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BMC Bioinformatics|May 11, 2016
SeqPurge: highly-sensitive adapter trimming for paired-end NGS dataMarc Sturm, Christopher Schroeder, Peter BauerMovement Disorders : Official Journal of the Movement Disorder Society|January 11, 2014
Screening of mutations in GNAL in sporadic dystonia patientsClaudia Dufke, Marc Sturm, Christopher Schroeder, et al.Molecular and Cellular Probes|May 17, 2015
Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathiesStephan Waldmüller, Christopher Schroeder, Marc Sturm, et al.Bioinformatics (Oxford, England)|April 17, 2013
UPDtool: a tool for detection of iso- and heterodisomy in parent-child trios using SNP microarraysChristopher Schroeder, Marc Sturm, Andreas Dufke, et al.Journal of Proteome Research|May 12, 2009
TOPPView: an open-source viewer for mass spectrometry dataMarc Sturm, Oliver KohlbacherPlos One|June 23, 2017
Next generation sequencing of the clonal IGH rearrangement detects ongoing mutations and interfollicular trafficking in in situ follicular neoplasiaPerikles Kosmidis, Irina Bonzheim, Claudia Dufke, et al.The Journal of Molecular Diagnostics : JMD|April 12, 2008
High-throughput homogeneous mass cleave assay technology for the diagnosis of autosomal recessive Parkinson's diseaseChristopher Schroeder, Michael Walter, Daniela Berg, et al.Breast Cancer Research and Treatment|May 30, 2015
HBOC multi-gene panel testing: comparison of two sequencing centersChristopher Schroeder, Ulrike Faust, Marc Sturm, et al.Molecular Genetics & Genomic Medicine|February 10, 2023
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndromeDennis Witt, Ulrike Faust, Gertrud Strobl-Wildemann, et al.Genes|October 26, 2024
Reply to Battke et al. Comment on "Park et al. Lessons Learned from Translating Genome Sequencing to Clinical Routine: Understanding the Accuracy of a Diagnostic Pipeline. <i>Genes</i> 2024, <i>15</i>, 136"Joohyun Park, Marc Sturm, Tobias B HaackPageof 67