Ethan D. Sperry

Medical Genetics | Pediatrics

3333 Burnet Ave # Mlc4006
Cincinnati, OH 45229

Last Updated: 09/26/2026

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Found 13 publications

Involvement of Tumor Suppressor Candidate 3 in Mouse Survival, Craniofacial, and Cortical Development.

Involvement of Tumor Suppressor Candidate 3 in Mouse Survival, Craniofacial, and Cortical Development.

Journal: G3 (Bethesda, Md.)

Published: June 12, 2026

The Lived Experience of Individuals with a Tracheostomy and their Caregivers: A Qualitative Analysis.

The Lived Experience of Individuals with a Tracheostomy and their Caregivers: A Qualitative Analysis.

Journal: Tracheostomy (Warrenville, Ill.)

Published: January 01, 2026

Mosaic X-linked adrenoleukodystrophy in males identified by newborn screening and next-generation sequencing.

Mosaic X-linked adrenoleukodystrophy in males identified by newborn screening and next-generation sequencing.

Journal: NPJ genomic medicine

Published: September 18, 2024

Long-read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalities.

Long-read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalities.

Journal: American journal of medical genetics. Part A

Published: March 07, 2024

Tracheostomy-related durable medical equipment: Insurance coverage, gaps, and barriers.

Tracheostomy-related durable medical equipment: Insurance coverage, gaps, and barriers.

Journal: American journal of otolaryngology

Published: October 08, 2023

Amplifying patient voices amid pandemic: Perspectives on tracheostomy care, communication, and connection.

Amplifying patient voices amid pandemic: Perspectives on tracheostomy care, communication, and connection.

Journal: American journal of otolaryngology

Published: May 27, 2022

Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Chd7 Mutant Mouse Ear.

Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Chd7 Mutant Mouse Ear.

Journal: Frontiers in genetics

Published: March 31, 2018

CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.

CHD7 represses the retinoic acid synthesis enzyme ALDH1A3 during inner ear development.

Journal: JCI insight

Published: September 18, 2017

Duplication 2p25 in a child with clinical features of CHARGE syndrome.

Duplication 2p25 in a child with clinical features of CHARGE syndrome.

Journal: American journal of medical genetics. Part A

Published: December 17, 2015

Chromodomain helicase DNA-binding proteins in stem cells and human developmental diseases.

Chromodomain helicase DNA-binding proteins in stem cells and human developmental diseases.

Journal: Stem cells and development

Published: January 09, 2015

The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.

The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development.

Journal: Developmental dynamics : an official publication of the American Association of Anatomists

Published: April 04, 2014

CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.

CHD7 and retinoic acid signaling cooperate to regulate neural stem cell and inner ear development in mouse models of CHARGE syndrome.

Journal: Human molecular genetics

Published: September 13, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026