Thomas M. Maynard - Publications

George Washington University, Washington, DC, United States 
22q11 Deletion Syndrome, cortical development, neural crest

22 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Fernandez A, Meechan DW, Karpinski BA, Paronett EM, Bryan CA, Rutz HL, Radin EA, Lubin N, Bonner ER, Popratiloff A, Rothblat LA, Maynard TM, LaMantia AS. Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment. Neuron. PMID 31079872 DOI: 10.1016/j.neuron.2019.04.013  1
2017 Sherman JH, Karpinski BA, Fralish MS, Cappuzzo JM, Dhindsa DS, Thal AG, Moody SA, LaMantia AS, Maynard TM. Foxd4 is essential for establishing neural cell fate and for neuronal differentiation. Genesis (New York, N.Y. : 2000). PMID 28316121 DOI: 10.1002/dvg.23031  1
2017 Maynard TM, Manzini MC. Balancing Act: Maintaining Amino Acid Levels in the Autistic Brain. Neuron. 93: 476-479. PMID 28182903 DOI: 10.1016/j.neuron.2017.01.015  0.32
2016 Gaur S, Mandelbaum M, Herold M, Majumdar HD, Neilson KM, Maynard TM, Mood K, Daar IO, Moody SA. Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm. Genesis (New York, N.Y. : 2000). PMID 27092474 DOI: 10.1002/dvg.22943  1
2016 Baker JL, Dunn K, Mingrone J, Wood BA, Karpinski BA, Sherwood CC, Wildman DE, Maynard TM, Bielawski JP. Functional Divergence of the Nuclear Receptor NR2C1 as a Modulator of Pluripotentiality During Hominid Evolution. Genetics. PMID 27075724 DOI: 10.1534/genetics.115.183889  1
2016 Tapocik JD, Ceniccola K, Mayo CL, Schwandt ML, Solomon M, Wang BD, Luu TV, Olender J, Harrigan T, Maynard TM, Elmer GI, Lee NH. MicroRNAs Are Involved in the Development of Morphine-Induced Analgesic Tolerance and Regulate Functionally Relevant Changes in Serpini1. Frontiers in Molecular Neuroscience. 9: 20. PMID 27047334 DOI: 10.3389/fnmol.2016.00020  1
2016 Karpinski BA, Bryan C, Paronett E, Baker J, Fernandez A, Horvath A, Maynard TM, Moody SA, LaMantia AS. A cellular and molecular mosaic establishes growth and differentiation states for cranial sensory neurons. Developmental Biology. PMID 26988119 DOI: 10.1016/j.ydbio.2016.03.015  1
2015 Baker JL, Wood B, Karpinski BA, LaMantia AS, Maynard TM. Testicular receptor 2, Nr2c1, is associated with stem cells in the developing olfactory epithelium and other cranial sensory and skeletal structures. Gene Expression Patterns : Gep. PMID 26712358 DOI: 10.1016/j.gep.2015.12.002  1
2015 LaMantia AS, Moody SA, Maynard T, Karpinski BA, Zohn I, Mendelowitz D, Lee NH, Popratiloff A. Hard to Swallow: Developmental Biological Insights into Pediatric Dysphagia. Developmental Biology. PMID 26554723 DOI: 10.1016/j.ydbio.2015.09.024  1
2015 Meechan DW, Maynard TM, Tucker ES, Fernandez A, Karpinski BA, Rothblat LA, LaMantia AS. Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development. Progress in Neurobiology. 130: 1-28. PMID 25866365 DOI: 10.1016/j.pneurobio.2015.03.004  1
2014 Paronett EM, Meechan DW, Karpinski BA, LaMantia AS, Maynard TM. Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation. Cerebral Cortex (New York, N.Y. : 1991). PMID 25452572 DOI: 10.1093/cercor/bhu285  1
2014 Karpinski BA, Maynard TM, Fralish MS, Nuwayhid S, Zohn IE, Moody SA, LaMantia AS. Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome. Disease Models & Mechanisms. 7: 245-57. PMID 24357327 DOI: 10.1242/dmm.012484  1
2013 Moody SA, Klein SL, Karpinski BA, Maynard TM, Lamantia AS. On becoming neural: what the embryo can tell us about differentiating neural stem cells. American Journal of Stem Cells. 2: 74-94. PMID 23862097  1
2013 Maynard TM, Gopalakrishna D, Meechan DW, Paronett EM, Newbern JM, LaMantia AS. 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development. Human Molecular Genetics. 22: 300-12. PMID 23077214 DOI: 10.1093/hmg/dds429  1
2012 Meechan DW, Tucker ES, Maynard TM, LaMantia AS. Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome. Proceedings of the National Academy of Sciences of the United States of America. 109: 18601-6. PMID 23091025 DOI: 10.1073/pnas.1211507109  1
2012 Manzini MC, Tambunan DE, Hill RS, Yu TW, Maynard TM, Heinzen EL, Shianna KV, Stevens CR, Partlow JN, Barry BJ, Rodriguez J, Gupta VA, Al-Qudah AK, Eyaid WM, Friedman JM, et al. Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome. American Journal of Human Genetics. 91: 541-7. PMID 22958903 DOI: 10.1016/j.ajhg.2012.07.009  1
2010 Manzini MC, Rajab A, Maynard TM, Mochida GH, Tan WH, Nasir R, Hill RS, Gleason D, Al Saffar M, Partlow JN, Barry BJ, Vernon M, LaMantia AS, Walsh CA. Developmental and degenerative features in a complicated spastic paraplegia. Annals of Neurology. 67: 516-25. PMID 20437587 DOI: 10.1002/ana.21923  1
2009 Meechan DW, Tucker ES, Maynard TM, LaMantia AS. Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome. Proceedings of the National Academy of Sciences of the United States of America. 106: 16434-45. PMID 19805316 DOI: 10.1073/pnas.0905696106  1
2006 Maynard TM, Meechan DW, Heindel CC, Peters AZ, Hamer RM, Lieberman JA, LaMantia AS. No evidence for parental imprinting of mouse 22q11 gene orthologs. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 822-32. PMID 16897343 DOI: 10.1007/s00335-006-0011-0  1
2002 Maynard TM, Haskell GT, Lieberman JA, LaMantia AS. 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 20: 407-19. PMID 12175881 DOI: 10.1016/S0736-5748(02)00050-3  1
2002 Maynard TM, Haskell GT, Bhasin N, Lee JM, Gassman AA, Lieberman JA, LaMantia AS. RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction. Mechanisms of Development. 111: 177-80. PMID 11804793 DOI: 10.1016/S0925-4773(01)00616-5  1
2002 Maynard TM, Jain MD, Balmer CW, LaMantia AS. High-resolution mapping of the Gli3 mutation extra-toes reveals a 51.5-kb deletion. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 13: 58-61. PMID 11773971 DOI: 10.1007/s00335-001-2115-X  1
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