Author

Olivera Spasić-Bošković

Cambridge University Hospitals NHS Foundation TrustORCID 0000-0003-1583-8132Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1 Assay:whole-genome sequencing· 1 Organism:zebrafish· 1

Frequent Co-Authors

Adam Jackson· 1 shared Catherine M. AbbottiD· 1 shared David R FitzPatrickiD· 1 shared Detelina GrozevaiD· 1 shared Emily K. OsterweiliD· 1 shared Frances Lucy RaymondiD· 1 shared Graeme R. GrimesiD· 1 shared Hemant BenganiiD· 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

Adam Jackson

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintAug 3, 2020

Functional Predictors of Causative Cis-Regulatory Mutations in Mendelian Disease

Hemant Bengani, Detelina Grozeva, Lambert Moyon…·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.

DOI 10.1101/2020.08.03.232926

humanzebrafish

𝕏 PostBluesky