Author

Erin Finnerty

Cincinnati Children's Hospital Medical Center

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 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Rolf W. StottmanniD· 2 shared Ryan P. LiegeliD· 2 shared Andrew DiStasio· 1 shared Bart O. WilliamsiD· 1 shared Cassandra R. DiegeliD· 1 shared Chelsea A. MenkeiD· 1 shared Cynthia A. ProwsiD· 1 shared Elizabeth BittermanniD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersDevelopmental Biology

Rolf W. StottmannORCID

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2 papers

Recent·Most cited

Dkk1 inhibition normalizes limb phenotypes in a mouse model of Fzd2 associated omodysplasia Robinow syndromes

Ryan P. Liegel, Megan N. Michalski, Sanika Vaidya, Elizabeth Bittermann, Erin Finnerty, Chelsea A. Menke, Cassandra R. Diegel, Zhendong A. Zhong, Bart O. Williams, Rolf W. Stottmann

This paper models a human FZD2 variant in mice, identifies limb and cleft palate phenotypes, and shows DKK1 inhibition can normalize limb defects.

bioRxiv · Jun 2, 2022 · PreprintDevelopmental Biology

Using human sequencing to guide craniofacial research.

Ryan P. Liegel, Erin Finnerty, Lauren E. Blizzard, Andrew DiStasio, Robert B. Hufnagel, Howard M. Saal, Kristen Lipscomb Sund, Cynthia A. Prows, Rolf W. Stottmann

The paper discusses using human sequencing and CRISPR-Cas9 to study a novel craniofacial syndrome, finding that a variant in AMOTL1 causes lethality in mice but its pathogenicity in humans remains unclear.

genesis · Oct 30, 2018Peer-reviewedGenetics