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	1	Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3 In: Breast cancer research and treatment 28.10.2016: 1-18
	2	Breast cancer risks associated with missense variants in breast cancer susceptibility genes Enthalten in Genome medicine Bd. 14, 18.5.2022, Nr. 1, date:12.2022: 1-17
	3	Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers Enthalten in Communications biology Bd. 5, 6.10.2022, Nr. 1, date:12.2022: 1-15
	4	Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer Enthalten in Nature Communications Bd. 10, 15.4.2019, Nr. 1, date:12.2019: 1-18
	5	Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women In: Breast cancer research Bd. 18, 11.11.2016, Nr. 1, date:12.2016: 1-19

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