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1 - Genes and behaviour: cognitive abilities and disabilities in normal populations

from Part I - Genes and behaviour

Published online by Cambridge University Press:  19 January 2010

Robert Plomin
Affiliation:
Institute of Psychiatry, King's College, London, UK
Maria A. Ron
Affiliation:
Institute of Neurology, London
Trevor W. Robbins
Affiliation:
University of Cambridge
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Summary

Introduction

During the past three decades, the behavioural sciences have emerged from an era of strict environmental explanations for differences in behaviour to a more balanced view that recognizes the importance of nature (genetics) as well as nurture (environment). This shift occurred first for behavioural disorders, including rare disorders such as autism (0.001 incidence), more common disorders such as schizophrenia (0.01), and very common disorders such as reading disability (0.05). More recently it has become increasingly accepted that genetic variation contributes importantly to differences among individuals in the normal range of variability as well as for abnormal behaviour. Moreover, many behavioural disorders, especially common ones, may represent the quantitative extreme of the same genetic and environmental factors responsible for variation in the normal range. That is, genetic influence on disorders such as reading disability may not be due to genes specific to the disorder but rather to genes that contribute to the normal range of individual differences in reading ability. This view, known as the quantitative trait locus (QTL) perspective, has important conceptual implications because it implies that some common disorders may not be disorders at all but rather the extremes of normal distributions. This QTL perspective has far-reaching implications for molecular genetics and for neuroscience. If many genes of small effect are involved, it will be much more difficult to find them. It will also be much more difficult to explore the brain mechanisms that mediate genetic effects on behaviour.

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Publisher: Cambridge University Press
Print publication year: 2003

