Publications by authors named "Ethan D Sperry"

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Mosaic X-linked adrenoleukodystrophy in males identified by newborn screening and next-generation sequencing.
Alexandra C Keefe, Dana M Jensen, Meranda M Pham, Natalie Y T Au, Erika Beckman, Ethan D Sperry

NPJ Genom Med· May 2025

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Tracheostomy-related durable medical equipment: Insurance coverage, gaps, and barriers.
Palmer L Foran, William J Benjamin, Ethan D Sperry, Simon R Best, Sarah E Boisen

Am J Otolaryngol· March 2024

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Amplifying patient voices amid pandemic: Perspectives on tracheostomy care, communication, and connection.
Vinciya Pandian, Brandon S Hopkins, Christina J Yang, Erin Ward, Ethan D Sperry

Am J Otolaryngol· September 2022

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Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Mutant Mouse Ear.
Robert Durruthy-Durruthy, Ethan D Sperry, Margot E Bowen, Laura D Attardi, Stefan Heller

Front Genet· October 2018

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CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.
Hui Yao, Sophie F Hill, Jennifer M Skidmore, Ethan D Sperry, Donald L Swiderski

JCI Insight· February 2018

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Duplication 2p25 in a child with clinical features of CHARGE syndrome.
Ethan D Sperry, Jane L Schuette, Conny M A van Ravenswaaij-Arts, Glenn E Green, Donna M Martin

Am J Med Genet A· May 2016

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Chromodomain helicase DNA-binding proteins in stem cells and human developmental diseases.
Joseph A Micucci, Ethan D Sperry, Donna M Martin

Stem Cells Dev· April 2015

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The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.
Ethan D Sperry, Elizabeth A Hurd, Mark A Durham, Elyse N Reamer, Adam B Stein

Dev Dyn· September 2014

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CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.
Joseph A Micucci, Wanda S Layman, Elizabeth A Hurd, Ethan D Sperry, Sophia F Frank

Hum Mol Genet· January 2014

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