Author

Ruth I.C. Glasgow

Karolinska InstitutetORCID 0000-0002-9522-2735Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Assay:long-read sequencing· 1 Organism:mouse· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Alessandro ReaiD· 1 shared Alexander J. M. BlakesiD· 1 shared Alexey AmuntsiD· 1 shared Alissa Wilhalm· 1 shared Amel Ben ChehidaiD· 1 shared Amir JahićiD· 1 shared Anju ShuklaiD· 1 shared Anna WedelliD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Alessandro ReaORCID

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2 papers

Recent·Most cited

Molecular BiologyNature CommunicationsPeer-reviewedJun 25, 2025

The mitochondrial methylation potential gates mitoribosome assembly

Ruth I.C. Glasgow, Vivek Singh, Lucía Peña‐Pérez…·Anna Wredenberg

The paper shows that mitochondrial SAM is essential for processing mitochondrial ribosomal RNA precursors and ribosome assembly.

14 citationstop 4%

mouselong-read sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintAug 19, 2024

Biallelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype

Thomas B. Smith, Robert Kopajtich, Leigh A. M. Demain…·William G. Newman

This study identifies biallelic DAP3 variants causing mitoribosomal dysfunction, leading to combined oxidative phosphorylation deficiency and Perrault syndrome-like features.

2 citations

humanproteomics

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