, a bio/informatics shared resource is still "open for business" - Visit the CDS website


James Sutcliffe
Last active: 2/20/2014

  1. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA (2004) Neurosci Lett 372(3): 209-14
    › Primary publication · 15542242 (PubMed)
  2. A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism. McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS (2004) Am J Med Genet B Neuropsychiatr Genet 131B(1): 51-9
    › Primary publication · 15389768 (PubMed)
  3. 'Severe' Prader-Willi syndrome with a large deletion of chromosome 15 due to an unbalanced t(15,22)(q14;q11.2) translocation. Matsumura M, Kubota T, Hidaka E, Wakui K, Kadowaki S, Ueta I, Shimizu T, Ueno I, Yamauchi K, Herzing LB, Nurmi EL, Sutcliffe JS, Fukushima Y, Katsuyama T (2003) Clin Genet 63(1): 79-81
    › Primary publication · 12519378 (PubMed)
  4. Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures. Sutcliffe JS, Han MK, Amin T, Kesterson RA, Nurmi EL (2003) BMC Genomics 4(1): 15
    › Primary publication · 12720574 (PubMed) · PMC156605 (PubMed Central)
  5. Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism. Sutcliffe JS, Nurmi EL, Lombroso PJ (2003) J Am Acad Child Adolesc Psychiatry 42(2): 253-6
    › Primary publication · 12544187 (PubMed)
  6. Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13. Nurmi EL, Dowd M, Tadevosyan-Leyfer O, Haines JL, Folstein SE, Sutcliffe JS (2003) J Am Acad Child Adolesc Psychiatry 42(7): 856-63
    › Primary publication · 12819446 (PubMed)
  7. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS (2003) Mol Psychiatry 8(6): 624-34, 570
    › Primary publication · 12851639 (PubMed)
  8. Defining the autism minimum candidate gene region on chromosome 7. Hutcheson HB, Bradford Y, Folstein SE, Gardiner MB, Santangelo SL, Sutcliffe JS, Haines JL (2003) Am J Med Genet B Neuropsychiatr Genet 117B(1): 90-6
    › Primary publication · 12555242 (PubMed)
  9. Possible dosage effect of maternally expressed genes on visual recognition memory in Prader-Willi syndrome. Joseph B, Egli M, Sutcliffe JS, Thompson T (2001) Am J Med Genet 105(1): 71-5
    › Primary publication · 11425004 (PubMed)
  10. Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation. Abou-Khalil B, Ge Q, Desai R, Ryther R, Bazyk A, Bailey R, Haines JL, Sutcliffe JS, George AL (2001) Neurology 57(12): 2265-72
    › Primary publication · 11756608 (PubMed)