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Stormy J Chamberlain PhD

TitleAssistant Professor
InstitutionUConn Health Center
DepartmentGenetics and Developmental Biology
AddressMC 6403
Cell and Genome Sciences Building, MC 6403
400 Farmington Avenue
Phone860-679-8351
Fax860-679-8345
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    Collapse Bibliographic 
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Smith OK, Kim R, Fu H, Martin MM, Lin CM, Utani K, Zhang Y, Marks AB, Lalande M, Chamberlain S, Libbrecht MW, Bouhassira EE, Ryan MC, Noble WS, Aladjem MI. Distinct epigenetic features of differentiation-regulated replication origins. Epigenetics Chromatin. 2016; 9:18. PMID: 27168766.
      View in: PubMed
    2. Chen PF, Hsiao JS, Sirois CL, Chamberlain SJ. RBFOX1 and RBFOX2 are dispensable in iPSCs and iPSC-derived neurons and do not contribute to neural-specific paternal UBE3A silencing. Sci Rep. 2016; 6:25368. PMID: 27146458.
      View in: PubMed
    3. Chamberlain SJ, Germain ND, Chen PF, Hsiao JS, Glatt-Deeley H. Modeling Genomic Imprinting Disorders Using Induced Pluripotent Stem Cells. Methods Mol Biol. 2016; 1353:45-64. PMID: 25520291.
      View in: PubMed
    4. LaSalle JM, Reiter LT, Chamberlain SJ. Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders. Epigenomics. 2015 Oct; 7(7):1213-28. PMID: 26585570.
      View in: PubMed
    5. Kalsner L, Chamberlain SJ. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes. Pediatr Clin North Am. 2015 Jun; 62(3):587-606. PMID: 26022164; PMCID: PMC4449422 [Available on 06/01/16].
    6. Germain ND, Chen PF, Plocik AM, Glatt-Deeley H, Brown J, Fink JJ, Bolduc KA, Robinson TM, Levine ES, Reiter LT, Graveley BR, Lalande M, Chamberlain SJ. Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1. Mol Autism. 2014; 5:44. PMID: 25694803; PMCID: PMC4332023.
    7. Cruvinel E, Budinetz T, Germain N, Chamberlain S, Lalande M, Martins-Taylor K. Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs. Hum Mol Genet. 2014 Sep 1; 23(17):4674-85. PMID: 24760766; PMCID: PMC4481691.
    8. Martins-Taylor K, Hsiao JS, Chen PF, Glatt-Deeley H, De Smith AJ, Blakemore AI, Lalande M, Chamberlain SJ. Imprinted expression of UBE3A in non-neuronal cells from a Prader-Willi syndrome patient with an atypical deletion. Hum Mol Genet. 2014 May 1; 23(9):2364-73. PMID: 24363065; PMCID: PMC3976333.
    9. King IF, Yandava CN, Mabb AM, Hsiao JS, Huang HS, Pearson BL, Calabrese JM, Starmer J, Parker JS, Magnuson T, Chamberlain SJ, Philpot BD, Zylka MJ. Topoisomerases facilitate transcription of long genes linked to autism. Nature. 2013 Sep 5; 501(7465):58-62. PMID: 23995680; PMCID: PMC3767287.
    10. Wang T, Wu H, Li Y, Szulwach KE, Lin L, Li X, Chen IP, Goldlust IS, Chamberlain SJ, Dodd A, Gong H, Ananiev G, Han JW, Yoon YS, Rudd MK, Yu M, Song CX, He C, Chang Q, Warren ST, Jin P. Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency. Nat Cell Biol. 2013 Jun; 15(6):700-11. PMID: 23685628; PMCID: PMC3998089.
    11. Chamberlain SJ. RNAs of the human chromosome 15q11-q13 imprinted region. Wiley Interdiscip Rev RNA. 2013 Mar-Apr; 4(2):155-66. PMID: 23208756; PMCID: PMC3578059.
    12. Smith EY, Futtner CR, Chamberlain SJ, Johnstone KA, Resnick JL. Transcription is required to establish maternal imprinting at the Prader-Willi syndrome and Angelman syndrome locus. PLoS Genet. 2011 Dec; 7(12):e1002422. PMID: 22242001; PMCID: PMC3248558.
    13. Chamberlain SJ. Comment on "Do repeated arrays of box C/D small nucleolar RNA and microRNA genes elicit genomic imprinting?" DOI 10.1002/bies201100032. Bioessays. 2011 Aug; 33(8):563-4. PMID: 21769903.
      View in: PubMed
    14. Leung KN, Chamberlain SJ, Lalande M, LaSalle JM. Neuronal chromatin dynamics of imprinting in development and disease. J Cell Biochem. 2011 Feb; 112(2):365-73. PMID: 21268055; PMCID: PMC3090268.
    15. Chamberlain SJ, Chen PF, Ng KY, Bourgois-Rocha F, Lemtiri-Chlieh F, Levine ES, Lalande M. Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes. Proc Natl Acad Sci U S A. 2010 Oct 12; 107(41):17668-73. PMID: 20876107; PMCID: PMC2955112.
    16. Chamberlain SJ, Lalande M. Angelman syndrome, a genomic imprinting disorder of the brain. J Neurosci. 2010 Jul 28; 30(30):9958-63. PMID: 20668179.
      View in: PubMed
    17. Chamberlain SJ, Lalande M. Neurodevelopmental disorders involving genomic imprinting at human chromosome 15q11-q13. Neurobiol Dis. 2010 Jul; 39(1):13-20. PMID: 20304067.
      View in: PubMed
    18. Chamberlain SJ, Li XJ, Lalande M. Induced pluripotent stem (iPS) cells as in vitro models of human neurogenetic disorders. Neurogenetics. 2008 Oct; 9(4):227-35. PMID: 18791750.
      View in: PubMed
    19. Sanz LA, Chamberlain S, Sabourin JC, Henckel A, Magnuson T, Hugnot JP, Feil R, Arnaud P. A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10. EMBO J. 2008 Oct 8; 27(19):2523-32. PMID: 18650936; PMCID: PMC2567399.
    20. Chamberlain SJ, Yee D, Magnuson T. Polycomb repressive complex 2 is dispensable for maintenance of embryonic stem cell pluripotency. Stem Cells. 2008 Jun; 26(6):1496-505. PMID: 18403752; PMCID: PMC2630378.
    21. Montgomery ND, Yee D, Chen A, Kalantry S, Chamberlain SJ, Otte AP, Magnuson T. The murine polycomb group protein Eed is required for global histone H3 lysine-27 methylation. Curr Biol. 2005 May 24; 15(10):942-7. PMID: 15916951.
      View in: PubMed
    22. Chamberlain SJ, Johnstone KA, DuBose AJ, Simon TA, Bartolomei MS, Resnick JL, Brannan CI. Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice. Hum Mol Genet. 2004 Dec 1; 13(23):2971-7. PMID: 15459179.
      View in: PubMed
    23. Chamberlain SJ, Brannan CI. The Prader-Willi syndrome imprinting center activates the paternally expressed murine Ube3a antisense transcript but represses paternal Ube3a. Genomics. 2001 May 1; 73(3):316-22. PMID: 11350123.
      View in: PubMed
    24. Lee S, Kozlov S, Hernandez L, Chamberlain SJ, Brannan CI, Stewart CL, Wevrick R. Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype. Hum Mol Genet. 2000 Jul 22; 9(12):1813-9. PMID: 10915770.
      View in: PubMed
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