Genomics and Precision Health Database

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Query Trace: all[original query]>>Tools/Methods[Product Type]

Publication
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 Similar articles in PubMed
SVAD: A genetic database curates non-ischemic sudden cardiac death-associated variants. Huang Wei-Chih et al. PloS one 2020 15(8) e0237731 Similar articles in PubMed
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 Similar articles in PubMed
Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritisation. King Charlotte et al. The pharmacogenomics journal 2020 Jan Similar articles in PubMed
High-throughput phenotyping with electronic medical record data using a common semi-supervised approach (PheCAP). Zhang Yichi et al. Nature protocols 2019 Nov Similar articles in PubMed
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 Similar articles in PubMed
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
The Community Counts Data Visualization Tool CDC, 2019
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 Similar articles in PubMed
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) Similar articles in PubMed
A Unified Model for the Analysis of Gene-Environment Interaction. Gauderman W James et al. American journal of epidemiology 2019 Apr 188(4) 760-767 Similar articles in PubMed
2019 Digital Toolkit: NATIONAL BIRTH DEFECTS PREVENTION MONTH
A Comprehensive Human Gastric Cancer Organoid Biobank Captures Tumor Subtype Heterogeneity and Enables Therapeutic Screening. Yan Helen H N et al. Cell stem cell 2018 Oct Similar articles in PubMed
ClinVar database of global familial hypercholesterolemia-associated DNA variants. Iacocca Michael A et al. Human mutation 2018 Nov 39(11) 1631-1640 Similar articles in PubMed
Polygenic approaches to detect gene-environment interactions when external information is unavailable. Lin Wan-Yu et al. Briefings in bioinformatics 2018 Sep Similar articles in PubMed
FH Awareness Day Media Kit, September 24, 2018 The FH Foundation, September 2018
Management of Individuals at Increased Hereditary Risk ASCO, 2018
ILDgenDB: integrated genetic knowledge resource for interstitial lung diseases (ILDs). Mishra Smriti et al. Database : the journal of biological databases and curation 2018 2018 Similar articles in PubMed
Prioritizing complex disease risk genes by integrating multiple data. Guo Shanshan et al. Genomics 2018 Apr Similar articles in PubMed
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.
Standard measures for sickle cell disease research: the PhenX Toolkit sickle cell disease collections. Eckman James R et al. Blood advances 2017 Dec 1(27) 2703-2711 Similar articles in PubMed
An educational booklet for patients with familial hypercholesterolemia Heart UK, 2017
Evidence-based practices on reducing transfusion complications in sickle cell disease Provider Training Video Series, Georgia Health Policy Center, 2017
Development of a communication aid for explaining hypertrophic cardiomyopathy genetic test results. Smagarinsky Yana et al. Pilot and feasibility studies 2017 353 Similar articles in PubMed
Sickle Cell Disease: What You Should Know CDC podcast, 2017
FH Diagnosis App From the FH foundation to help providers and patients