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Home All issues Volume 19 / No 11 (Novembre 2003) Med Sci (Paris), 19 11 (2003) 1081-1090 References
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Issue
Med Sci (Paris)
Volume 19, Number 11, Novembre 2003
Page(s) 1081 - 1090
Section M/S Revues
DOI https://doi.org/10.1051/medsci/200319111081
Published online 15 November 2003
  1. Kanner L. Autistic disturbances of affective contact. Nervous Child 1943; 2: 217–50. [Google Scholar]
  2. American psychiatric association. Diagnostic and statistical manual of mental disorders, 4th ed. Washington, DC: APA, 1994. [Google Scholar]
  3. Folstein SE, Rosen-Sheidley B. Genetics of autism: complex aetiology for a heterogeneous disorder. Nat Rev Genet 2001; 2: 943–55. [Google Scholar]
  4. Lord C, Rutter M, Le Couteur A. Autism diagnostic interviewrevised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 1994; 24: 659–85. [Google Scholar]
  5. Piven J. The biological basis of autism. Curr Opin Neurobiol 1997; 7: 708–12. [Google Scholar]
  6. Filipek PA, Accardo PJ, Baranek GT, et al. The screening and diagnosis of autistic spectrum disorders. J Autism Dev Disord 1999; 29: 439–84. [Google Scholar]
  7. Ashley-Koch AE, Carney RJ, Wolpert CM, et al. Screening for MECP2 mutations in females with autistic disorder. IXth World Congress of Psychiatric Genetics. St. Louis, MO, USA, 2001. [Google Scholar]
  8. Gillberg C. Chromosomal disorders and autism. J Autism Dev Disord 1998; 28: 415–25. [Google Scholar]
  9. Wassink TH, Piven J, Patil SR. Chromosomal abnormalities in a clinic sample of individuals with autistic disorder. Psychiatr Genet 2001; 11: 57–63. [Google Scholar]
  10. Leboyer M, Philippe A, Bouvard M, et al. Whole blood serotonin and plasma beta-endorphin in autistic probands and their firstdegree relatives. Biol Psychiatry 1999; 45: 158–63. [Google Scholar]
  11. Betancur C, Corbex M, Spielewoy C, et al. Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder. Mol Psychiatry 2002; 7: 67–71. [Google Scholar]
  12. International molecular genetic study of autism consortium (IMGSAC). A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 1998; 7: 571–8. [Google Scholar]
  13. Philippe A, Martinez M, Guilloud-Bataille M, et al. Genome-wide scan for autism susceptibility genes. Paris autism research international sibpair study. Hum Mol Genet 1999; 8: 805–12. [Google Scholar]
  14. Risch N, Spiker D, Lotspeich L, et al. A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet 1999; 65: 493–507. [Google Scholar]
  15. Barrett S, Beck JC, Bernier R, et al. An autosomal genomic screen for autism. Collaborative linkage study of autism. Am J Med Genet 1999; 88: 609–15. [Google Scholar]
  16. Buxbaum JD, Silverman JM, Smith CJ, et al. Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity. Am J Hum Genet 2001; 68: 1514–20. [Google Scholar]
  17. Liu J, Nyholt DR, Magnussen P, et al. A genomewide screen for autism susceptibility loci. Am J Hum Genet 2001; 69: 327–40. [Google Scholar]
  18. International molecular genetic study of autism consortium (IMGSAC). A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 2001; 69: 570–81. [Google Scholar]
  19. Shao Y, Wolpert CM, Raiford KL, et al. Genomic screen and follow-up analysis for autistic disorder. Am J Med Genet 2002; 114: 99–105. [Google Scholar]
  20. Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995; 11: 241–7. [Google Scholar]
  21. Shao YJ, Raiford KL, Wolpert CM, et al. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder. Am J Hum Genet 2002; 70: 1058–61. [Google Scholar]
  22. Jamain S, Betancur C, Quach H, et al. Linkage and association of the glutamate receptor 6 gene with autism. Mol Psychiatry 2002; 7: 302–10. [Google Scholar]
  23. Bradford Y, Haines J, Hutcheson H, et al. Incorporating language phenotypes strengthens evidence of linkage to autism. Am J Med Genet 2001; 105: 539–47. [Google Scholar]
  24. Ashley-Koch A, Wolpert CM, Menold MM, et al. Genetic studies of autistic disorder and chromosome 7. Genomics 1999; 61: 227–36. [Google Scholar]
  25. International molecular genetic study of autism consortium (IMGSAC). Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. Hum Mol Genet 2001; 10: 973–82. [Google Scholar]
  26. Vincent JB, Herbrick JA, Gurling HM, Bolton PF, Roberts W, Scherer SW. Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual. Am J Hum Genet 2000; 67: 510–4. [Google Scholar]
  27. Persico AM, D’Agruma L, Maiorano N, et al. Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder. Mol Psychiatry 2001; 6: 150–9. [Google Scholar]
  28. Krebs MO, Betancur C, Leroy S, et al. Absence of association between a polymorphic GGC repeat in the 5’ untranslated region of the reelin gene and autism. Mol Psychiatry 2002; 7: 801–4. [Google Scholar]
  29. Wassink TH, Piven J, Vieland VJ, et al. Evidence supporting WNT2 as an autism susceptibility gene. Am J Med Genet 2001; 105: 406–13. [Google Scholar]
  30. Newbury DF, Bonora E, Lamb JA, et al. FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet 2002; 70: 1318–27. [Google Scholar]
  31. Bass MP, Menold MM, Wolpert CM, et al. Genetic studies in autistic disorder and chromosome 15. Neurogenetics 2000; 2: 219–26. [Google Scholar]
  32. Veenstra-VanderWeele J, Gonen D, Leventhal BL, Cook EH, Jr. Mutation screening of the UBE3A/E6- AP gene in autistic disorder. Mol Psychiatry 1999; 4: 64–7. [Google Scholar]
  33. Cook EH, Courchesne RY, Cox NJ, et al. Linkagedisequilibrium mapping of autistic disorder, with 15q11-13 markers. Am J Hum Genet 1998; 62: 1077–83. [Google Scholar]
  34. Buxbaum JD, Silverman JM, Smith CJ, et al. Association between a GABRB3 polymorphism and autism. Mol Psychiatry 2002; 7: 311–6. [Google Scholar]
  35. Miles JH, Hillman RE. Value of a clinical morphology examination in autism. Am J Med Genet 2000; 91: 245–53. [Google Scholar]
  36. Ishikawa-Brush Y, Powell JF, Bolton P, et al. Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3’ to the SDC2 gene. Hum Mol Genet 1997; 6: 1241–50. [Google Scholar]
  37. Thomas NS. Xp deletions associated with autism in three females. Lancet 1999; 353: 541–5. [Google Scholar]
  38. Skuse DH, James RS, Bishop DV, et al. Evidence from Turner’s syndrome of an imprinted X-linked locus affecting cognitive function. Nature 1997; 387: 705–8. [Google Scholar]
  39. Jamain S, Quach H, Quintana-Murci L, et al. Y chromosome haplogroups in autistic subjects. Mol Psychiatry 2002; 7: 217–9. [Google Scholar]
  40. Goussé V, Plumet MH, Chabane N, Mouren- Siméoni MC, Ferradian N, Leboyer M. Fringe phenotypes in autism: review of clinical, biochemical and cognitive studies. Eur Psychiatry 2002; 17: 1–9. [Google Scholar]
  41. Jamain S, Quach H, Betancur C, et al. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet 2003; 34 : 27–9. [Google Scholar]

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