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 (47393)
CDC/NIH Web Information Database (32181)
CDC-Authored Genomics and Precision Health Publications Database (6021)
Precision Health Database (63675)
Tier-Classified Guidelines Database (534)
Pathogen Advanced Molecular Detection Database (26775)
All of Us Reports and Publications Database (676)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226505)
Epigenetic Epidemiology Publications Database (22770)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 25, 2024
. (Total: 63675 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 4231 Records)
Next
Query Trace:
all[original query]>>Chronic Disease[Category]
Identifying dementia from cognitive footprints in hospital records among Chinese older adults: a machine-learning study.
Jiayi Zhou et al. Lancet Reg Health West Pac 2024 46101060
Similar articles in PubMed
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.
Emil K Gustavsson et al. Lancet Neurol 2024
Similar articles in PubMed
Cross-Sectional Analysis of Exome Sequencing Diagnosis in Patients With Neurologic Phenotypes Facing Barriers to Clinical Testing.
Sonya Watson et al. Neurol Genet 2024 10(3) e200133
Similar articles in PubMed
The Significance of Screening Family Members in Glaucoma: Opportunities and Challenges.
Siddharth Bhargava et al. J Glaucoma 2024
Similar articles in PubMed
Accuracy of Artificial Intelligence Models in the Prediction of Periodontitis: A Systematic Review.
A Polizzi et al. JDR Clin Trans Res 2024 23800844241232318
Similar articles in PubMed
Using an Interpretable Amino Acid-Based Machine Learning Method to Enhance the Diagnosis of Major Depressive Disorder.
Cyrus Su Hui Ho et al. J Clin Med 2024 13(5)
Similar articles in PubMed
Predictive analytics support for complex chronic medical conditions: An experience-based co-design study of physician managers' needs and preferences.
Muhammad Rafiq et al. Int J Med Inform 2024 187105447
Similar articles in PubMed
Artificial intelligence in multiple sclerosis management: Challenges in a new era.
Sebastián Rodríguez et al. Mult Scler Relat Disord 2024 86105611
Similar articles in PubMed
Development and validation of machine learning models to predict frailty risk for elderly.
Wei Zhang et al. J Adv Nurs 2024
Similar articles in PubMed
Exploring deep learning radiomics for classifying osteoporotic vertebral fractures in X-ray images.
Jun Zhang et al. Front Endocrinol (Lausanne) 2024 151370838
Similar articles in PubMed
Progression from Prediabetes to Diabetes in a Diverse US Population: a Machine Learning Model.
Joseph Aoki et al. Diabetes Technol Ther 2024
Similar articles in PubMed
Association of Obesity with Telomere Length in Human Sperm.
Efthalia Moustakli et al. J Clin Med 2024 13(7)
Similar articles in PubMed
Factors Influencing Patient Disclosure of Parkinson's Disease Genetic Testing Results to Relatives.
Jeanine Schulze et al. Mov Disord Clin Pract 2024
Similar articles in PubMed
Development and validation of a machine learning model for prediction of type 2 diabetes in patients with mental illness.
Martin Bernstorff et al. Acta Psychiatr Scand 2024
Similar articles in PubMed
Performance Evaluation of Deep, Shallow and Ensemble Machine Learning Methods for the Automated Classification of Alzheimer's Disease.
Noushath Shaffi et al. Int J Neural Syst 2024 2450029
Similar articles in PubMed
Machine Learning for prediction of violent behaviors in schizophrenia spectrum disorders: a systematic review.
Mohammadamin Parsaei et al. Front Psychiatry 2024 151384828
Similar articles in PubMed
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
Radiomics-based prediction of nonalcoholic fatty liver disease following pancreatoduodenectomy.
Takehiro Fujii et al. Surg Today 2024
Similar articles in PubMed
Familial aggregation and heritability of childhood-onset and adult-onset type 1 diabetes: a Swedish register-based cohort study.
Yuxia Wei et al. Lancet Diabetes Endocrinol 2024
Similar articles in PubMed
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
Similar articles in PubMed
Physical Activity and Incident Obesity Across the Spectrum of Genetic Risk for Obesity.
Evan L Brittain et al. JAMA Netw Open 2024 7(3) e243821
Similar articles in PubMed
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
Similar articles in PubMed
Development and External Validation of Machine Learning Models for Diabetic Microvascular Complications: Cross-Sectional Study With Metabolites.
Feng He et al. J Med Internet Res 2024 26e41065
Similar articles in PubMed
Utilizing ultra-early continuous physiologic data to develop automated measures of clinical severity in a traumatic brain injury population.
Shiming Yang et al. Sci Rep 2024 14(1) 7618
Similar articles in PubMed
Fluctuating salience in those living with genetic risk of motor neuron disease: A qualitative interview study.
Jade Howard et al. Health Expect 2024 27(2) e14024
Similar articles in PubMed
The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops.
Tiera Mack et al. Am J Med Genet B Neuropsychiatr Genet 2024 e32978
Similar articles in PubMed
Accessibility, availability and common practices regarding genetic testing for epilepsy across Europe: A survey of the European Reference Network EpiCARE.
Maria T Papadopoulou et al. Epilepsia Open 2024
Similar articles in PubMed
Spondyloarthritis in first-degree relatives and spouses of patients with inflammatory bowel disease: A nationwide population-based cohort study from Sweden.
Sarita Shrestha et al. J Crohns Colitis 2024
Similar articles in PubMed
Artificial intelligence insights into osteoporosis: assessing ChatGPT's information quality and readability.
Yakup Erden et al. Arch Osteoporos 2024 19(1) 17
Similar articles in PubMed
Ensemble-imbalance-based classification for amyotrophic lateral sclerosis prognostic prediction: identifying short-survival patients at diagnosis.
Fabiano Papaiz et al. BMC Med Inform Decis Mak 2024 24(1) 80
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 25, 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