Publications by authors named "Devon Knight"

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IKZF3/Aiolos H195Y mutation identified in a mouse model of B cell leukemia results in altered DNA binding and altered STAT5-dependent gene expression.
Bruno Rodrigues de Oliveira, James Iansavitchous, Heidi Rysan, Wei Cen Wang, Mia P Sams, Devon Knight

Gene· March 2024

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Ezogabine impacts seizures and development in patients with KCNQ2 developmental and epileptic encephalopathy.
Devon Knight, Sonal Mahida, Mckenna Kelly, Annapurna Poduri, Heather E Olson

Epilepsia· July 2023

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Utility of Exome Sequencing for Diagnosis in Unexplained Pediatric-Onset Epilepsy.
Hyun Yong Koh, Lacey Smith, Kimberly N Wiltrout, Archana Podury, Nitish Chourasia, Devon Knight

JAMA Netw Open· July 2023

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The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2.
Abbe Lai, Aubrie Soucy, Christelle Moufawad El Achkar, Anthony J Barkovich, Yang Cao, Devon Knight

Genet Med· November 2022

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A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy.
Min Ni, Bushra Afroze, Chao Xing, Chunxiao Pan, Yanqiu Shao, Devon Knight

Genet Med· May 2021

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Janus Kinase Mutations in Mice Lacking PU.1 and Spi-B Drive B Cell Leukemia through Reactive Oxygen Species-Induced DNA Damage.
Michelle Lim, Carolina R Batista, Bruno R de Oliveira, Rachel Creighton, Jacob Ferguson, Devon Knight

Mol Cell Biol· August 2020

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Children's rare disease cohorts: an integrative research and clinical genomics initiative.
Shira Rockowitz, Nicholas LeCompte, Mary Carmack, Andrew Quitadamo, Lily Wang, Devon Knight

NPJ Genom Med· July 2020

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