Author

Meinolf Suttorp

Technische Universität DresdenORCID 0000-0002-9522-8838Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:benchmarking· 1 Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Arndt BorkhardtiD· 1 shared Arne JahniD· 1 shared Carolin WalteriD· 1 shared Claudia Zinke· 1 shared Evelin SchröckiD· 1 shared Franziska AueriD· 1 shared Jonas Langanke· 1 shared Judith Lohse· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Arndt BorkhardtORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 22, 2022

Clinical criteria for genetic testing in pediatric oncology show a low specificity and miss every 4th child carrying a cancer predisposition

Ulrike Anne Friedrich, Marc Bienias, Claudia Zinke…·Franziska Auer

The paper evaluates clinical checklists for genetic testing in pediatric oncology, finding low specificity and missing 25% of children with cancer predisposition variants.

DOI 10.1101/2022.10.22.22281392

humanwhole-exome sequencing

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