Author

Barbara Meissner

BC Cancer AgencyORCID 0000-0002-5242-5559Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Christian SteidliD· 3 shared Merrill BoyleiD· 3 shared Ryan D. MoriniD· 3 shared Aixiang JiangiD· 2 shared Andrew J. J. MungalliD· 2 shared Bruno M. GrandeiD· 2 shared Christopher K. RushtoniD· 2 shared David W. ScottiD· 2 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenomics

Christian SteidlORCID

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3 papers

Recent·Most cited

Cancer BiologybioRxivPreprintOct 20, 2026

Developmental origins of thymic B-cell lymphomas

Shinya Rai, Yifan Yin, Manabu Fujisawa…·Christian Steidl

This study identifies a thymus-specific B-cell differentiation program linked to thymic B-cell lymphomagenesis through single-cell multiomics and spatial profiling.

DOI 10.64898/2026.10.17.759359

humanscRNA-seq

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GenomicsBloodPeer-reviewedMar 11, 2020

Coding and regulatory drivers of mantle cell lymphoma identified through exome and genome sequencing

Prasath Pararajalingam, Krysta Mila Coyle, Sarah E. Arthur…·Ryan D. Morin

This study identifies genetic drivers of mantle cell lymphoma through exome and genome sequencing, revealing novel mutations in genes involved in RNA splicing and regulation.

71 citationstop 2%

humanwhole-exome sequencing

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GenomicsNature CommunicationsPeer-reviewedSep 25, 2018

Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma

Sarah E. Arthur, Aixiang Jiang, Bruno M. Grande…·Ryan D. Morin

This study identifies somatic coding and regulatory variants in DLBCL, revealing novel mechanisms of oncogene deregulation and potential therapeutic targets.

146 citationstop 1%

humanwhole-exome sequencing

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