Autism: Common, heritable, but not harmful

Gernsbacher, M. A., Dawson, M., & Mottron, L. (2006). Autism: Common, heritable, but not harmful. Behavioral and Brain Sciences, 29(4), 413-414. https://doi.org/10.1017/s0140525x06319097

Publication date: 1 Aug 2006 Added to AutiHub: 3 Jul 2026 Type: Article Article language: English

This publication is integrated into AutiHub through:

Authors

Publication authors
3
Publication authors identified as autistic
1 / 3 (33.3%)

Abstract

We assert that one of the examples used by Keller & Miller (K&M), namely, autism, is indeed common, and heritable, but we question whether it is harmful. We provide a brief review of cognitive science literature in which autistics perform superiorly to non-autistics in perceptual, reasoning, and comprehension tasks; however, these superiorities are often occluded and are instead described as dysfunctions.

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Bibliography inclusion overview

These indicators describe the cited bibliography imported for this publication. Cited-reference metrics use the cited-reference total as denominator. Cited-author metrics state whether they use all cited-author occurrences or only occurrences linked to authors already integrated in the AutiHub database. They use cached links between cited authors and authors integrated in the AutiHub database. Last computed: 16 Aug 2026 11:30.

Cited references
43
Total cited references integrated for this publication.
Cited references with an identified autistic author
2 / 43 (4.7%)
Cited author occurrences identified as autistic
2 / 189 (1.1%)
Among occurrences linked to AutiHub author records: 2 / 11 (18.2%). Distinct cited authors identified as autistic: 1 / 184 (0.5%).
Cited author occurrences linked to AutiHub author records
11 / 189 (5.8%)
Distinct linked cited authors: 10 / 184 (5.4%)
Linked cited-author occurrences not identified as autistic
9 / 11 (81.8%)
Among linked cited-author occurrences only. Across all cited-author occurrences: 9 / 189 (4.8%). Distinct linked cited authors not identified as autistic: 9 / 10 (90.0%).
  1. George C. Williams (2018). Adaptation and Natural Selection . Princeton University Press.
    OpenAlex
  2. Danielle Ropar , Peter Mitchell (2002). Shape constancy in autism: the role of prior knowledge and perspective cues . Journal of Child Psychology and Psychiatry, 43(5), 647-653. Wiley.
    OpenCitations
  3. Peter J. Richerson , Robert Boyd (2004). Not By Genes Alone . University of Chicago Press.
    OpenAlex
  4. Motomi Toichi , Yoko Kamio , Takashi Okada , Morimitsu Sakihama , Eric A. Youngstrom , Robert L. Findling et al. (2002). A Lack of Self-Consciousness in Autism . American Journal of Psychiatry, 159(8), 1422-1424. American Psychiatric Association Publishing.
    OpenAlex OpenCitations
  5. Endler, John A. 1947- , Mousseau, Timothy A. , Sinervo, Barry (2000). Adaptive Genetic Variation In The Wild . Oxford University PressNew York, NY.
    OpenAlex
  6. Amitta Shah , Uta Frith (1993). Why Do Autistic Individuals Show Superior Performance on the Block Design Task? Journal of Child Psychology and Psychiatry, 34(8), 1351-1364. Wiley.
    OpenCitations
  7. Eugen Bleuler (1911). Dementia Praecox oder Gruppe der Schizophrenien .
    Type: Book OpenAlex: https://openalex.org/W1530582387
    OpenAlex
  8. A. Jablensky , N. Sartorius , G. Ernberg , M. Anker , A. Korten , J. E. Cooper et al. (1992). Schizophrenia: manifestations, incidence and course in different cultures A World Health Organization Ten-Country Study . Psychological Medicine. Monograph Supplement, 20, 1-97. Cambridge University Press (CUP).
    OpenAlex
