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Continued: -----Original Message-----
From: Wertz, Dorothy [mailto:Dorothy.Wertz@umassmed.edu]
Sent: Tuesday, October 30, 2001 8:56 PM
To: 'Leggett, David'
Subject: RE: website
Dear David,
Yes, I finally got into the website. I'll have to send you more details
about the people so you can flesh it out. For starters, my father's people
were the Dietlys, not Deitlys. They originally came from Canton Solothurn in
Switzerland and were Catholics over there. I have a rather complete
genealogy and some Swiss third cousins (all professionals) near Zuerich. My
grandmother (Dietly ) lived in Erie, Ohio, along with her family, who became
wealthy by making asphalt rolling machines.. Her stay in Kingston was very
brief, as she was only married a few years before getting a divorce in 1898.
Grandfather Corbett went west and was never heard from again until his death
in Edmonton in 1926. Kate B. Leggett was President of the William T. Leggett
Company from the time of her husband's death in 1909 until your grandfather
was ready to take over (your father can fill you in on the year). Grandma
Leggett made the policy decisions about the company and scrutinized all the
accounts, which Mr. Croyle brought out from town on the train every week.
They fought for years. By the way, she hated both her names--Kate and
Adelia--and made her children promise that they would never attach these
names to their own children.
Congratulations on finding an 11th cousin. Maybe now it's time for DNA
testing. I'd like to come with you to see the sites when you place the
stones on the 6th, but whether I can get away depends on several matters.
I'll call you later in the week. Dorothy
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BIOGRAPHICAL SKETCH
NAMEDOROTHY CORBETT WERTZ POSITION TITLESenior Scientist; Research Professor of Psychiatry
EDUCATION/TRAINING
INSTITUTION AND LOCATION DEGREE YEAR(s) FIELD OF STUDY
Radcliffe College A.B. 1958 Social Relations
London School of Economics 1959 Social Anthropology
Radcliffe College A.M. 1961 Sociology of Religion
Harvard University Ph.D 1966 Study of Religion
RESEARCH AND PROFESSIONAL EXPERIENCE:
A. Positions and Honors:
1963-1965 Instructor, Bryn Mawr College
1965-1966 Instructor in Social Science, Kingsborough Community College, CUNY
1966-1968 Assistant Professor of Sociology, Boston College
1968-1969 Assistant Professor of Sociology, Rhode Island College
1969-1972 Assistant Professor of Sociology, Bridgewater State College, MA
1972-1973 Assistant Professor of Sociology, University of Bridgeport
1973-1974 Associate Professor of Sociology, University of New Haven
1975-1981 Associate Professor of Sociology, Suffolk University, Boston, MA
Boston University School of Public Health, Health Services Dept.
1981-1982 NSF Science Faculty Professional Development Fellow
1982-1984 NSF Interdisciplinary Incentive Award Fellow in Ethics and Values in Science and Technology
1983-1985 Adjunct Associate Professor of Public Health
1988-1992 Research Professor of Public Health
1993- Adjunct Research Professor of Public Health
1991-2000 Senior Scientist, Div of Social Science, Ethics and Law, Shriver Center for Mental Retardation, Waltham, MA
2000- Research Professor, Psychiatry, University of Massachusetts Medical School, Shriver Division, Waltham, MA
2002- Senior Scientist, American Society of Law, Medicine and Ethics, Boston, MA
American Bar Association Silver Gavel Award, 1991, for "Privacy and the Public Interest" (The World and I)
Rockefeller Foundation Fellow, Bellagio Study Center, August, 2000
B. Selected peer-reviewed publications
Wertz DC, Fletcher JC. Genetics and Ethics in Global Perspective. Washington, DC.: Georgetown University Press, in press.
Wertz DC, Knoppers BM. Serious genetic disorders: Can or should they be defined? Am. J. Med. Genet. 2002; 108: 29-35.
Wertz DC. Embryo and stem cell research in the USA: A political history. Trends in Molecular Medicine 2002; 8: 143-146.
Wertz DC. Testing of Children and Adolescents. In: Burley JC, Harris J (eds), A Companion to Genethics: Philosophy and the Genetic Revolution. Oxford: Basil Blackwell, 2002, pp. 92-113.
Caulfield T, Wertz DC. Creating needs? A review of survey data and concerns relevant to the commercialization of genetic testing. Community Genet. 2001; 4: 68-76.
Wertz DC. Pre-conception sex selection: A question of consequences. Am. J. Bioethics 2001: 1: 36-37.
