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	41	Publisher Correction: Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes Enthalten in Basic research in cardiology Bd. 117, 5.4.2022, Nr. 1, date:12.2022: 1-2
	42	Qtlizer: comprehensive QTL annotation of GWAS results Enthalten in Scientific reports Bd. 10, 24.11.2020, Nr. 1, date:12.2020: 1-8
	43	Serum microRNA-1233 is a specific biomarker for diagnosing acute pulmonary embolism Enthalten in Journal of translational medicine Bd. 14, 5.5.2016, Nr. 1, date:12.2016: 1-10
	44	Stimulators of the soluble guanylyl cyclase: promising functional insights from rare coding atherosclerosis-related GUCY1A3 variants Enthalten in Basic research in cardiology Bd. 111, 24.6.2016, Nr. 4, date:7.2016: 1-13
	45	The assertion that a G21V mutation in AGTR2 causes mental retardation is not supported by other studies Enthalten in Human genetics Bd. 114, 13.1.2004, Nr. 4, date:3.2004: 396
	46	The CAD risk locus 9p21 increases the risk of vascular calcification in an iPSC-derived VSMC model Enthalten in Stem cell research & therapy Bd. 12, 6.3.2021, Nr. 1, date:12.2021: 1-12
	47	The DZHK research platform: maximisation of scientific value by enabling access to health data and biological samples collected in cardiovascular clinical studies Enthalten in Clinical research in cardiology Bd. 112, 8.3.2023, Nr. 7, date:7.2023: 923-941
	48	The interleukin-11 receptor variant p.W307R results in craniosynostosis in humans Enthalten in Scientific reports Bd. 13, 18.8.2023, Nr. 1, date:12.2023: 1-14
	49	Transcriptome-wide association study of coronary artery disease identifies novel susceptibility genes Enthalten in Basic research in cardiology Bd. 117, 17.2.2022, Nr. 1, date:12.2022: 1-20
	50	What can we learn from common variants associated with unexpected phenotypes in rare genetic diseases? Enthalten in Orphanet journal of rare diseases Bd. 16, 21.1.2021, Nr. 1, date:12.2021: 1-5

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