Katalog der Deutschen Nationalbibliothek

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	31	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
	32	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
	33	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
	34	Whole-exome sequencing in an extended family with myocardial infarction unmasks familial hypercholesterolemia Enthalten in BMC cardiovascular disorders Bd. 14, 26.8.2014, Nr. 1, date:12.2014: 1-6

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