Last Posted: Jun 19, 2024
- Using Wearable Sensors and Machine Learning to Assess Upper Limb Function in Huntington's Disease.
Ashkan Vaziri et al. Res Sq 2024 - A wearable sensor and machine learning estimate step length in older adults and patients with neurological disorders.
Assaf Zadka et al. NPJ Digit Med 2024 7(1) 142 - Utility of next generation sequencing in paediatric neurological disorders: experience from South Africa.
Magriet van Niekerk et al. Eur J Hum Genet 2024 - Explainable machine learning for predicting conversion to neurological disease: Results from 52,939 medical records.
Christina Felix et al. Digit Health 2024 1020552076241249286 - Prospective evaluation of NGS-based sequencing in epilepsy patients: results of seven NASGE-associated diagnostic laboratories.
Maximilian G W Witzel et al. Front Neurol 2023 141276238 - QALYs and rare diseases: exploring the responsiveness of SF-6D, EQ-5D-5L and AQoL-8D following genomic testing for childhood and adult-onset rare genetic conditions in Australia.
Tianxin Pan et al. Health Qual Life Outcomes 2023 21(1) 132 - Clinical and Demographic Characteristics of Families Attending the Epilepsy, Neuromuscular, and Child Wellbeing Clinics.
Ahmed K Bamaga et al. Cureus 2023 15(8) e43651 - Caffeine intake interacts with Asian gene variants in Parkinson's disease: a study in 4488 subjects.
Yi-Lin Ong et al. Lancet Reg Health West Pac 2023 40100877 - Machine learning using multimodal clinical, electroencephalographic, and magnetic resonance imaging data can predict incident depression in adults with epilepsy: A pilot study.
Guillermo Delgado-García et al. Epilepsia 2023 - Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders.
María Isabel Alvarez-Mora et al. Genes (Basel) 2023 14(4) - Application of optimized convolutional neural networks for early aided diagnosis of essential tremor: Automatic handwriting recognition and feature analysis.
Yanwen Wang et al. Medical engineering & physics 2023 113103962 - Short-term outcome prediction for myasthenia gravis: an explainable machine learning model.
Huahua Zhong et al. Therapeutic advances in neurological disorders 2023 1617562864231154976 - Artificial Intelligence Tools to Evaluate Language and Speech Patterns in Alzheimer's Disease.
Favaro Anna et al. Alzheimer's & dementia : the journal of the Alzheimer's Association 2022 18 Suppl 2e064913 - A Machine Learning Approach for Detecting Idiopathic REM Sleep Behavior Disorder.
Salsone Maria et al. Diagnostics (Basel, Switzerland) 2022 12(11) - Artificial intelligence-based methods for fusion of electronic health records and imaging data.
Mohsen Farida et al. Scientific reports 2022 12(1) 17981 - The White Matter Rounds experience: The importance of a multidisciplinary network to accelerate the diagnostic process for adult patients with rare white matter disorders.
Huang Yu Tong et al. Frontiers in neurology 2022 13928493 - Association of Genetic Variant Linked to Hemochromatosis With Brain Magnetic Resonance Imaging Measures of Iron and Movement Disorders.
Loughnan Robert et al. JAMA neurology 2022 - Shared mechanisms across the major psychiatric and neurodegenerative diseases
TS Wingo et al, Nat Comm, July 26, 2022 - An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities.
Slaby Isabella et al. Journal of neurodevelopmental disorders 2022 14(1) 37 - Genetic therapies for neurological disease: state of the art and opportunities for next-generation approaches.
Morris Gareth et al. Neuroscience 2022 - Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study.
Ibañez Kristina et al. The Lancet. Neurology 2022 21(3) 234-245 - Genetic Analysis of Neuroligin 4Y Gene in Autism Population of India.
Hegde Rajat et al. Global medical genetics 2022 9(1) 18-22 - Accurate detection of autism using Douglas-Peucker algorithm, sparse coding based feature mapping and convolutional neural network techniques with EEG signals.
Ari Berna et al. Computers in biology and medicine 2022 143105311 - DNA Methylation in Genetic and Sporadic Forms of Neurodegeneration: Lessons from Alzheimer's, Related Tauopathies and Genetic Tauopathies.
