DNA Is Not Destiny When It Comes To Heart Risk
![a stethoscope and heart](https://www.cdc.gov/genomics/images/2015-02_heart.jpg)
HEART DISEASE
![](https://phgkb.cdc.gov/GAPPKB/images/Whats_new.jpg)
Last Updated: Nov 16, 2016
- Precision Public Health in Action: How to Prevent Heart Disease and Cancer Associated with Inherited Mutations
NCI Webinar, December 14, 2-3 pm, - DNA Is Not Destiny When It Comes To Heart Risk
R Harris, NPR News, November 13, 2016 - Genetic Heart Disease Risk Eased by Healthy Habits, Study Finds
G Kolata, New York Times, November 11, 2016 - Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease
AV Khera et al, NEJM< November 12, 2016 - Testing toddlers for inherited heart disease
Genomics Education UK, October 31, 2016 - Proof of concept study: renal sympathetic denervation for treatment of polymorphic premature ventricular complexes.
Kiuchi Márcio Galindo, et al. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2016 11 (2) 221-229 - Evaluation of family history of permanent hearing loss in childhood as a risk indicator in universal screening.
Valido Quintana Mercedes, et al. Acta otorrinolaringologica espanola 2016 10 - Correlation of angiotensin I-converting enzyme gene insertion/deletion polymorphism with rheumatic heart disease: a meta-analysis.
Tian Yulong, et al. Bioscience reports 2016 10 - Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
Preuss Christoph, et al. PLoS genetics 2016 10 (10) e1006335 - APSH YI-02 THE POLYMORPHISM IN ALDEHYDE DEHYDROGENASE-2 (ALDH2) GENE IS ASSOCIATED WITH MYOCARDIAL INFARCTION AND STROKE IN A CHINESE POPULATION.
Liu Xin, et al. Journal of hypertension 2016 9 e385 - Circulating Apolipoprotein E Concentration and Cardiovascular Disease Risk: Meta-analysis of Results from Three Studies.
Sofat Reecha, et al. PLoS medicine 2016 10 (10) e1002146 - OS 30-05 GENETIC RISK SCORE DETERMINES DIPPING PROFILE IN PATIENTS WITH CORONARY HEART DISEASE.
Wirtwein Marcin, et al. Journal of hypertension 2016 9 e256 - CDKN2BAS polymorphisms: are associated with coronary heart disease risk a Han Chinese population.
Zhao Qingbin, et al. Oncotarget 2016 10 - Emerging Field of Cardiomics: High-Throughput Investigations into Transcriptional Regulation of Cardiovascular Development and Disease.
Slagle Christopher E et al. Trends in genetics : TIG 2016 Oct - Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease
C Preus et al, PLOS Genetics, October 2016
![CDC Resources with and image of DNA](https://phgkb.cdc.gov/GAPPKBImage/images/CDC_resources.jpg)
![Seletced Insights & Reviews with various images of researchers in labortory environments](https://phgkb.cdc.gov/GAPPKBImage/images/discovery.jpg)
![Epidemiology with an image of a crowd of people with a double helix](https://phgkb.cdc.gov/GAPPKBImage/images/epidemiology.jpg)
- Human (7389)
- Pathogen (0)
![Translational Research with two images of people talking to a genetic counselor and an image of a hand with wrapped sequecing around it](https://phgkb.cdc.gov/GAPPKBImage/images/translational.jpg)
- Human (147)
- Pathogen (0)
![Evidence Synthesis with an image of sequencing and a double helix](https://phgkb.cdc.gov/GAPPKBImage/images/evidence.jpg)
![Practice & Implementation with images of people taking to a doctor and a nurse examining a child](https://phgkb.cdc.gov/GAPPKBImage/images/practice.jpg)
- Huamn (54)
- Pathogen (0)
No hay comentarios:
Publicar un comentario