All Stories

  1. Distinct cellular and transcriptional mechanisms mediate an antioxidant therapeutic response in 22q11-deleted upper layer cortical projection neurons

    Article • December 2025, openRxiv

    Dr Thomas M Maynard

  2. 22q11 deletion selectively alters progenitor states and projection neuron identities in the developing cerebral cortex

    Article • May 2025, Springer Science + Business Media

    Dr Thomas M Maynard

  3. 22q11 deletion selectively alters progenitor states and projection neuron identities in the developing cerebral cortex

    Article • May 2025, Cold Spring Harbor Laboratory Press

    Dr Thomas M Maynard

  4. Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder

    Article • Developmental Neuroscience, May 2023, Karger Publishers

    Dr Thomas M Maynard

  5. Identity, lineage and fates of a temporally distinct progenitor population in the embryonic olfactory epithelium

    Article • Developmental Biology, March 2023, Elsevier

    Dr Thomas M Maynard

  6. Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome

    Article • Human Molecular Genetics, February 2023, Oxford University Press (OUP)

    Dr Thomas M Maynard

  7. Lineage, Identity, and Fate of Distinct Progenitor Populations in the Embryonic Olfactory Epithelium

    Article • October 2021, Cold Spring Harbor Laboratory Press

    Dr Thomas M Maynard

  8. Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome

    Article • Disease Models & Mechanisms, May 2021, The Company of Biologists

    Dr Thomas M Maynard

  9. Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome

    Article • Human Molecular Genetics, September 2020, Oxford University Press (OUP)

    Dr Thomas M Maynard

  10. Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome

    Article • Birth Defects Research, May 2020, Wiley

    Dr Thomas M Maynard

  11. Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology

    Article • Annual Review of Neuroscience, February 2020, Annual Reviews

    Dr Thomas M Maynard

  12. Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome

    Article • Human Molecular Genetics, February 2020, Oxford University Press (OUP)

    Dr Thomas M Maynard

  13. Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome

    Article • Frontiers in Neurology, January 2020, Frontiers

    Dr Thomas M Maynard

  14. In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?

    Article • Journal of Neurodevelopmental Disorders, June 2019, Springer Science + Business Media

    Dr Thomas M Maynard

  15. Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment

    Article • Neuron, May 2019, Elsevier

    Dr Thomas M Maynard

  16. Foxd4 is essential for establishing neural cell fate and for neuronal differentiation

    Article • genesis, April 2017, Wiley

    Dr Thomas M Maynard

  17. Oxidative stress-driven parvalbumin interneuron impairment as a common mechanism in models of schizophrenia

    Article • Molecular Psychiatry, March 2017, Nature

    Dr Thomas M Maynard

  18. Balancing Act: Maintaining Amino Acid Levels in the Autistic Brain

    Article • Neuron, February 2017, Elsevier

    Dr Thomas M Maynard

  19. A cellular and molecular mosaic establishes growth and differentiation states for cranial sensory neurons

    Article • Developmental Biology, July 2016, Elsevier

    Dr Thomas M Maynard

  20. Functional Divergence of the Nuclear Receptor NR2C1 as a Modulator of Pluripotentiality During Hominid Evolution

    Article • Genetics, June 2016, Genetics Society of America

    Dr Thomas M Maynard

  21. Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm

    Article • genesis, May 2016, Wiley

    Dr Thomas M Maynard

  22. MicroRNAs Are Involved in the Development of Morphine-Induced Analgesic Tolerance and Regulate Functionally Relevant Changes in Serpini1

    Article • Frontiers in Molecular Neuroscience, March 2016, Frontiers

    Dr Thomas M Maynard

  23. Hard to swallow: Developmental biological insights into pediatric dysphagia

    Article • Developmental Biology, January 2016, Elsevier

    Dr Thomas M Maynard

  24. Testicular receptor 2, Nr2c1, is associated with stem cells in the developing olfactory epithelium and other cranial sensory and skeletal structures

    Article • Gene Expression Patterns, January 2016, Elsevier

    Dr Thomas M Maynard

  25. Progressive Differentiation and Instructive Capacities of Amniotic Fluid and Cerebrospinal Fluid Proteomes following Neural Tube Closure

    Article • Developmental Cell, December 2015, Elsevier

    Dr Thomas M Maynard

  26. Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development

    Article • Progress in Neurobiology, July 2015, Elsevier

    Dr Thomas M Maynard

  27. 22q11 Deletion Syndrome

    Article • January 2015, Elsevier

    Dr Thomas M Maynard

  28. Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development

    Article • Developmental Dynamics, December 2014, Wiley

    Dr Thomas M Maynard

  29. Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation

    Article • Cerebral Cortex, December 2014, Oxford University Press (OUP)

