James Sutcliffe
Last active: 2/20/2014

  1. Enhanced activity of human serotonin transporter variants associated with autism. Prasad HC, Steiner JA, Sutcliffe JS, Blakely RD (2009) Philos Trans R Soc Lond B Biol Sci 364(1514): 163-73
    › Primary publication · 18957375 (PubMed) · PMC2674096 (PubMed Central)
  2. Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions. Campbell DB, Buie TM, Winter H, Bauman M, Sutcliffe JS, Perrin JM, Levitt P (2009) Pediatrics 123(3): 1018-24
    › Primary publication · 19255034 (PubMed)
  3. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H (2009) Nature 459(7246): 528-33
    › Primary publication · 19404256 (PubMed) · PMC2943511 (PubMed Central)
  4. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Glessner JT, Wang K, Cai G, Korvatska O, Kim CE, Wood S, Zhang H, Estes A, Brune CW, Bradfield JP, Imielinski M, Frackelton EC, Reichert J, Crawford EL, Munson J, Sleiman PM, Chiavacci R, Annaiah K, Thomas K, Hou C, Glaberson W, Flory J, Otieno F, Garris M, Soorya L, Klei L, Piven J, Meyer KJ, Anagnostou E, Sakurai T, Game RM, Rudd DS, Zurawiecki D, McDougle CJ, Davis LK, Miller J, Posey DJ, Michaels S, Kolevzon A, Silverman JM, Bernier R, Levy SE, Schultz RT, Dawson G, Owley T, McMahon WM, Wassink TH, Sweeney JA, Nurnberger JI, Coon H, Sutcliffe JS, Minshew NJ, Grant SF, Bucan M, Cook EH, Buxbaum JD, Devlin B, Schellenberg GD, Hakonarson H (2009) Nature 459(7246): 569-73
    › Primary publication · 19404257 (PubMed) · PMC2925224 (PubMed Central)
  5. Association and mutation analyses of 16p11.2 autism candidate genes. Kumar RA, Marshall CR, Badner JA, Babatz TD, Mukamel Z, Aldinger KA, Sudi J, Brune CW, Goh G, Karamohamed S, Sutcliffe JS, Cook EH, Geschwind DH, Dobyns WB, Scherer SW, Christian SL (2009) PLoS One 4(2): e4582
    › Primary publication · 19242545 (PubMed) · PMC2644762 (PubMed Central)
  6. A genome-wide linkage and association scan reveals novel loci for autism. Weiss LA, Arking DE, Gene Discovery Project of Johns Hopkins & the Autism Consortium, Daly MJ, Chakravarti A (2009) Nature 461(7265): 802-8
    › Primary publication · 19812673 (PubMed) · PMC2772655 (PubMed Central)
  7. Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. Mefford HC, Sharp AJ, Baker C, Itsara A, Jiang Z, Buysse K, Huang S, Maloney VK, Crolla JA, Baralle D, Collins A, Mercer C, Norga K, de Ravel T, Devriendt K, Bongers EM, de Leeuw N, Reardon W, Gimelli S, Bena F, Hennekam RC, Male A, Gaunt L, Clayton-Smith J, Simonic I, Park SM, Mehta SG, Nik-Zainal S, Woods CG, Firth HV, Parkin G, Fichera M, Reitano S, Lo Giudice M, Li KE, Casuga I, Broomer A, Conrad B, Schwerzmann M, Räber L, Gallati S, Striano P, Coppola A, Tolmie JL, Tobias ES, Lilley C, Armengol L, Spysschaert Y, Verloo P, De Coene A, Goossens L, Mortier G, Speleman F, van Binsbergen E, Nelen MR, Hochstenbach R, Poot M, Gallagher L, Gill M, McClellan J, King MC, Regan R, Skinner C, Stevenson RE, Antonarakis SE, Chen C, Estivill X, Menten B, Gimelli G, Gribble S, Schwartz S, Sutcliffe JS, Walsh T, Knight SJ, Sebat J, Romano C, Schwartz CE, Veltman JA, de Vries BB, Vermeesch JR, Barber JC, Willatt L, Tassabehji M, Eichler EE (2008) N Engl J Med 359(16): 1685-99
    › Primary publication · 18784092 (PubMed) · PMC2703742 (PubMed Central)
  8. Our vision for Autism Research. Bailey A, Sutcliffe JS, Schultz R, Rogers S (2008) Autism Res 1(2): 71-2
    › Primary publication · 19360653 (PubMed)
  9. Molecular genetics of the platelet serotonin system in first-degree relatives of patients with autism. Cross S, Kim SJ, Weiss LA, Delahanty RJ, Sutcliffe JS, Leventhal BL, Cook EH, Veenstra-Vanderweele J (2008) Neuropsychopharmacology 33(2): 353-60
    › Primary publication · 17406648 (PubMed) · PMC2739682 (PubMed Central)
  10. Heterogeneity and the design of genetic studies in autism. Sutcliffe JS (2008) Autism Res 1(4): 205-6
    › Primary publication · 19360669 (PubMed)