All Stories

  1. Reply to: a quantitative trait locus for reduced microglial APOE expression associates with reduced cerebral amyloid angiopathy
  2. A bioinformatic survey of RNA isoform diversity and expression across 9 GTEx tissues using long-read sequencing data
  3. Genome annotations matter: characterizing Ensembl hg38 annotations from 2014 to 2023
  4. Genetic association analyses of cognitive performance across multi-ancestry older adults: Application of Tobit models
  5. Systematic review and meta-analysis of bulk RNAseq studies in human Alzheimer’s disease brain tissue
  6. Medicare medication therapy Management: Beneficiary characteristics and utilization patterns in a national CMS Medicare fee-for-service sample (2013 to 2016)
  7. Limbic-predominant age-related TDP-43 encephalopathy (LATE-NC): Co-pathologies and genetic risk factors provide clues about pathogenesis
  8. Novel multi-omics deconfounding variational autoencoders can obtain meaningful disease subtyping
  9. Atorvastatin rescues hyperhomocysteinemia-induced cognitive deficits and neuroinflammatory gene changes
  10. A neuropathologic feature of brain aging: multi-lumen vascular profiles
  11. Different cohort, disparate results: Selection bias is a key factor in autopsy cohorts
  12. LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry
  13. Urinary Incontinence in a Community-Based Autopsy Cohort Is Associated with Limbic Predominant Age-Related TDP-43 Encephalopathy Neuropathologic Changes
  14. Associations of potential ADRD plasma biomarkers in cognitively normal volunteers
  15. Estimating random effects in a finite Markov chain with absorbing states: Application to cognitive data
  16. Genome-wide association study of multiple neuropathology endophenotypes identifies novel risk loci and provides insights into known Alzheimer’s risk loci
  17. Evaluation of pathologies associated with hyperhomocysteinemia in human autopsy brain tissue
  18. The association of gabapentin initiation and neurocognitive changes in older adults with normal cognition
  19. Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities
  20. Sex differences in the genetic architecture of cognitive resilience to Alzheimer’s disease
  21. Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90
  22. Limbic-Predominant Age-Related TDP-43 Encephalopathy
  23. New insights into the genetic etiology of Alzheimer’s disease and related dementias
  24. Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2
  25. Association between WWOX/MAF variants and dementia-related neuropathologic endophenotypes
  26. Genetic expression changes and pathologic findings associated with hyperhomocysteinemia in human autopsy brain tissue
  27. Type 2 Diabetes and association with neuropathological changes and domain specific cognitive decline
  28. Analysis of genes (TMEM106B, GRN, ABCC9, KCNMB2, and APOE) implicated in risk for LATE-NC and hippocampal sclerosis provides pathogenetic insights: a retrospective genetic association study
  29. Inflammatory Pathways Are Impaired in Alzheimer Disease and Differentially Associated With Apolipoprotein E Status
  30. Predictors of chronic opioid therapy in Medicaid beneficiaries with HIV who initiated antiretroviral therapy
  31. Four Common Late-Life Cognitive Trajectories Patterns Associate with Replicable Underlying Neuropathologies
  32. Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
  33. Analysis of Genetic Variants Associated with Levels of Immune Modulating Proteins for Impact on Alzheimer’s Disease Risk Reveal a Potential Role for SIGLEC14
  34. Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2
  35. A New Functional F-Statistic for Gene-Based Inference Involving Multiple Phenotypes
  36. A Highly Predictive MicroRNA Panel for Determining Delayed Cerebral Vasospasm Risk Following Aneurysmal Subarachnoid Hemorrhage
  37. Age and sex are associated with the plasma lipidome: findings from the GOLDN study
  38. Reduced rank multinomial logistic regression in Markov chains with application to cognitive data
  39. Longitudinal cognitive performance of Alzheimer's disease neuropathological subtypes
  40. Brain arteriolosclerosis
  41. Prevalence and Clinical Phenotype of Quadruple Misfolded Proteins in Older Adults
  42. Distinct clinicopathologic clusters of persons with TDP-43 proteinopathy
  43. Quantitative phenotype scan statistic (QPSS) reveals rare variant associations with Alzheimer’s disease endophenotypes
  44. The MUC6/AP2A2 Locus and Its Relevance to Alzheimer’s Disease: A Review
  45. Genetic Variants and Functional Pathways Associated with Resilience to Alzheimer’s Disease
  46. Hierarchical Clustering Analyses of Plasma Proteins in Subjects With Cardiovascular Risk Factors Identify Informative Subsets Based on Differential Levels of Angiogenic and Inflammatory Biomarkers
  47. Alzheimer Disease Pathology-Associated Polymorphism in a Complex Variable Number of Tandem Repeat Region Within the MUC6 Gene, Near the AP2A2 Gene
  48. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
  49. Reply: LATE to the PART-y
  50. Tau and TDP-43 proteinopathies: kindred pathologic cascades and genetic pleiotropy
  51. Erratum
  52. Evaluation of CD33 as a genetic risk factor for Alzheimer’s disease
  53. Tobacco Smoking and Dementia in a Kentucky Cohort: A Competing Risk Analysis
  54. Socioemotional selectivity and psychological health in amyotrophic lateral sclerosis patients and caregivers: a longitudinal, dyadic analysis
  55. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
  56. Translating Alzheimer's disease–associated polymorphisms into functional candidates: a survey of IGAP genes and SNPs
  57. Characterization of Squamous Cell Lung Cancers from Appalachian Kentucky
  58. Correction: Genetic data and cognitively defined late-onset Alzheimer’s disease subgroups
  59. Patterns and predictors of chronic opioid use in older adults: A retrospective cohort study
  60. Noninvasive sleep monitoring in large-scale screening of knock-out mice reveals novel sleep-related genes
  61. Estimation of multi-state models with missing covariate values based on observed data likelihood
  62. Genetic data and cognitively defined late-onset Alzheimer’s disease subgroups
  63. Dichotomous scoring of TDP-43 proteinopathy from specific brain regions in 27 academic research centers: associations with Alzheimer’s disease and cerebrovascular disease pathologies
  64. Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease
  65. Longitudinal data methods for evaluating genome-by-epigenome interactions in families
  66. Association analyses of repeated measures on triglyceride and high-density lipoprotein levels: insights from GAW20
  67. GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics
  68. Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau
  69. Genetic data and cognitively-defined late-onset Alzheimer’s disease subgroups
  70. Sex-specific genetic predictors of Alzheimer’s disease biomarkers
  71. Visual Arts Education improves self-esteem for persons with dementia and reduces caregiver burden: A randomized controlled trial
  72. Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing
  73. Genetically elevated high‐density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease
  74. Detergent Insoluble Proteins and Inclusion Body-Like Structures Immunoreactive for PRKDC/DNA-PK/DNA-PKcs, FTL, NNT, and AIFM1 in the Amygdala of Cognitively Impaired Elderly Persons
  75. The Amygdala as a Locus of Pathologic Misfolding in Neurodegenerative Diseases
  76. Impact of home visit capacity on genetic association studies of late-onset Alzheimer's disease
  77. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
  78. Peripheral Inflammation, Apolipoprotein E4 , and Amyloid-β Interact to Induce Cognitive and Cerebrovascular Dysfunction
  79. Gene-based association study of genes linked to hippocampal sclerosis of aging neuropathology: GRN , TMEM106B , ABCC9 , and KCNMB2
  80. Functional human GRIN2B promoter polymorphism and variation of mental processing speed in older adults
  81. CSF protein changes associated with hippocampal sclerosis risk gene variants highlight impact of GRN /PGRN
  82. Overlapping but distinct TDP‐43 and tau pathologic patterns in aged hippocampi
  83. Outcomes after diagnosis of mild cognitive impairment in a large autopsy series
  84. Systems biology approach to late‐onset Alzheimer's disease genome‐wide association study identifies novel candidate genes validated using brain expression data and Caenorhabditis elegans experiments
  85. Multi-state models and missing covariate data: expectation–maximization algorithm for likelihood estimation
  86. Risk of incident clinical diagnosis of Alzheimer's disease–type dementia attributable to pathology‐confirmed vascular disease
  87. Genomics and CSF analyses implicate thyroid hormone in hippocampal sclerosis of aging
  88. On combining family- and population-based sequencing data
  89. Causal effect estimation in sequencing studies: a Bayesian method to account for confounder adjustment uncertainty
  90. Comparing performance of non–tree-based and tree-based association mapping methods
  91. Diabetes is associated with cerebrovascular but not Alzheimer's disease neuropathology
  92. Automated quality control for genome wide association studies
  93. Risk factors and global cognitive status related to brain arteriolosclerosis in elderly individuals
  94. Crowdsourced estimation of cognitive decline and resilience in Alzheimer's disease
  95. “New Old Pathologies”: AD, PART, and Cerebral Age-Related TDP-43 With Sclerosis (CARTS)
  96. The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable
  97. Assessment of the genetic variance of late-onset Alzheimer's disease
  98. ABCC9/SUR2 in the brain: Implications for hippocampal sclerosis of aging and a potential therapeutic target
  99. Genetics ignite focus on microglial inflammation in Alzheimer’s disease
  100. Openness to Change: Experiential and Demographic Components of Change in Local Health Department Leaders
  101. Genetics and non-syndromic facial growth
  102. Novel humanABCC9/SUR2brain-expressed transcripts and an eQTL relevant to hippocampal sclerosis of aging
  103. Self-reported memory complaints: A comparison of demented and unimpaired outcomes
  104. Genetic differences between symptomatic and asymptomatic persons with Alzheimer's disease neuropathologic change
  105. Integrating human protein-protein interaction network with results from gwas in whites and african-americans identifies common genes underlying late-onset Alzheimer’s disease
  106. A Summary Score for the Framingham Heart Study Neuropsychological Battery
  107. Genetics of CD33 in Alzheimer's disease and acute myeloid leukemia
  108. Should They Stay or Should They Go? Leader Duration and Financial Performance in Local Health Departments
  109. Reassessment of Risk Genotypes (GRN,TMEM106B, andABCC9Variants) Associated With Hippocampal Sclerosis of Aging Pathology
  110. Assessing the Discriminant Ability, Reliability, and Comparability of Multiple Short Forms of the Boston Naming Test in an Alzheimer's Disease Center Cohort
  111. Analysis of sleep traits in knockout mice from the large-scale KOMP2 population using a non-invasive, high-throughput piezoelectric system
  112. Impact of Population Stratification on Family-Based Association in an Admixed Population
  113. An Ecological Systems Examination of Elder Abuse: A Week in the Life of Adult Protective Services
  114. Longitudinal Trajectories of Cholesterol from Midlife through Late Life according to Apolipoprotein E Allele Status
  115. Self-reported memory complaints: Implications from a longitudinal cohort with autopsies
  116. Effects of Alcohol Consumption on Cognition and Regional Brain Volumes Among Older Adults
  117. Governance Practices and Performance in US Academic Medical Centers
  118. Complex Pedigrees in the Sequencing Era: To Track Transmissions or Decorrelate?
  119. Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees
  120. ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology
  121. Comparison of BMI, AHI, and Apolipoprotein E ε4 (APOE-ε4) Alleles among Sleep Apnea Patients with Different Skeletal Classifications
  122. Low Plasma Leptin in Cognitively Impaired ADNI Subjects: Gender Differences and Diagnostic and Therapeutic Potential
  123. Genetics of PICALM Expression and Alzheimer's Disease
  124. Assessment of appalachian region pediatric hearing healthcare disparities and delays
  125. Delays in Diagnosis of Congenital Hearing Loss in Rural Children
  126. An intronic PICALM polymorphism, rs588076, is associated with allelic expression of a PICALM isoform
  127. A 2-step penalized regression method for family-based next-generation sequencing association studies
  128. Modeling of multivariate longitudinal phenotypes in family genetic studies with Bayesian multiplicity adjustment
  129. On family-based genome-wide association studies with large pedigrees: observations and recommendations
  130. Using Mendelian inheritance errors as quality control criteria in whole genome sequencing data set
  131. Self-Reported Head Injury and Risk of Late-Life Impairment and AD Pathology in an AD Center Cohort
  132. ABCA7 expression is associated with Alzheimer's disease polymorphism and disease status
  133. The Relationship Between Midlife and Late Life Alcohol Consumption, APOE e4 and the Decline in Learning and Memory Among Older Adults
  134. CD33 Alzheimer's Risk-Altering Polymorphism, CD33 Expression, and Exon 2 Splicing
  135. Hippocampal sclerosis of aging, a prevalent and high-morbidity brain disease
  136. Vascular neuropathology in dementia patients receiving antipsychotic therapy
  137. Vascular disease, vascular risk factors and risk of late-onset Alzheimer's disease: Mendelian randomization analyses in the combined ADGC dataset
  138. Early-to mid-life formal training in music is associated with improved late-life semantic and episodic memory among cognitively normal older adults
  139. Clinical correlates of hippocampal sclerosis of aging: The University of Kentucky experience
  140. Self-reported head injury and risk of cognitive impairment and Alzheimer's-type pathology in a longitudinal Alzheimer’s disease center cohort
  141. Genome-wide SNP analysis finds executive-prominent late-onset Alzheimer's disease is highly heritable
  142. GWAS of the joint ADGC data set identifies novel common variants associated with late-onset Alzheimer's disease
  143. APOE-ε2 and APOE-ε4 Correlate With Increased Amyloid Accumulation in Cerebral Vasculature
  144. Self-reported memory decline predicts mild cognitive impairment and dementia
  145. Adjusting for Mortality when Identifying Risk Factors for Transitions to Mild Cognitive Impairment and Dementia
  146. Board Oversight of Patient Care Quality in Large Nonprofit Health Systems
  147. Levels of Soluble Apolipoprotein E/Amyloid-  (A ) Complex Are Reduced and Oligomeric A  Increased with APOE4 and Alzheimer Disease in a Transgenic Mouse Model and Human Samples
  148. Generic antiepileptic drug prescribing: A cross-sectional study
  149. Combining genetic association study designs: a GWAS case study
  150. Paradoxical Relationship Between the Degree of EGFR Amplification and Outcome in Glioblastomas
  151. Effect of gene-environment interactions between APOE-ɛ4 and lifetime alcohol consumption on cognition in older adults
  152. Genetics of Clusterin Isoform Expression and Alzheimer's Disease Risk
  153. Families or Unrelated: The Evolving Debate in Genetic Association Studies
  154. Mild Cognitive Impairment: Statistical Models of Transition Using Longitudinal Clinical Data
  155. Gene-environment interaction testing in family-based association studies with phenotypically ascertained samples: a causal inference approach
  156. PATHOLOGY
  157. Evaluation of retention protocols among members of the American Association of Orthodontists in the United States
  158. Race-ethnicity as an effect modifier of the association between HbAlc and mortality in U.S. adults without diagnosed diabetes
  159. Sclerostin and Dickkopf-1 in Renal Osteodystrophy
  160. Exploration and comparison of methods for combining population- and family-based genetic association using the Genetic Analysis Workshop 17 mini-exome
  161. On Quality Control Measures in Genome-Wide Association Studies: A Test to Assess the Genotyping Quality of Individual Probands in Family-Based Association Studies and an Application to the HapMap Data
  162. Recovering unused information in genome-wide association studies: the benefit of analyzing SNPs out of Hardy–Weinberg equilibrium
  163. Predictors of an Accurate Preoperative Sestamibi Scan for Single-Gland Parathyroid Adenomas
  164. On dichotomizing phenotypes in family‐based association tests: quantitative phenotypes are not always the optimal choice
  165. Guest Commentary by Dr. David H. Johnson