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The Journal of Pediatrics|June 3, 2023
Rapid Genome Sequencing Diagnosis in Pediatric Patients with Liver DysfunctionDanielle Bonser, Sabrina Malone Jenkins, Rachel Palmquist, et al.
The Journal of Clinical Investigation|March 10, 2021
Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophyQuentin Raas, Malu-Clair van de Beek, Sonja Forss-Petter, et al.
Epilepsia Open|October 28, 2024
Factors impacting time to genetic diagnosis for children with epilepsyMegan Rimmasch, Carey A Wilson, Nephi A Walton, et al.
Pediatric Neurology|November 23, 2022
SARS-CoV-2 Infection and Increased Risk for Pediatric StrokeMaryGlen J Vielleux, Shanna Swartwood, Dan Nguyen, et al.
Eneuro|February 1, 2020
Dopaminergic Co-Regulation of Locomotor Development and Motor Neuron Synaptogenesis is Uncoupled by Hypoxia in ZebrafishJong-Hyun Son, Tamara J Stevenson, Miranda D Bowles, et al.
BMC Genomics|May 6, 2016
Temporal Dysynchrony in brain connectivity gene expression following hypoxiaBrett Milash, Jingxia Gao, Tamara J Stevenson, et al.
HGG Advances|January 20, 2022
Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological diseaseAlexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Biomedical Microdevices|March 17, 2015
Microfluidic-aided genotyping of zebrafish in the first 48 h with 100% viabilityRaheel Samuel, Regan Stephenson, Paula Roy, et al.
The Journal of Pediatrics|October 17, 2012
Determinants of health care use in a population-based leukodystrophy cohortClint Nelson, Michael B Mundorff, E Kent Korgenski, et al.
BMC Developmental Biology|October 28, 2008
Domain-specific regulation of foxP2 CNS expression by lef1Joshua L Bonkowsky, Xu Wang, Esther Fujimoto, et al.
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