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James Sutcliffe
Last active: 2/20/2014

  1. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism. Celestino-Soper PB, Violante S, Crawford EL, Luo R, Lionel AC, Delaby E, Cai G, Sadikovic B, Lee K, Lo C, Gao K, Person RE, Moss TJ, German JR, Huang N, Shinawi M, Treadwell-Deering D, Szatmari P, Roberts W, Fernandez B, Schroer RJ, Stevenson RE, Buxbaum JD, Betancur C, Scherer SW, Sanders SJ, Geschwind DH, Sutcliffe JS, Hurles ME, Wanders RJ, Shaw CA, Leal SM, Cook EH, Goin-Kochel RP, Vaz FM, Beaudet AL (2012) Proc Natl Acad Sci U S A 109(21): 7974-81
    › Primary publication · 22566635 (PubMed) · PMC3361440 (PubMed Central)
  2. Accuracy of phenotyping children with autism based on parent report: what specifically do we gain phenotyping "rapidly"? Warren Z, Vehorn A, Dohrmann E, Nicholson A, Sutcliffe JS, Veenstra-Vanderweele J (2012) Autism Res 5(1): 31-8
    › Primary publication · 21972233 (PubMed)
  3. Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Celestino-Soper PB, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH, Stankiewicz P, State MW, Beaudet AL (2011) Hum Mol Genet 20(22): 4360-70
    › Primary publication · 21865298 (PubMed) · PMC3196886 (PubMed Central)
  4. Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Pagnamenta AT, Khan H, Walker S, Gerrelli D, Wing K, Bonaglia MC, Giorda R, Berney T, Mani E, Molteni M, Pinto D, Le Couteur A, Hallmayer J, Sutcliffe JS, Szatmari P, Paterson AD, Scherer SW, Vieland VJ, Monaco AP (2011) J Med Genet 48(1): 48-54
    › Primary publication · 20972252 (PubMed) · PMC3003876 (PubMed Central)
  5. Parent-of-origin effects of the serotonin transporter gene associated with autism. Kistner-Griffin E, Brune CW, Davis LK, Sutcliffe JS, Cox NJ, Cook EH (2011) Am J Med Genet B Neuropsychiatr Genet 156(2): 139-44
    › Primary publication · 21302342 (PubMed) · PMC3438509 (PubMed Central)
  6. Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. Vieland VJ, Hallmayer J, Huang Y, Pagnamenta AT, Pinto D, Khan H, Monaco AP, Paterson AD, Scherer SW, Sutcliffe JS, Szatmari P, Autism Genome Project (AGP) (2011) J Neurodev Disord 3(2): 113-23
    › Primary publication · 21484201 (PubMed) · PMC3105232 (PubMed Central)
  7. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, Davis L, Wright NR, Dhodapkar RM, DiCola M, DiLullo NM, Fernandez TV, Fielding-Singh V, Fishman DO, Frahm S, Garagaloyan R, Goh GS, Kammela S, Klei L, Lowe JK, Lund SC, McGrew AD, Meyer KA, Moffat WJ, Murdoch JD, O'Roak BJ, Ober GT, Pottenger RS, Raubeson MJ, Song Y, Wang Q, Yaspan BL, Yu TW, Yurkiewicz IR, Beaudet AL, Cantor RM, Curland M, Grice DE, G√ľnel M, Lifton RP, Mane SM, Martin DM, Shaw CA, Sheldon M, Tischfield JA, Walsh CA, Morrow EM, Ledbetter DH, Fombonne E, Lord C, Martin CL, Brooks AI, Sutcliffe JS, Cook EH, Geschwind D, Roeder K, Devlin B, State MW (2011) Neuron 70(5): 863-85
    › Primary publication · 21658581 (PubMed) · PMC3939065 (PubMed Central)
  8. Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism. Delahanty RJ, Kang JQ, Brune CW, Kistner EO, Courchesne E, Cox NJ, Cook EH, Macdonald RL, Sutcliffe JS (2011) Mol Psychiatry 16(1): 86-96
    › Primary publication · 19935738 (PubMed) · PMC3428055 (PubMed Central)
  9. Genetic analysis of biological pathway data through genomic randomization. Yaspan BL, Bush WS, Torstenson ES, Ma D, Pericak-Vance MA, Ritchie MD, Sutcliffe JS, Haines JL (2011) Hum Genet 129(5): 563-71
    › Primary publication · 21279722 (PubMed) · PMC3107984 (PubMed Central)
  10. Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders. Anney RJ, Kenny EM, O'Dushlaine C, Yaspan BL, Parkhomenka E, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L, Autism Genome Project, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L (2011) Eur J Hum Genet 19(10): 1082-9
    › Primary publication · 21522181 (PubMed) · PMC3190264 (PubMed Central)