  9. M. A. Just (2004). Cortical activation and synchronization during sentence comprehension in high-functioning autism: evidence of underconnectivity . Brain, 127(8), 1811-1821. Oxford University Press (OUP).
    OpenCitations
  10. Irene Tiemann-Boege , William Navidi , Raji Grewal , Dan Cohn , Brenda Eskenazi , Andrew J. Wyrobek et al. (2002). The observed human sperm mutation frequency cannot explain the achondroplasia paternal age effect . Proceedings of the National Academy of Sciences, 99(23), 14952-14957. National Academy of Sciences.
    OpenAlex
  11. Carolina Johansson , Mårten Jansson , Love Linnér , Qiu-Ping Yuan , Nancy L Pedersen , Douglas Blackwood et al. (2001). Genetics of affective disorders . European Neuropsychopharmacology, 11(6), 385-394. Elsevier BV.
    OpenAlex
  12. David Q. Beversdorf , Brian W. Smith , Gregory P. Crucian , Jeffrey M. Anderson , Jocelyn M. Keillor , Anna M. Barrett et al. (2000). Increased discrimination of “false memories” in autism spectrum disorder . Proceedings of the National Academy of Sciences, 97(15), 8734-8737. National Academy of Sciences.
    OpenCitations
  13. A.D. Børglum , G. Kirov , N. Craddock , O. Mors , W. Muir , V. Murray et al. (2003). Possible parent‐of‐origin effect of Dopa decarboxylase in susceptibility to bipolar affective disorder . American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 117B(1), 18-22. Wiley.
    OpenAlex
  14. Amitta Shah , Uta Frith (1983). AN ISLET OF ABILITY IN AUTISTIC CHILDREN: A RESEARCH NOTE . Journal of Child Psychology and Psychiatry, 24(4), 613-620. Wiley.
    OpenCitations
  15. David Metzgar , Christopher Wills (2000). Evidence for the Adaptive Evolution of Mutation Rates . Cell, 101(6), 581-584. Elsevier BV.
    OpenAlex
  16. Suniti Chakrabarti , Éric Fombonne (2005). Pervasive Developmental Disorders in Preschool Children: Confirmation of High Prevalence . American Journal of Psychiatry, 162(6), 1133-1141. American Psychiatric Association Publishing.
    OpenCitations
  17. Rachel Raybould , Elaine K. Green , Stuart MacGregor , Katherine Gordon-Smith , Jess Heron , Sally Hyde et al. (2005). Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1) . Biological Psychiatry, 57(7), 696-701. Elsevier BV.
    OpenAlex
  18. Nicholas B. Allen , Paul B. T. Badcock (2003). The Social Risk Hypothesis of Depressed Mood: Evolutionary, Psychosocial, and Neurobiological Perspectives. Psychological Bulletin, 129(6), 887-913. American Psychological Association (APA).
    OpenAlex
  19. A. Vogels , M. De Hert , M.J. Descheemaeker , V. Govers , K. Devriendt , E. Legius et al. (2004). Psychotic disorders in Prader–Willi syndrome . American Journal of Medical Genetics Part A, 127A(3), 238-243. Wiley.
    OpenAlex
  20. R. M. CORBO , R. SCACCHI (1999). Apolipoprotein E (APOE) allele distribution in the world. Is APOE * 4 a ‘thrifty’ allele? Annals of Human Genetics, 63(4), 301-310. Wiley.
    OpenAlex
  21. Lee Anna Clark (2005). Temperament as a Unifying Basis for Personality and Psychopathology. Journal of Abnormal Psychology, 114(4), 505-521. American Psychological Association (APA).
    OpenAlex
  22. Peter McGuffin , Fruhling Rijsdijk , Martin Andrew , Pak Sham , Randy Katz , Alastair Cardno (2003). The Heritability of Bipolar Affective Disorder and the Genetic Relationship to Unipolar Depression . Archives of General Psychiatry, 60(5), 497. American Medical Association (AMA).
    OpenAlex
  23. Annamari Tuulio-Henriksson , Ritva Arajärvi , Timo Partonen , Jari Haukka , Teppo Varilo , Marjut Schreck et al. (2003). Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients . Biological Psychiatry, 54(6), 623-628. Elsevier BV.
    OpenAlex
