Hostname: page-component-586b7cd67f-g8jcs Total loading time: 0 Render date: 2024-11-30T17:52:43.210Z Has data issue: false hasContentIssue false
  • English
  • Français

A geneticist's approach to psychiatric disease1

Published online by Cambridge University Press:  09 July 2009

Edmond A. Murphy
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content so a preview has been provided. As you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Editorial
Information
Psychological Medicine , Volume 17 , Issue 4 , November 1987 , pp. 805 - 815
Copyright
Copyright © Cambridge University Press 1987

References

Blass, J. P. & Gibson, G. E. (1977). Abnormality of a thiamine-requiring enzyme in patients with Wernicke-Korsakoff syndrome. New England Journal of Medicine 297, 1367–1370.CrossRefGoogle ScholarPubMed
Bodmer, W. F. & Cavalli-Sforza, L. L. (1970). Intelligence and race. Scientific American 223, 419–429.CrossRefGoogle ScholarPubMed
Breitner, J. C. S., Folstein, M. F. & Murphy, E. A. (1986). Familial aggregation in Alzheimer dementia I. A model for the age-dependent expression of the autosomal dominant gene. Journal of Psychiatric Research 20, 31–43.CrossRefGoogle Scholar
Cadoret, R. J. (1978). Evidence for the genetic inheritance of primary affective disorder in adoptees. American Journal of Psychiatry 135, 463–466.Google ScholarPubMed
Dickenson, A. & Mackintosh, N. J. (1978). Classical conditioning in animals. Annual Review of Psychology 29, 587–612.Google Scholar
Farmer, D., Roffoli, T. & Wolfram, S. (eds) (1984). Cellular Automata (Proceedings of an Interdisciplinary Workshop).North-Holland:Amsterdam.Google Scholar
Feinstein, A. R. (1974). The derangements of the ‘range of normal’. Clinical Pharmacology and Therapeutics 15, 528–540. Reprinted in Feinstein, A. R. (1977). Clinical Biostatistics. Mosby: St Louis.CrossRefGoogle ScholarPubMed
Fisher, R. A. (1918). The correlation between relatives on the supposition of Mendelian inheritance. Transactions of the Royal Society of Edinburgh 52, 399–433.CrossRefGoogle Scholar
Fisher, R. A. (1958). The Genetic Theory of Natural Selection. Dover: New York.Google Scholar
Folstein, M. F., De Paulo, J. R. & Trepp, K. (1982). Unusual mood stability in patients taking lithium. British Journal of Psychiatry 140, 188–191.CrossRefGoogle ScholarPubMed
Galen, R. S. & Gambino, S. R. (1975). Beyond Normality. The Predictive Value and Efficiency of Medical Diagnosis. Wiley: New York.Google Scholar
Garrod, A. E. (1909). Inborn Errors of Metabolism. Frowde, Hodder and Stoughton: London.Google Scholar
Gusella, J. F., Wexler, N. S., Conneally, P. M, Naylor, S. L., Anderson, M. A., Tanzi, R. E., Watkins, P. S., Ottina, K., Wallace, M. R., Sakaguchi, A. Y., Young, A. B., Shoulson, F., Bonilla, E. & Martin, J. B. (1983). A polymorphic DNA marker genetically linked to Huntington's disease. Nature 306, 234–238.CrossRefGoogle ScholarPubMed
Harker, L. A. & Scott, C. R. (1977). Platelets in homocystinuria. New England Journal of Medicine 296, 818.Google ScholarPubMed
Jensen, A. R. (1969). How much can we boost IQ and scholastic achievement? Harvard Educational Review 39, 1–123.CrossRefGoogle Scholar
Judd, L. L., Hubbard, B. & Janowski, D. S. (1977). The effect of lithium carbonate on affect, mood, and personality of normal subjects. Archives of General Psychiatry 34, 346–351.CrossRefGoogle ScholarPubMed
Klawans, H. L. & Goetz, C. G. (1980). Levodopa and presymptomatic detection of Huntington's disease. Eight year follow-up. New England Journal of Medicine 302, 1090.Google ScholarPubMed
