Abstract
Human behavioural genetics is an established research discipline of the genomic age, and applications for behavioural genetic information are most likely to emerge in areas such as criminal justice, education, employment and insurance. However, behavioural genetic research into personality traits and antisocial behaviour poses several risks; for example, tentative or preliminary research findings might be misused in legal and commercial settings. Scientific caution, public and media education, expert consultation and confidentiality protection are essential for the responsible use of behavioural genetics.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$189.00 per year
only $15.75 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
References
Rothstein, M. in Behavioural Genetics: the Clash of Culture and Biology (eds Carson, R. & Rothstein, M.) 98–100 (Johns Hopkins Univ. Press, Baltimore, 1999).
Kevles, D. In the Name of Eugenics: Genetics and the Use of Human Heredity (Knopf, New York, 1985).
Nelkin, D. & Lindee, S. The DNA Mystique: the Gene as a Cultural Icon (W.H. Freeman, New York, 1995).
Horgan, J. Do our genes influence behaviour? Chron. High. Educ. 51, 62 (2004).
Clark, W. & Grunstein, M. Are We Hardwired? The Role of Genes in Human Behaviour (Oxford Univ. Press, Oxford, 2000).
Condit, C. M., Ofulue, N. & Sheedy, K. M. Determinism and mass-media portrayals of genetics. Am. J. Hum. Genet. 63, 662–663 (1998).
Petersen, A. Biofantasies: genetics and medicine in the print news media. Soc. Sci. Med. 52, 1255–1268 (2004).
Geller, G., Bernhardt, B. & Holtzman, N. A. The media and public reaction to genetic research. JAMA 287, 713 (2002).
Plomin, R., DeFries, J. C., Craig, I. W. & McGuffin, P. (eds) Behavioural Genetics in the Post-Genomic Era (American Psychological Association, Washington DC, 2003).
Parens, E. (ed.) Genetic differences and human identities: on why talking about behavioural genetics is important and difficult. Hastings Cent. Rep. 34, S1–S35 (2004).
Sherman, S. L. & Waldman, I. D. in Behavioural Genetics: The Clash of Culture and Biology 55. (eds Carson, R. A. & Rothstein, M. A.) 35–60 (Johns Hopkins Univ. Press, Baltimore, 1999).
Hamer, D. Rethinking behaviour genetics. Science 298, 71–72 (2002).
Arias, B. et al. The 5-HT(2A) receptor gene 102T/C polymorphism is associated with suicidal behaviour in depressed patients. Am. J. Med. Genet. 105, 801–804 (2001).
Sjoholt, G. et al. Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder. Mol. Psychiatry 9, 621–629 (2004).
Barondes, S. H. et al. Workshop on schizophrenia. Proc. Natl Acad. Sci. USA 94, 1612–1614 (1997).
Ozelius, L. et al. Human monoamine oxidase gene (MAOA) chromosome position (Xp21–p11) and DNA polymorphism. Genomics 3, 53–58 (1988).
Brunner, H. G. in Genetics of Criminal Behaviour (Wiley, Chichester 1996).
Goldman, D., Oroszi, G. & Ducci, F. The genetics of addictions: uncovering the genes. Nature Rev. Genet. 6, 521–532 (2005).
Fowler, J. S. et al. Inhibition of monoamine oxidase B in the brains of smokers. Nature 379, 733–736 (1996).
Preisig, M. et al. Association between bipolar disorder and monoamine oxidase A gene polymorphisms: results of a multicenter study. Am. J. Psychiatry 157, 948–955 (2000).
Sobell, J. L. et al. Screening the monoamine oxidase B gene in 100 male patients with schizophrenia: a cluster of polymorphisms in African-Americans but lack of functionally significant sequence changes. Am. J. Med. Genet. 74, 44–49 (1997).
Valavka, J., Bilder, R. & Nolan, K. Catecholamine and aggression: the role of COMT and MAO polymorphisms. Ann. NY Acad. Sci. 1036, 393–398 (2004).
Brunner, H. G. et al. Abnormal behaviour associated with a point mutation in the structural gene for monoamine oxidase A. Science 262, 578–580 (1993).
