The National Institute on Aging Genetics of Alzheimer's Disease Data Storage Site
Publications
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2025
2025,  
Alzheimer's & Dementia (New York, N. Y.)
LD-informed deep learning for Alzheimer's gene loci detection using WGS data
Jo, T., et al.
2024
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Project
Lee, W., et al.
2024,  
bioRxiv: The Preprint Server for Biology
CHARMER: detecting and harmonizing high-confidence chromatin interactions across tissues and Hi-C protocols
Cole, S., et al.
2024,  
Nature Genetics
GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia
Shade, LMP., et al.
2024,  
Alzheimer's Research & Therapy
Blood-derived mitochondrial DNA copy number is associated with Alzheimer disease, Alzheimer-related biomarkers and serum metabolites
Tong, T., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Whole-genome sequencing study in Koreans identifies novel loci for Alzheimer's disease
Kang, M., et al.
2024,  
NIAGADS: A Comprehensive National Data Repository for Alzheimer's Disease and Related Dementia Genetics and Genomics Research
Kuzma, A., et al.
2024,  
Translational Psychiatry
Causal relationships between dyslexia and the risk of eight dementias
Zhu, P., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Cognitive resilience to Alzheimer's disease characterized by cell-type abundance
O'Neill, N., et al.
2024,  
Nature Communications
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Farrell, K., et al.
2024,  
Molecular Neurodegeneration
Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Wang, H., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Extended genome-wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry
Ray, NR., et al.
2024,  
medRxiv: The Preprint Server for Health Sciences
A Specialized Reference Panel with Structural Variants Integration for Improving Genotype Imputation in Alzheimer's Disease and Related Dementias (ADRD)
Cheng, P., et al.
2024,  
Journal of Medical Imaging (Bellingham, Wash.)
Field-of-view extension for brain diffusion MRI via deep generative models
Gao, C., et al.
2024,  
bioRxiv: The Preprint Server for Biology
Sex, racial, and APOE-ε4 allele differences in longitudinal white matter microstructure in multiple cohorts of aging and Alzheimer's disease
Peterson, A., et al.
2024,  
Research Square
Novel early-onset Alzheimer-associated genes influence risk through dysregulation of glutamate, immune activation, and intracell signaling pathways
Cruchaga, C., et al.
2024,  
eLife
Biobank-wide association scan identifies risk factors for late-onset Alzheimer's disease and endophenotypes
Yan, D., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data
Wang, Y., et al.
2024,  
Life Science Alliance
A comparative study of structural variant calling in WGS from Alzheimer's disease families
Malamon, JS., et al.
2024,  
medRxiv: The Preprint Server for Health Sciences
The Role of Genomic-Informed Risk Assessments in Predicting Dementia Outcomes
Andrews, SJ., et al.
2024,  
Journal of Neurology, Neurosurgery, and Psychiatry
Genetics impact risk of Alzheimer's disease through mechanisms modulating structural brain morphology in late life
Korologou-Linden, R., et al.
2024,  
medRxiv: The Preprint Server for Health Sciences
The Role of X Chromosome in Alzheimer's Disease Genetics
Belloy, ME., et al.
2024,  
medRxiv: The Preprint Server for Health Sciences
Comparative gene regulatory networks modulating APOE expression in microglia and astrocytes
Brase, L., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Whole genome-wide sequence analysis of long-lived families (Long-Life Family Study) identifies MTUS2 gene associated with late-onset Alzheimer's disease
Xicota, L., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Genetic associations with dementia-related proteinopathy: Application of item response theory
Katsumata, Y., et al.
2024,  
iScience
AI-enabled evaluation of genome-wide association relevance and polygenic risk score prediction in Alzheimer's disease
Platt, DE., et al.
2024,  
American Journal of Human Genetics
The association of GNB5 with Alzheimer disease revealed by genomic analysis restricted to variants impacting gene function
Zhang, J., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Genome-wide association studies identify novel loci in rapidly progressive Alzheimer's disease
Wang, P., et al.
2024,  
medRxiv: The Preprint Server for Health Sciences
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes
Wang, H., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Sex-specific genetic architecture of late-life memory performance
Eissman, JM., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Longitudinal change in memory performance as a strong endophenotype for Alzheimer's disease
Archer, DB., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
NIAGADS Alzheimer's GenomicsDB: A resource for exploring Alzheimer's disease genetic and genomic knowledge
Greenfest-Allen, E., et al.
2024,  
medRxiv: The Preprint Server for Health Sciences
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy
Wang, H., et al.
