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	11	A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A Enthalten in Scientific reports Bd. 9, 27.2.2019, Nr. 1, date:12.2019: 1-12
	12	A genomic exploration identifies mechanisms that may explain adverse cardiovascular effects of COX-2 inhibitors Enthalten in Scientific reports Bd. 7, 31.8.2017, Nr. 1, date:12.2017: 1-9
	13	Abstracts from the 8th International Conference on cGMP Generators, Effectors and Therapeutic Implications Enthalten in BMC pharmacology & toxicology Bd. 18, 10.10.2017, Nr. 1, date:10.2017: 1-35
	14	Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease Enthalten in Nature Communications Bd. 9, 24.4.2018, Nr. 1, date:12.2018: 1-8
	15	Assessing the causal association of glycine with risk of cardio-metabolic diseases Enthalten in Nature Communications Bd. 10, 5.3.2019, Nr. 1, date:12.2019: 1-13
	16	Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants Enthalten in Nature genetics Bd. 54, 6.12.2022, Nr. 12, date:12.2022: 1803-1815
	17	Etidronate prevents dystrophic cardiac calcification by inhibiting macrophage aggregation Enthalten in Scientific reports Bd. 8, 11.4.2018, Nr. 1, date:12.2018: 1-13
	18	Genetic insights into resting heart rate and its role in cardiovascular disease Enthalten in Nature Communications Bd. 14, 2.8.2023, Nr. 1, date:12.2023: 1-21
	19	Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus Enthalten in Scientific reports Bd. 8, 12.9.2018, Nr. 1, date:12.2018: 1-10
	20	Homozygous splice-site variant in ENPP1 underlies generalized arterial calcification of infancy Enthalten in BMC pediatrics Bd. 24, 13.11.2024, Nr. 1, date:12.2024: 1-11

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