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Precision Health Database


Precision Health Database|Search|PHGKB

Heart, Lung, Blood and Sleep Disorders

Last data update: Dec 02, 2023. (Total: 62228 Documents since 2012)
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Query Trace: all[original query]>>Tools/Methods [Product Type]
A Framework for a Health Economic Evaluation Model for Patients with Sickle Cell Disease to Estimate the Value of New Treatments in the United States of America.
Aaron Winn et al. PharmacoEconomics - open 2023
Implementing Cardiogenomics in Clinical Practice
Northwestern University and the Jackson Labs, 2023
Calculating variant penetrance from family history of disease and average family size in population-scale data.
Spargo Thomas P et al. Genome medicine 2022 14(1) 141
An ML-Enabled Internet of Things Framework for Early Detection of Heart Disease.
Muhammad Yar et al. BioMed research international 2022 20223372296
CHDbase: A comprehensive knowledgebase for congenital heart disease-related genes and clinical manifestations.
Zhou Wei-Zhen et al. Genomics, proteomics & bioinformatics 2022
A Clinical Framework for Evaluating Machine Learning Studies.
Ghazi Lama et al. JACC. Heart failure 2022
Congenital Heart Disease Gene: a Curated Database for Congenital Heart Disease Genes
A Yang et al, CIrc Gen Prec Medicine, May 6, 20222
A preliminary application of a haemophilia value framework to emerging therapies in haemophilia.
Skinner Mark W et al. Haemophilia : the official journal of the World Federation of Hemophilia 2022 28 Suppl 29-18
A Framework for Augmented Intelligence in Allergy and Immunology Practice and Research-A Work Group Report of the AAAAI Health Informatics, Technology and Education Committee.
Khoury Paneez et al. The journal of allergy and clinical immunology. In practice 2022
GWAS of longitudinal trajectories at biobank scale.
Ko Seyoon et al. American journal of human genetics 2022
GRNDaD: big data and sickle cell disease.
Lanzkron Sophie et al. Blood advances 2022 6(3) 1088
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
Pharmacogenomic associations of adverse drug reactions in asthma: systematic review and research prioritisation.
King Charlotte et al. The pharmacogenomics journal 2020 Jan
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
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
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)
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
2019 Digital Toolkit: NATIONAL BIRTH DEFECTS PREVENTION MONTH
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