2024,  
Nature Communications
Human whole-exome genotype data for Alzheimer's disease
Leung, YY., et al.
2024,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
DNA from multiple viral species is associated with Alzheimer's disease risk
Tejeda, M., et al.
2024,  
Alzheimer's & Dementia (New York, N. Y.)
Genetic and multi-omic risk assessment of Alzheimer's disease implicates core associated biological domains
Cary, GA., et al.
2024,  
Journal of Alzheimer's disease: JAD
Epistatic Features and Machine Learning Improve Alzheimer's Disease Risk Prediction Over Polygenic Risk Scores
Hermes, S., et al.
2024,  
Journal of Alzheimer's disease: JAD
African Ancestry Individuals with Higher Educational Attainment Are Resilient to Alzheimer's Disease Measured by pTau181
Rajabli, F., et al.
2023
2023,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Novel loci for Alzheimer's disease identified by a genome-wide association study in Ashkenazi Jews
Li, D., et al.
2023,  
medRxiv: The Preprint Server for Health Sciences
Polygenic burden of short tandem repeat expansions promote risk for Alzheimer's disease
Guo, MH., et al.
2023,  
PLoS genetics
Transfer learning with false negative control improves polygenic risk prediction
Jeng, XJ., et al.
2023,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
A haptoglobin (HP) structural variant alters the effect of APOE alleles on Alzheimer's disease
Bai, H., et al.
2023,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Alzheimer's disease heterogeneity explained by polygenic risk scores derived from brain transcriptomic profiles
Chung, J., et al.
2023,  
Bioinformatics (Oxford, England)
hipFG: high-throughput harmonization and integration pipeline for functional genomics data
Cifello, J., et al.
2023,  
Research Square
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects
Lee, W., et al.
2023,  
medRxiv: The Preprint Server for Health Sciences
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects
Wang, H., et al.
2023,  
medRxiv: The Preprint Server for Health Sciences
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
Lee, W., et al.
2023,  
Aging Cell
Sex- and APOE-specific genetic risk factors for late-onset Alzheimer's disease: Evidence from gene-gene interaction of longevity-related loci
Dato, S., et al.
2023,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
The Early-Onset Alzheimer's Disease Whole-Genome Sequencing Project: Study design and methodology
Ray, NR., et al.
2023,  
medRxiv: The Preprint Server for Health Sciences
Key variants via Alzheimer's Disease Sequencing Project whole genome sequence data
Wang, Y., et al.
2023,  
Journal of Neuropathology and Experimental Neurology
LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry
Katsumata, Y., et al.
2023,  
International Journal of Stroke: Official Journal of the International Stroke Society
Pleiotropy analysis between lobar intracerebral hemorrhage and CSF β-amyloid highlights new and established associations
Marini, S., et al.
2023,  
medRxiv: The Preprint Server for Health Sciences
APOE loss-of-function variants: Compatible with longevity and associated with resistance to Alzheimer's Disease pathology
Chemparathy, A., et al.
2023,  
HGG advances
Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations
Horimoto, ARVR., et al.
2023,  
medRxiv: The Preprint Server for Health Sciences
Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies LRRC4C, LHX5-AS1 and nominates ancestry-specific loci PTPRK , GRB14 , and KIAA0825 as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium
Rajabli, F., et al.
2023,  
Nature Medicine
Clonal hematopoiesis is associated with protection from Alzheimer's disease
Bouzid, H., et al.
2023,  
Molecular Neurodegeneration
A genome-wide search for pleiotropy in more than 100,000 harmonized longitudinal cognitive domain scores
Kang, M., et al.
2023,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Admixture mapping identifies novel Alzheimer's disease risk regions in African Americans
Rajabli, F., et al.
2023,  
Translational Psychiatry
Circulating S100B levels at birth and risk of six major neuropsychiatric or neurological disorders: a two-sample Mendelian Randomization Study
Pan, M., et al.
2023,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Metabolomic and lipidomic signatures in autosomal dominant and late-onset Alzheimer's disease brains
Novotny, BC., et al.
2023,  
bioRxiv: The Preprint Server for Biology
hipFG: High-throughput harmonization and integration pipeline for functional genomics data
Cifello, J., et al.
2023,  
Genes
Interaction between KLOTHO-VS Heterozygosity and APOE ε4 Allele Predicts Rate of Cognitive Decline in Late-Onset Alzheimer's Disease
Chen, XR., et al.
2023,  
Communications Medicine
Deep learning-based polygenic risk analysis for Alzheimer's disease prediction
Zhou, X., et al.
