| Year |
Citation |
Score |
| 2023 |
Rukh S, Meechan DW, Maynard TM, Lamantia AS. Out of Line or Altered States? Neural Progenitors as a target in a Polygenic Neurodevelopmental Disorder. Developmental Neuroscience. 1. PMID 37231803 DOI: 10.1159/000530898 |
0.313 |
|
| 2023 |
Paronett EM, Bryan CA, Maynard ME, Goroff JA, Meechan DW, LaMantia AS, Maynard TM. Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome. Human Molecular Genetics. PMID 36790128 DOI: 10.1093/hmg/ddad030 |
0.42 |
|
| 2021 |
Karpinski BA, Maynard TM, Bryan CA, Yitsege G, Horvath A, Lee NH, Moody SA, LaMantia AS. Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome. Disease Models & Mechanisms. PMID 33722956 DOI: 10.1242/dmm.047357 |
0.411 |
|
| 2020 |
Motahari Z, Maynard TM, Popratiloff A, Moody SA, LaMantia AS. 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. PMID 32901287 DOI: 10.1093/Hmg/Ddaa199 |
0.631 |
|
| 2020 |
Yitsege G, Stokes BA, Sabatino JA, Sugrue KF, Banyai G, Paronett EM, Karpinski BA, Maynard TM, LaMantia AS, Zohn IE. Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome. Birth Defects Research. PMID 32431076 DOI: 10.1002/bdr2.1709 |
0.616 |
|
| 2020 |
Maynard TM, Horvath A, Bernot JP, Karpinski BA, Tavares ALP, Shah A, Zheng Q, Spurr L, Olender J, Moody SA, Fraser CM, LaMantia AS, Lee NH. Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome. Human Molecular Genetics. PMID 32358605 DOI: 10.1093/hmg/ddaa067 |
0.674 |
|
| 2020 |
Maynard TM, Zohn IE, Moody SA, LaMantia AS. Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology. Annual Review of Neuroscience. PMID 32101484 DOI: 10.1146/Annurev-Neuro-100419-100636 |
0.587 |
|
| 2020 |
Maynard TM, Horvath A, Bernout J, Karpinski BA, Tavares ALP, Shah A, Zheng Q, Spurr L, Olender J, Moody SA, Fraser CM, LaMantia AS, Lee NH. Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 Deletion Syndrome. Human Molecular Genetics. PMID 32047912 DOI: 10.1093/Hmg/Ddaa024 |
0.73 |
|
| 2019 |
Motahari Z, Moody SA, Maynard TM, LaMantia AS. In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects? Journal of Neurodevelopmental Disorders. 11: 7. PMID 31174463 DOI: 10.1186/S11689-019-9267-Z |
0.433 |
|
| 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 |
0.366 |
|
| 2017 |
Steullet P, Cabungcal JH, Coyle J, Didriksen M, Gill K, Grace AA, Hensch TK, LaMantia AS, Lindemann L, Maynard TM, Meyer U, Morishita H, O'Donnell P, Puhl M, Cuenod M, et al. Oxidative stress-driven parvalbumin interneuron impairment as a common mechanism in models of schizophrenia. Molecular Psychiatry. PMID 28322275 DOI: 10.1038/Mp.2017.47 |
0.306 |
|
| 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 |
0.674 |
|
| 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 |
0.391 |
|
| 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 |
0.36 |
|
| 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 |
0.669 |
|
| 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 |
0.668 |
|
| 2015 |
Chau KF, Springel MW, Broadbelt KG, Park HY, Topal S, Lun MP, Mullan H, Maynard T, Steen H, LaMantia AS, Lehtinen MK. Progressive Differentiation and Instructive Capacities of Amniotic Fluid and Cerebrospinal Fluid Proteomes following Neural Tube Closure. Developmental Cell. 35: 789-802. PMID 26702835 DOI: 10.1016/J.Devcel.2015.11.015 |
0.619 |
|
| 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 |
0.667 |
|
| 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 |
0.776 |
|
| 2015 |
Yan B, Neilson KM, Ranganathan R, Maynard T, Streit A, Moody SA. Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 244: 181-210. PMID 25403746 DOI: 10.1002/Dvdy.24229 |
0.394 |
|
| 2015 |
Meechan DW, Rutz HL, Fralish MS, Maynard TM, Rothblat LA, LaMantia AS. Cognitive ability is associated with altered medial frontal cortical circuits in the LgDel mouse model of 22q11.2DS. Cerebral Cortex (New York, N.Y. : 1991). 25: 1143-51. PMID 24217989 DOI: 10.1093/Cercor/Bht308 |
0.663 |
|
| 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 |
0.725 |
|
| 2014 |
Sarkar AA, Nuwayhid SJ, Maynard T, Ghandchi F, Hill JT, Lamantia AS, Zohn IE. Hectd1 is required for development of the junctional zone of the placenta. Developmental Biology. 392: 368-80. PMID 24855001 DOI: 10.1016/J.Ydbio.2014.05.007 |
0.64 |
|
| 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 |
0.727 |
|
| 2014 |
Fernandez A, Meechan D, Baker JL, Karpinski BA, LaMantia AS, Maynard TM. 22q11 Deletion Syndrome: Copy Number Variations and Development. Principles of Developmental Genetics: Second Edition. 677-696. DOI: 10.1016/B978-0-12-405945-0.00036-3 |
0.652 |
|
| 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 |
0.633 |
|
| 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 |
0.79 |
|
| 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 |
0.809 |