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References

Abecasis, G R, Noguchi, E, Heinzmann, A et al. (2001). Extent and distribution of linkage disequilibrium in three genomic regions. Am J Hum Genet, 68, 191–7Google Scholar
American Psychiatric Association (1994). Diagnostic and Statistical Manual of Mental Disorders, 4th edn (DSM–IV). Washington, DC: APA
Anderson B (2000). The g factor in non-human animals. In The Nature of Intelligence, ed. G R Bock, J A Goode and K Webb, pp. 79–95. Chichester: John Wiley and Sons (Novartis Foundation Symposium 233)
Anderson M (1992). The Development of Intelligence: Studies in Developmental Psychology. Hove: Psychology Press
Andreasen N C (2001). Brave New Brain: Conquering Mental Illness in the Era of the Genome. Oxford: Oxford University Press
Andrews, G, Morris-Yates, A, Howie, P and Martin, N (1991). Genetic factors in stuttering confirmed. Arch Gen Psychiatry, 48, 1034–5Google Scholar
Baddeley A and Gathercole S (1999). Individual differences in learning and memory: psychometrics and the single case. In Learning and Individual Differences: Process, Trait, and Content Determinants, ed. P L Ackerman, P C Kyllonen and R D Roberts, pp. 31–55. Washington, DC: American Psychological Association
Bakwin, H (1973). Reading disability in twins. Dev Med Child Neurol, 15, 184–7CrossRefGoogle Scholar
Baron, M (2001). Genetics of schizophrenia and the new millennium: progress and pitfalls. Am J Hum Genet, 68, 299–312Google Scholar
Bishop, D V M, North, T and Donlan, C (1995). Genetic basis of specific language impairment: evidence from a twin study. Dev Med Child Neurol, 37, 56–71Google Scholar
Cardon, L R and Bell, J (2001). Association study designs for complex diseases. Nat Genet, 2, 91–9CrossRefGoogle Scholar
Cardon, L R, Smith, S D, Fulker, D W, Kimberling, W J, Pennington, B F and DeFries, J C (1994). Quantitative trait locus for reading disability on chromosome 6. Science, 266, 276–9Google Scholar
Carroll J B (1993). Human Cognitive Abilities. New York: Cambridge University Press
Carroll, J B (1997). Psychometrics, intelligence, and public policy. Intelligence, 24, 25–52CrossRefGoogle Scholar
Chorney, M J, Chorney, K, Seese, N et al. (1998). A quantitative trait locus (QTL) associated with cognitive ability in children. Psychol Sci, 9, 1–8Google Scholar
Corder, E H, Saunders, A M, Strittmatter, W J et al. (1993). Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science, 261, 921–3Google Scholar
Crusio W E and Gerlai R T (1999). Handbook of Molecular-Genetic Techniques for Brain and Behavior Research. Amsterdam: Elsevier
Dale, P S, Simonoff, E, Bishop, D V M et al. (1998). Genetic influence on language delay in 2-year-old children. Nat Neurosci, 1, 324–8Google Scholar
Dale, P S, Dionne, G, Eley, T C and Plomin, R (2000). Lexical and grammatical development: a behavioral genetic perspective. J Child Lang, 27, 619–42CrossRefGoogle Scholar
Daniels, J, Holmans, P, Plomin, R, McGuffin, P and Owen, M J (1998). A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. Am J Hum Genet, 62, 1189–97Google Scholar
Deary I (2000). Looking Down on Human Intelligence: From Psychometrics to the Brain. Oxford: Oxford University Press
Deary, I J, Whalley, L J, Lemmon, H, Crawford, J R and Starr, J M (2000). The stability of individual differences in mental ability from childhood to old age: follow-up of the 1932 Scottish Mental Survey. Intelligence, 28, 49–55CrossRefGoogle Scholar
Decker S N and Vandenberg S G (1985). Colorado twin study of reading disability. In Biobehavioral Measures of Dyslexia, ed. D B Gray and J F Kavanagh, pp. 123–35. Parkton, MD: York Press
DeFries, J C and Fulker, D W (1985). Multiple regression analysis of twin data. Behav Genet, 15, 467–73CrossRefGoogle Scholar
DeFries, J C and Fulker, D W (1988). Multiple regression analysis of twin data: etiology of deviant scores versus individual differences. Acta Genet Med Gemellol, 37, 205–16Google Scholar
DeFries J C and Gillis J J (1993). Genetics and reading disability. In Nature, Nurture and Psychology, ed. R Plomin and G E McClearn, pp. 121–45. Washington, DC: American Psychological AssociationCrossRef
DeFries J C, Vogler G P and LaBuda M C (1986). Colorado Family Reading Study: an overview. In Perspectives in Behavior Genetics, ed. J L Fuller and E C Simmel, pp. 29–56. Hillsdale, NJ: Lawrence Erlbaum
DeFries J C, Knopik V S and Wadsworth S J (1999). Colorado Twin Study of reading disability. In Reading and Attention Disorders: Neurobiological Correlates, ed. D D Duane, pp. 17–41. Baltimore, MD: York Press
Duncan, J, Seitz, R J, Kolodny, J et al. (2000). A neural basis for general intelligence. Science, 289, 457–60CrossRefGoogle Scholar
Felsenfeld S (1994). Developmental speech and language disorders. In Nature and Nurture During Middle Childhood, ed. J C DeFries, R Plomin and D W Fulker, pp. 102–19. Oxford: Blackwell