Wertz DC, Gregg R. Genetic Services in a Social, Ethical and Policy Context: A Collaboration Between Consumers and Providers. Journal of Medical Ethics, 2000; 26: 261-265.
Wertz DC. Drawing Lines: Notes for Policymakers. In: Parens E, Asch A (eds) Prenatal Genetic Testing and Disability Rights. Washington, DC: Georgetown University Press, 2000, pp. 261-287.
Wertz DC. Genetic Discrimination: Results of a Survey of Genetics Professionals, Primary Care Physicians, Patients and Public. Health Law Review 1999; 7(3):7-8.
Wertz DC. Archived Specimens: A Platform for Discussion. Community Genetics 1999; 2:51-60.
Wertz DC. et al. Stored DNA Samples: What You Should Know. The Genetic Resource 12 (1&2); 1999:92-96.
Wertz DC. Patient and Professional Views on Autonomy: A survey in the United States and Canada. Health Law Review 7(3); 1999:9-10.
Wertz DC. Views of Chinese Medical Geneticists; How They Differ from 35 other Nations. In: Doering O (ed.) Chinese Scienticists and Responsibility: Ethical Issues of Human Geneticists in Chinese and International Contests. Mitteilungen des Instituts fuer Asienkunde, Hamburg, Germany, 1999.
Wertz DC. Eugenics is Alive and Well. Science in Context, 11 (3/4); 1998; 493-510. Special Issue on Eugenic Thought and Practice, ed. Falk, R., Paul, D.
Wertz DC. The difficulties of recruiting minorities to studies of ethics and values in genetics. Community Genetics 1 (3); 1998:175-179. .
Wertz DC. Ethical Issues in Pediatric Genetics: Views of Geneticists, Parents and Primary Care Physicians. Health Law Journal 6:1998:1-42.
Wertz DC. Patients' and Professionals' Views on Autonomy, Disability and "Discrimination". In: Williams-Jones B, Caufield T (eds). The Commercialization of Genetic Research. New York. Plenum Press, 1999, pp. 171-181.
Wertz DC. International Perspectives. In: Clarke AJ (ed.), The Genetic Testing of Children. Oxford: Bios Scientific Publishers, 1998: pp. 271-287.
Wertz DC, Fletcher JC, Berg, K. Guidelines on Ethical Issues in Medical Genetics and the Provision of Genetics Services. (WHO/HDP/CONS/95.1) Geneva: World Health Organization Hereditary Diseases Programme, 1995, Proposed International Guidelines on Ethical Issues in Medical Genetics and Genetic Services, WHO, 1998..
Wertz DC, Fletcher JC. Ethics and Human Genetics: A Cross-Cultural Perspective. Berlin and New York: Springer-Verlag, 1989.
Wertz DC. Is There a "Women's Ethic" in Genetics: A 37-Nation Survey of Providers. Journal of the American Medical Women's Association 52 (1): 1997; 33-38.
Wertz DC. International Perspectives on Privacy and Access to Genetic Information. Microbial and Comparative Genomics 2 (1); 1997: 33-41.
Wertz DC, Reilly PR, Laboratory policies and practices for the genetic testing of children; a survey of the Helix network. American Journal of Human Genetics 61; 1997: 1163-1168.
Wertz DC. Society and the Not-So-New Genetics: What Are We Afraid Of? Journal of Contemporary Health Law and Policy 13 (2), 1997, 299-346.
Wertz DC. Ethical and Social Issues in Prenatal Sex Selection: A Survey of Geneticists in 37 Nations. Social Science and Medicine, 46(2); 1998: 255-273.
Wertz RW, Wertz DC. Lying-In: A History of Childbirth in America. New York: Free Press, 1977. (Paperback by Schocken Books). Expanded Edition: New Haven: Yale University Press, 1989.
Wertz DC, Fanos JH, Reilly PR. Genetic testing for children and adolescents: who decides? JAMA 272(11); Sept. 21, 1994: 875-881.
Wertz DC. Provider gender and moral reasoning: the politics of an "ethics of care". Journal of Genetic Counseling 3(2); 1994: 95-112.
Wertz DC. Prenatal diagnosis and society. In: New Reproductive Technologies:
Ethical Aspects. Research Studies, Vol. 1, Ch. 4, pp. 191-332. Ottawa, Canada: The Royal Commission on New Reproductive Technologies, 1993.
Wertz DC, Fletcher JC. Proposed: An International Code of Ethics for Medical Genetics. Clinical Genetics 44; 1993: 37-43.
