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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Neurological Disorders
Last data update: Apr 18, 2024
. (Total: 63623 Documents since 2012)
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all[original query]>>Reviews/Commentaries[Product Type]
Many Models, Little Adoption-What Accounts for Low Uptake of Machine Learning Models for Atrial Fibrillation Prediction and Detection?
Yuki Kawamura et al. J Clin Med 2024 13(5)
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Artificial intelligence in multiple sclerosis management: Challenges in a new era.
Sebastián Rodríguez et al. Mult Scler Relat Disord 2024 86105611
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Clinically significant changes in genes and variants associated with epilepsy over time: implications for re-analysis.
Alan J Robertson et al. Sci Rep 2024 14(1) 7717
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Harnessing Big Data in Amyotrophic Lateral Sclerosis: Machine Learning Applications for Clinical Practice and Pharmaceutical Trials.
Ee Ling Tan et al. J Integr Neurosci 2024 23(3) 58
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Emerging artificial intelligence-aided diagnosis and management methods for ischemic strokes and vascular occlusions: A comprehensive review.
G A U R I Parvathy et al. World Neurosurg X 2024 22100303
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A Communication and Decision-Making Framework for Pediatric Precision Medicine.
Brittany L Greene et al. Pediatrics 2024
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Predictive deep learning models for cognitive risk using accessible data.
Kenji Karako et al. Biosci Trends 2024
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A review of machine learning and deep learning algorithms for Parkinson's disease detection using handwriting and voice datasets.
Md Ariful Islam et al. Heliyon 2024 10(3) e25469
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Evaluation of Informative Content on Cerebral Palsy in the Era of Artificial Intelligence: The Value of ChatGPT.
Ayse Merve Ata et al. Phys Occup Ther Pediatr 2024 1-10
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Applications of Artificial Intelligence in Pain Medicine.
Alaa Abd-Elsayed et al. Curr Pain Headache Rep 2024
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Connecting clinical and genetic heterogeneity in ADHD.
Chloe X Yap et al. Nat Genet 2024
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Building CRISPR Gene Therapies for the Central Nervous System: A Review.
Sally E Salomonsson et al. JAMA Neurol 2024
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Challenges and opportunities in spinal muscular atrophy therapeutics.
Crystal J J Yeo et al. Lancet Neurol 2024 23(2) 205-218
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FDA Review of Radiologic AI Algorithms: Process and Challenges.
Kuan Zhang et al. Radiology 2024 310(1) e230242
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Rethinking Dementia Risk Prediction: A Critical Evaluation of a Multimodal Machine Learning Predictive Model.
Silvia Ottaviani et al. J Alzheimers Dis 2024
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The Early Care (0-3 Years) In Duchenne Muscular Dystrophy Meeting Report.
Niki Armstrong et al. J Neuromuscul Dis 2024
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Genetics in Ischemic Stroke: Current Perspectives and Future Directions.
Ka Zhang et al. J Cardiovasc Dev Dis 2023 10(12)
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Direct to Consumer Biomarker Testing for Alzheimer Disease—Are We Ready for the Insurance Consequences?
JJ Arias et al, JAMA Neurology, December 18, 2023
Machine Learning and Artificial Intelligence Applications to Epilepsy: a Review for the Practicing Epileptologist.
Wesley T Kerr et al. Curr Neurol Neurosci Rep 2023
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Detecting early signs in Duchenne muscular dystrophy: comprehensive review and diagnostic implications.
Eugenio Mercuri et al. Front Pediatr 2023 111276144
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The Monitoring with Advanced Sensors, Transmission and E-Resuscitation in Traumatic Brain Injury (MASTER-TBI) collaborative: bringing data science to the ICU bedside.
Robert McNamara et al. Crit Care Resusc 2023 24(1) 39-42
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EEG-Based Epilepsy Prediction: Evaluation Metrics, Data Deficiency and Limitation of Current Methods.
Bowen Xiong et al. Stud Health Technol Inform 2023 3083-10
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Public Health Genetics, Gene Therapy, and Duchenne Muscular Dystrophy
CDC Webinar, December 18, 2023
Gene therapy-based strategies for spinal muscular atrophy-an Asia-Pacific perspective.
Michelle A Farrar et al. Mol Cell Pediatr 2023 10(1) 17
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Public engagement with genomics.
Anna Middleton et al. Wellcome Open Res 2023 8310
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The implications of DNA methylation for amyotrophic lateral sclerosis.
Adriana Helena DE Oliveira Reis et al. An Acad Bras Cienc 2023 95(suppl 2) e20230277
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Artificial Intelligence Applications in Diagnosing and Managing Non-syndromic Craniosynostosis: A Comprehensive Review.
Amna Qamar et al. Cureus 2023 15(9) e45318
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Challenges of Parkinson's disease GWASs in African people.
Samia Ben Sassi et al. Lancet Neurol 2023 22(11) 975-976
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Machine learning applications in stroke medicine: advancements, challenges, and future prospectives.
Mario Daidone et al. Neural Regen Res 2023 19(4) 769-773
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Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders.
Chelsea Chambers et al. Neurol Clin Pract 2023 13(5) e200201
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 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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