Author

Ryan P. Liegel

Cincinnati Children's Hospital Medical CenterORCID 0000-0001-7480-5459Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 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· 3 shared Chelsea A. MenkeiD· 2 shared Elizabeth BittermanniD· 2 shared Erin Finnerty· 2 shared Howard M. SaaliD· 2 shared Andrew DiStasio· 1 shared Andrew Timms· 1 shared Bart O. WilliamsiD· 1 shared

Activity by Year

2018-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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3 shared papersDevelopmental Biology

Rolf W. StottmannORCID

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3 papers

Recent·Most cited

Developmental BiologybioRxivPreprintJun 2, 2022

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

Ryan P. Liegel, Megan N. Michalski, Sanika Vaidya…·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.

DOI 10.1101/2022.06.02.494481

mouseexperimental assay

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Developmental BiologyPLoS GeneticsPeer-reviewedAug 6, 2019

Differential requirements of tubulin genes in mammalian forebrain development.

Elizabeth Bittermann, Ryan P. Liegel, Chelsea A. Menke…·Rolf W. Stottmann

The paper investigates the differential requirements of tubulin genes in mouse forebrain development, showing that some are essential while others are not.

59 citations

mouseexperimental assay

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GeneticsgenesisPeer-reviewedOct 30, 2018

Using human sequencing to guide craniofacial research.

Ryan P. Liegel, Erin Finnerty, Lauren E. Blizzard…·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.

7 citations

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