James Sutcliffe
Last active: 2/20/2014

  1. A genetic variant that disrupts MET transcription is associated with autism. Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P (2006) Proc Natl Acad Sci U S A 103(45): 16834-9
    › Primary publication · 17053076 (PubMed) · PMC1838551 (PubMed Central)
  2. The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures. Ma S, Abou-Khalil B, Sutcliffe JS, Haines JL, Hedera P (2005) BMC Med Genet : 13
    › Primary publication · 15799783 (PubMed) · PMC1079842 (PubMed Central)
  3. Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase. Prasad HC, Zhu CB, McCauley JL, Samuvel DJ, Ramamoorthy S, Shelton RC, Hewlett WA, Sutcliffe JS, Blakely RD (2005) Proc Natl Acad Sci U S A 102(32): 11545-50
    › Primary publication · 16055563 (PubMed) · PMC1183547 (PubMed Central)
  4. Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates. McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS (2005) BMC Med Genet : 1
    › Primary publication · 15647115 (PubMed) · PMC546213 (PubMed Central)
  5. Analysis of the RELN gene as a genetic risk factor for autism. Skaar DA, Shao Y, Haines JL, Stenger JE, Jaworski J, Martin ER, DeLong GR, Moore JH, McCauley JL, Sutcliffe JS, Ashley-Koch AE, Cuccaro ML, Folstein SE, Gilbert JR, Pericak-Vance MA (2005) Mol Psychiatry 10(6): 563-71
    › Primary publication · 15558079 (PubMed)
  6. Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors. Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD (2005) Am J Hum Genet 77(2): 265-79
    › Primary publication · 15995945 (PubMed) · PMC1224529 (PubMed Central)
  7. Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism. McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS (2004) Am J Med Genet B Neuropsychiatr Genet 127B(1): 104-12
    › Primary publication · 15108191 (PubMed)
  8. Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes. Hutcheson HB, Olson LM, Bradford Y, Folstein SE, Santangelo SL, Sutcliffe JS, Haines JL (2004) BMC Med Genet : 12
    › Primary publication · 15128462 (PubMed) · PMC420465 (PubMed Central)
  9. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene. Hedera P, Abou-Khalil B, Crunk AE, Taylor KA, Haines JL, Sutcliffe JS (2004) Epilepsia 45(3): 218-22
    › Primary publication · 15009222 (PubMed)
  10. Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues. Dykens EM, Sutcliffe JS, Levitt P (2004) Ment Retard Dev Disabil Res Rev 10(4): 284-91
    › Primary publication · 15666333 (PubMed)