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Bioinformatics (Oxford, England)|January 19, 2018
VIPER: a web application for rapid expert review of variant callsMarius Wöste, Martin Dugas
BMC Bioinformatics|July 26, 2023
OGRE: calculate, visualize, and analyze overlap between genomic input regions and public annotationsSven Berres, Jörg Gromoll, Marius Wöste, et al.
BMC Bioinformatics|May 3, 2020
wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing dataMarius Wöste, Elsa Leitão, Sandra Laurentino, et al.
Gigascience|November 2, 2020
CopyDetective: Detection threshold-aware copy number variant calling in whole-exome sequencing dataSarah Sandmann, Marius Wöste, Aniek O de Graaf, et al.
Clinical Epigenetics|May 8, 2020
The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesisElsa Leitão, Sara Di Persio, Sandra Laurentino, et al.
Blood Advances|September 24, 2021
Calcitonin receptor-like (CALCRL) is a marker of stemness and an independent predictor of outcome in pediatric AMLLinus Angenendt, Marius Wöste, Jan-Henrik Mikesch, et al.
The Journal of Clinical Endocrinology and Metabolism|March 19, 2022
A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone LevelsMaria Schubert, Lina Pérez Lanuza, Marius Wöste, et al.
Clinical Epigenetics|August 22, 2021
Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changesSara Di Persio, Elsa Leitão, Marius Wöste, et al.
Geroscience|July 14, 2026
Normal spermatogenesis in older men is associated with compensatory transcriptome changesYihan Wang, Sven Berres, Henrike Krenz, et al.
Human Genetics|November 19, 2020
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermiaAlbert Salas-Huetos, Frank Tüttelmann, Margot J Wyrwoll, et al.
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