Author

Stephanie Hill

University of Oxford

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Genetics· 1

Signature Assays, Organisms & Methods

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Assay:ATAC-seq· 1 Organism:human· 1 Approach:machine learning (classical)· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

A. Marieke OudelaariD· 1 shared Andrew John KingiD· 1 shared Antony J. CutleriD· 1 shared Calliope Athena DendrouiD· 1 shared Caroline ScottiD· 1 shared Chris Q. EijsboutsiD· 1 shared Christopher A. Fisher· 1 shared Damien J. DownesiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

A. Marieke OudelaarORCID

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1 paper

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