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 (47475)
CDC/NIH Web Information Database (32208)
CDC-Authored Genomics and Precision Health Publications Database (6094)
Precision Health Database (63881)
Tier-Classified Guidelines Database (535)
Pathogen Advanced Molecular Detection Database (26916)
All of Us Reports and Publications Database (698)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (227294)
Epigenetic Epidemiology Publications Database (22891)
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: May 18, 2024
. (Total: 63881 Documents since 2012)
All
Cancer
Diabetes
Economic
Environmental
Equity
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 89 Records)
Next
Query Trace:
Family history, socioeconomic factors, comorbidities, health behaviors, and the risk of sudden cardiac arrest.
Eujene Jung et al. Sci Rep 2023 13(1) 21341
Similar articles in PubMed
Rare Genetic Variants Associated With Sudden Cardiac Arrest in the Young: A Prospective, Population-Based Study.
Lauri Holmstrom et al. Circ Genom Precis Med 2023 e004105
Similar articles in PubMed
Management of Inherited Arrhythmia Syndromes: A HiRO Consensus Handbook on Process of Care.
Mikyla L Janzen et al. CJC Open 2023 5(4) 268-284
Similar articles in PubMed
Phenotypes of Overdiagnosed Long QT Syndrome.
Sahej Bains et al. Journal of the American College of Cardiology 2023 81(5) 477-486
Similar articles in PubMed
Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest.
Brendan J Floyd et al. Circulation. Genomic and precision medicine 2023
Similar articles in PubMed
Genetic characterization of juvenile sudden cardiac arrest and death in Tuscany: The ToRSADE registry.
Girolami Francesca et al. Frontiers in cardiovascular medicine 2023 91080608
Similar articles in PubMed
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant.
Hoorntje Edgar T et al. Circulation. Genomic and precision medicine 2022 e003672
Similar articles in PubMed
Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy.
Nauffal Victor et al. European heart journal 2022 42(38) 3932-3944
Similar articles in PubMed
The Outcome of Long QT Syndrome, a Korean Single Center Study.
Ahn Kyung Jin et al. Korean circulation journal 2022 52(10) 771-781
Similar articles in PubMed
Genetic variants in Colombian patients with inherited cardiac conditions.
Rucinski Cynthia et al. Molecular genetics & genomic medicine 2022 e2046
Similar articles in PubMed
Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics.
Nafissi Navid A et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003675
Similar articles in PubMed
Pharmacogenetics-guided dalcetrapib therapy after an acute coronary syndrome: the dal-GenE trial.
Tardif Jean Claude et al. European heart journal 2022
Similar articles in PubMed
Secondary Findings Using Broad Pan Cardiomyopathy and Arrhythmia Panels in Patients With a Personal or Family History of Inherited Cardiomyopathy or Arrhythmia Syndrome.
Smith Emily et al. The American journal of cardiology 2022
Similar articles in PubMed
Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for Management.
Dusi Veronica et al. JACC. Clinical electrophysiology 2022 8(3) 281-294
Similar articles in PubMed
Out-of-hospital pediatric sudden cardiac arrest and inherited arrhythmia syndromes in Hungary.
Környei László et al. Orvosi hetilap 2022 163(12) 473-477
Similar articles in PubMed
Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death.
Neves Raquel et al. Circulation. Genomic and precision medicine 2021 CIRCGEN121003497
Similar articles in PubMed
Worldwide differences in primary prevention implantable cardioverter defibrillator utilization and outcomes in hypertrophic cardiomyopathy.
Nauffal Victor et al. European heart journal 2021
Similar articles in PubMed
Yield and clinical significance of genetic screening in elite and amateur athletes.
Limongelli Giuseppe et al. European journal of preventive cardiology 2021 28(10) 1081-1090
Similar articles in PubMed
A college student’s near fatal collapse uncovered a frightening family legacy
SG Boodman, Washington Post, August 23, 2021
Sudden cardiac death in childhood hypertrophic cardiomyopathy is best predicted by a combination of ECG Risk-score and HCMRisk-Kids score.
Östman-Smith Ingegerd et al. Acta paediatrica (Oslo, Norway : 1992) 2021
Similar articles in PubMed
Sudden Death in the Young: Information for the Primary Care Provider.
Erickson Christopher C et al. Pediatrics 2021
Similar articles in PubMed
2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.
Stiles Martin K et al. Journal of arrhythmia 2021 37(3) 481-534
Similar articles in PubMed
Non-Ischemic Sudden Cardiac Arrest: Role of 12 Lead Holter, Family Screening and Genetic Testing.
Blich Miry et al. Pacing and clinical electrophysiology : PACE 2021
Similar articles in PubMed
Genetics and genomics of arrhythmic risk: current and future strategies to prevent sudden cardiac death.
Scrocco Chiara et al. Nature reviews. Cardiology 2021
Similar articles in PubMed
Clinical and genetic characteristics and course of congenital long QT syndrome in children: A nine-year single-center experience.
Ergül Yakup et al. Anatolian journal of cardiology 2021 25(4) 250-257
Similar articles in PubMed
Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT.
Dubé Marie-Pierre et al. Circulation. Genomic and precision medicine 2021 Feb
Similar articles in PubMed
Health data research on sudden cardiac arrest: perspectives of survivors and their next-of-kin.
Bak Marieke A R et al. BMC medical ethics 2021 Jan 22(1) 7
Similar articles in PubMed
Sudden cardiac death in sports: could we save Pheidippides?
Deligiannis Asterios et al. Acta cardiologica 2021 Jan 1-15
Similar articles in PubMed
[Clinical pathway for cardiomyopathies: a genetic testing strategy proposed by ANMCO in Tuscany].
Girolami Francesca et al. Giornale italiano di cardiologia (2006) 2020 Dec 21(12) 926-934
Similar articles in PubMed
The End Unexplained Cardiac Death (EndUCD) Registry for Young Australian Sudden Cardiac Arrest.
Paratz Elizabeth D et al. Heart, lung & circulation 2020 Nov
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:
May 18, 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