Publications
The CAD risk locus 9p21 increases the risk of vascular calcification in an iPSC-derived VSMC model
Stem Cell Res Ther. 2021 Mar 6;12(1):166. doi: 10.1186/s13287-021-02229-5.
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23
Eur Heart J. 2021 Mar 3:ehab030. doi: 10.1093/eurheartj/ehab030.
sGC Activity and Regulation of Blood Flow in a Zebrafish Model System
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Front. Physiol., 25 February 2021. doi.org/10.3389/fphys.2021.633171.
Unfolding and disentangling coronary vascular disease through genome-wide association studies
Eur Heart J 2021 Feb 9;ehaa1089. doi: 10.1093/eurheartj/ehaa1089.
What can we learn from common variants associated with unexpected phenotypes in rare genetic diseases?
Orphanet J Rare Dis 16, 41 (2021). https://doi.org/10.1186/s13023-021-01684-w.
Population bias in polygenic risk prediction models for coronary artery disease.
Circ Genom Precis Med. 2020 Nov 10. doi: 10.1161/CIRCGEN.120.002932.
Identifying multimodal signatures underlying the somatic comorbidity of psychosis: the COMMITMENT roadmap.
Mol Psychiatry. 2020 Oct 15. doi: 10.1038/s41380-020-00915-z.
Qtlizer: comprehensive QTL annotation of GWAS results.
Sci Rep. 2020 Nov 24;10(1):20417. doi: 10.1038/s41598-020-75770-7.
An integrated personal and population-based Egyptian genome reference.
Nat Commun. 2020 Sep 18;11(1):4719. doi: 10.1038/s41467-020-17964-1.