Brunner, H. G. et al. X-linked borderline mental retardation with prominent behavioural disturbance: phenotype, genetic localization, and evidence for disturbed monoamine oxidase metabolism. Am. J. Hum. Genet. 52, 1032–1039 (1993).
Garpenstrand, H. et al. Low platelet monoamine oxidase activity in Swedish imprisoned criminal offenders. Eur. Neuropsychopharmacol. 12, 135–140 (2002).
Klinteberg, B. A. Biology, norms, and personality: a developmental perspective. Neuropsychobiology 34, 146–154 (1996).
Berman, M. E. & Coccaro, E. F. Neurobiological correlates of violence: relevance to criminal responsibility. Behav. Sci. Law 16, 303–318 (1998).
Cravchik, A. & Goldman, D. Neurochemical individuality: genetic diversity among human dopamine and serotonin receptors and transporters. Arch. Gen. Psychiatry 57, 1105–1114 (2000).
Rueter, L. E. et al. A critical review of 5-HT brain microdialysis and behaviour. Rev. Neurosci. 8, 117–137 (1997).
Davidson, R. J. et al. Dysfunction in the neural circuitry of emotion regulation — a possible prelude to violence. Science 289, 591–594 (2000).
Stanley, B. et al. Association of aggressive behaviour with altered serotonergic function in patients who are not suicidal. Am. J. Psychiatry 157, 609–614 (2000).
Virkkunen, M. et al. A prospective follow-up study of alcoholic violent offenders and fire setters. Arch. Gen. Psychiatry 53, 523–529 (1996).
Maron, E. et al. Associations between serotonin-related gene polymorphisms and panic disorder. Int. J. Neuropsychopharmacol. 8, 261–266 (2005).
Evans, J. et al. Impulsiveness, serotonin genes and repetition of deliberate self-harm (DSH). Psychol. Med. 30, 1327–1334 (2000).
Bjork, J. M. et al. Serotonin 2a receptor T102C polymorphism and impaired impulse control. Am. J. Med. Genet. 114, 336–339 (2002).
Jarvie, K. R., Tiberi, M. & Caron, M. G. in Dopamine Receptors and Transporters (ed. Niznik, H. B.) 133–150 (Dekker, New York, 1994).
Blum, K. et al. Reward deficiency syndrome: a biogenetic model for the diagnosis and treatment of impulsive, addictive, and compulsive behaviours. J. Psychoactive Drugs 32 (Suppl. 1–4), 1–112 (2000).
Retz, W., Retz Junginger, P., Supprian, T., Thome, J. & Rosler, M. Association of serotonin transporter promoter gene polymorphism with violence: relation with personality disorders, impulsivity, and childhood ADHD psychopathology. Behav. Sci. Law 22, 415–425 (2004).
Soderstrom, H. et al. CSF studies in violent offenders: I. 5-HIAA as a negative and HVA as a positive predictor of psychopathy. J. Neural Transm. 108, 869–878 (2001).
Caron, L., Karkazis, K., Raffin, T., Swan, G. & Koenig, B. Nicotine addiction through a neurogenomic prism: ethics, public health, and smoking. Nicotine Tob. Res. 7, 181–197 (2005).
Beirut, L. J. et al. Familial transmission of substance dependence: alcohol, marijuana, cocaine, and habitual smoking: a report from a collaborative study on the genetics of alcoholism. Arch. Gen. Psychiatry 55, 982–988 (1998).
Ellickson, P. et al. Profiles of violent youth: substance use and other concurrent problems. Am. J. Public Health 87, 1327–1334 (2000).
Hamer, D. The heritability of happiness. Nature Genet. 14, 125–126 (1996).
Bartels, M., Rietveld, M. J., Van Baal, G. C. & Boomsma, D. I. Genetic and environmental influences on the development of intelligence. Behav. Genet. 32, 237–249 (2002).
Benjamin, J. et al. Population and familial association between the D4 dopamine receptor gene and measures of novelty seeking. Nature Genet. 12, 81–84 (1996).
Pillard, R. C. & Bailey, J. M. Human sexual orientation has heritable component. Hum. Biol. 70, 347 (1998).
Joyce, P. R. et al. Polymorphisms of DRD4 and DRD3 and risk of avoidant and obsessive personality traits and disorders. Psychiatry Res. 119, 1–10 (2003).
