Genetic Epidemiology

The Basis for a New Health Service Delivery Model
  • Marcia Phillips
  • Jack Goldberg


Genetic Testing Segregation Analysis Congenital Hypothyroidism Human Genome Project Health Care Manager 
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  1. Bell, J., and Haldane, J. B. S., 1937, The linkage between the genes for color-blindness and haemophilia in men, Proc. R. Soc. Lond. [Biol] 123:119–150.CrossRefGoogle Scholar
  2. Boulyjenkow, V., 1998, WHO Human Genetics Programme: A brief overview, Commun. Genet. 1:57–60.Google Scholar
  3. Bowman, J. E., 1998, To screen or not to screen: When should screening be offered? Commun. Genet. 1:145–147.Google Scholar
  4. Casselbrandt, M. L., Mandel, E. M., Fall, P. A., Rockette, H. E., Kurs-Lasky, M., Bluestone, C. D., and Ferrel, R. E., 1999, The heritability of otitis media: A twin and triplet study, JAMA 282:2125–2130.Google Scholar
  5. Claus, E. B., Risen, N., and Thompson, W. D., 1991, Genetic analysis of breast cancer in the cancer and steroid hormone study, Am. J. Hum. Genet. 48:232–242.PubMedGoogle Scholar
  6. Decruyenaere, M., Evers-Kiebooms, G., Denayer, L., and Welkenhuysen, M., 1998, Uptake and impact of carrier testing for cystic fibrosis, Commun. Genet. 1:23–35.Google Scholar
  7. Eeles, R., Taylor, R., Lunt, P., and Baum, M., 1996, Prophylactic mastectomy for genetic predisposition to breast cancer: The proband’s story, Clin. Oncol. 8:222–225.CrossRefGoogle Scholar
  8. El-Serag, H. B., Inadomi, J. M., and Kowdley, K. V., 2000, Screening for hereditary hemochromatosis in siblings and children of affected patients: A cost-effectiveness analysis, Ann. Intern. Med. 15:261–269.Google Scholar
  9. Hall, J. M., Lee, J. K., Morrow, J. E., Anderson, L. A., Huey, B., and King, M. C., 1990, Linkage of early-onset familial breast cancer to chromosome 17q21, Science 250:1684–1689.PubMedGoogle Scholar
  10. Hwang, S. J., Beaty, T. H., Panny, S. R., Street, N. A., Joseph, J. M., Gordon, S., McIntosh, I., and Francomano, C. A., 1995, Association study of transforming growth factor alpha TaqI polymorphisms and oral clefts: Indication of gene-environment interaction in a population-based sample of infants with birth defects, Am. J. Epidemiol. 141:629–636.PubMedGoogle Scholar
  11. Kahn, P., 1996, Coming to grips with genes and risk, Science 274:496–498.PubMedGoogle Scholar
  12. Kaplan, F., 1998, Tay-Sachs disease carrier screening: A model for prevention of genetic disease, Commun. Genet. 2:271–292.Google Scholar
  13. Khoury, M. J., and Dorman, J. S., 1998, The Human Genome Epidemiology Network (HuGE Net), Am. J. Epidemiol. 148:1–3.PubMedGoogle Scholar
  14. Neel, J. V., 1995, Physician to the Gene Pool, John Wiley & Sons, New York.Google Scholar
  15. Ostrer, H., 1998, Non-Mendelian Genetics in Humans, Oxford University Press, New York.Google Scholar
  16. Ott, J., 1999, Analysis of Human Genetic Linkage, 3rd ed., Johns Hopkins University Press, Baltimore, MD.Google Scholar
  17. Parmigiani, G., Berry, D. A., and Aguilar, O., 1998, Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2, Am. J. Hum. Genet. 62:145–158.PubMedCrossRefGoogle Scholar
  18. Pedersen, J., and Berg, K., 1989, Interaction between low density lipoprotein receptor (LDLR) and apolipoprotein E (apoE) alleles contributes to normal variation in lipid levels, Clin. Genet. 35:331–337.PubMedGoogle Scholar
  19. Pernick, M. S., 1996, The Black Stork, Oxford University Press, New York.Google Scholar
  20. Rajab, A., and Patton, M. A., 1999, Analysis of the population structure in Oman, Commun. Genet. 2:23–25.Google Scholar
  21. Rothenberg, K. H., and Rutkin, A. B., 1998, Toward a framework of mutualism: The Jewish community in genetics research, Commun. Genet. 1:148–153.Google Scholar
  22. Viel, A., Genuardi, M., Lucci-Cordisco, E., Capozzi, E., Rovella, V., Fornasarig, M., Ponz de Leon, M., Anti, M., Pedroni, M., Bellacosa, A., Percesepe, A., Covino, M., Benatti, P., Del Tin, L., Roncucci, L., Valentini, M., Boiocchi, M., and Neri, G., 1998, Hereditary nonpolyposis colorectal cancer: An approach to the selection of candidates to genetic testing based on clinical and molecular characteristics, Community Genet. 1:229–235.PubMedCrossRefGoogle Scholar
  23. Wilson, E. B., 1911, The sex chromosomes, Arch. Mikrosk. Anat. Enwicklungmec 77:249–271.Google Scholar

Copyright information

© Kluwer Academic Publishers 2002

Authors and Affiliations

  • Marcia Phillips
    • 1
  • Jack Goldberg
    • 2
  1. 1.Department of Health Systems ManagementRush UniversityChicago
  2. 2.Epidemiology/Biostatistics Division, School of Public HealthUniversity of Illinois at ChicagoChicago

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