Author

Susan Vermeulen

Radboud University Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2

Frequent Co-Authors

Alexander HoischeniD· 2 shared Dominique SmeetsiD· 2 shared Ellen Kater‐Baats· 2 shared Guillaume van de Zande· 2 shared Kornelia NevelingiD· 2 shared Marc PauperiD· 2 shared Marian Stevens‐KroefiD· 2 shared Michiel Oorsprong· 2 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Alexander HoischenORCID

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2 papers

Recent·Most cited

Next generation cytogenetics: genome-imaging enables comprehensive structural variant detection for 100 constitutional chromosomal aberrations in 85 samples

Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard, Marion Benoist, Guillaume van de Zande, Ellen Kater‐Baats, Imane Baatout, Ronald van Beek, Tony Yammine, Michiel Oorsprong, Daniel Olde-Weghuis, Wed Majdali, Susan Vermeulen, Marc Pauper, Aziza Lebbar, , Laïla El Khattabi

This study evaluates high-resolution optical mapping for detecting chromosomal aberrations in 85 samples, achieving 100% concordance with standard tests for non-centromeric breakpoints.

bioRxiv · Jul 15, 2020 · PreprintGenetics

Next generation cytogenetics: comprehensive assessment of 48 leukemia genomes by genome imaging

Kornelia Neveling, Tuomo Mantere, Susan Vermeulen, Michiel Oorsprong, Ronald van Beek, Ellen Kater‐Baats, Marc Pauper, Guillaume van de Zande, Dominique Smeets, Daniël Olde Weghuis, Marian Stevens‐Kroef, Alexander Hoischen

This study assesses genome imaging in 48 leukemia cases, showing it can detect complex structural variants and chromosomal aberrations with high accuracy, potentially replacing traditional cytogenetic methods.

bioRxiv · Feb 6, 2020 · PreprintGenomics