Levy, H. L. (1973). Genetic screening. Advances in Human Genetics 4, 1–104.Google ScholarPubMed
Morales, A. J., Murphy, E. A. & Krush, A. J. (1984). The bingo model of survivorship II. Statistical aspects of the bingo model of multiplicity I with application to hereditary polyposis of the colon. American Journal of Medical Genetics 17, 783–801.CrossRefGoogle ScholarPubMed
Murphy, E. A. (1966). A scientific viewpoint on normalcy. Perspectives in Biology and Medicine 9, 333–348.CrossRefGoogle ScholarPubMed
Murphy, E. A. (1971). The estimation of blood platelet survival III. The robustness of the basic models. Thrombosis et Diathesis Haemorrhagica 26, 431–449.Google Scholar
Murphy, E. A. (1981 a). The pursuit of the minor premise. A comment on normality. Metamedicine 2, 283–299.CrossRefGoogle Scholar
Murphy, E. A. (1981 a). The genetic dynamics of disease. American Journal of Medical Genetics 8, 35–52.CrossRefGoogle ScholarPubMed
Murphy, E. A. & Francis, M. E. (1971). The estimation of blood platelet survival II. The multiple hit model. Thrombosis et Diathesis Haemorrhagica 25, 53–80.Google ScholarPubMed
Murphy, E. A. & Pyeritz, R. E. (1986). Homeostasis VII. A conspectus. American Journal of Medical Genetics 24, 735–751.CrossRefGoogle ScholarPubMed
Murphy, E. A., Francis, M. E. & Bollong, D. R. (1973). The estimation of blood platelet survival V. A method for the analysis of population data. Journal of Chronic Disease 26, 797–815.CrossRefGoogle Scholar
Murphy, E. A., Trojak, J. E., Hou, W. & Rohde, C. A (1981). The bingo model of survivorship. 1. Probabilistic aspects. American Journal of Medical Genetics 10, 261–277.CrossRefGoogle ScholarPubMed
Opitz, J. M. (1977). The American Journal of Medical Genetics Foreword. American Journal of Medical Genetics 1, 1–2.CrossRefGoogle Scholar
Penrose, L. S. (1951). Measurement of pleotropic effects in phenylketonuria. Annals of Eugenics, London 16, 134–138.CrossRefGoogle Scholar
Reimann, H. A., Moadie, J, Semerdijian, S. & Sahyoun, P. F. (1954). Periodic peritonitis, heredity and pathology. Report of seventy-two cases. Journal of American Medical Association 154, 1254–1259.CrossRefGoogle ScholarPubMed
Russell, B. (1950). An Enquiry into Meaning and Truth. Allen and Unwin: London.Google Scholar
Seckel, H. P. G. (1960). Bird-headed Dwarfs. Studies in Developmental Anthropology Including Human Proportions. Charles C. Thomas: Springfield.Google Scholar
Strahan, N. V., Murphy, E. A., Fortuin, N. J., Come, P. C. & Humphries, J. O. (1983). Inheritance of mitral valve prolapse syndrome. Discussion of a three-compartmental penetrance model. American Journal of Medicine 74, 967–972.CrossRefGoogle ScholarPubMed
Trojak, J. E. & Murphy, E. A. (1983). Paradoxical fixation of deleterious alleles in two-locus systems with epistasis. American Journal of Medical Genetics 16, 493–502.CrossRefGoogle ScholarPubMed
Turner, G. & Jacobs, P. (1983). Marker X-linked mental retardation. Advances in Human Genetics 13, 83–112.CrossRefGoogle ScholarPubMed
Turner, G. & Turner, B. (1974). X-linked mental retardation. Journal of Medical Genetics 11, 109–113.CrossRefGoogle ScholarPubMed
Vogel, F. & Motulsky, G. (1979). Human Genetics: Problems and Approaches. (pp. 527–531). Springer: New York.Google Scholar
Walderstrom, J. & Haeger-Aronsen, B. (1963). Different patterns of human prophyria. British Medical Journal ii 272–276.CrossRefGoogle Scholar
Webb, W. B. & Cartwright, R. D. (1978). Sleep and dreams. Annual Review of Psychology 29, 223–252.CrossRefGoogle ScholarPubMed