Author

Anita Langerød

Oslo University Hospital

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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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:drug response / drug discovery· 1 Research Focus:protein structure prediction· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Anne‐Lise Børresen‐DaleiD· 2 shared Anthony MathelieriD· 2 shared Miriam R. R. AureiD· 2 shared Ole Christian LingjærdeiD· 2 shared Arne V. PladseniD· 1 shared Arnoldo FrigessiiD· 1 shared Carlos CaldasiD· 1 shared David C. WedgeiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Anne‐Lise Børresen‐DaleORCID

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Author profile →

2 papers

Recent·Most cited

Cis-regulatory mutations associate with transcriptional and post-transcriptional deregulation of the gene regulatory program in cancers

Jaime Abraham Castro-Mondragon, Miriam R. R. Aure, Ole Christian Lingjærde, Anita Langerød, John W.M. Martens, Anne‐Lise Børresen‐Dale, Vessela Nedelcheva Kristensen, Anthony Mathelier

The paper identifies cis-regulatory mutations in cancer that disrupt gene regulatory programs by affecting both transcriptional and post-transcriptional regulation.

Nucleic Acids Research · Nov 17, 2022Peer-reviewedGenomics

Copy number motifs expose genome instability type and predict driver events and disease outcome in breast cancer

Arne V. Pladsen, Gro Nilsen, Oscar M. Rueda, Miriam R. R. Aure, Ørnulf Borgan, Knut Liestøl, Valeria Vitelli, Arnoldo Frigessi, Anita Langerød, OSBREAC, Anthony Mathelier, Olav Engebråten, David C. Wedge, Peter Van Loo, Carlos Caldas, , Ole Christian Lingjærde

The paper identifies copy number motifs in breast cancer genomes that predict disease outcome and driver events, outperforming existing clinical and genomic markers.

bioRxiv · Sep 14, 2019 · PreprintBioinformatics