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 (47415)
CDC/NIH Web Information Database (32174)
CDC-Authored Genomics and Precision Health Publications Database (5825)
Precision Health Database (63627)
Tier-Classified Guidelines Database (533)
Pathogen Advanced Molecular Detection Database (26729)
All of Us Reports and Publications Database (656)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226255)
Epigenetic Epidemiology Publications Database (22724)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Heart, Lung, Blood and Sleep Disorders
Last data update: Apr 19, 2024
. (Total: 63627 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 437 Records)
Next
Query Trace:
Integration of a polygenic score into guideline-recommended prediction of cardiovascular disease.
Ling Li et al. Eur Heart J 2024
Similar articles in PubMed
Physical signs and atherosclerotic cardiovascular disease in familial hypercholesterolemia: the HELLAS-FH Registry.
Loukianos S Rallidis et al. J Cardiovasc Med (Hagerstown) 2024
Similar articles in PubMed
Measuring Costs of Cardiovascular Disease Prevention for Patients with Familial Hypercholesterolemia in Administrative Claims Data.
Lauren E Passero et al. High Blood Press Cardiovasc Prev 2024
Similar articles in PubMed
Genetics in Ischemic Stroke: Current Perspectives and Future Directions.
Ka Zhang et al. J Cardiovasc Dev Dis 2023 10(12)
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
Impact of CYP2C19 Genotype on Efficacy and Safety of Clopidogrel-based Antiplatelet Therapy in Stroke or Transient Ischemic Attack Patients: An Updated Systematic Review and Meta-analysis of Non-East Asian Studies.
Sarah Cargnin et al. Cardiovasc Drugs Ther 2023
Similar articles in PubMed
Genetic risk, adherence to healthy lifestyle and acute cardiovascular and thromboembolic complications following SARS-COV-2 infection.
Junqing Xie et al. Nat Commun 2023 14(1) 4659
Similar articles in PubMed
Familial hypercholesterolemia is related to cardiovascular disease, heart failure and atrial fibrillation. Results from a population-based study.
Hayato Tada et al. Eur J Clin Invest 2023 e14119
Similar articles in PubMed
Research participants' perception of ethical issues in stroke genomics and neurobiobanking research in Africa.
Ayodele Jegede et al. medRxiv 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 and Nongenetic Components of Stroke Family History: A Population Study of Adopted and Nonadopted Individuals.
Ernst Mayerhofer et al. J Am Heart Assoc 2023 12(20) e031566
Similar articles in PubMed
Implementation of Hospital-Based Sickle Cell Newborn Screening and Follow-Up Programs in Haiti.
Ofelia A Alvarez et al. Blood Adv 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
Screening for Lipid Disorders in Children and Adolescents: US Preventive Services Task Force Recommendation Statement.
et al. JAMA 2023 330(3) 253-260
Similar articles in PubMed
The causal effects of education on adult health, mortality and income: evidence from Mendelian randomization and the raising of the school leaving age.
Neil M Davies et al. Int J Epidemiol 2023
Similar articles in PubMed
Lipoprotein(a): a Case for Universal Screening in Youth.
Aparna Alankar et al. Curr Atheroscler Rep 2023
Similar articles in PubMed
Clinical Profiles of Children With Sickle Cell Anaemia Presenting With Acute Clinical Events: A Single-Center Study.
Anwesha Singh et al. Cureus 2023 15(5) e39008
Similar articles in PubMed
Genetic and non-genetic components of family history of stroke and heart disease: a population-based study among adopted and non-adopted individuals.
Ernst Mayerhofer et al. medRxiv 2023
Similar articles in PubMed
Mendelian randomization evidence for the causal effects of socio-economic inequality on human longevity among Europeans.
Chao-Jie Ye et al. Nat Hum Behav 2023
Similar articles in PubMed
BA.1 Bivalent COVID-19 Vaccine Use and Stroke in England.
Nick Andrews et al. JAMA 2023
Similar articles in PubMed
Tumor Genomic Profile Is Associated With Arterial Thromboembolism Risk in Patients With Solid Cancer.
Stephanie Feldman et al. JACC CardioOncol 2023 5(2) 246-255
Similar articles in PubMed
Thrombophilia screening in the routine clinical care of children with arterial ischemic stroke.
Kristin Maher et al. Pediatr Blood Cancer 2023 e30381
Similar articles in PubMed
Cardiovascular Disease Risk Assessment Using Traditional Risk Factors and Polygenic Risk Scores in the Million Veteran Program.
Jason L Vassy et al. JAMA Cardiol 2023
Similar articles in PubMed
Stroke, Myocardial Infarction, and Pulmonary Embolism after Bivalent Booster.
Marie-Joelle Jabagi et al. N Engl J Med 2023 388(15) 1431-1432
Similar articles in PubMed
Genetic Susceptibility to Mood Disorders and Risk of Stroke: A Polygenic Risk Score and Mendelian Randomization Study.
Jiangming Sun et al. Stroke 2023
Similar articles in PubMed
Assessing the performance of genetic risk score for stratifying risk of post-sepsis cardiovascular complications.
Brian McElligott et al. Frontiers in cardiovascular medicine 2023 101076745
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
Predicting Pain in People With Sickle Cell Disease in the Day Hospital Using the Commercial Wearable Apple Watch: Feasibility Study.
Rebecca Sofia Stojancic et al. JMIR formative research 2023 7e45355
Similar articles in PubMed
ASOC Osuntokun Award Lecture 2022: Partnership for stroke prevention and treatment in Africa: Qualitative research processes and findings.
Carolyn Jenkins et al. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2023 107060
Similar articles in PubMed
Genetic variation supports a causal role for valproate in prevention of ischemic stroke.
Ernst Mayerhofer et al. medRxiv : the preprint server for health sciences 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 19, 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