2023,  
medRxiv: The Preprint Server for Health Sciences
Epistatic Features and Machine Learning Improve Alzheimer's Risk Prediction Over Polygenic Risk Scores
Hermes, S., et al.
2023,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women
Chung, J., et al.
2023,  
Neurobiology of Aging
Investigation of the independent role of a rare APOE variant (L28P; APOE*4Pittsburgh) in late-onset Alzheimer disease
Fan, K., et al.
2023,  
Molecular Psychiatry
Neuroimmune transcriptome changes in patient brains of psychiatric and neurological disorders
Chen, Y., et al.
2023,  
Neuron
TREM2-independent microgliosis promotes tau-mediated neurodegeneration in the presence of ApoE4
Gratuze, M., et al.
2023,  
Scientific Reports
Explainable machine learning aggregates polygenic risk scores and electronic health records for Alzheimer's disease prediction
Gao, XR., et al.
2023,  
Molecular Neurodegeneration
Genome-wide association study of brain biochemical phenotypes reveals distinct genetic architecture of Alzheimer's disease related proteins
Oatman, SR., et al.
2023,  
Journal of Alzheimer's disease: JAD
Visit-to-Visit Blood Pressure Variability and Cognitive Decline in Apolipoprotein ɛ4 Carriers versus Apolipoprotein ɛ3 Homozygotes
Sible, IJ., et al.
2023,  
Alzheimer's & Dementia (Amsterdam, Netherlands)
Early-onset Alzheimer's disease explained by polygenic risk of late-onset disease?
Mantyh, WG., et al.
2023,  
Journal of Alzheimer's disease: JAD
Polygenic Liability to Alzheimer's Disease Is Associated with a Wide Range of Chronic Diseases: A Cohort Study of 312,305 Participants
Wu, B., et al.
2022
2022,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Progranulin mutations in clinical and neuropathological Alzheimer's disease
Vardarajan, BN., et al.
2022,  
Journal of Psychiatric Research
Association of autoimmune diseases with Alzheimer's disease: A mendelian randomization study
Yeung, CHC., et al.
2022,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Protein phosphatase 2A and complement component 4 are linked to the protective effect of APOE ɛ2 for Alzheimer's disease
Jun, GR., et al.
2022,  
Neurobiology of Disease
Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities
Katsumata, Y., et al.
2022,  
Human Molecular Genetics
Scalable approaches for functional analyses of whole-genome sequencing non-coding variants
Kuksa, PP., et al.
2022,  
HGG advances
A scalable Bayesian functional GWAS method accounting for multivariate quantitative functional annotations with applications for studying Alzheimer disease
Chen, J., et al.
2022,  
Movement Disorders: Official Journal of the Movement Disorder Society
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System Atrophy
Hopfner, F., et al.
2022,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Integration of GWAS and brain transcriptomic analyses in a multiethnic sample of 35,245 older adults identifies DCDC2 gene as predictor of episodic memory maintenance
Gao, Y., et al.
2022,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Mendelian randomization highlights causal association between genetically increased C-reactive protein levels and reduced Alzheimer's disease risk
Hu, Y., et al.
2022,  
Molecular Psychiatry
Cognitive performance protects against Alzheimer's disease independently of educational attainment and intelligence
Hu, Y., et al.
2022,  
Bioinformatics (Oxford, England)
Omnibus and robust deconvolution scheme for bulk RNA sequencing data integrating multiple single-cell reference sets and prior biological knowledge
Chen, C., et al.
2022,  
Nature Communications
The causes and consequences of Alzheimer's disease: phenome-wide evidence from Mendelian randomization
Korologou-Linden, R., et al.
2022,  
Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism
Genome-wide association study of brain arteriolosclerosis
Shade, LM., et al.
2022,  
Brain: A Journal of Neurology
Sex differences in the genetic architecture of cognitive resilience to Alzheimer's disease
Eissman, JM., et al.
2022,  
Scientific Reports
Using a two-sample mendelian randomization analysis to explore the relationship between physical activity and Alzheimer's disease
Zhang, B., et al.
2022,  
PLoS genetics
A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer's Disease in African Ancestry
Rajabli, F., et al.
2022,  
PLoS genetics
Integrated analysis of direct and proxy genome wide association studies highlights polygenicity of Alzheimer's disease outside of the APOE region
de la Fuente, J., et al.
2022,  
BMC medical genomics
Integrative analysis of eQTL and GWAS summary statistics reveals transcriptomic alteration in Alzheimer brains
Varathan, P., et al.
2022,  
Scientific Reports
ODACH: a one-shot distributed algorithm for Cox model with heterogeneous multi-center data
Luo, C., et al.
