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 (47219)
CDC/NIH Web Information Database (32125)
CDC-Authored Genomics and Precision Health Publications Database (5510)
Precision Health Database (63390)
Tier-Classified Guidelines Database (532)
Pathogen Advanced Molecular Detection Database (26537)
All of Us Reports and Publications Database (634)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (225926)
Epigenetic Epidemiology Publications Database (22563)
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: Mar 28, 2024
. (Total: 63390 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 77 Records)
Next
Query Trace:
Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study.
Kimberly Martin et al. Prenat Diagn 2023
Similar articles in PubMed
Using a polygenic score to account for genomic risk factors in a model to detect individuals with dilated ascending thoracic aortas.
John DePaolo et al. medRxiv 2023
Similar articles in PubMed
Prenatal diagnosis and early childhood outcome of fetuses with extremely large nuchal translucency.
Hang Zhou et al. Mol Cytogenet 2023 16(1) 22
Similar articles in PubMed
[Association between clinical phenotypes of hypertrophic cardiomyopathy and Ca gene variation gene variation].
J Zhao et al. Zhonghua Xin Xue Guan Bing Za Zhi 2023 51(5) 497-503
Similar articles in PubMed
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
Family Screening in Dilated Cardiomyopathy: Prevalence, Incidence, and Potential for Limiting Follow-Up.
Vissing Christoffer R et al. JACC. Heart failure 2022 10(11) 792-803
Similar articles in PubMed
Delphi Panel Consensus Recommendations for Screening and Managing Childhood Cancer Survivors at Risk for Cardiomyopathy.
Aziz-Bose Rahela et al. JACC. CardioOncology 2022 4(3) 354-367
Similar articles in PubMed
Transthyretin cardiac amyloidosis.
Porcari Aldostefano et al. Cardiovascular research 2022
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
Loss-of-Function FLNC Variants Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes When Identified Through Exome Sequencing of a General Clinical Population.
Carruth Eric D et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003645
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
Importance of Echocardiography and Clinical "Red Flags" in Guiding Genetic Screening for Fabry Disease.
Citro Rodolfo et al. Frontiers in cardiovascular medicine 2022 9838200
Similar articles in PubMed
Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality.
Patel Aniruddh P et al. JAMA cardiology 2022
Similar articles in PubMed
Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands.
Borg Sanna Á et al. BMJ open 2022 12(4) e050857
Similar articles in PubMed
Gender Related Differences in the Clinical Presentation of Hypertrophic Cardiomyopathy-An Analysis from the SILICOFCM Database.
Preveden Andrej et al. Medicina (Kaunas, Lithuania) 2022 58(2)
Similar articles in PubMed
Diagnosis and Evaluation of Hypertrophic Cardiomyopathy: JACC State-of-the-Art Review.
Maron Barry J et al. Journal of the American College of Cardiology 2022 79(4) 372-389
Similar articles in PubMed
Main Physical Features, Echocardiographic and Renal Ultrasonographic Findings of Turner Syndrome in 107 Pediatric Patients.
Akalin Akçahan et al. Molecular syndromology 2021 12(6) 335-341
Similar articles in PubMed
Combined Non-Invasive Cardiac Imaging and Genetic Testing of Elite Volleyball Players: A Ten-Year Experience.
Grossfeld Paul et al. Cardiology and cardiovascular medicine 2021 5(5) 545-550
Similar articles in PubMed
Prevalence and potential genetic determinants of young sudden unexplained death victims with suspected arrhythmogenic mitral valve prolapse syndrome.
Giudicessi John R et al. Heart rhythm O2 2021 2(5) 431-438
Similar articles in PubMed
Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey.
Behr Elijah R et al. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2021
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
Clinical and genetic findings in patients with congenital cataract and heart diseases.
Li Xinru et al. Orphanet journal of rare diseases 2021 16(1) 242
Similar articles in PubMed
Analysis of Copy Number Variations by Low-Depth Whole-Genome Sequencing in Fetuses with Congenital Cardiovascular Malformations.
Huang Jiwei et al. Cytogenetic and genome research 2021 1-7
Similar articles in PubMed
Spectrum of transthyretin gene mutations and clinical characteristics of Polish patients with cardiac transthyretin amyloidosis.
Gawor Monika et al. Cardiology journal 2020 Aug
Similar articles in PubMed
Influence of hereditary haemochromatosis on left ventricular wall thickness: does iron overload exacerbate cardiac hypertrophy?
Rozwadowska K et al. Folia morphologica 2019 78(4) 746-753
Similar articles in PubMed
Left Ventricular Strain and Progression of Hypertrophy in Danon Disease Cardiomyopathy: Insights from a Global Registry.
Ma G S et al. The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation 2020 Apr 39(4S) S154
Similar articles in PubMed
Management of Women With Phenylalanine Hydroxylase Deficiency (Phenylketonuria): ACOG Committee Opinion Summary, Number 802.
et al. Obstetrics and gynecology 2020 Apr 135(4) 987-988
Similar articles in PubMed
Management of Women With Phenylalanine Hydroxylase Deficiency (Phenylketonuria): ACOG Committee Opinion, Number 802.
et al. Obstetrics and gynecology 2020 Apr 135(4) e167-e170
Similar articles in PubMed
Genetic screening for hypertrophic cardiomyopathy in large, asymptomatic military cohorts.
Brough Joe et al. American journal of medical genetics. Part C, Seminars in medical genetics 2020 Feb
Similar articles in PubMed
Familial Dilated Cardiomyopathy.
Peters Stacey et al. Heart, lung & circulation 2019 Dec
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:
Mar 28, 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