Predicting Sensation Seeking From Dopamine Genes

Burton P.R. Clayton D.G. Cardon L.R. Craddock N. Deloukas P. Duncanson A. . (2007). Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature, 447, 661–678.

Cloninger C.R. Przybeck T.R. Svrakic D.M. (1991). The Tridimensional Personality Questionnaire: United States normative data. Psychological Reports, 69, 1047–1057.

Costa P.T. Jr. McCrae R.R. (1994). NEO PI-R professional manual: Revised (NEO PI-R) and NEO Five-Factor Inventory (NEO-FFI). Lutz, FL: Psychological Assessment Resources.

Derringer J. Krueger R.F. Dick D.M. Saccone S. Grucza R.A. Agrawal A. . (2010). Predicting sensation seeking from dopamine genes: A candidate-system approach. Psychological Science, 21, 1282–1290.

Evans D.M. Visscher P.M. Wray N.R. (2009). Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. Human Molecular Genetics, 18, 3525–3531.

Eysenck S.B.G. Eysenck H.J. Barrett P. (1985). A revised version of the Psychoticism Scale. Personality and Individual Differences, 6, 21–29.

Goddard M.E. Wray N.R. Verbyla K. Visscher P.M. (2009). Estimating effects and making predictions from genome-wide marker data. Statistical Science, 24, 517–529.

Hettema J.M. van den Oord E. An S.S. Kendler K.S. Chen X.N. (2009). Follow-up association study of novel neuroticism gene MAMDC1 . Psychiatric Genetics, 19, 213–214.

Jang K.L. Livesley W.J. Vernon P.A. (1996). Heritability of the big five personality dimensions and their facets: A twin study. Journal of Personality, 64, 577–591.

Janssens A. Gwinn M. Bradley L.A. Oostra B.A. van Duijn C.M. Khoury M.J. (2008). A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions. American Journal of Human Genetics, 82, 593–599.

Keller M.C. Coventry W.L. Heath A.C. Martin N.G. (2005). Widespread evidence for non-additive genetic variation in Cloninger’s and Eysenck’s personality dimensions using a twin plus sibling design. Behavior Genetics, 35, 707–721.

Koopmans J.R. Boomsma D.I. Heath A.C. Van Doornen L.J.P. (1995). A multivariate genetic analysis of sensation seeking. Behavior Genetics, 25, 349–356.

Loehlin J.C. (1992). Genes and environment in personality development. Newbury Park, CA: Sage.

Maher B. (2008). Personal genomes: The case of the missing heritability. Nature, 456, 18–21.

Manolio T.A. (2010). Genomewide association studies and assessment of the risk of disease. New England Journal of Medicine, 363, 166–176.

Manolio T.A. Collins F.S. Cox N.J. Goldstein D.B. Hindorff L.A. Hunter D.J. . (2009). Finding the missing heritability of complex diseases. Nature, 461, 747–753.

Moskvina V. Schmidt K.M. (2008). On multiple-testing correction in genome-wide association studies. Genetic Epidemiology, 32, 567–573.

Nyholt D.R. (2004). A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other. American Journal of Human Genetics, 74, 765–769.

Purcell S.M. Wray N.R. Stone J.L. Visscher P.M. O’Donovan M.C. Sullivan P.F. . (2009). Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature, 460, 748–752.

Shifman S. Bhomra A. Smiley S. Wray N.R. James M.R. Martin N.G. . (2008). A whole genome association study of neuroticism using DNA pooling. Molecular Psychiatry, 13, 302–312.

Terracciano A. Balaci L. Thayer J. Scally M. Kokinos S. Ferrucci L. . (2009). Variants of the serotonin transporter gene and NEO-PI-R neuroticism: No association in the BLSA and SardiNIA samples. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 150, 1070–1077.

Verweij K.J.H. Zietsch B.P. Medland S.E. Gordon S.D. Benyamin B. Nyholt D.R. . (2010). A genome-wide association study of Cloninger’s Temperament scales: Implications for the evolutionary genetics of personality. Biological Psychology, 85, 306–317.

Wray N.R. Goddard M.E. Visscher P.M. (2007). Prediction of individual genetic risk to disease from genome-wide association studies. Genome Research, 17, 1520–1528.