Skip to main content
NCBI home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1979 Nov;31(6):655–661.

Major locus analysis for quantitative traits.

R C Elston
PMCID: PMC1686044  PMID: 517517

Full text

PDF
655

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Berg K., Heiberg A. Linkage studies on familial hyperlipoproteinemia with xanthomatosis: normal lipoprotein markers and the C3 polymorphism. Birth Defects Orig Artic Ser. 1976;12(7):266–270. [PubMed] [Google Scholar]
  2. Boyle C. R., Elston R. C. Multifactorial genetic models for quantitative traits in humans. Biometrics. 1979 Mar;35(1):55–68. [PubMed] [Google Scholar]
  3. Elston R. C., Lange K. The prior probability of autosomal linkage. Ann Hum Genet. 1975 Jan;38(3):341–350. doi: 10.1111/j.1469-1809.1975.tb00619.x. [DOI] [PubMed] [Google Scholar]
  4. Elston R. C. Letter: Reply to "message from a referee on the Elston method". Behav Genet. 1973 Sep;3(3):319–320. doi: 10.1007/BF01067609. [DOI] [PubMed] [Google Scholar]
  5. Elston R. C., Namboodiri K. K., Glueck C. J., Fallat R., Tsang R., Leuba V. Study of the genetic transmission of hypercholesterolemia and hypertriglyceridemia in a 195 member kindred. Ann Hum Genet. 1975 Jul;39(1):67–87. doi: 10.1111/j.1469-1809.1975.tb00109.x. [DOI] [PubMed] [Google Scholar]
  6. Elston R. C., Namboodiri K. K., Go R. C., Siervogel R. M., Glueck C. J. Probable linkage between essential familial hypercholesterolemia and third complement component (C3). Birth Defects Orig Artic Ser. 1976;12(7):294–297. [PubMed] [Google Scholar]
  7. Elston R. C., Rao D. C. Statistical modeling and analysis in human genetics. Annu Rev Biophys Bioeng. 1978;7:253–286. doi: 10.1146/annurev.bb.07.060178.001345. [DOI] [PubMed] [Google Scholar]
  8. Elston R. C., Sobel E. Sampling considerations in the gathering and analysis of pedigree data. Am J Hum Genet. 1979 Jan;31(1):62–69. [PMC free article] [PubMed] [Google Scholar]
  9. Elston R. C., Stewart J. A general model for the genetic analysis of pedigree data. Hum Hered. 1971;21(6):523–542. doi: 10.1159/000152448. [DOI] [PubMed] [Google Scholar]
  10. Fain P. R. Characteristics of simple sibship variance tests for the detection of major loci and application to height, weight and spatial performance. Ann Hum Genet. 1978 Jul;42(1):109–120. doi: 10.1111/j.1469-1809.1978.tb00935.x. [DOI] [PubMed] [Google Scholar]
  11. Gerrard J. W., Rao D. C., Morton N. E. A genetic study of immunoglobulin E. Am J Hum Genet. 1978 Jan;30(1):46–58. [PMC free article] [PubMed] [Google Scholar]
  12. Go R. C., Elston R. C., Kaplan E. B. Efficiency and robustness of pedigree segregation analysis. Am J Hum Genet. 1978 Jan;30(1):28–37. [PMC free article] [PubMed] [Google Scholar]
  13. Haseman J. K., Elston R. C. The investigation of linkage between a quantitative trait and a marker locus. Behav Genet. 1972 Mar;2(1):3–19. doi: 10.1007/BF01066731. [DOI] [PubMed] [Google Scholar]
  14. Hill A. P. Quantitative linkage: a statistical procedure for its detection and estimation. Ann Hum Genet. 1975 May;38(4):439–449. doi: 10.1111/j.1469-1809.1975.tb00633.x. [DOI] [PubMed] [Google Scholar]
  15. Jensen J., Blankenhorn D. H. The inheritance of familial hypercholesterolemia. Am J Med. 1972 Apr;52(4):499–516. doi: 10.1016/0002-9343(72)90041-1. [DOI] [PubMed] [Google Scholar]
  16. Kempthorne O. Logical, epistemological and statistical aspects of nature-nurture data interpretation. Biometrics. 1978 Mar;34(1):1–23. [PubMed] [Google Scholar]
  17. Kravitz K., Skolnick M., Cannings C., Carmelli D., Baty B., Amos B., Johnson A., Mendell N., Edwards C., Cartwright G. Genetic linkage between hereditary hemochromatosis and HLA. Am J Hum Genet. 1979 Sep;31(5):601–619. [PMC free article] [PubMed] [Google Scholar]
  18. Lange K., Elston R. C. Extensions to pedigree analysis I. Likehood calculations for simple and complex pedigrees. Hum Hered. 1975;25(2):95–105. doi: 10.1159/000152714. [DOI] [PubMed] [Google Scholar]
  19. Lange K., Spence M. A., Frank M. B. Application of the lod method to the detection of linkage between a quantitative trait and a qualitative marker: a simulation experiment. Am J Hum Genet. 1976 Mar;28(2):167–173. [PMC free article] [PubMed] [Google Scholar]
  20. MURPHY E. A. ONE CAUSE?MANY CAUSES?THE ARGUMENT FROM THE BIMODAL DISTRIBUTION. J Chronic Dis. 1964 Apr;17:301–324. doi: 10.1016/0021-9681(64)90073-6. [DOI] [PubMed] [Google Scholar]
  21. MacLean C. J., Morton N. E., Lew R. Analysis of family resemblance. IV. Operational characteristics of segregation analysis. Am J Hum Genet. 1975 May;27(3):365–384. [PMC free article] [PubMed] [Google Scholar]
  22. Maclean C. J., Morton N. E., Elston R. C., Yee S. Skewness in commingled distributions. Biometrics. 1976 Sep;32(3):695–699. [PubMed] [Google Scholar]
  23. Morton N. E., MacLean C. J. Analysis of family resemblance. 3. Complex segregation of quantitative traits. Am J Hum Genet. 1974 Jul;26(4):489–503. [PMC free article] [PubMed] [Google Scholar]
  24. Namboodiri K. K., Elston R. C., Hames C. Segregation and linkage analyses of a large pedigree with hypertriglyceridemia. Am J Med Genet. 1977;1(2):157–171. doi: 10.1002/ajmg.1320010203. [DOI] [PubMed] [Google Scholar]
  25. Ott J. Maximum likelihood estimation by counting methods under polygenic and mixed models in human pedigrees. Am J Hum Genet. 1979 Mar;31(2):161–175. [PMC free article] [PubMed] [Google Scholar]
  26. Smith C. A. A non-parametric test for linkage with a quantitative character. Ann Hum Genet. 1975 May;38(4):451–460. doi: 10.1111/j.1469-1809.1975.tb00634.x. [DOI] [PubMed] [Google Scholar]
  27. Weinshilboum R. M., Raymond F. A. Inheritance of low erythrocyte catechol-o-methyltransferase activity in man. Am J Hum Genet. 1977 Mar;29(2):125–135. [PMC free article] [PubMed] [Google Scholar]
  28. Weinshilboum R. M., Schorott H. G., Raymond F. A., Weidman W. H., Elveback L. R. Inheritance of very low serum dopamine-beta-hydroxylase activity. Am J Hum Genet. 1975 Sep;27(5):573–585. [PMC free article] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES