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Precision Health Database


Genomics & Health Impact Scan Database|Search|PHGKB

Heart, Lung, Blood, and Sleep Disorders

Last data update: Jun 29, 2022. (Total: 47967 Documents since 2012)
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Query Trace: Heart And Vascular Diseases[original query]>>Tools/Methods [Product Type]
GWAS of longitudinal trajectories at biobank scale.
Ko Seyoon et al. American journal of human genetics 2022
Insurance payment for artificial intelligence technology: Methods used by a stroke artificial intelligence system and strategies to qualify for the new technology add-on payment.
Murray Nick M et al. The neuroradiology journal 2022 19714009211067408
An update on the CHDGKB for the systematic understanding of risk factors associated with non-syndromic congenital heart disease.
Yang Lan et al. Computational and structural biotechnology journal 2021 195741-5751
IMPACT webinars: Improving Patient Access to genetic Counselling and Testing using webinars-the Alberta experience with hypertrophic cardiomyopathy.
Christian Susan et al. Journal of community genetics 2021
FH Awareness Day Toolkit 2021
The FH Foundation September 2021
Clinical utility gene card for: Long-QT syndrome.
Beckmann Britt M et al. European journal of human genetics : EJHG 2021
The early warning research on nursing care of stroke patients with intelligent wearable devices under COVID-19.
Li Fengxia et al. Personal and ubiquitous computing 2021 Jan 1-13
Color Data v2: a user-friendly, open-access database with hereditary cancer and hereditary cardiovascular conditions datasets.
Berger Mark J et al. Database : the journal of biological databases and curation 2020 Jan 2020
SVAD: A genetic database curates non-ischemic sudden cardiac death-associated variants.
Huang Wei-Chih et al. PloS one 2020 15(8) e0237731
CHDGKB: a knowledgebase for systematic understanding of genetic variations associated with non-syndromic congenital heart disease.
Yang Lan et al. Database : the journal of biological databases and curation 2020 Jan 2020
A database for using machine learning and data mining techniques for coronary artery disease diagnosis.
Alizadehsani R et al. Scientific data 2019 Oct 6(1) 227
New CRISPR tool has the potential to correct almost all disease-causing DNA glitches, scientists report
S Begley. Stat News, October 21, 2019
Heart Disease and Stroke Map Widget
CDC, 2019
InheRET
Some diseases run in families - knowing your family history can lead to early detection and prevention
A checklist for clinical trials in rare disease: obstacles and anticipatory actions-lessons learned from the FOR-DMD trial.
Crow Rebecca A et al. Trials 2018 May 19(1) 291
The Transcriptomic Toolbox: Resources for Interpreting Large Gene Expression Data within a Precision Medicine Context for Metabolic Disease Atherosclerosis.
Marín de Evsikova Caralina et al. Journal of personalized medicine 2019 Apr 9(2)
ClinVar database of global familial hypercholesterolemia-associated DNA variants.
Iacocca Michael A et al. Human mutation 2018 Nov 39(11) 1631-1640
Polygenic approaches to detect gene-environment interactions when external information is unavailable.
Lin Wan-Yu et al. Briefings in bioinformatics 2018 Sep
FH Awareness Day Media Kit, September 24, 2018
The FH Foundation, September 2018
Management of Individuals at Increased Hereditary Risk
ASCO, 2018
Beyond the Data - Million Hearts® 2022: A Compelling Call to Action
CDC You Tube Video, Feb 2018
Find FH Patients in your practice
Machine learning tool from the FH Foundation
CardioClassifier
An automated and interactive web tool that supports disease specific interpretation of genetic variants in genes associated with Inherited Cardiac Conditions.
An educational booklet for patients with familial hypercholesterolemia
Heart UK, 2017
Development of a communication aid for explaining hypertrophic cardiomyopathy genetic test results.
Smagarinsky Yana et al. Pilot and feasibility studies 2017 353
FH Diagnosis App
From the FH foundation to help providers and patients
Do you #KnowFH?
YouTube video, FH Foundation, August 2017
CardioClassifier: demonstrating the power of disease- and gene-specific computational decision support for clinical genome interpretation
N Whiffin et al, BioRxiV preprints, August 2017
How Studying Familial Hypercholesterolemia Resulted in the Discovery of Statins as an Effective Treatment for High Cholesterol
JAMA Podcast, July 25, 2017
Using Workflow Modeling to Identify Areas to Improve Genetic Test Processes in the University of Maryland Translational Pharmacogenomics Project.
Cutting Elizabeth M et al. AMIA ... Annual Symposium proceedings. AMIA Symposium 2015466-74
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