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Molecular Genetics & Genomic Medicine|November 30, 2016
A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2AGuoling Tian, Ana G Cristancho, Holly A Dubbs, et al.
STAR Protocols|August 17, 2021
Protocol for isolating young adult parvalbumin interneurons from the mouse brain for extraction of high-quality RNADonald J Joseph, Markus Von Deimling, Yuiko Hasegawa, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 4, 2021
An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypesTal Yardeni, Ana G Cristancho, Almedia J McCoy, et al.
Journal of Child Neurology|June 23, 2025
Agenesis of Corpus Callosum: A Clinical Study of Complete Versus Partial Agenesis in a 20-Year Retrospective CohortRudmila Rashid, Ashley Bach, Juliana Gebb, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 2011
Repressor transcription factor 7-like 1 promotes adipogenic competency in precursor cellsAna G Cristancho, Michael Schupp, Martina I Lefterova, et al.
Iscience|January 25, 2021
Postnatal Arx transcriptional activity regulates functional properties of PV interneuronsDonald J Joseph, Markus Von Deimling, Yuiko Hasegawa, et al.
Developmental Neuroscience|March 13, 2022
Deficits in Seizure Threshold and Other Behaviors in Adult Mice without Gross Neuroanatomic Injury after Late Gestation Transient Prenatal HypoxiaAna G Cristancho, Elyse C Gadra, Ima M Samba, et al.
Biorxiv : the Preprint Server for Biology|December 15, 2025
Chromatin Disruption After Prenatal Hypoxia Predicts Lasting Neuron DeficitsAna G Cristancho, Donald J Joseph, Margaret M Cassidy, et al.
Clinical Genetics|September 8, 2022
Six new cases of CRB2-related syndrome and a review of clinical findings in 28 reported patientsMichelle Adutwum, Anna Hurst, Ghayda Mirzaa, et al.
Plos One|August 6, 2025
DNA methylation differences stratified by normalized fetal/placental weight ratios suggest neurodevelopmental deficits in neonates with congenital heart diseaseMarin Jacobwitz, Michael Xie, Jamie Catalano, et al.
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