Author

Stephanie Oerum

Centre National de la Recherche ScientifiqueORCID 0000-0001-9525-7295Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Albert Amberger· 1 shared Andrea J. Deutschmann· 1 shared Andrew E. FirthiD· 1 shared Ben F. LuisiiD· 1 shared Emma M. JenkinsoniD· 1 shared Felix RandowiD· 1 shared Helena Jane MaieriD· 1 shared Inna A. BelyantsevaiD· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Albert Amberger

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2 papers

Recent·Most cited

Molecular BiologyJournal of VirologyPeer-reviewedMay 6, 2021

The stem loop 2 motif is a site of vulnerability for SARS-CoV-2

Valeria Lulla, Michal P. Wandel, Katarzyna Justyna Bandyra…·Ben F. Luisi

The paper identifies the stem loop 2 motif as a vulnerable site in SARS-CoV-2 that can be targeted by antisense oligonucleotides to inhibit replication and infection.

101 citationstop 3%

experimental assaydrug response / drug discovery

𝕏 PostBluesky

GeneticsbioRxivPreprintJul 25, 2017

A homozygous variant in mitochondrial RNase P subunit PRORP is associated with Perrault syndrome characterized by hearing loss and primary ovarian insufficiency

Irit Hochberg, Leigh A. M. Demain, Jill E. Urquhart…·William G. Newman

The paper identifies a homozygous variant in KIAA0391 (PRORP) as a cause of Perrault syndrome, showing reduced mitochondrial RNase P activity and impaired tRNA processing.

7 citations

humanstatistical model

𝕏 PostBluesky