Author

Sarah E. Arthur

Simon Fraser UniversityORCID 0000-0002-5341-7868Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Andrew J. J. MungalliD· 2 shared Barbara MeissneriD· 2 shared Bruno M. GrandeiD· 2 shared Christian SteidliD· 2 shared Christopher K. RushtoniD· 2 shared David W. ScottiD· 2 shared Graham W. SlackiD· 2 shared Joseph Michael ConnorsiD· 2 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenomics

Andrew J. J. MungallORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

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

Prasath Pararajalingam, Krysta Mila Coyle, Sarah E. Arthur, Nicole Thomas, Miguel Alcaide, Barbara Meissner, Merrill Boyle, Quratulain Qureshi, Bruno M. Grande, Christopher K. Rushton, Graham W. Slack, Andrew J. J. Mungall, Constantine Si Lun Tam, Rishu Agarwal, Sarah‐Jane Dawson, , 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.

Blood · Mar 11, 2020Peer-reviewedGenomics

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

Sarah E. Arthur, Aixiang Jiang, Bruno M. Grande, Miguel Alcaide, Razvan Cojocaru, Christopher K. Rushton, Anja Mottok, Laura K. Hilton, Prince Kumar Lat, Eric Y. Stutheit-Zhao, Luka Culibrk, Daisuke Ennishi, Selin Jessa, Lauren C. Chong, Nicole Thomas, , Ryan D. Morin

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

Nature Communications · Sep 25, 2018Peer-reviewedGenomics