Thomas M. Maynard

Biomedical Research Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

34h-index4.5kcitations85works0.32yr avg
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Research Topics

Congenital heart defects research(42), Developmental Biology and Gene Regulation(11), Olfactory and Sensory Function Studies(9), Congenital Heart Disease Studies(8), Neurogenesis and neuroplasticity mechanisms(8)

Publications84 total

Distinct cellular and transcriptional mechanisms mediate an antioxidant therapeutic response in 22q11-deleted upper layer cortical projection neurons
2025Open Access
22q11 deletion selectively alters progenitor states and projection neuron identities in the developing cerebral cortex
2025Open Access
22q11 deletion selectively alters progenitor states and projection neuron identities in the developing cerebral cortex
2025· 1 citedOpen Access
Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder
Developmental Neuroscience·2023· 2 citedOpen Access
<i>Ranbp1</i>modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome
Human Molecular Genetics·2023· 4 citedOpen Access
Identity, lineage and fates of a temporally distinct progenitor population in the embryonic olfactory epithelium
Developmental Biology·2023· 4 citedOpen Access
184 Managing vitamin D supplementation in elite academy footballers
Poster presentations·2021Open Access
RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction
UNC Libraries·2021Open Access
Lineage, Identity, and Fate of Distinct Progenitor Populations in the Embryonic Olfactory Epithelium
2021Open Access
Mesenchymal/epithelial regulation of retinoic acid signaling in the olfactory placode
UNC Libraries·2021Open Access
Development and implementation of a scalable and versatile test for COVID-19 diagnostics in rural communities
Nature Communications·2021· 20 citedOpen Access
Proliferative and transcriptional identity of distinct classes of neural precursors in the mammalian olfactory epithelium
UNC Libraries·2021Open Access
Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome
Disease Models & Mechanisms·2021· 14 citedOpen Access
Development and Implementation of a scalable and versatile test for COVID-19 diagnostics in rural communities
2021· 2 citedOpen Access
Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
UNC Libraries·2020· 7 citedOpen Access
The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells
UNC Libraries·2020Open Access
No evidence for parental imprinting of mouse 22q11 gene orthologues
UNC Libraries·2020Open Access
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development
UNC Libraries·2020· 1 citedOpen Access
Developmental and degenerative features in a complicated spastic paraplegia
UNC Libraries·2020Open Access
Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome
Human Molecular Genetics·2020· 7 citedOpen Access
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Frequent Co-authors

Anthony‐Samuel LaMantia(23), Daniel W. Meechan(12), Beverly A. Karpinski(11), Sally A. Moody(11), Eric S. Tucker(7), Irene E. Zohn(6), Gloria Haskell(5), Jeffrey A. Lieberman(5), Anthony S. LaMantia(4), James A. Weston(4), Elizabeth M. Paronett(4), Norman H. Lee(4), Maria K. Lehtinen(3), Christopher A. Walsh(3), Yoshio Wakamatsu(3), M. Chiara Manzini(3), Alejandra Fernandez(3), Corey A. Bryan(3), Lawrence A. Rothblat(3), Amanda Z. Peters(3)