Zimmer-Bensch Geraldine et al. Cells 2021 10(11) - Genetic therapies for neurological disorders.
FitzPatrick Laura et al. Human genetics 2021 - Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.
Schon Katherine R et al. BMJ (Clinical research ed.) 2021 375e066288 - Advanced Machine Learning Tools to Monitor Biomarkers of Dysphagia: A Wearable Sensor Proof-of-Concept Study.
O'Brien Megan K et al. Digital biomarkers 2021 5(2) 167-175 - Aging with Down Syndrome-Where Are We Now and Where Are We Going?
Alldred Melissa J et al. Journal of clinical medicine 2021 10(20) - Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study.
Mergnac Jean-Philippe et al. Human genetics 2021 - Diagnostic yield and recognized barriers of an adult neurogenetics clinic.
Peleg Amir et al. Journal of community genetics 2021 - NGS in Hereditary Ataxia: When Rare Becomes Frequent.
Galatolo Daniele et al. International journal of molecular sciences 2021 22(16) - Utility of Gene Panels for the Diagnosis of Inborn Errors of Metabolism in a Metabolic Reference Center.
Barbosa-Gouveia Sofia et al. Genes 2021 12(8) - Unraveling the Ethical, Legal, and Social Implications of Neurobiobanking and Stroke Genomic Research in Africa: A Study Protocol of the African Neurobiobank for Precision Stroke Medicine ELSI Project.
Akinyemi Rufus O et al. International journal of qualitative methods 2020 19 - An insight into the role of Artificial Intelligence in the early diagnosis of Alzheimer's disease.
Verma Rohit Kumar et al. CNS & neurological disorders drug targets 2021 - Recent Advancements in the Diagnosis and Treatment of Leukodystrophies.
Bradbury Allison M et al. Seminars in pediatric neurology 2021 37100876 - Artificial intelligence-assisted phenotype discovery of fragile X syndrome in a population-based sample.
Movaghar Arezoo et al. Genetics in medicine : official journal of the American College of Medical Genetics 2021 - Deep learning applications for the classification of psychiatric disorders using neuroimaging data: Systematic review and meta-analysis.
Quaak Mirjam et al. NeuroImage. Clinical 2021 30102584 - A policy analysis of the national phenylketonuria screening program in Iran.
Heidari Alireza et al. BMC health services research 2021 Feb 21(1) 120 - The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective.
Eratne Dhamidhu et al. Journal of the neurological sciences 2020 Dec 420117260 - Gait Analysis with Wearables Can Accurately Classify Fallers from Non-Fallers: A Step toward Better Management of Neurological Disorders.
Rehman Rana Zia Ur et al. Sensors (Basel, Switzerland) 2020 Dec 20(23) - Diagnostic yield and treatment impact of whole-genome sequencing in paediatric neurological disorders.
Lee Hsiu-Fen et al. Developmental medicine and child neurology 2020 Nov - A new index for multiple chronic conditions predicts functional outcome in ischemic stroke.
Jiang Xiaqing et al. Neurology 2020 Oct - Current scenario of the genetic testing for rare neurological disorders exploiting next generation sequencing.
Di Resta Chiara et al. Neural regeneration research 2021 Mar 16(3) 475-481 - A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome.
Ghosh Shereen G et al. European journal of human genetics : EJHG 2020 Sep - The value of genomic sequencing in complex pediatric neurological disorders: a discrete choice experiment.
Goranitis Ilias et al. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Aug - Smart diagnostics devices through artificial intelligence and mechanobiological approaches.
Yadav Dinesh et al. 3 Biotech 2020 Aug 10(8) 351 - [Ethical Issues of Genetic Testing towards Hereditary Neurological Disorders].
Muto Kaori et al. Brain and nerve = Shinkei kenkyu no shinpo 2020 Jul 72(7) 719-725 - Clinical application of next-generation sequencing to the practice of neurology.
Rexach Jessica et al. The Lancet. Neurology 2019 18(5) 492-503 - The Polygenic Score Catalog: an open database for reproducibility and systematic evaluation
SA Lambert et al, MEDRXIV, May 23, 2020 - The use of next-generation sequencing to unravel new genes: overcoming challenges posed by rare neurological disorders such as myoclonus-dystonia.
Gannamani Rahul et al. European journal of neurology 2020 May
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