Author

Jacqueline K. Rainger

Institute of Genetics and Cancer

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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Developmental Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David R FitzPatrickiD· 2 shared Hemant BenganiiD· 2 shared Liusaidh J. OweniD· 2 shared Adam Jackson· 1 shared Andrew Sofronis PapanastasiouiD· 1 shared Catherine M. AbbottiD· 1 shared Detelina GrozevaiD· 1 shared Emily K. OsterweiliD· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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2 shared papersDevelopmental Biology

David R FitzPatrickORCID

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2 papers

Recent·Most cited

Characterization of an Eye Field-like State during Optic Vesicle Organoid Development

Liusaidh J. Owen, Jacqueline K. Rainger, Hemant Bengani, Fiona M. Kilanowski, David R FitzPatrick, Andrew Sofronis Papanastasiou

The paper uses optic vesicle organoids to study gene expression and chromatin changes during eye field specification, identifying key transcription factors and regulatory elements.

Development · Jun 12, 2023Peer-reviewedDevelopmental Biology

Functional Predictors of Causative Cis-Regulatory Mutations in Mendelian Disease

Hemant Bengani, Detelina Grozeva, Lambert Moyon, Shipra Bhatia, Susana R. Louros, Jilly E. Hope, Adam Jackson, James G. D. Prendergast, Liusaidh J. Owen, Magali Naville, Jacqueline K. Rainger, Graeme R. Grimes, Mihail R. Halachev, Laura C. Murphy, Olivera Spasić-Bošković, , David R FitzPatrick

The paper identifies rare CRE variants associated with X-linked intellectual disability by combining sequencing, functional assays in zebrafish and mice, and phenotypic analysis.

bioRxiv · Aug 3, 2020 · PreprintGenetics