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.
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Strong evidence has emerged recently for the concept that herpes simplex virus type 1 (HSV1) is a major risk for Alzheimer's disease (AD).
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Further analysis of the AD brain proteome will continue to yield new insights into the biological basis of AD.
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A pathogenic mutation in the PSEN2 gene in a Korean patient associated with EOAD was identified.
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Genetics can provide a systematic approach to discovering the tissues and cell types relevant for a complex disease or trait.
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Health risk factors such as body mass index (BMI) and serum cholesterol are associated with many common diseases.
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These results provide support that higher educational attainment is associated with a reduced risk of Alzheimer's disease.
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The Alzheimer's disease risk gene apolipoprotein E epsilon 4 (APOE ε4) is associated with increased cerebral amyloid.
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The identification of subjects at high risk for Alzheimer's disease is important for prognosis and early intervention.
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Presenilin 2 gene (PSEN2) mutations account for <5% of all early-onset familial Alzheimer's disease (EOFAD) cases and only 13 have strong evidence for pathogenicity.
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Our data indicated that the levels of triglyceride, total cholesterol, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, apolipoprotein A-I (ApoA-I), ApoB, ApoE, lipoprotein (a) (Lp(a)) of mutant genotypes in ApoE c.61G > A and c.761T > A genetic variants were different from those subjects with wild genotype in HD patients and healthy controls.
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Alzheimer's disease (AD) is a severe age-related neurodegenerative disorder characterized by accumulation of amyloid-β plaques and neurofibrillary tangles, synaptic and neuronal loss, and cognitive decline.
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Apolipoprotein E type 4 allele (ApoE∊4) is known as a risk gene for the late-onset Alzheimer’s disease, and the relationship between ApoE∊4 and cognitive function of the elderly people has drawn the attention of the scientists.
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Children with Down syndrome (DS) experience congenital and functional medical issues that predispose them to obstructive sleep apnea (OSA).
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To extend our understanding of the genetic basis of human immune function and dysfunction, we performed an expression quantitative trait locus (eQTL) study of purified CD4(+) T cells and monocytes, representing adaptive and innate immunity, in a multi-ethnic cohort of 461 healthy individuals.
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Epigenetic dysregulation of gene expression is thought to be critically involved in the pathophysiology of Alzheimer's disease (AD).
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45/100
The apolipoprotein E (APOE) genotype is the major genetic risk factor for Alzheimer's disease (AD).
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Cognitive decline is a debilitating feature of most neurodegenerative diseases of the central nervous system, including Alzheimer's disease.
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A genome-wide, whole brain approach to investigate genetic effects on neuroimaging phenotypes for identifying quantitative trait loci is described.
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We identified two novel heterozygous mutations in two unrelated patients, Cys139Arg in the PGRN gene and Val412Ile in the PSEN1 gene.
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Based on the folding energy (ΔΔG) calculations, mutations G165W and L155W were particularly destabilizing in APOE4.
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43/100
The study of transcriptomic and epigenomic variations in neurodegenerative diseases, particularly tauopathies like Pick's disease (PiD) and Alzheimer's disease (AD), offers insights into their underlying regulatory mechanisms.
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The brain is the most cholesterol-rich organ in the body, and ApoE is the main lipid carrier protein in the brain.
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Previous studies in humans and humanized APOE mice have demonstrated APOE-genotype-specific differences in the GMB.
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While preclinical studies suggest that Phosphodiesterase 5 (PDE5) inhibition may reduce cognitive impairment, findings from observational studies on whether PDE5 inhibitors reduce Alzheimer's disease (AD) risk have been inconsistent.
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43/100
Somatic mutations are DNA sequence changes that occur in non-reproductive cells during an organism's life and are not inherited by offspring.
From across this topic
10 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 10. The same 10 appear here every time.
- A novel multi-tissue RNA diagnostic of healthy ageing relates to cognitive health status
- deepDR: a network-based deep learning approach to in silico drug repositioning
- Targeting Apolipoprotein E for Alzheimer's Disease: An Industry Perspective
- APOE Lipoprotein Particles: Pathophysiology, Therapy, and the Crosstalk in Alzheimer's Disease and Cardiovascular Disease
- Mechanisms of sex differences in Alzheimer's disease
- Human apolipoprotein E ɛ4 expression impairs cerebral vascularization and blood-brain barrier function in mice
- Integrating spatial transcriptomics data across different conditions, technologies and developmental stages
- The roles of apolipoprotein E ε4 on neuropathology and neuroinflammation in patients with Alzheimer's disease
- Associations of genetic predisposition to Alzheimer’s disease with blood-based biomarkers: a community-based study
- Genetic effects and gene-by-education interactions on episodic memory performance and decline in an aging population