Stormy J Chamberlain

Summary

Affiliation: University of Connecticut Health Center
Country: USA

Publications

  1. doi request reprint Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells
    Stormy J Chamberlain
    University of Connecticut Health Center, 400 Farmington Avenue, Farmington, CT, 06030 6403, USA
    Methods Mol Biol 1353:45-64. 2016
  2. pmc RNAs of the human chromosome 15q11-q13 imprinted region
    Stormy J Chamberlain
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, CT, USA
    Wiley Interdiscip Rev RNA 4:155-66. 2013
  3. doi request reprint Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13
    Stormy J Chamberlain
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, MC3301, 263 Farmington Ave, Farmington, CT 06030, USA
    Neurobiol Dis 39:13-20. 2010
  4. pmc Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
    Stormy J Chamberlain
    University of Connecticut Stem Cell Institute and Departments of Genetics and Developmental Biology and Neuroscience, University of Connecticut Health Center, Farmington, CT 06030, USA
    Proc Natl Acad Sci U S A 107:17668-73. 2010
  5. pmc Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion
    Kristen Martins-Taylor
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, CT, USA
    Hum Mol Genet 23:2364-73. 2014
  6. pmc Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1
    Noélle D Germain
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, 400 Farmington Avenue, Farmington, CT 06032, USA
    Mol Autism 5:44. 2014
  7. doi request reprint Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders
    Stormy J Chamberlain
    Department of Genetics and Developmental Biology, Stem Cell Institute, University of Connecticut Health Center, Farmington, CT, USA
    Neurogenetics 9:227-35. 2008
  8. pmc RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing
    Pin Fang Chen
    Department of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, Connecticut, 06030, USA
    Sci Rep 6:25368. 2016

Collaborators

  • Xue Jun Li
  • ERIC LEVINE
  • Pin Fang Chen
  • Jack S Hsiao
  • Noélle D Germain
  • Marc Lalande
  • Heather Glatt-Deeley
  • Kristen Martins-Taylor
  • Carissa L Sirois
  • Alex M Plocik
  • Judith Brown
  • Adam J de Smith
  • James J Fink
  • Brenton R Graveley
  • Alexandra I F Blakemore
  • Tiwanna M Robinson
  • Lawrence T Reiter
  • Kaitlyn A Bolduc

Detail Information

Publications8

  1. doi request reprint Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells
    Stormy J Chamberlain
    University of Connecticut Health Center, 400 Farmington Avenue, Farmington, CT, 06030 6403, USA
    Methods Mol Biol 1353:45-64. 2016
    ....
  2. pmc RNAs of the human chromosome 15q11-q13 imprinted region
    Stormy J Chamberlain
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, CT, USA
    Wiley Interdiscip Rev RNA 4:155-66. 2013
    ..This review summarizes what is known about the various RNAs within the imprinted domain, including a novel type of RNA that was only very recently identified...
  3. doi request reprint Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13
    Stormy J Chamberlain
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, MC3301, 263 Farmington Ave, Farmington, CT 06030, USA
    Neurobiol Dis 39:13-20. 2010
    ....
  4. pmc Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
    Stormy J Chamberlain
    University of Connecticut Stem Cell Institute and Departments of Genetics and Developmental Biology and Neuroscience, University of Connecticut Health Center, Farmington, CT 06030, USA
    Proc Natl Acad Sci U S A 107:17668-73. 2010
    ..These iPSC models of genomic imprinting disorders will facilitate investigation of the AS and PWS disease processes and allow study of the developmental timing and mechanism of UBE3A repression in human neurons...
  5. pmc Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion
    Kristen Martins-Taylor
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, CT, USA
    Hum Mol Genet 23:2364-73. 2014
    ..These data also suggest that a boundary element lying within the PWS critical region prevents UBE3A-ATS expression in non-neural tissues. ..
  6. pmc Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1
    Noélle D Germain
    Department of Genetics and Developmental Biology, University of Connecticut Health Center, 400 Farmington Avenue, Farmington, CT 06032, USA
    Mol Autism 5:44. 2014
    ..1 duplication (Dup15q) syndrome...
  7. doi request reprint Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders
    Stormy J Chamberlain
    Department of Genetics and Developmental Biology, Stem Cell Institute, University of Connecticut Health Center, Farmington, CT, USA
    Neurogenetics 9:227-35. 2008
    ....
  8. pmc RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing
    Pin Fang Chen
    Department of Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, Connecticut, 06030, USA
    Sci Rep 6:25368. 2016
    ..Our data show that while RBFOX1 and RBFOX2 do not mediate neuron-specific processing of UBE3A-ATS, these proteins play important roles in developing neurons and are not completely functionally redundant...