Publications by authors named "Christopher Simotas"

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Homozygous variants in EIF3K associated with neurodevelopmental delay, microcephaly, and growth retardation.
Bobbi McGivern, Tess Holling, Maria J Guillen Sacoto, Hákon Gudbjartsson, Ibrahim M Abdelrazek, Christopher Simotas

HGG Adv· July 2025

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Flow interruption compared to forced oscillatory maneuvers and esophageal balloon/pneumotachography for measurement of respiratory resistance in the horse.
Melissa R Mazan, Christopher Simotas, Thomas Coons, Brian Barrow, Daniela Bedenice

J Appl Physiol (1985)· September 2024

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Autosomal Recessive Infantile Hyaline Fibromatosis Identified Using Artificial Intelligence-Assisted Rapid Whole Genome Sequencing: A Rare, Multisystemic, Hereditary Disorder.
George X Ye, Eric Ontiveros, Axel Ivander, Milen Velinov, Christopher Simotas

Cureus· June 2024

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Haploinsufficiency of the basic helix-loop-helix transcription factor HAND2 causes congenital heart defects.
Ana S A Cohen, Christopher Simotas, Bryn D Webb, Huanzhi Shi, Wahab A Khan

Am J Med Genet A· May 2020

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