Wertz DC, Janes SR, Rosenfield JM, Erbe RW. Attitudes toward the prenatal diagnosis of cystic fibrosis: factors in decision making among affected families. American Journal of Human Genetics 50; 1992: 222-235.
Wertz DC, Rosenfield JM, Janes SR, Erbe RW. Attitudes toward abortion among parents of children with cystic fibrosis. American Journal of Public Health 81 (8); 1991: 992-996.
Wertz DC, Fletcher JC. Privacy and disclosure in medical genetics examined in an ethics of care. Bioethics 5 (3); 1991: 212-232.
Wertz DC, Fletcher JC. Fatal Knowledge? Prenatal Diagnosis and Sex Selection. Hastings Center Report 19: 3; (May/June, 1989): 21-27.
Wertz DC, Fletcher JC, Mulvihill JJ, Medical geneticists confront ethical dilemmas: cross-cultural comparisions among 18 nations. American Journal of Human Genetics 46; 1990: 1200-1213.
Wertz DC, Fletcher JC. Ethical Problems in Prenatal Diagnosis: A Cross-Cultural Survey of Medical Geneticists in 18 Nations. Prenatal Diagnosis 9 (3); 1989: 145-157.
Wertz DC, Fletcher JC. An International Survey of Attitudes of Medical Geneticists Toward Mass Screening and Access to Results. Public Health Reports 4 (1); January/February 1989: 34-44.
Wertz DC, Fletcher JC. Disclosing Genetic Information: Who Should Know? Technology Review 92 (5); July, 1989: 22-23.
Wertz DC, Fletcher JC. Ethics and Medical Genetics in the United States: A National Survey. American Journal of Medical Genetics 29; April, 1988: 815-827.
C. Research Support
"Distance-learning for IRB's on Ethical Issues in Genetics". Grant #5 T15 AI07545. National Institute of Allergy and Infectious Diseases, NIH (PA: Short-term Courses in Research Ethics), 09/301/1998-09/30/02. Goals: To educate members of Institutional Review Boards about ethical and social issues in genetics, using a 16-week course on the Internet. Role: Principal Investigator.
:::::::::::::::::::::::::::::::::::::::::::::::::::::::::
Updated June, 2002
DOROTHY CORBETT WERTZ
39 Rutland Square
Boston, Massachusetts 02118
SUMMER: BUSINESS:
2002 Main Road, Box 95 Division of Social Science, Ethics, Law
Westport Point, MA 02791 The Shriver Center
Phone and fax 508 636-8943 200 Trapelo Road
Waltham, MA 02452
Tel: 781 642-0292 fax: 781 642-0130
e-mail: dorothy.wertz@umassmed.edu
PRESENT POSITION:
Research Professor of Psychiatry, University of Massachusetts Medical School, Shriver Division
Senior Scientist, Division of Social Science, Ethics, and Law
The Shriver Center
Waltham, Massachusetts 02452
Senior Scientist, American Society of Law, Medicine, and Ethics, Boston, MA
Adjunct Research Professor, Maternal and Child Health
School of Public Health
Boston University
EDUCATION
Ph.D. 1966 Harvard University Study of Religion
A.M. 1961 Radcliffe College History and Philosophy of Religion
1959 London School of Economics Social Anthropology
A.B. 1958 Radcliffe College Social Relations
RECENT ACTIVITIES
1. Genedit. New quarterly review of international social/ethical issues. Part of www.humgen.umontreal.ca, an international ethics/law site with 20,000 visitors a day .
2. The Geneletter: An Internet-based newsletter on ethical, legal, social and scientific issues in genetics. Published bimonthly 1996-1999, over 2,106,000 hits, 778,000 page impressions, and 394,000 user sessions. Now part of Genesage.com
3. Ethics and Human Genetics: A Survey in the United States and Canada. Questionnaire survey of 1084 geneticists and genetic counselors, 499 non-geneticist physicians, 476 patients at 13 genetics clinics, and 988 members of the general public with regard to ethical issues such as privacy and disclosure, prenatal diagnosis, disclosure of genetic information to relatives, sex selection, views on disability. Supported by contract NO 1-HD-1-3136 from the Mental Retardation and Developmental Disorders Branch, National Institute of Child Health and Human Development (NIH). 7/1991-6/1996.
4. Geneticists Approach Ethics: An International Survey in 36 Nations. Extends the North American Survey of geneticists' ethical views in all countries with ten or more medical geneticists. 7/1992 - 4/1995. Supported by grant # HG0045-540-02, Ethical, Legal and Social Implications Branch, National Human Genome Research Institute (NIH).
