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	11	Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits Frankfurt am Main : Univ.-Bibliothek Frankfurt am Main, 2013
	12	Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy Stark, Klaus. - Augsburg : Universität Augsburg, 2010
	13	Genetik des Herzinfarktes. Der lange Weg von der positiven Familienanamnese zum Gen Enthalten in Chemie in unserer Zeit Bd. 43, 2009, Nr. 5: 288-295. 8 S.
	14	Hypertrophe Kardiomyopathie Enthalten in Herz Bd. 30, Nr. 6, date:9.2005: 550-557
	15	Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia Enthalten in Human genetics Bd. 97, Nr. 5, date:5.1996: 614-619
	16	Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome) Enthalten in Human genetics Bd. 92, Nr. 4, date:10.1993: 347-349
	17	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
	18	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
	19	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
	20	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

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