Swerdlow, DI;
Humphries, SE;
(2017)
Genetics of CHD in 2016: Common and rare genetic variants and risk of CHD.
Nat Rev Cardiol
, 14
(2)
pp. 73-74.
10.1038/nrcardio.2016.209.
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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 |
| DOI: | 10.1038/nrcardio.2016.209 |
| Publisher version: | http://dx.doi.org/10.1038/nrcardio.2016.209 |
| Language: | English |
| Additional information: | Copyright © 2016 Macmillan Publishers Limited, part of Springer Nature. All rights reserved. The final publication is available at [Journal title] via http://dx.doi.org/10.1038/nrcardio.2016.209 |
| 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-pp.ucl.ac.uk/id/eprint/1535593 |
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