Author

Erica K. Creighton

University of Missouri

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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Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1 Organism:mouse· 1

Frequent Co-Authors

Leslie A. LyonsiD· 2 shared Reuben M. BuckleyiD· 2 shared Barbara Gandolfi· 1 shared Connor Pyne· 1 shared David A. Senter· 1 shared Delia M. Bouhan· 1 shared Johnny R. Gobble· 1 shared Marie AbitboliD· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenetics

Leslie A. LyonsORCID

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2 papers

Recent·Most cited

GeneticsGenesPeer-reviewedJun 22, 2020

Werewolf, there wolf: variants in Hairless associated with hypotrichia and roaning in the lykoi cat breed

Reuben M. Buckley, Barbara Gandolfi, Erica K. Creighton…·Leslie A. Lyons

The paper identifies variants in the Hairless gene associated with hypotrichia and roaning in lykoi cats by comparing whole genome sequencing data from a lykoi cat to a non-lykoi dataset.

30 citationstop 3%

mousewhole-genome sequencing

𝕏 PostBluesky

GeneticsGenesPeer-reviewedJun 19, 2020

A deletion in GDF7 is associated with a heritable forebrain commissural malformation concurrent with ventriculomegaly and interhemispheric cysts in cats.

Yoshihiko Yu, Erica K. Creighton, Reuben M. Buckley, Leslie A. Lyons

The paper identifies a 7 bp deletion in GDF7 causing a heritable forebrain commissural malformation in cats, validated through genomic analysis and pedigree studies.

10 citations

whole-genome sequencingstatistical model

𝕏 PostBluesky