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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 19, 2024
. (Total: 63627 Documents since 2012)
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Records 1 - 21 (of 21 Records)
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Dementia[original query]>>Evidence Synthesis [Product Type]
Applications of Artificial Intelligence in the Neuropsychological Assessment of Dementia: A Systematic Review.
Isabella Veneziani et al. J Pers Med 2024 14(1)
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Radiomics and Artificial Intelligence for the Diagnosis and Monitoring of Alzheimer's Disease: A Systematic Review of Studies in the Field.
Roberta Bevilacqua et al. J Clin Med 2023 12(16)
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Artificial intelligence for diagnostic and prognostic neuroimaging in dementia: A systematic review.
Robin J Borchert et al. Alzheimers Dement 2023
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Rationale for the selection of dual primary endpoints in prevention studies of cognitively unimpaired individuals at genetic risk for developing symptoms of Alzheimer's disease.
Angelika Caputo et al. Alzheimer's research & therapy 2023 15(1) 45
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Genetic propensity for cerebral amyloidosis and risk of mild cognitive impairment and Alzheimer's disease within a cognitive reserve framework.
Niki Mourtzi et al. Alzheimer's & dementia : the journal of the Alzheimer's Association 2023
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Identification of High Likelihood of Dementia in Population-Based Surveys using Unsupervised Clustering: a Longitudinal Analysis.
Amin Gharbi-Meliani et al. medRxiv : the preprint server for health sciences 2023
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Interpretable machine learning for dementia: A systematic review.
Sophie A Martin et al. Alzheimer's & dementia : the journal of the Alzheimer's Association 2023
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Machine Learning for Dementia Prediction: A Systematic Review and Future Research Directions.
Ashir Javeed et al. Journal of medical systems 2023 47(1) 17
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Dialogue agents for artificial intelligence-based conversational systems for cognitively disabled: a systematic review.
Huq Syed Mahmudul et al. Disability and rehabilitation. Assistive technology 2022 1-20
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Epigenetic aging as a biomarker of dementia and related outcomes: a systematic review.
Zhou Aoshuang et al. Epigenomics 2022
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Machine learning methods for predicting progression from mild cognitive impairment to Alzheimer's disease dementia: a systematic review.
Grueso Sergio et al. Alzheimer's research & therapy 2021 13(1) 162
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Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD: A Systematic Scoping Review.
Crook Ashley et al. Alzheimer disease and associated disorders 2021
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The Use of Motor Cognitive Dual-Task Quantitative Assessment on Subjects with Mild Cognitive Impairment: A systematic Review.
Mancioppi Gianmaria et al. Mechanisms of ageing and development 2020 Nov 111393
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Accuracy of Biomarker Testing for Neuropathologically Defined Alzheimer Disease in Older Adults With Dementia: A Systematic Review.
Fink Howard A et al. Annals of internal medicine 2020 Apr
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CLINGEN Actionability Report for Hereditary transthyretin-related amyloidosis - TTR
ClinGen Actionability Working Group
CLINGEN Actionability Report for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukocenphalopathy, type 1 - NOTCH3
ClinGen Actionability Working Group
Using data science to diagnose and characterize heterogeneity of Alzheimer's disease.
Ang Ting F A et al. Alzheimer's & dementia (New York, N. Y.) 2019 5264-271
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Clinical implications of APOE genotyping for late-onset Alzheimer's disease (LOAD) risk estimation: a review of the literature.
Marshe Victoria S et al. Journal of neural transmission (Vienna, Austria : 1996) 2018 Oct
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Effect of Apolipoprotein E ?4 Carrier Status on Cognitive Response to Acetylcholinesterase Inhibitors in Patients with Alzheimer's Disease: A Systematic Review and Meta-Analysis.
Cheng Ying-Chih et al. Dementia and geriatric cognitive disorders 2018 Jul 45(5-6) 335-352
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Genetic counselling in ALS: facts, uncertainties and clinical suggestions.
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Risk estimations, risk factors, and genetic variants associated with Alzheimer's disease in selected publications from the Framingham Heart Study.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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