Swerdlow, DI;
Humphries, SE;
(2017)
Genetics of CHD in 2016: Common and rare genetic variants and risk of CHD.
Nature Reviews Cardiology
, 14
(2)
pp. 73-74.
10.1038/nrcardio.2016.209.
Preview |
Text
Humphries_Swerdlow and Humphries Nat cardiol Final.pdf - Accepted Version Download (439kB) | Preview |
Abstract
Much of the progress in cardiovascular genetics in 2016 has been driven by next-generation sequencing studies, and the clinical utility of knowing an individual's genotype for predicting their risk of cardiovascular disease is gaining credibility, both for monogenic and polygenic disorders. Additionally, phenotype data are increasingly abundant, although databases linking genotype with clinically relevant phenotypes require optimization.
| Type: | Article |
|---|---|
| Title: | Genetics of CHD in 2016: Common and rare genetic variants and risk of CHD |
| Location: | England |
| Open access status: | An open access version is available from UCL Discovery |
| DOI: | 10.1038/nrcardio.2016.209 |
| Publisher version: | http://dx.doi.org/10.1038/nrcardio.2016.209 |
| Language: | English |
| Additional information: | This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions. |
| Keywords: | Cardiomyopathies, Cardiovascular genetics, Coronary artery disease and stable angina, Dyslipidaemias, Population screening, |
| UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science |
| URI: | https://discovery.ucl.ac.uk/id/eprint/1535593 |
Loading...
Loading...Loading...Loading...Archive Staff Only
 |
View Item |