5. Distance-learning for Institutional Review Boards (IRBs) on Ethical Issues in Genetics. An interactive, online course for IRB members, including how to write an informed consent and involve the community. 9/30/98 - 9/29/2001. Supported by grant T15 A107545-01 from the National Institute of Allergy and Infectious Diseases. (NIH).
6. Exploring Quality Assurance in Genetics Encounters: A Pilot Study of Consumers and Providers. Using focus groups of consumers, physicians, and genetic counselors, this project developed a document outlining minimal and ideal standards for genetics services, supplemented by an educational videotape for providers and consumers 10/1/93 - 9/30/97. Supported by the New England Regional Genetics Group.
7. Cost-benefit/Cost-effectiveness Analysis in Genetics. What can be done? What Should be Done? New England Regional Genetics Group. A one-day public conference of consumers, providers, health economists, managed health care executives, ethicists, and social scientists, March 30, 1996.
LISTINGS
Who's Who in America, 57th Edition, 2003 International Who's Who of Business and Professional Women, 2001
2000 Intellectuals of the 21st Century, 2001 The World's Women, 1995
Who's Who in the East, 1994 - 2000
Who's Who in the World, 1995
Who's Who in Science and Engineering, 1995-97
American Men and Women of Science, 1994-97
Dictionary of International Biography, 1995
500 Leaders of Science, 2002
PUBLICATIONS - BOOKS:
1. Wertz DC, Fletcher JC. Genetics and Ethics in Global Perspective. Washington, DC, Georgetown University Press, 2003, in press.
2. Wertz, DC, Fletcher JC, Berg K. Review of Ethical Issues in Medical Genetics. Geneva: WHO, 2001.
3. Wertz, DC, Fletcher JC, Berg K. Guidelines on Ethical Issues in Medical Genetics and the Provision of Genetics Services. (WHO/HDP/EPH/95.1) Geneva; World Health Organization, Hereditary Diseases Program, 1995.
4. Wertz DC, Fletcher JC. Ethics and Human Genetics: A Cross-Cultural Perspective. Berlin and New York: Springer-Verlag, 1989.
5. Wertz RW, Wertz DC. Lying-In: A History of Childbirth in America. New York: Free Press, 1977. (Paperback by Schocken Books). Expanded Edition: New Haven: Yale University Press, 1989.
6. Wertz DC (ed.). Research in the Sociology of Health Care, Vol. 7. Greenwich, Connecticut: JAI Press, 1988.
7. Wertz DC, (ed.). Research in the Sociology of Health Care, Vol. 8. Greenwich, Connecticut: JAI Press, 1989.
8. Wertz DC, (ed.). Research in the Sociology of Health Care, Vol 9. Greenwich, Connecticut: JAI Press, 1991.
9. Miller DM, Wertz DC. Hindu Monastic Life: The Monks and Monasteries and Bhubaneswar. Montreal and London: McGill Queen's University Press, 1976. 2nd edition: New Delhi, India and Columbia MO: Manahar Press and South Asia Press, 1996.
PUBLICATIONS-MONOGRAPHS:
1. Wertz, DC, Principal Investigator. Optimizing Genetics Services in a Social, Ethical, and Policy Context. Suggestions from Consumers and Providers in the New England Regional Genetics Group. The Genetic Resource, Vol. 10, No. 2 Special Issue, 1996.
PUBLICATIONS - ARTICLES
Articles, 2002
1. Wertz DC, Fletcher JC, Ayme S, Nippert I, Wolff G. Has patient autonomy gone too far? Geneticists' views in 36 nations. In Focus, American Journal of Bioethics 2(4), Fall 2002, in press.
2. Wertz DC. Embryo and stem cell research in the United States: history and politics. Gene Therapy 9(11), June, 2002:674-678.
3. Wertz DC. Genetic discrimination-an overblown fear? Ethicswatch, Nature Reviews Genetics, July, 2002, in press.
4. Wertz DC. Did eugenics ever die? Ethicswatch, Nature Reviews Genetics 3(6); June, 2002: 408.
5. Wertz DC. Embryo and stem cell research: Views from the USA. Journal of Commercial Biotechnology 8(3); Winter 2002: 200-208.
6. Wertz DC. Embryo and stem cell research in the United Stares: A political history. Trends in Molecular Medicine 8(3); March 2002: 143-146.
7. Wertz DC, Knoppers BM. "Serious" Genetic Disorders: Can or Should They Be Defined? American Journal of Medical Genetics, 108 (1); 2002: 29-35.
