Author

Susan J. Monkley

AstraZeneca (Sweden)ORCID 0000-0001-9174-6278Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Abhishek NagiD· 1 shared Adam PlattiD· 1 shared Alex Mackay· 1 shared Andrew Robert HarperiD· 1 shared AstraZeneca Genomics Initiative· 1 shared Carolina HaefligeriD· 1 shared Daniel MuthasiD· 1 shared Dimitrios VitsiosiD· 1 shared

Activity by Year

2020-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenomics

Abhishek NagORCID

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2 papers

Recent·Most cited

Cell BiologybioRxivPreprintMar 31, 2026

Extracellular Vesicle microRNAs From Small Airways Promote Senescence and Fibrosis in COPD

Justine V. Devulder, Peter S Fenwick, Susan J. Monkley…·Peter John Barnes

This study identifies miRNA changes in COPD small airway cells and EVs, linking them to cellular senescence and fibrosis pathways.

DOI 10.64898/2026.03.30.713627

humanbulk RNA-seq

𝕏 PostBluesky

GenomicsbioRxivPreprintDec 13, 2020

Surveying the contribution of rare variants to the genetic architecture of human disease through exome sequencing of 177,882 UK Biobank participants

Quanli Wang, Ryan S. Dhindsa, Keren Carss…·AstraZeneca Genomics Initiative

This study uses exome sequencing of 177,882 UK Biobank participants to assess the role of rare variants in 10,533 phenotypes, identifying 911 significant gene-phenotype relationships.

10 citations

humanwhole-exome sequencing

𝕏 PostBluesky