James Sutcliffe
Last active: 2/20/2014

  1. Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus. Jinno Y, Sengoku K, Nakao M, Tamate K, Miyamoto T, Matsuzaka T, Sutcliffe JS, Anan T, Takuma N, Nishiwaki K, Ikeda Y, Ishimaru T, Ishikawa M, Niikawa N (1996) Hum Mol Genet 5(8): 1155-61
    › Primary publication · 8842735 (PubMed)
  2. Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region. Ning Y, Roschke A, Christian SL, Lesser J, Sutcliffe JS, Ledbetter DH (1996) Genome Res 6(8): 742-6
    › Primary publication · 8858349 (PubMed)
  3. Detection of imprinting mutations in Angelman syndrome using a probe for exon alpha of SNRPN. Beuten J, Sutcliffe JS, Casey BM, Beaudet AL, Hennekam RC, Willems PJ (1996) Am J Med Genet 63(2): 414-5
    › Primary publication · 8725798 (PubMed)
  4. Angelman syndrome in an inbred family. Beuten J, Hennekam RC, Van Roy B, Mangelschots K, Sutcliffe JS, Halley DJ, Hennekam FA, Beaudet AL, Willems PJ (1996) Hum Genet 97(3): 294-8
    › Primary publication · 8786067 (PubMed)
  5. Advantages of RT-PCR and denaturing gradient gel electrophoresis for analysis of genomic imprinting: detection of new mouse and human expressed polymorphisms. Nakao M, Sutcliffe JS, Beaudet AL (1996) Hum Mutat 7(2): 144-8
    › Primary publication · 8829631 (PubMed)
  6. Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region. Gunaratne PH, Nakao M, Ledbetter DH, Sutcliffe JS, Chinault AC (1995) Genes Dev 9(7): 808-20
    › Primary publication · 7705658 (PubMed)
  7. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E). Nakao M, Sutcliffe JS, Durtschi B, Mutirangura A, Ledbetter DH, Beaudet AL (1994) Hum Mol Genet 3(2): 309-15
    › Primary publication · 8004100 (PubMed)
  8. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Sutcliffe JS, Nakao M, Christian S, Orstavik KH, Tommerup N, Ledbetter DH, Beaudet AL (1994) Nat Genet 8(1): 52-8
    › Primary publication · 7987392 (PubMed)
  9. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M (1993) Nat Genet 3(1): 36-43
    › Primary publication · 8490651 (PubMed)
  10. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat. Ashley CT, Sutcliffe JS, Kunst CB, Leiner HA, Eichler EE, Nelson DL, Warren ST (1993) Nat Genet 4(3): 244-51
    › Primary publication · 8358432 (PubMed)