Felsenfeld, S and Plomin, R (1997). Epidemiological and offspring analyses of developmental speech disorders using data from the Colorado Adoption Project. J Speech Lang Hear Res, 40, 778–91Google Scholar
Fisher, S E, Vargha-Khadem, F, Watkins, K E, Monaco, A P and Pembrey, M E (1998). Localisation of a gene implicated in a severe speech and language disorder. Nat Genet, 18, 168–70Google Scholar
Fodor J A (1983). The Modularity of Mind. Cambridge, MA: MIT Press
Gardner H (1983). Frames of Mind: The Theory of Multiple Intelligences. New York: Basic Books
Gayán, J, Smith, S D, Cherny, S S et al. (1999). Quantitative-trait locus for specific language and reading deficits on chromosome 6p. Am J Hum Genet, 64, 157–64Google Scholar
Gazzaniga M S E (2000). Cognitive Neuroscience: A Reader. Oxford: Blackwell
Gilger J W (1997). How can behavioral genetic research help us understand language development and disorders? In Towards A Genetics of Language, ed. M L Rice, pp. 77–110. Hillsdale, NJ: Lawrence Erlbaum
Goleman D (1995). Emotional Intelligence. New York: Bantam Books
Gottfredson, L S (1997). Why g matters: the complexity of everyday life. Intelligence, 24, 79–132CrossRefGoogle Scholar
Gould S J (1996). The Mismeasure of Man, 2nd edn. New York: W W Norton
Grigorenko, E L, Wood, F B, Meyer, M S et al. (1997). Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15. Am J Hum Genet, 60, 27–39Google Scholar
Hill, L, Chorney, M J, Chorney, K et al. (in press). A quantitative trait locus not associated with cognitive ability in children: a failure to replicate. Psychol Sci
Howie, P (1981) Concordance for stuttering in monozygotic and dizygotic twin pairs. J Speech Hear Res, 5, 343–8Google Scholar
International Molecular Genetics Study of Autism Consortium (1998). A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet, 7, 571–8
Jensen, A R (1998). The g Factor: The Science of Mental Ability. Wesport: Praeger
Kidd K (1983). Recent progress on the genetics of stuttering. In Genetic Aspects of Speech and Language Disorders, ed. C Ludlow and J Cooper, pp. 197–213. New York: Academic Press
Kosslyn S and Plomin R (2001). Towards a neuro-cognitive genetics: goals and issues. In Psychiatric Neuroimaging Research: Contemporary Strategies, ed. D Doughert, S L Rauch and J F Rosenbaum, pp. 491–515. Washington, DC: American Psychiatric Press
Kruglyak, L (1999). Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nat Genet, 22, 139–44CrossRefGoogle Scholar
Lai, C S, Fisher, S E, Hurst, J A, Vargha-Khadem, F and Monaco, A P (2001). A forkhead-domain gene is mutated in a severe speech and language disorder. Nature, 413, 519–23Google Scholar
Lewis, B A and Thompson, L A (1992). A study of developmental speech and language disorders in twins. J Speech Hear Res, 35, 1086–94Google Scholar
McClearn, G E, Johansson, B, Berg, S et al. (1997). Substantial genetic influence on cognitive abilities in twins 80+ years old. Science, 276, 1560–63Google Scholar
McGue M, Bouchard T J Jr, Iacono W G and Lykken D T (1993). Behavioral genetics of cognitive ability: a life-span perspective. In Nature, Nurture, and Psychology, ed. R Plomin and G E McClearn, pp. 59–76. Washington, DC: American Psychological Association
Neisser, U, Boodoo, G, Bouchard, T J Jr et al. (1996). Intelligence: knowns and unknowns. Am Psychol, 51, 77–101Google Scholar
Nichols, P L (1984). Familial mental retardation. Behav Genet, 14, 161–70CrossRefGoogle Scholar
Petrill, S A (1997). Molarity versus modularity of cognitive functioning? A behavioral genetic perspective. Curr Directions Psychol Sci, 6, 96–9CrossRefGoogle Scholar
Pfaff D W, Berrettini W H, Joh T H and Maxson S C (2000). Genetic influences on neural and behavioral functions. Boca Raton, FL: CRC Press
Pinker S (1994). The Language Instinct. New York, NY: William Morrow and Co
Plomin R (1994). Genetics and Experience: The Interplay Between Nature and Nurture. Thousand Oaks, CA: Sage Publications
Plomin, R (1999 a). Genetic research on general cognitive ability as a model for mild mental retardation. Int Rev Psychiatry, 11, 34–6Google Scholar
Plomin R (1999b). Genetics and general cognitive ability. Nature, 402, C25–9
Plomin, R (2001). The genetics of g in human and mouse. Nat Rev Neurosci, 2, 136–41Google Scholar
Plomin R (2002). Quantitative trait loci (QTLs) and general cognitive ability. In Molecular Genetics of Human Personality, ed. J Benjamin, R Ebstein and R H Belmaker, pp. 211–30. Washington, DC: American Psychiatric Press
Plomin, R and Crabbe, J C (2000). DNA. Psychol Bull, 126, 806–28CrossRefGoogle Scholar
Plomin R and Dale P S (2000). Genetics and early language development: a UK study of twins. In Speech and Language Impairments In Children: Causes, Characteristics, Intervention and Outcome, ed. D V M Bishop and B E Leonard, pp. 35–51. Hove: Psychology Press