Eid, M., Riemann, R., Angleitner, A. & Borkenau, P. Sociability and positive emotionality: genetic and environmental contributions to the covariation between different facets of extroversion. J. Personality 71, 319–346 (2003).
Ando, J., Ono, Y. & Wright, M. J. Genetic structure of spatial and verbal working memory. Behav. Genet. 31, 615–624 (2001).
Schulte, P. A. & Lomax, G. Assessment of the scientific basis for genetic testing of railroad workers with carpal tunnel syndrome. J. Occup. Environ. Med. 45, 592–600 (2003).
Rothstein, M. A., Craver, C. B., Schroeder, E. P. & Shoben, E. W. Employment Law Vol. 2, 67–118 (Thomson/West, St Paul, Minneapolis, 2004).
Wiggins v. Smith, 539 US 510 (2003).
Botkin, J. R., McMahon, W. M. & Francis, L. P. (eds) Genetics and Criminality (American Psychological Association, Washington DC, 1999).
Nuffield Council on Bioethics. Genetics and Human Behaviour: the Ethical Context 165 (Nuffield Council, London, 2002).
Hill v. Ozmint, 339 F. 3d 187 (4th Cir. 2003).
Winnick, B. J. & LaFond, J. Q. Protecting Society from Sexually Dangerous Offenders: Law, Justice, and Therapy. (American Psychological Association, Washington DC, 2003).
Tost, H. et al. Pedophilia: neuropsychological evidence encouraging a brain network perspective. Med. Hypotheses 63, 528–531 (2004).
Stone, R. D. The cloudy crystal ball: genetics, child abuse, and the perils of predicting behaviour. Vanderbilt Law Rev. 56, 1557–1590 (2004).
Reiss, A. L., Eliez, S., Schmitt, J. E. & Haberecht, M. Brain imaging in neurogenetic conditions: realizing the potential of behavioural neurogenetics research. Ment. Retard. Dev. Disabil. Res. Rev. 6, 186–197 (2000).
Junaid, M. A. et al. Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor. Am. J. Med. Genet. 131, 11–17 (2004).
Kaminen, N. et al. A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32. J. Med. Genet. 40, 340–345 (2003).
Shalev, R. S. et al. Developmental dyscalculia is a familial learning disability. J. Learn. Disabil. 34, 59–65 (2001).
DiMaio, S., Grizenko, N. & Joober, R. Dopamine genes and attention-deficit hyperactivity disorder: a review. J. Psychiatry Neurosci. 28, 27–38 (2003).
Kuo, P. H., Lin, C. C., Yang, H. J., Soong, W. T. & Chen, W. J. A twin study of competence and behavioural/emotional problems among adolescents in Taiwan. Behav. Genet. 34, 63–74 (2004).
Rothstein, L. F. in Genetic Secrets: Protecting Privacy and Confidentiality in the Genetic Era (ed. Rothstein, M. A.) 317–331 (Yale Univ. Press, New Haven, 1997).
Nuffield Council on Bioethics. Genetics and Human Behaviour: The Ethical Context 74–75 (Nuffield Council, London, 2002).
Turkheimer, E., Haley, A. Waldron, M., D'onofrio, B & Gottesman, I. I. Socioeconomic status modifies heritability of IQ in young children. Psychol. Sci. 14, 623–628 (2003).
Hooker W. D. Psychological testing in the workplace. Occup. Med. 11, 699–717 (1996).
Stabile, S. J. The use of personality tests as a hiring tool: is the benefit worth the cost? Univ. Pennsylvania J. Labor Employ. Law 4, 279–313 (2002).
Travis, M. A. Psychological health tests for violence-prone police officers: objectives, shortcomings, and alternatives. Stanford Law Rev. 46, 1717–1770 (1994).
Ibanez, A., Blanco, C., deCastro, I. P., Fernandez-Piqueras, J. & Saiz-Ruiz, J. Genetics of pathological gambling. J. Gambling Stud. 19, 11–22 (2003).
Comings, D. E. et al. Studies of the 48 bp repeat polymorphism of the DRD4 gene in impulsive, compulsive, addictive behaviours: Tourette syndrome, ADHD, pathological gambling, and substance abuse. Am. J. Med. Genet. 88, 358–368 (1999).