2022,  
Scientific Reports
Manifestations of Alzheimer's disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90
Heath, L., et al.
2022,  
Genome Research
An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns
Jin, B., et al.
2022,  
Nature Genetics
New insights into the genetic etiology of Alzheimer's disease and related dementias
Bellenguez, C., et al.
2022,  
Nature Neuroscience
Integrating whole-genome sequencing with multi-omic data reveals the impact of structural variants on gene regulation in the human brain
Vialle, RA., et al.
2022,  
NAR genomics and bioinformatics
FILER: a framework for harmonizing and querying large-scale functional genomics knowledge
Kuksa, PP., et al.
2022,  
Epilepsia
Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study
Koko, M., et al.
2022,  
Neurobiology of Aging
Association between WWOX/MAF variants and dementia-related neuropathologic endophenotypes
Dugan, AJ., et al.
2022,  
BMJ open
Association of social isolation, loneliness and genetic risk with incidence of dementia: UK Biobank Cohort Study
Elovainio, M., et al.
2022,  
Alzheimer's Research & Therapy
Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping
Belloy, ME., et al.
2022,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Association of mitochondrial variants and haplogroups identified by whole exome sequencing with Alzheimer's disease
Zhang, X., et al.
2022,  
Alzheimer's Research & Therapy
Mendelian randomization highlights significant difference and genetic heterogeneity in clinically diagnosed Alzheimer's disease GWAS and self-report proxy phenotype GWAX
Liu, H., et al.
2022,  
Nature Communications
Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants
Sanders, B., et al.
2022,  
Journal of Alzheimer's disease: JAD
The Advisory Group on Risk Evidence Education for Dementia: Multidisciplinary and Open to All
Rosen, AC., et al.
2022,  
Frontiers in Aging Neuroscience
The role of structural variations in Alzheimer's disease and other neurodegenerative diseases
Wang, H., et al.
2022,  
Journal of Alzheimer's disease: JAD
Investigating Causal Relations Between Circulating Metabolites and Alzheimer's Disease: A Mendelian Randomization Study
Huang, S., et al.
2022,  
Dementia and Geriatric Cognitive Disorders Extra
Early-Stage MRI Volumetric Differences in White Matter Hyperintensity and Temporal Lobe Volumes between Autopsy-Confirmed Alzheimer's Disease, Cerebral Small Vessel Disease, and Mixed Pathologies
Yang, D.
2022,  
Journal of Alzheimer's disease: JAD
Parkinson's Disease rs117896735 Variant Regulates INPP5F Expression in Brain Tissues and Increases Risk of Alzheimer's Disease
Xue, F., et al.
2022,  
Journal of Alzheimer's disease: JAD
Polygenic Risk Scores in Alzheimer's Disease Genetics: Methodology, Applications, Inclusion, and Diversity
Clark, K., et al.
2022,  
Journal of Alzheimer's disease: JAD
Alzheimer's Disease Variant Portal: A Catalog of Genetic Findings for Alzheimer's Disease
Kuksa, PP., et al.
2021
2021,  
Biomedicines
Systems Analysis Reveals Ageing-Related Perturbations in Retinoids and Sex Hormones in Alzheimer's and Parkinson's Diseases
Lam, S., et al.
2021,  
Neurobiology of Aging
Genetic variants in glutamate-, Aβ-, and tau-related pathways determine polygenic risk for Alzheimer's disease
Lawingco, T., et al.
2021,  
Scientific Reports
Reconcile the debate over protective effects of BCG vaccine against COVID-19
Fu, W., et al.
2021,  
Acta Neuropathologica
Lack of evidence supporting a role for DPP6 sequence variants in Alzheimer's disease in the European American population
Kirola, L., et al.
2021,  
Cytometry. Part A: The Journal of the International Society for Analytical Cytology
Tailor: Targeting heavy tails in flow cytometry data with fast, interpretable mixture modeling
Ionita, M., et al.
2021,  
Genetic Epidemiology
Set-based genetic association and interaction tests for survival outcomes based on weighted V statistics
Li, C., et al.
2021,  
Heart & Lung: The Journal of Critical Care
Testing influences of APOE and BDNF genes and heart failure on cognitive function
Jung, M., et al.
2021,  
Methods in Molecular Biology (Clifton, N.J.)
Using INFERNO to Infer the Molecular Mechanisms Underlying Noncoding Genetic Associations
Amlie-Wolf, A., et al.
2021,  
Journal of Neurogenetics
Analysis of whole genome sequenced cases and controls shows that the association of variants in TOMM40, BCAM, NECTIN2 and APOC1 with late onset Alzheimer's disease is driven by linkage disequilibrium with APOE ε2/ε3/ε4 alleles
Curtis, D.
