Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
About
Public Health Genomics Branch
PHGKB Weekly Horizon Scan
Genomics Precision Health Scan
Advanced Molecular Detection Clips
Non-Genomics Precision Health Scan
CDC-authored Publications Scan
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
Family Health History PHGKB
Health Equity PHGKB
HLBS-PopOmics
Infectious Diseases PHGKB
Implementation Science PHGKB
Neurological Disorders PHGKB
Pharmacogenomics PHGKB
Primary Immune Deficiency Diseases PHGKB
Rare Diseases PHGKB
Reproductive and Child Health PHGKB
All Databases
COVID-19 GPH (47317)
CDC/NIH Web Information Database (32178)
CDC-Authored Genomics and Precision Health Publications Database (5836)
Precision Health Database (63650)
Tier-Classified Guidelines Database (533)
Pathogen Advanced Molecular Detection Database (26729)
All of Us Reports and Publications Database (672)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226390)
Epigenetic Epidemiology Publications Database (22739)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Neurological Disorders
Last data update: Apr 23, 2024
. (Total: 63650 Documents since 2012)
All
Cancer
Diabetes
Economic
Equity
Environmental
FHH
HLBS
ID
Implementation
ND
PGx
PI
Rare
RCH
dataset
All
GPH
Non-GPH
Filtered By
:
Select to fine-tune your search
Disease
Gene
Product Type
Category
Year
Previous
Records 1 - 30 (of 330 Records)
Next
Query Trace:
all[original query]>>Evidence Synthesis [Product Type]
Interpreting artificial intelligence models: a systematic review on the application of LIME and SHAP in Alzheimer's disease detection.
Viswan Vimbi et al. Brain Inform 2024 11(1) 10
Similar articles in PubMed
Integration of a polygenic score into guideline-recommended prediction of cardiovascular disease.
Ling Li et al. Eur Heart J 2024
Similar articles in PubMed
Unveiling the Diagnostic Potential of Linguistic Markers in Identifying Individuals with Parkinson's Disease through Artificial Intelligence: A Systematic Review.
Cinzia Palmirotta et al. Brain Sci 2024 14(2)
Similar articles in PubMed
Diagnostic Accuracy of Creatine Kinase Isoenzyme-MM Test in Newborn Screening for Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis.
Liang Tang et al. Pediatr Neurol 2024 15384-91
Similar articles in PubMed
The effect of machine learning algorithms in the prediction, and diagnosis of meningitis: A systematic review.
Kosar Ghaddaripouri et al. Health Sci Rep 2024 7(2) e1893
Similar articles in PubMed
Applications of Artificial Intelligence in the Neuropsychological Assessment of Dementia: A Systematic Review.
Isabella Veneziani et al. J Pers Med 2024 14(1)
Similar articles in PubMed
Cost-effectiveness of spinal muscular atrophy newborn screening based on real-world data in Belgium.
Tamara Dangouloff et al. Neuromuscul Disord 2023 3461-67
Similar articles in PubMed
Impact of GLA Variant Classification on the Estimated Prevalence of Fabry Disease: A Systematic Review and Meta-Analysis of Screening Studies.
Emanuele Monda et al. Circ Genom Precis Med 2023 e004252
Similar articles in PubMed
Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus: A Systematic Review and Meta-Analysis.
Ana B W Greenberg et al. JAMA Netw Open 2023 6(11) e2343384
Similar articles in PubMed
Machine learning algorithms for the prognostication of abdominal aortic aneurysm progression: a systematic review.
Nazifa Ullah et al. Minerva Surg 2023
Similar articles in PubMed
Genetic Variation and Sickle Cell Disease Severity: A Systematic Review and Meta-Analysis.
Justin K Kirkham et al. JAMA Netw Open 2023 6(10) e2337484
Similar articles in PubMed
Genetic literacy and attitude towards genetic testing in patients with Parkinson's disease and their caregivers: A review of literature.
Sneha D Kamath et al. Parkinsonism Relat Disord 2023 105853
Similar articles in PubMed
Using Neural Networks Algorithm in Ischemic Stroke Diagnosis: A Systematic Review.
Suebsarn Ruksakulpiwat et al. J Multidiscip Healthc 2023 162593-2602
Similar articles in PubMed
Carrier Screening Programs for Cystic Fibrosis, Fragile X Syndrome, Hemoglobinopathies and Thalassemia, and Spinal Muscular Atrophy: A Health Technology Assessment.
et al. Ont Health Technol Assess Ser 2023 23(4) 1-398
Similar articles in PubMed
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)
Similar articles in PubMed
Genome-wide Analysis of Motor Progression in Parkinson Disease.
Alejandro Martínez Carrasco et al. Neurol Genet 2023 9(5) e200092
Similar articles in PubMed
Artificial intelligence for diagnostic and prognostic neuroimaging in dementia: A systematic review.
Robin J Borchert et al. Alzheimers Dement 2023
Similar articles in PubMed
Cost-effectiveness analysis of implementing polygenic risk score in a workplace cardiovascular disease prevention program.
Deo Mujwara et al. Front Public Health 2023 111139496
Similar articles in PubMed
The differential diagnosis value of radiomics-based machine learning in Parkinson's disease: a systematic review and meta-analysis.
Jiaxiang Bian et al. Front Aging Neurosci 2023 151199826
Similar articles in PubMed
The impacts of adrenoleukodystrophy newborn screening on the evaluation of adrenal dysfunction in male children: An integrative literature review.
Leslie Pitts et al. J Pediatr Nurs 2023
Similar articles in PubMed
Knowledge, attitudes and experiences of genetic testing for autism spectrum disorders among caregivers, patients, and health providers: A systematic review.
Meng Zhou et al. World J Psychiatry 2023 13(5) 247-261
Similar articles in PubMed
Integrating real-world data in cost-effectiveness analysis of universal HLA-B*15:02 screening in Malaysia.
Huey Yi Chong et al. Br J Clin Pharmacol 2023
Similar articles in PubMed
Passive digital markers for Alzheimer's disease and other related dementias: A systematic evidence review.
Britain Taylor et al. J Am Geriatr Soc 2023
Similar articles in PubMed
Cost-Effectiveness of Newborn Screening for Spinal Muscular Atrophy in England.
Diana Weidlich et al. Neurol Ther 2023
Similar articles in PubMed
Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature.
Luca Soliani et al. Mov Disord Clin Pract 2023 10(4) 547-557
Similar articles in PubMed
Thrombophilia Testing - a Systematic Review.
Lars Asmis et al. Clin Lab 2023 69(4)
Similar articles in PubMed
Use of artificial intelligence techniques for detection of mild cognitive impairment: A systematic scoping review.
Li JuanVivian Quek et al. J Clin Nurs 2023
Similar articles in PubMed
Polygenic risk score penetrance & recurrence risk in familial Alzheimer disease.
Min Qiao et al. Annals of clinical and translational neurology 2023
Similar articles in PubMed
KCNQ2 - Related Epilepsy: geno - phenotype relationship with tailorized anti seizures medication (ASM): Systematic review.
Raffaele Falsaperla et al. Neuropediatrics 2023
Similar articles in PubMed
Impact of Genetic polymorphisms on the risk of epilepsy amongst patients with acute brain injury: a systematic review.
Shubham Misra et al. European journal of neurology 2023
Similar articles in PubMed
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 23, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
TOP