    Dr Thomas M Maynard

  30. Hectd1 is required for development of the junctional zone of the placenta

    Article • Developmental Biology, August 2014, Elsevier

    Dr Thomas M Maynard

  31. Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome

    Article • Disease Models & Mechanisms, December 2013, The Company of Biologists

    Dr Thomas M Maynard

  32. Cognitive Ability is Associated with Altered Medial Frontal Cortical Circuits in the LgDel Mouse Model of 22q11.2DS

    Article • Cerebral Cortex, November 2013, Oxford University Press (OUP)

    Dr Thomas M Maynard

  33. 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development

    Article • Human Molecular Genetics, October 2012, Oxford University Press (OUP)

    Dr Thomas M Maynard

  34. Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome

    Article • Proceedings of the National Academy of Sciences, October 2012, Proceedings of the National Academy of Sciences

    Dr Thomas M Maynard

  35. Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome

    Article • The American Journal of Human Genetics, September 2012, Elsevier

    Dr Thomas M Maynard

  36. Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: Patterning, proliferation, and mitochondrial functions of 22q11 genes

    Article • International Journal of Developmental Neuroscience, May 2011, Elsevier

    Dr Thomas M Maynard

  37. The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells

    Article • Neuron, March 2011, Elsevier

    Dr Thomas M Maynard

  38. Comt1 genotype and expression predicts anxiety and nociceptive sensitivity in inbred strains of mice

    Article • Genes Brain & Behavior, November 2010, Wiley

    Dr Thomas M Maynard

  39. Proliferative and transcriptional identity of distinct classes of neural precursors in the mammalian olfactory epithelium

    Article • Development, June 2010, The Company of Biologists

    Dr Thomas M Maynard

  40. Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotropin-releasing hormone (GnRH) neurons

    Article • Developmental Dynamics, May 2010, Wiley

    Dr Thomas M Maynard

  41. Developmental and degenerative features in a complicated spastic paraplegia

    Article • Annals of Neurology, November 2009, Wiley

    Dr Thomas M Maynard

  42. Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome

    Article • Proceedings of the National Academy of Sciences, September 2009, Proceedings of the National Academy of Sciences

    Dr Thomas M Maynard

  43. Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes

    Article • Molecular and Cellular Neuroscience, October 2008, Elsevier

    Dr Thomas M Maynard

  44. Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome

    Article • Molecular and Cellular Neuroscience, December 2006, Elsevier

    Dr Thomas M Maynard

  45. No evidence for parental imprinting of mouse 22q11 gene orthologs

    Article • Mammalian Genome, August 2006, Springer Science + Business Media

    Dr Thomas M Maynard

  46. When Half Is Not Enough: Gene Expression and Dosage in the 22q11 Deletion Syndrome

    Article • Gene Expression, June 2006, Xia & He Publishing

    Dr Thomas M Maynard

  47. Limited influence of olanzapine on adult forebrain neural precursors in vitro

    Article • Neuroscience, January 2006, Elsevier

    Dr Thomas M Maynard

  48. A comprehensive analysis of 22q11 gene expression in the developing and adult brain

    Article • Proceedings of the National Academy of Sciences, November 2003, Proceedings of the National Academy of Sciences

    Dr Thomas M Maynard

  49. Mesenchymal/epithelial regulation of retinoic acid signaling in the olfactory placode

    Article • Developmental Biology, September 2003, Elsevier

    Dr Thomas M Maynard

  50. Retinoic acid signaling at sites of plasticity in the mature central nervous system

    Article • The Journal of Comparative Neurology, September 2002, Wiley

    Dr Thomas M Maynard

  51. 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome

    Article • International Journal of Developmental Neuroscience, June 2002, Elsevier

    Dr Thomas M Maynard

  52. RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction

    Article • Mechanisms of Development, February 2002, Elsevier

    Dr Thomas M Maynard

  53. High-resolution mapping of the Gli3 mutation Extra-toesJ reveals a 51.5-kb deletion

    Article • Mammalian Genome, January 2002, Springer Science + Business Media

    Dr Thomas M Maynard

  54. Neural Development, Cell-Cell Signaling, and the "Two-Hit" Hypothesis of Schizophrenia

    Article • Schizophrenia Bulletin, January 2001, Oxford University Press (OUP)

    Dr Thomas M Maynard

  55. Avian transitin expression mirrors glial cell fate restrictions during neural crest development

    Article • Developmental Dynamics, May 2000, Wiley

    Dr Thomas M Maynard

  56. NUMB Localizes in the Basal Cortex of Mitotic Avian Neuroepithelial Cells and Modulates Neuronal Differentiation by Binding to NOTCH-1

    Article • Neuron, May 1999, Elsevier

    Dr Thomas M Maynard

  57. Glial domains and axonal reordering in the chiasmatic region of the developing ferret

    Article • The Journal of Comparative Neurology, November 1994, Wiley

    Dr Thomas M Maynard