Author

Caroline Scott

University of OxfordORCID 0000-0002-1708-7427Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Assay:ATAC-seq· 1 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Douglas R. HiggsiD· 3 shared Christian BabbsiD· 2 shared Christopher A. Fisher· 2 shared Damien J. DownesiD· 2 shared Jim R. HughesiD· 2 shared Matthew E. GosdeniD· 2 shared Noemi B. A. RoyiD· 2 shared Ron SchweßingeriD· 2 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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3 shared papersGenetics

Douglas R. HiggsORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicineDevelopmental CellPeer-reviewedAug 15, 2023

RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation

Danya J. Martell, Hope E. Merens, Alexis Caulier…·L. Stirling Churchman

This study shows that SUPT5H mutations disrupt RNA polymerase II pausing, delaying erythroid differentiation and cell cycle progression in human cells.

34 citationstop 2%

humanbulk RNA-seq

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GeneticsbioRxivPreprintJan 15, 2020

An integrated platform to systematically identify causal variants and genes for polygenic human traits.

Damien J. Downes, Ron Schweßinger, Stephanie Hill…·Jim R. Hughes

The paper develops a platform combining ATAC-seq, DNaseI footprints, NG Capture-C, and machine learning to identify causal variants and genes for polygenic human traits.

19 citations

humanATAC-seq

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GeneticsbioRxivPreprintAug 30, 2019

Modelling erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I)

Caroline Scott, Damien J. Downes, Jill M. Brown…·Veronica J. Buckle

This study models erythropoiesis in CDA-I by analyzing patient-derived erythroblasts, identifying abnormalities in DNA accessibility, proliferation, and enucleation, with genotype-phenotype correlations.

3 citations

humanproteomics

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