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	1	2012 highlights in translational 'omics In: Genome medicine Bd. 5, 31.1.2013, Nr. 1, date:1.2013: 1-5
	2	3D clusters of somatic mutations in cancer reveal numerous rare mutations as functional targets In: Genome medicine Bd. 9, 23.1.2017, Nr. 1, date:12.2017: 1-13
	3	5′-tRF-GlyGCC: a tRNA-derived small RNA as a novel biomarker for colorectal cancer diagnosis Enthalten in Genome medicine Bd. 13, 9.2.2021, Nr. 1, date:12.2021: 1-12
	4	A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases In: Genome medicine Bd. 7, 30.9.2015, Nr. 1, date:12.2015: 1-16
	5	A bioinformatic framework for immune repertoire diversity profiling enables detection of immunological status Enthalten in Genome medicine Bd. 7, 28.5.2015, Nr. 1, date:12.2015: 1-15
	6	A BRCA1-mutation associated DNA methylation signature in blood cells predicts sporadic breast cancer incidence and survival In: Genome medicine Bd. 6, 27.6.2014, Nr. 6, date:12.2014: 1-11
	7	A case study of an integrative genomic and experimental therapeutic approach for rare tumors: identification of vulnerabilities in a pediatric poorly differentiated carcinoma In: Genome medicine Bd. 8, 31.10.2016, Nr. 1, date:12.2016: 1-17
	8	A cell-of-origin epigenetic tracer reveals clinically distinct subtypes of high-grade serous ovarian cancer Enthalten in Genome medicine Bd. 12, 30.10.2020, Nr. 1, date:12.2020: 1-20
	9	A chromosomal connectome for psychiatric and metabolic risk variants in adult dopaminergic neurons Enthalten in Genome medicine Bd. 12, 19.2.2020, Nr. 1, date:12.2020: 1-19
	10	A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing Enthalten in Genome medicine Bd. 11, 26.7.2019, Nr. 1, date:12.2019: 1-11

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