Rothstein, M. A. Genetics and the work force of the next hundred years. Columb. Bus. Law Rev. 2000, 371–402 (2000).
Rothstein, M. A. & Anderlik, M. R. What is genetic discrimination and when and how can it be prevented? Genet. Med. 3, 354–358 (2001).
McGuffin, P., Owen, M. J. & Gottesman, I. I. Psychiatric Genetics and Genomics (Oxford Univ. Press, New York, 2004).
Nestler, E. Genes and addiction. Nature Genet. 26, 277–281 (2000).
Rothstein, M. A. Genetics and Life Insurance: Medical Underwriting and Social Policy (MIT Press, Cambridge, Massachusetts, 2004).
Zuckerman, M. & Kuhlman, D. M. Personality and risk-taking: common biosocial factors. J. Personality 68, 999–1029 (2000).
Kluger, A. N., Siegried, Z. & Ebstein, R. P. A meta-analysis of the association between DRD4 polymorphism and novelty seeking. Mol. Psychiatry 7, 712–717 (2002).
Caspi, A. et al. Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science 301, 386–389 (2003).
Comings, D. E. A multivariate analysis of 59 candidate genes in personality traits: the temperament and character inventory. Clin. Genet. 58, 375 (2000).
Knoppers, B. M., Godard, B. & Joly, Y. in Genetics and Life Insurance: Medical Underwriting and Social Policy (ed. Rothstein, M. A.) (MIT Press, Cambridge, Massachusetts, 2004).
Nuffield Council on Bioethics. Genetics and Human Behaviour: The Ethical Context 113–115 (Nuffield Council, London, 2002).
Dixon, M. Brave new choices? Behavioural genetics and public policy — a discussion document. Institute for Public Policy Research [online], <http://www.ippr.org.uk/ecomm/files/SJ%20genetics.pdf> (2005).
Acknowledgements
The author is indebted to I.I. Gottesman and D. Kaye for their helpful comments on an earlier draft of this article.
Author information
Authors and Affiliations
Ethics declarations
Competing interests
The author declares no competing financial interests.
Related links
Glossary
- ATTENTION-DEFICIT HYPERACTIVITY DISORDER
-
A persistent pattern of inattention and/or hyperactivity or impulsivity that is more frequently displayed and more severe than is typically observed in individuals that are at a comparable level of development.
- BIPOLAR DISORDER
-
A mood disorder that is characterized by periodic swings between exaggerated elation and depression.
- BRAINSTEM
-
A portion of the deep posterior part of the brain that consists of the midbrain, pons and medulla.
- CARPAL TUNNEL SYNDROME
-
Compression of the median nerve as it passes through the carpal tunnel in the wrist, which is often caused by repetitive flexion and extension of the wrist.
- FRAGILE X SYNDROME
-
X-linked mental retardation. It occurs in both genders, but with a higher frequency in males.
- FRIEND OF THE COURT
-
An individual or group that has an interest in a case, but is not a party to it.
- HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
-
A disorder of the peripheral nerves that results in unusual sensitivity to touch, numbness and loss of muscle strength.
- KLINEFELTER SYNDROME
-
A disorder in which males have an XXY-chromosomal constitution. It is associated with a predisposition to learning disabilities and other symptoms.
- LINKAGE ANALYSIS
-
A method for tracking the transmission of genetic information across generations to identify the map location of genetic loci on the basis of co-inheritance of genetic markers and discernable phenotypes in families.
- RECIDIVISM
-
The tendency to relapse into a behavioural condition, especially criminal behaviour.
- TURNER SYNDROME
-
An aneuploidy disorder in which females have a single X-chromosome constitution. It is associated with a diminution in perceptual abilities.
- WILLIAMS SYNDROME
-
A disorder that is caused by deletion in chromosome 7, resulting in mental retardation, aortic stenosis and other symptoms.
Rights and permissions
About this article
Cite this article
Rothstein, M. Applications of behavioural genetics: outpacing the science?. Nat Rev Genet 6, 793–798 (2005). https://doi.org/10.1038/nrg1687
Published:
Issue Date:
DOI: https://doi.org/10.1038/nrg1687
This article is cited by
-
Paediatric MRI Research Ethics: The Priority Issues
Journal of Bioethical Inquiry (2007)