Author

Esther Kinning

NHS Greater Glasgow and ClydeORCID 0009-0002-9505-5954Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Bronwyn A. KerriD· 1 shared Caroline Fiona WrightiD· 1 shared David R FitzPatrickiD· 1 shared Diana S. JohnsoniD· 1 shared Elizabeth H. Wynn· 1 shared Emma McCann· 1 shared Frances A. Flinter· 1 shared Giuseppe GalloneiD· 1 shared

Activity by Year

2019-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Bronwyn A. KerrORCID

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1 paper

Recent·Most cited

Pathogenicity and selective constraint on variation near splice sites

Jenny Lord, Giuseppe Gallone, Patrick Short, Jeremy F. McRae, Holly Ironfield, Elizabeth H. Wynn, Sebastian S. Gerety, Liu He, Bronwyn A. Kerr, Diana S. Johnson, Emma McCann, Esther Kinning, Frances A. Flinter, I. Karen Temple, Jill Clayton‐Smith, , on behalf of the Deciphering Developmental Disorders study

The paper analyzes exome sequencing data to assess the contribution of splice site mutations to developmental disorders and estimates their pathogenicity and underrepresentation in public databases.

Genome Research · Feb 1, 2019Peer-reviewedGenetics