Author

Christopher A. Fisher

John Radcliffe 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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Genetics· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:ATAC-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Approach:machine learning (classical)· 1 Assay:proteomics· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Caroline ScottiD· 2 shared Damien J. DownesiD· 2 shared Douglas R. HiggsiD· 2 shared Jim R. HughesiD· 2 shared Matthew E. GosdeniD· 2 shared Ron SchweßingeriD· 2 shared Veronica J. BuckleiD· 2 shared A. Marieke OudelaariD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersGenetics

Caroline ScottORCID

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2 papers

Recent·Most cited

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

Damien J. Downes, Ron Schweßinger, Stephanie Hill, Lea Nußbaum, Caroline Scott, Matthew E. Gosden, Priscila P. Hirschfeld, Jelena M. Telenius, Chris Q. Eijsbouts, Simon J. McGowan, Antony J. Cutler, Jon Kerry, Jessica L. Davies, Calliope Athena Dendrou, Jamie R. J. Inshaw, , 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.

bioRxiv · Jan 15, 2020 · PreprintGenetics

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

Caroline Scott, Damien J. Downes, Jill M. Brown, Christian Babbs, Aude-Anaïs Olijnik, Matthew E. Gosden, Robert A. Beagrie, Ron Schweßinger, Christopher A. Fisher, Anna M. Rose, David J. P. Ferguson, Errin Johnson, Quentin A. Hill, Steven Okoli, Raffaele Renella, , 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.

bioRxiv · Aug 30, 2019 · PreprintGenetics