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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

Naj, AC., et al.