Search

Search Constraints

You searched for: Author/Creator Body, Simon C.

Search Results

1. Association of Factor V Leiden With Subsequent Atherothrombotic Events: A GENIUS-CHD Study of Individual Participant Data. Issue 6 (11th August 2020)

2. Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry. Issue 12 (8th September 2016)

3. Calcium Signaling Pathway Genes RUNX2 and CACNA1C Are Associated With Calcific Aortic Valve Disease. (December 2015)

5. Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation. (February 2015)

6. Genetic and Clinical Risk Prediction Model for Postoperative Atrial Fibrillation. (February 2015)

7. Spatiotemporal Multi-Omics Mapping Generates a Molecular Atlas of the Aortic Valve and Reveals Networks Driving Disease. Issue 4 (24th July 2018)

8. The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study. (January 2017)

10. Using Next-generation RNA Sequencing to Examine Ischemic Changes Induced by Cold Blood Cardioplegia on the Human Left Ventricular Myocardium Transcriptome. (March 2015)