James Sutcliffe
Last active: 2/20/2014

  1. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, Folstein SE, Haines JL, Sutcliffe JS (2001) Genomics 77(1-2): 105-13
    › Primary publication · 11543639 (PubMed)
  2. Appetitive behavior, compulsivity, and neurochemistry in Prader-Willi syndrome. Dimitropoulos A, Feurer ID, Roof E, Stone W, Butler MG, Sutcliffe J, Thompson T (2000) Ment Retard Dev Disabil Res Rev 6(2): 125-30
    › Primary publication · 10899805 (PubMed) · PMC6777566 (PubMed Central)
  3. The spectrum of mutations in UBE3A causing Angelman syndrome. Fang P, Lev-Lehman E, Tsai TF, Matsuura T, Benton CS, Sutcliffe JS, Christian SL, Kubota T, Halley DJ, Meijers-Heijboer H, Langlois S, Graham JM, Beuten J, Willems PJ, Ledbetter DH, Beaudet AL (1999) Hum Mol Genet 8(1): 129-35
    › Primary publication · 9887341 (PubMed)
  4. Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb. Christian SL, Bhatt NK, Martin SA, Sutcliffe JS, Kubota T, Huang B, Mutirangura A, Chinault AC, Beaudet AL, Ledbetter DH (1998) Genome Res 8(2): 146-57
    › Primary publication · 9477342 (PubMed) · PMC310691 (PubMed Central)
  5. The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region. Sutcliffe JS, Jiang YH, Galijaard RJ, Matsuura T, Fang P, Kubota T, Christian SL, Bressler J, Cattanach B, Ledbetter DH, Beaudet AL (1997) Genome Res 7(4): 368-77
    › Primary publication · 9110176 (PubMed) · PMC139148 (PubMed Central)
  6. Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity. Huq AH, Sutcliffe JS, Nakao M, Shen Y, Gibbs RA, Beaudet AL (1997) Genome Res 7(6): 642-8
    › Primary publication · 9199937 (PubMed) · PMC310659 (PubMed Central)
  7. Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndrome. Sutcliffe JS, Han M, Christian SL, Ledbetter DH (1997) Lancet 350(9090): 1520-1
    › Primary publication · 9388406 (PubMed)
  8. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Albrecht U, Sutcliffe JS, Cattanach BM, Beechey CV, Armstrong D, Eichele G, Beaudet AL (1997) Nat Genet 17(1): 75-8
    › Primary publication · 9288101 (PubMed)
  9. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome. Matsuura T, Sutcliffe JS, Fang P, Galjaard RJ, Jiang YH, Benton CS, Rommens JM, Beaudet AL (1997) Nat Genet 15(1): 74-7
    › Primary publication · 8988172 (PubMed)
  10. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome. Kubota T, Sutcliffe JS, Aradhya S, Gillessen-Kaesbach G, Christian SL, Horsthemke B, Beaudet AL, Ledbetter DH (1996) Am J Med Genet 66(1): 77-80
    › Primary publication · 8957518 (PubMed)