2020
2020,  
Neuromolecular Medicine
Transcriptomic Heterogeneity of Alzheimer's Disease Associated with Lipid Genetic Risk
Miao, X., et al.
2020,  
Aging Cell
Underlying features of epigenetic aging clocks in vivo and in vitro
Liu, Z., et al.
2020,  
Molecular Psychiatry
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation
Bis, JC., et al.
2020,  
Bioinformatics (Oxford, England)
SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variants
Kuksa, PP., et al.
2020,  
Nature Communications
Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study
Reiman, EM., et al.
2020,  
Acta Neuropathologica
Overlapping genetic architecture between Parkinson disease and melanoma
Dube, U., et al.
2020,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Two-stage Bayesian GWAS of 9576 individuals identifies SNP regions that are targeted by miRNAs inversely expressed in Alzheimer's and cancer
Pathak, GA., et al.
2020,  
Journal of Alzheimer's disease: JAD
Whole-Exome Sequencing Analysis of Alzheimer's Disease in Non-APOE*4 Carriers
Fan, K., et al.
2019
2019,  
Brain: A Journal of Neurology
Sex differences in the genetic predictors of Alzheimer's pathology
Dumitrescu, L., et al.
2019,  
Genome Biology
Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight
Ebbert, MTW., et al.
2019,  
Bioinformatics (Oxford, England)
VCPA: genomic variant calling pipeline and data management tool for Alzheimer's Disease Sequencing Project
Leung, YY., et al.
2019,  
Neurobiology of Aging
Translating Alzheimer's disease-associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs
Katsumata, Y., et al.
2019,  
The American Journal of Clinical Nutrition
Circulating antioxidants and Alzheimer disease prevention: a Mendelian randomization study
Williams, DM., et al.
2018
2018,  
Acta Neuropathologica
Sex-specific genetic predictors of Alzheimer's disease biomarkers
Deming, Y., et al.
2018,  
JAMA neurology
Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau
Hohman, TJ., et al.
2018,  
Nucleic Acids Research
SPAR: small RNA-seq portal for analysis of sequencing experiments
Kuksa, PP., et al.
2018,  
Genes, Brain, and Behavior
Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease
Blue, EE., et al.
2018,  
Annals of Clinical and Translational Neurology
Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease
Raghavan, NS., et al.
2018,  
Annals of Clinical and Translational Neurology
Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease
Vardarajan, BN., et al.
2018,  
Alzheimer's Research & Therapy
Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease
Chung, J., et al.
2018,  
Proceedings of the National Academy of Sciences of the United States of America
Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer's disease pathogenesis
Zhou, X., et al.
2018,  
American Journal of Alzheimer's Disease and Other Dementias
Val66Met Polymorphism in BDNF Has No Sexual and APOE ε4 Status-Based Dimorphic Effects on Susceptibility to Alzheimer's Disease: Evidence From an Updated Meta-Analysis of Case-Control Studies and High-Throughput Genotyping Cohorts
Zhao, Q., et al.
2017
2017,  
Neurology. Genetics
The Alzheimer's Disease Sequencing Project: Study design and sample selection
Beecham, GW., et al.
2017,  
PLoS medicine
Fine-mapping of the human leukocyte antigen locus as a risk factor for Alzheimer disease: A case-control study
Steele, NZR., et al.
2017,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans
Mez, J., et al.
2016
2016,  
Neurology. Genetics
SORL1 mutations in early- and late-onset Alzheimer disease
Cuccaro, ML., et al.
2016,  
Biological Psychiatry
Genetic Markers of Human Evolution Are Enriched in Schizophrenia
Srinivasan, S., et al.
2016,  
Neurobiology of Aging
The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable
Mez, J., et al.
2016,  
Neurobiology of Aging
Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium
Hohman, TJ., et al.
2015
2015,  
Alzheimer's & Dementia: The Journal of the Alzheimer's Association
Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease
Barral, S., et al.
2015,  
PloS One
Transcriptomic Changes Due to Cytoplasmic TDP-43 Expression Reveal Dysregulation of Histone Transcripts and Nuclear Chromatin
Amlie-Wolf, A., et al.
2014
2014,  
Methods (San Diego, Calif.)
Using machine learning and high-throughput RNA sequencing to classify the precursors of small non-coding RNAs
Ryvkin, P., et al.
2014,  
PloS One
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease
Escott-Price, V., et al.
2013
2013,  
Nature Genetics
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Lambert, JC., et al.
2011
2011,  
Nature Genetics
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease