Each study has a usefulness score out of 100 (rubric version 4.0). Tap a score to see what makes it up.
Highest usefulness score first. Studies without a score come last.
-
Previous studies showed that U1 small nuclear RNA (snRNA) was selectively enriched in the brain of individuals with familial Alzheimer's disease (AD), resulting in widespread changes in RNA splicing.
-
As predicted, we observed a differential impact of CBE status on cognition as a function of APOE ε4 status, in which CBE ε4 carriers displayed significantly worse neuropsychological performance, specifically in the domain of memory.
-
Alzheimer's disease (AD) lacks protein biomarkers reflective of its diverse underlying pathophysiology, hindering diagnostic and therapeutic advancements.
-
The deaf group showed considerably lower scores on the OPT, OLT, and Y-maze test than the control group.
-
Alzheimer's disease is a progressive neurodegenerative disorder, with the strongest disease-associated changes observed at clinical or end-stage disease.
-
Aetiological and clinical heterogeneity is increasingly recognized as a common characteristic of Alzheimer's disease and related dementias.
-
Recent research efforts provided compelling evidence of genome-wide DNA methylation alterations in aging and age-related disease.
-
Genes play a strong role in Alzheimer's disease (AD), with late-onset AD showing heritability of 58-79% and early-onset AD showing over 90%.
-
41/100
Neuronal intranuclear inclusion disease (NIID) is a slowly progressing neurodegenerative disease characterized by eosinophilic intranuclear inclusions in the nervous system and multiple visceral organs.
-
We devise a conceptually different computational framework based on a holistic view, where single-cell datasets are used to infer global, large-scale regulatory networks.
-
Apolipoprotein E ( APOE ) genotype is the strongest prevalent genetic risk factor for Alzheimer's disease (AD).
-
Emerging evidence suggests that these morphological changes reflect functional alterations that affect disease.
-
Both social and genetic factors contribute to cognitive impairment and decline, yet genetic factors identified through genome-wide association studies (GWAS) explain only a small portion of trait variability.
-
Differentially methylated positions (DMPs) between persons with and without late-onset Alzheimer's disease (LOAD) were observed at 477 of 769,190 loci in a plurality of genes.
-
Graphs are widely used as a natural framework that captures interactions between individual elements represented as nodes in a graph.
-
Identifying reliable biomarkers of aging is a major goal in geroscience.
-
Aging is the strongest risk factor for Alzheimer's disease (AD), although the underlying mechanisms remain unclear.
-
Our results suggest that RAB10 could be a promising therapeutic target for AD prevention.
-
Early expression disturbance of hub genes is an important feature of AD development, and interfering with this process may reverse the disease progression.
-
Here, we report proteomic analyses of 129 human cortical tissues to define changes associated with the asymptomatic and symptomatic stages of Alzheimer's disease (AD).
-
Disruptions of normal circadian rhythms and sleep cycles are consequences of aging and can profoundly affect health.
-
Apolipoprotein E (apoE) is associated with lipoproteins in the cerebrospinal fluid (CSF).
-
41/100
Genome-wide association studies (GWAS) have traditionally been undertaken in homogeneous populations from the same ancestry group.
-
The bacterial CRISPR/Cas9 system allows sequence-specific gene editing in many organisms and holds promise as a tool to generate models of human diseases, for example, in human pluripotent stem cells.
-
41/100
SMC ε4+ showed greater amyloid deposition than SMC ε4-, but no hypometabolism or medial temporal lobe (MTL) atrophy.
From across this topic
9 of the 933 studies in this topic, picked by a fixed rule (a hash of each study's address), not by score or date; each page of this list shows a different 9. The same 9 appear here every time.
- The Caenorhabditis elegans IMPAS gene, imp-2, is essential for development and is functionally distinct from related presenilins
- Sex differences in interacting genetic and functional connectivity biomarkers in Alzheimer's disease
- Differential Gene Expression and DNA Methylation in the Risk of Depression in LOAD Patients
- Atrial Fibrillation Genetics Update: Toward Clinical Implementation
- Reduced GLP-1R availability in the caudate nucleus with Alzheimer's disease
- The Caribbean-Hispanic Alzheimer's disease brain transcriptome reveals ancestry-specific disease mechanisms
- Protein-Protein interactions uncover candidate 'core genes' within omnigenic disease networks
- Comprehensive Screening for Disease Risk Variants in Early-Onset Alzheimer's Disease Genes in African Americans Identifies Novel PSEN Variants
- Apolipoprotein E genotype, Alzheimer's pathologies and related gene expression in the aged population