetic regulation of splicing.

Polygenic burden of short tandem repeat expansions promote risk for Alzheimer's disease.

Temporal tau asymmetry spectrum influences divergent behavior and language patterns in Alzheimer`s disease.

Cross-phenotype associations between Alzheimer's Disease and its comorbidities may provide clues to progression.

Frequency of Variants in Mendelian Alzheimer's Disease Genes within the Alzheimer's Disease Sequencing Project (ADSP).

Characterizing Treatment Non-responders vs. Responders in Completed Alzheimer's Disease Clinical Trials.

Research participants' perception of ethical issues in stroke genomics and neurobiobanking research in Africa.

Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects.

Extended genome-wide association study employing the African Genome Resources Panel identifies novel susceptibility loci for Alzheimer's Disease in individuals of African ancestry.

Association of Common and Rare Variants with Alzheimer's Disease in over 13,000 Diverse Individuals with Whole-Genome Sequencing from the Alzheimer's Disease Sequencing Project.

Key variants via Alzheimer's Disease Sequencing Project whole genome sequence data.

Characterizing patterns of diffusion tensor imaging variance in aging brains.

AORTA Gene: Polygenic prediction improves detection of thoracic aortic aneurysm.

Lysophosphatidylcholines are associated with P-tau181 levels in early stages of Alzheimer's Disease.

Risk of Alzheimer's Disease is Associated with Longitudinal Changes in Plasma Biomarkers in the Multiethnic Washington Heights, Inwood Columbia Aging Project Cohort.

Improving Genetic Association Studies with a Novel Methodology that Unveils the Hidden Complexity of All-Cause Heart Failure.

APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer's Disease pathology.

A 3'UTR Insertion Is a Candidate Causal Variant at the TMEM106B Locus Associated with Increased Risk for FTLD-TDP.

GRPa-PRS: A risk stratification method to identify genetically-regulated pathways in polygenic diseases.

SR-TWAS: Leveraging Multiple Reference Panels to Improve TWAS Power by Ensemble Machine Learning.

Single-cell RNA sequencing data reveals rewiring of transcriptional relationships in Alzheimer's Disease associated with risk variants.

White matter integrity is associated with cognition and amyloid burden in older adult Koreans along the Alzheimer's disease continuum.

A single-nucleus transcriptome-wide association study implicates novel genes in depression pathogenesis.

MS4A4A modifies the risk of Alzheimer disease by regulating lipid metabolism and immune response in a unique microglia state.

Epistatic Features and Machine Learning Improve Alzheimer's Risk Prediction Over Polygenic Risk Scores.

Chromosome 10q24.32 Variants Associate with Brain Arterial Diameters in Diverse Populations: A Genome-Wide Association Study.

Plasma proteomics of SARS-CoV-2 infection and severity reveals impact on Alzheimer and coronary disease pathways.

Olfactory Bulb and Amygdala Gene Expression Changes in Subjects Dying with COVID-19.

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