Publications
A novel missense mutation in TNNI3K causes recessively inherited cardiac conduction disease in a consanguineous Pakistani family
Ramzan S, Tennstedt S, Tariq M, Khan S, Ul Ayan HN, Ali A, Munz M, Thiele H, Korejo AA, Mughal AR, Jamal SZ, Nürnberg P, Baig SM, Erdmann J, Ahmad I.
Genes 2021, 12(8), 1282
The C5a/C5a receptor 1 axis controls tissue neovascularization through CXCL4 release from platelets
Nat Commun. 2021 Jun 7;12(1):3352. doi: 10.1038/s41467-021-23499-w.
Effect of Differences in the Microbiome of Cyp17a1-Deficient Mice on Atherosclerotic Background
Cells. 2021 May 23;10(6):1292. doi: 10.3390/cells10061292.
Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans
Orphanet J Rare Dis. 2021 May 19;16(1):228. doi: 10.1186/s13023-021-01863-9.
Cis-epistasis at the LPA locus and risk of cardiovascular diseases
Cardiovasc Res. 2021 Apr 20:cvab136. doi: 10.1093/cvr/cvab136.
The fibrillin-1 RGD motif posttranscriptionally regulates ERK1/2 signaling and fibroblast proliferation via miR-1208
FASEB J. 2021 May;35(5):e21598. doi: 10.1096/fj.202100282R.
A proteomic atlas of the neointima identifies novel druggable targets for preventive therapy
European Heart Journal, ehab140, https://doi.org/10.1093/eurheartj/ehab140