  24. C.P Somnath , Y.C Janardhan Reddy , S Jain (2002). Is there a familial overlap between schizophrenia and bipolar disorder? Journal of Affective Disorders, 72(3), 243-247. Elsevier BV.
    OpenAlex
  25. W. Bodmer (1999). Familial adenomatous polyposis (FAP) and its gene, APC . Cytogenetic and Genome Research, 86(2), 99-104. S. Karger AG.
    OpenAlex
  26. Q RAHMAN (2005). The neurodevelopment of human sexual orientation . Neuroscience & Biobehavioral Reviews, 29(7), 1057-1066. Elsevier BV.
    OpenAlex
  27. SU Peters , AL Beaudet , N Madduri , CA Bacino (2004). Autism in Angelman syndrome: implications for autism research . Clinical Genetics, 66(6), 530-536. Wiley.
    OpenAlex
  28. Wolfgang Enard , Molly Przeworski , Simon E. Fisher , Cecilia S. L. Lai , Victor Wiebe , Takashi Kitano et al. (2002). Molecular evolution of FOXP2, a gene involved in speech and language . Nature, 418(6900), 869-872. Springer Science and Business Media LLC.
    OpenAlex
  29. T Crow (1995). A continuum of psychosis, one human gene, and not much else — the case for homogeneity . Schizophrenia Research, 17(2), 135-145. Elsevier BV.
    OpenAlex
  30. W Reik , E R Maher , P J Morrison , A E Harding , S A Simpson (1993). Age at onset in Huntington's disease and methylation at D4S95. Journal of Medical Genetics, 30(3), 185-188. BMJ.
    OpenAlex
  31. Jordan W. Smoller , Christine T. Finn (2003). Family, twin, and adoption studies of bipolar disorder . American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 123C(1), 48-58. Wiley.
    OpenAlex
  32. Kenneth S. Kendler (1987). Symptoms of Anxiety and Symptoms of Depression . Archives of General Psychiatry, 44(5), 451. American Medical Association (AMA).
    OpenAlex
  33. N H Barton (1990). Pleiotropic models of quantitative variation. Genetics, 124(3), 773-782. Oxford University Press (OUP).
    OpenAlex
  34. Lynn E. DeLisi , Sarah H. Shaw , Timothy J. Crow , Gail Shields , Angela B. Smith , Veronica W. Larach et al. (2002). A Genome-Wide Scan for Linkage to Chromosomal Regions in 382 Sibling Pairs With Schizophrenia or Schizoaffective Disorder . American Journal of Psychiatry, 159(5), 803-812. American Psychiatric Association Publishing.
    OpenAlex
  35. Peter J. Bentley (2004). Evolving beyond perfection: an investigation of the effects of long-term evolution on fractal gene regulatory networks . Biosystems, 76(1-3), 291-301. Elsevier BV.
    OpenAlex
  36. Michael W Nachman , Susan L Crowell (2000). Estimate of the Mutation Rate per Nucleotide in Humans . Genetics, 156(1), 297-304. Oxford University Press (OUP).
    OpenAlex
  37. Alan S. Brown , Catherine A. Schaefer , Richard J. Wyatt , Melissa D. Begg , Raymond Goetz , Michaeline A. Bresnahan et al. (2002). Paternal Age and Risk of Schizophrenia in Adult Offspring . American Journal of Psychiatry, 159(9), 1528-1533. American Psychiatric Association Publishing.
    OpenAlex
  38. Susan L. Smalley , Sandra K. Loo , May H. Yang , Rita M. Cantor (2005). Toward localizing genes underlying cerebral asymmetry and mental health . American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 135B(1), 79-84. Wiley.
    OpenAlex
  39. Kenneth S. Kendler , Margaret Gatz , Charles O. Gardner , Nancy L. Pedersen (2006). A Swedish National Twin Study of Lifetime Major Depression . American Journal of Psychiatry, 163(1), 109-114. American Psychiatric Association Publishing.
    OpenAlex
  40. Trevor Price , Dolph Schluter (1991). ON THE LOW HERITABILITY OF LIFE-HISTORY TRAITS . Evolution, 45(4), 853-861. Oxford University Press (OUP).
    OpenAlex
  41. Leda Cosmides , Jerome H. Barkow (1992). The Adapted Mind .
    Type: Book OpenAlex: https://openalex.org/W2798670267
    OpenAlex