|
| 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 |
0.346 |
|
| 2011 |
Lehtinen MK, Zappaterra MW, Chen X, Yang YJ, Hill AD, Lun M, Maynard T, Gonzalez D, Kim S, Ye P, D'Ercole AJ, Wong ET, LaMantia AS, Walsh CA. The cerebrospinal fluid provides a proliferative niche for neural progenitor cells. Neuron. 69: 893-905. PMID 21382550 DOI: 10.1016/J.Neuron.2011.01.023 |
0.617 |
|
| 2011 |
Meechan DW, Maynard TM, Tucker ES, LaMantia AS. Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 29: 283-94. PMID 20833244 DOI: 10.1016/J.Ijdevneu.2010.08.005 |
0.823 |
|
| 2010 |
Segall SK, Nackley AG, Diatchenko L, Lariviere WR, Lu X, Marron JS, Grabowski-Boase L, Walker JR, Slade G, Gauthier J, Bailey JS, Steffy BM, Maynard TM, Tarantino LM, Wiltshire T. Comt1 genotype and expression predicts anxiety and nociceptive sensitivity in inbred strains of mice. Genes, Brain, and Behavior. 9: 933-46. PMID 20659173 DOI: 10.1111/J.1601-183X.2010.00633.X |
0.336 |
|
| 2010 |
Tucker ES, Lehtinen MK, Maynard T, Zirlinger M, Dulac C, Rawson N, Pevny L, Lamantia AS. Proliferative and transcriptional identity of distinct classes of neural precursors in the mammalian olfactory epithelium. Development (Cambridge, England). 137: 2471-81. PMID 20573694 DOI: 10.1242/Dev.049718 |
0.775 |
|
| 2010 |
Rawson NE, Lischka FW, Yee KK, Peters AZ, Tucker ES, Meechan DW, Zirlinger M, Maynard TM, Burd GB, Dulac C, Pevny L, LaMantia AS. Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotropin-releasing hormone (GnRH) neurons. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 1723-38. PMID 20503368 DOI: 10.1002/Dvdy.22315 |
0.757 |
|
| 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 |
0.679 |
|
| 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 |
0.815 |
|
| 2008 |
Maynard TM, Meechan DW, Dudevoir ML, Gopalakrishna D, Peters AZ, Heindel CC, Sugimoto TJ, Wu Y, Lieberman JA, Lamantia AS. Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes. Molecular and Cellular Neurosciences. 39: 439-51. PMID 18775783 DOI: 10.1016/J.Mcn.2008.07.027 |
0.803 |
|
| 2007 |
Meechan DW, Maynard TM, Gopalakrishna D, Wu Y, LaMantia AS. When half is not enough: gene expression and dosage in the 22q11 deletion syndrome. Gene Expression. 13: 299-310. PMID 17708416 DOI: 10.3727/000000006781510697 |
0.82 |
|
| 2006 |
Meechan DW, Maynard TM, Wu Y, Gopalakrishna D, Lieberman JA, LaMantia AS. Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome. Molecular and Cellular Neurosciences. 33: 412-28. PMID 17097888 DOI: 10.1016/J.Mcn.2006.09.001 |
0.825 |
|
| 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 |
0.708 |
|
| 2006 |
Councill JH, Tucker ES, Haskell GT, Maynard TM, Meechan DW, Hamer RM, Lieberman JA, LaMantia AS. Limited influence of olanzapine on adult forebrain neural precursors in vitro. Neuroscience. 140: 111-22. PMID 16564641 DOI: 10.1016/J.Neuroscience.2006.02.014 |
0.769 |
|
| 2003 |
Maynard TM, Haskell GT, Peters AZ, Sikich L, Lieberman JA, LaMantia AS. A comprehensive analysis of 22q11 gene expression in the developing and adult brain. Proceedings of the National Academy of Sciences of the United States of America. 100: 14433-8. PMID 14614146 DOI: 10.1073/Pnas.2235651100 |
0.818 |
|
| 2003 |
Bhasin N, Maynard TM, Gallagher PA, LaMantia AS. Mesenchymal/epithelial regulation of retinoic acid signaling in the olfactory placode. Developmental Biology. 261: 82-98. PMID 12941622 DOI: 10.1016/S0012-1606(03)00295-1 |
0.58 |
|
| 2002 |
Thompson Haskell G, Maynard TM, Shatzmiller RA, Lamantia AS. Retinoic acid signaling at sites of plasticity in the mature central nervous system. The Journal of Comparative Neurology. 452: 228-41. PMID 12353219 DOI: 10.1002/Cne.10369 |
0.644 |
|
| 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 |
0.802 |
|
| 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 |
0.79 |
|
| 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 |
0.693 |
|
| 2001 |
Maynard TM, Sikich L, Lieberman JA, LaMantia AS. Neural development, cell-cell signaling, and the "two-hit" hypothesis of schizophrenia. Schizophrenia Bulletin. 27: 457-76. PMID 11596847 DOI: 10.1093/Oxfordjournals.Schbul.A006887 |
0.658 |
|
| 2000 |
Henion PD, Blyss GK, Luo R, An M, Maynard TM, Cole GJ, Weston JA. Avian transitin expression mirrors glial cell fate restrictions during neural crest development Developmental Dynamics. 218: 150-159. PMID 10822267 DOI: 10.1002/(Sici)1097-0177(200005)218:1<150::Aid-Dvdy13>3.0.Co;2-6 |
0.662 |
|
| 1999 |
Wakamatsu Y, Maynard TM, Jones SU, Weston JA. NUMB localizes in the basal cortex of mitotic avian neuroepithelial cells and modulates neuronal differentiation by binding to NOTCH-1. Neuron. 23: 71-81. PMID 10402194 DOI: 10.1016/S0896-6273(00)80754-0 |
0.622 |
|
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