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	21	Protein C Deficiency caused by Homozygosity for a Novel PROC D180G Mutation – in vitro Expression and Structural Analysis of the Mutation Enthalten in Thrombosis and haemostasis Bd. 87, 2002, Nr. 04: 632-638
	22	Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk Enthalten in Nature genetics Bd. 55, 25.9.2023, Nr. 10, date:10.2023: 1778-1779
	23	Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries Enthalten in Nature genetics Bd. 51, 20.5.2019, Nr. 6, date:6.2019: 1067
	24	Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries Enthalten in Nature genetics Bd. 56, 19.4.2024, Nr. 5, date:5.2024: 1032-1033
	25	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals Enthalten in Nature genetics Bd. 52, 23.11.2020, Nr. 12, date:12.2020: 1314-1332
	26	Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression Enthalten in Nature genetics Bd. 50, 26.4.2018, Nr. 5, date:5.2018: 668-681
	27	Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention Enthalten in Nature genetics Bd. 54, 7.9.2022, Nr. 9, date:9.2022: 1332-1344
	28	GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes Enthalten in Nature Communications Bd. 9, 3.12.2018, Nr. 1, date:12.2018: 1-14
	29	How rural and urban parents describe convenience in the context of school-based influenza vaccination: a qualitative study Enthalten in BMC health services research Bd. 15, 22.1.2015, Nr. 1, date:12.2015: 1-7
	30	Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk Enthalten in Nature genetics Bd. 55, 13.3.2023, Nr. 3, date:3.2023: 410-422

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