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 (47318)
CDC/NIH Web Information Database (32178)
CDC-Authored Genomics and Precision Health Publications Database (5836)
Precision Health Database (63653)
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)
Heart, Lung, Blood and Sleep Disorders
Last data update: Apr 23, 2024
. (Total: 63653 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 - 19 (of 19 Records)
Query Trace:
Echocardiography[original query]>>Evidence Synthesis [Product Type]
Global research trends of hypertrophic cardiomyopathy from 2000 to 2022: Insights from bibliometric analysis.
Xifeng Zheng et al. Frontiers in cardiovascular medicine 2023 101039098
Similar articles in PubMed
Automated multi-beat tissue Doppler echocardiography analysis using deep neural networks.
Lane Elisabeth S et al. Medical & biological engineering & computing 2023
Similar articles in PubMed
The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy-A systematic review and meta-analysis.
Cirino Allison L et al. Journal of genetic counseling 2022
Similar articles in PubMed
Usefullness of MicroRNAs in Predicting the Clinical Outcome of Patients with Acute Myocardial Infarction During Follow-Up: A Systematic Review.
Venugopal Priyanka et al. Genetic testing and molecular biomarkers 2022 26(5) 277-289
Similar articles in PubMed
Machine learning methods for perioperative anesthetic management in cardiac surgery patients: a scoping review.
Rellum Santino R et al. Journal of thoracic disease 2022 13(12) 6976-6993
Similar articles in PubMed
Cost-effectiveness analysis of screening for first-degree relatives of patients with bicuspid aortic valve.
Tessler Idit et al. European heart journal. Quality of care & clinical outcomes 2021
Similar articles in PubMed
CLINGEN Actionability Report for Marfan Syndrome - FBN1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary Hemorrhagic Telangiectasia - ENG, ACVRL1, SMAD4, GDF2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Phenylketonuria (PKU) - PAH
ClinGen Actionability Working Group
CLINGEN Actionability Report for Ehlers-Danlos syndrome, classic type - COL5A1, COL5A2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Alkaptonuria-HGD
ClinGen Actionability Working Group
CLINGEN Actionability Report for Autosomal Dominant Polycystic Kidney Disease - DNAJB11, GANAB, PKD1, PKD2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Primary pulmonary hypertension 1- BMPR2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Arterial tortuosity syndrome - SLC2A10
ClinGen Actionability Working Group
CLINGEN Actionability Report for Very Long Chain Actyl-CoA Dehydrogenase Deficiency (ACADVLD) - ACADVL
ClinGen Actionability Working Group
CLINGEN Actionability Report for Emery-Dreifuss Muscular Dystrophy (AD, XL) - LMNA, EMD, FHL1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Hereditary transthyretin-related amyloidosis - TTR
ClinGen Actionability Working Group
CLINGEN Actionability Report for Myofibrillar Myopathy -DES, BAG3, FLNC
ClinGen Actionability Working Group
Sudden cardiac death in young athletes with long QT syndrome: the role of genetic testing and cardiovascular screening.
Longo Umile Giuseppe et al. British medical bulletin 2018 Jun
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