Plomin, R and DeFries, J C (1998). Genetics of cognitive abilities and disabilities. Sci Am, May, 62–9CrossRefGoogle Scholar
Plomin, R and Rutter, M (1998). Child development, molecular genetics, and what to do with genes once they are found. Child Dev, 69, 1223–42Google Scholar
Plomin, R, Owen, M J and McGuffin, P (1994). The genetic basis of complex human behaviors. Science, 264, 1733–9CrossRefGoogle Scholar
Plomin, R, McClearn, G E, Smith, D L et al. (1995). Allelic associations between 100 DNA markers and high versus low IQ. Intelligence, 21, 31–48Google Scholar
Plomin R, DeFries J C, McClearn G E and McGuffin P (2001a). Behavioral Genetics, 4th edn. New York: Worth Publishers
Plomin, R, Asbury, K and Dunn, J (2001 b). Why are children in the same family so different? Nonshared environment a decade later. Can J Psychiatry, 46, 225–33Google Scholar
Plomin, R, Hill, L, Craig, I, McGuffin, P et al. (2001 c). A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling. Behav Genet, 31, 497–509Google Scholar
Price, T S, Eley, T C, Dale, P S, Stevenson, J and Plomin, R (2000). Genetic and environmental covariation between verbal and non-verbal cognitive development in infancy. Child Dev, 71, 948–59Google Scholar
Reed E W and Reed S C (1965). Mental Retardation: A Family Study. Philadelphia: Saunders
Reich, D E, Cargill, M, Bolk, S et al. (2001). Linkage disequilibrium in the human genome. Nature, 411, 199–204Google Scholar
Rice M L (1996). Toward a Genetics of Language. Hillsdale, NJ: Lawrence Erlbaum
Risch, N and Merikangas, K R (1996). The future of genetic studies of complex human diseases. Science, 273, 1516–17CrossRefGoogle Scholar
Rutter, M and Plomin, R (1997). Opportunities for psychiatry from genetic findings. Br J Psychiatry, 171, 209–19CrossRefGoogle Scholar
Salthouse, T A and Czaja, S J (2000). Structural constraints on process explanations in cognitive aging. Psychol Aging, 15, 44–55Google Scholar
Schulte-Körne, G, Grimm, T, Nöthen, M M, Müller-Myhsok, B, Propping, P and Remschmidt, H (1997). Evidence for linkage of spelling disability to chromosome 15. Am J Med Genet (Neuropsychiatric Genet), 74, 661 (abstract)Google Scholar
Smith, S D, Kimberling, W J, Pennington, B F and Lubs, H A (1983). Specific reading disability: identification of an inherited form through linkage analysis. Science, 219, 1345–47CrossRefGoogle Scholar
Smith, S D, Kimberling, W J and Pennington, B F (1991). Screening for multiple genes influencing dyslexia. Read Writ, 3, 285–98CrossRefGoogle Scholar
Smith, S D, Kelley, P M and Brower, A M (1998). Molecular approaches to the genetic analysis of specific reading disability. Hum Biol, 70, 239–56Google Scholar
Snyderman, M and Rothman, S (1987). Survey of expert opinion on intelligence and aptitude testing. Am Psychol, 42, 137–44CrossRefGoogle Scholar
Spearman, C (1904). General intelligence, objectively determined and measured. Am J Psychol, 15, 201–93CrossRefGoogle Scholar
Spearman C (1927). The Abilities of Man: Their Nature and Measurement. New York: Macmillan
Stauffer, J M, Ree, M J and Carretta, T R (1996). Cognitive-components tests are not much more than g: an extension of Kyllonen's analyses. J Gen Psychol193–205Google Scholar
Sternberg R J (1985). Beyond IQ: A Triarchic Theory of Human Intelligence. Cambridge: Cambridge University Press
Sternberg R J and Gardner M K (1983). A componential interpretation of the general factor in human intelligence. In A Model for Intelligence, ed. H J Eysenck, pp. 231–54. Berlin: Springer Verlag
Stevenson, J, Graham, P, Fredman, G and McLoughlin, V (1987). A twin study of genetic influences on reading and spelling ability and disability. J Child Psychol Psychiatry, 28, 229–47CrossRefGoogle Scholar
Stromswold, K (2001). The heritability of language: a review and meta-analysis of twin, adoption and linkage studies. Language, 77, 647–723CrossRefGoogle Scholar
Thompson R F (2000). The Brain: a Neuroscience Primer, 3rd edn. New York: Worth
Tomblin, J B and Buckwalter, P R (1998). Heritability of poor language achievement among twins. J Speech Lang Hear Res, 41, 188–99Google Scholar
Wahlström, J (1990). Gene map of mental retardation. J Ment Deficiency Res, 34, 11–27Google Scholar
Watson, S J and Akil, H (1999). Gene chips and arrays revealed: a primer on their power and their uses. Biol Psychiatry, 45, 533–43Google Scholar
Wickelgren, I (1998). Tracking insulin to the mind. Science, 280, 517–19Google Scholar
Willcutt E G, DeFries J C, Pennington B F, Smith S D, Cardon L R and Olson R K (2002). Genetic etiology of comorbid reading difficulties and ADHD. In Behavioral Genetics in the Postgenomic Era, ed. R Plomin, J DeFries, I C Craig and P McGuffin, pp. 227–46. Washington, DC: APA Books
Yairi, E, Ambrose, N and Cox, N (1996). Genetics of stuttering: a critical review. J Speech Lang Hear Res, 39, 771–84CrossRefGoogle Scholar

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