| Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome DW Meechan, ES Tucker, TM Maynard, AS LaMantia Proceedings of the National Academy of Sciences 106 (38), 16434-16445, 2009 | 182 | 2009 |
| Mitochondrial dysfunction leads to cortical under-connectivity and cognitive impairment A Fernandez, DW Meechan, BA Karpinski, EM Paronett, CA Bryan, ... Neuron 102 (6), 1127-1142. e3, 2019 | 129 | 2019 |
| Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes TM Maynard, DW Meechan, ML Dudevoir, D Gopalakrishna, AZ Peters, ... Molecular and Cellular Neuroscience 39 (3), 439-451, 2008 | 114 | 2008 |
| Cxcr4 regulation of interneuron migration is disrupted in 22q11. 2 deletion syndrome DW Meechan, ES Tucker, TM Maynard, AS LaMantia Proceedings of the National Academy of Sciences 109 (45), 18601-18606, 2012 | 110 | 2012 |
| Modeling a model: Mouse genetics, 22q11. 2 Deletion Syndrome, and disorders of cortical circuit development DW Meechan, TM Maynard, ES Tucker, A Fernandez, BA Karpinski, ... Progress in neurobiology 130, 1-28, 2015 | 97 | 2015 |
| When half is not enough: gene expression and dosage in the 22q11 deletion syndrome DW Meechan, TM Maynard, D Gopalakrishna, Y Wu, AS LaMantia Gene expression 13 (6), 299, 2007 | 79 | 2007 |
| Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes DW Meechan, TM Maynard, ES Tucker, AS LaMantia International Journal of Developmental Neuroscience 29 (3), 283-294, 2011 | 76 | 2011 |
| Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation EM Paronett, DW Meechan, BA Karpinski, AS LaMantia, TM Maynard Cerebral cortex 25 (10), 3977-3993, 2015 | 54 | 2015 |
| Cognitive Ability is Associated with Altered Medial Frontal Cortical Circuits in the LgDel Mouse Model of 22q11.2DS DW Meechan, HLH Rutz, MS Fralish, TM Maynard, LA Rothblat, ... Cerebral cortex 25 (5), 1143-1151, 2015 | 51 | 2015 |
| Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome DW Meechan, TM Maynard, Y Wu, D Gopalakrishna, JA Lieberman, ... Molecular and Cellular Neuroscience 33 (4), 412-428, 2006 | 44 | 2006 |
| 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development TM Maynard, D Gopalakrishna, DW Meechan, EM Paronett, JM Newbern, ... Human molecular genetics 22 (2), 300-312, 2013 | 41 | 2013 |
| Cortical interneurons require Jnk1 to enter and navigate the developing cerebral cortex AK Myers, DW Meechan, DR Adney, ES Tucker Journal of Neuroscience 34 (23), 7787-7801, 2014 | 36 | 2014 |
| Single nucleotide polymorphisms in the leptin receptor gene: studies in anorexia nervosa ND Quinton, DW Meechan, K Brown, H Eastwood, AIF Blakemore Psychiatric Genetics 14 (4), 191-194, 2004 | 33 | 2004 |
| Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotropin‐releasing hormone (GnRH) neurons NE Rawson, FW Lischka, KK Yee, AZ Peters, ES Tucker, DW Meechan, ... Developmental Dynamics 239 (6), 1723-1738, 2010 | 19 | 2010 |
| Limited influence of olanzapine on adult forebrain neural precursors in vitro JH Councill, ES Tucker, GT Haskell, TM Maynard, DW Meechan, ... Neuroscience 140 (1), 111-122, 2006 | 17 | 2006 |
| No evidence for parental imprinting of mouse 22q11 gene orthologs TM Maynard, DW Meechan, CC Heindel, AZ Peters, RM Hamer, ... Mammalian genome 17, 822-832, 2006 | 8 | 2006 |
| 22q11 deletion syndrome: copy number variations and development A Fernandez, D Meechan, JL Baker, BA Karpinski, AS LaMantia, ... Principles of Developmental Genetics, 677-696, 2015 | 5 | 2015 |
| Out of Line or Altered States? Neural Progenitors as a Target in a Polygenic Neurodevelopmental Disorder SRDWM Thomas, M Maynarda, AS LaMantiaa Dev Neurosci 46, 1-21, 2024 | | 2024 |
| Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome EM Paronett, CA Bryan, ME Maynard, JA Goroff, DW Meechan, ... Human Molecular Genetics 32 (12), 1959-1974, 2023 | | 2023 |
| Perspectives on Neuroscience and Behavior A Fernandez, DW Meechan, BA Karpinski, EM Paronett, CA Bryan, ... pain 22 (10), 1649-58, 2020 | | 2020 |
Thomas MaynardVirginia Tech Carilion, Fralin Biomedical Research InstituteVerified email at vtc.vt.edu
