Author

Emily M. A. Lewis

Washington University in St. LouisORCID 0000-0002-0301-3427Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Assay:bulk RNA-seq· 1 Research Focus:cell-cell communication· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Kristen L. KrolliD· 2 shared Paul M. GontarziD· 2 shared Azad BonniiD· 1 shared Bo ZhangiD· 1 shared Bo ZhangiD· 1 shared Caili TongiD· 1 shared David M. OrnitziD· 1 shared Dustin BaldridgeiD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersDevelopmental Biology

Kristen L. KrollORCID

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2 papers

Recent·Most cited

Developmental BiologyDevelopmental BiologyPeer-reviewedMay 22, 2020

Geminin is required for Hox gene regulation to pattern the developing limb

Emily M. A. Lewis, Savita Sankar, Caili Tong…·Kristen L. Kroll

This paper identifies Geminin as a regulator of Hox gene expression in mouse limb development, showing its role in patterning limb skeletal elements through effects on Hox gene expansion and SHH signaling.

5 citations

mouseexperimental assay

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NeuroscienceMolecular AutismPeer-reviewedDec 1, 2019

Cellular and molecular characterization of multiplex autism in human induced pluripotent stem cell-derived neurons

Emily M. A. Lewis, Kesavan Meganathan, Dustin Baldridge…·Kristen L. Kroll

This study models multiplex autism using iPSC-derived neurons from a family with varying ASD liability, identifying morphological, physiological, and transcriptomic changes linked to polygenic susceptibility.

31 citations

humanbulk RNA-seq

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