Articles, 2001
8. Wertz DC. Emerging risks of genetic testing. Journal of Medical Practice Management 17(3), Nov-Dec. 2001: 166-168.
9. Wertz DC. Archived Specimens: Ethics Concerns . Acta Tropica 78 (suppl. 1), Proceedings Seminar on Health research Ethics in Africa,15 January, 2001: S77-S84.
10. Wertz DC. On the Need for Fictive Lines. (Comment on Peter Singer). Society, July/August 2001; 26-29.
11. Wertz DC. Pre-conception Sex Selection: A Question of Consequences. American Journal of Bioethics 1 (1); 2001:36-37.
12. Wertz DC. No Consensus Worldwide. American Journal of Bioethics 1(3); 2001; 14-15.
13. Caulfield TA, Wertz DC. Creating Needs? A Review of Survey Data and Concerns Relevant to the Commercialization of Genetic Testing. Community Genetics 4(2); 2001: 68-78.
14. Wertz DC. Some definitions needed: Comment on N. Daniels, "Justice, Health, and Health Care." American Journal of Bioethics 1 (2):online.
15. Wertz DC. No consensus worldwide: Comment on D.J. Doukas and J.W. Berg, The family covenant and genetic testing. American Journal of Bioethics 1(3): 14-15.
16. Ralston SJ, Wertz DC, Chelmow D, Craigo SD, Bianchi D. Pregnancy Outcomes Following Prenatal Diagnosis of Aneuploidy. Obstetrics and Gynecology 97; 2001: 729-33.
17. Knoppers BM, Takebe H, Berg K, Chadwick R, Qiu, RZ, Verma IC, Macer D, Murray TH, Daar A, Cantu JM, Engels EM, Kirby, M, Wertz DC. HUGO Urges Genetic Benefit Sharing. Community Genetics 3; 2000 (released March 2001): 88-92.
18. Saraiva JM, Anionwu E, Belo M, Jenkins T, Kristoffersson U, Marques I, Santos HG, Sequeiros J, Simpson SA, Wertz DC, Monteiro C. Issues in human Genethics. Genetics in Medicine 3(3); May-June 2001: 218-219.
Articles, 2000
19. Wertz, DC, Gregg, R. Genetic Services in a Social, Ethical, and Policy Context: A Collaboration Between Consumers and Providers. Journal of Medical Ethics, 26: 261-265.
20. Wertz, DC. Emerging Risks of Genetic Testing. Forum: Risk Management Foundation of the Harvard Medical Institutions. 20 (4): 8-9.
Articles, 1999
21. Wertz, DC, "Genetic Discrimination": Results of a Survey of Genetics Professionals, Primary Care Physicians, Patients, and Public. Health Law Review 7(3): 7-8.
22. Wertz, DC. Archived Specimens: A Platform for Discussion. Community Genetics 1999; 2:51-60 (released in March, 2000)
23. Wertz, DC. Patient and Professional Views on Autonomy: A Survey in the United States and Canada. Health Law Review 7(3): 9-10.
24. Wertz, DC, et al. Stored DNA Samples: What You Should Know. The Genetic Resource 12 (1&2): 92-96.
25. Wolff, G, Wertz DC, Nippert I. Ergebnisse der Umfrage zu Problemaspekten angewandter Humangenetik. (Results of a Survey on Problematic Aspects in the Practice of Human Genetics). Medizinischegenetik (Medical Genetics) 11; 1999: 308-318.
26. Wertz DC. Genetics and eugenics. New Scientist 161; Feb. 19, 1999:55-56.
27. Wertz, DC. A Needed Boost for the Human Genome Diversity Project. Politics and the Life Sciences 18 (2); 1999: 336-337.
28. Wertz DC. Guidelines point the way on genetics ethics. Nature 399, 27 May 1999: 297.
Articles, 1998
29. Wertz DC. Eugenics is Alive and Well. Science in Context, 11 (3/4): 493-510. Special issue on Eugenic Thought and Practice, ed. Falk, R., Paul, D.
30. Wertz DC. The difficulties of recruiting minorities to studies of ethics and values in genetics. Community Genetics 1 (3): 175-179.
31. Wertz DC. Ethical Issues in Pediatric Genetics: Views of Geneticists, Parents and Primary Care Physicians. Health Law Journal 6:1-42.
32. Wertz DC, Fletcher J.C. Ethical and Social Issues in Prenatal Sex Selection: A Survey of Geneticists in 37 Nations. Social Science and Medicine. 46 (2): 255-273.
33. Wertz DC. Editorial Comment: Genetic Counseling in Mexico. American Journal of Medical Genetics. 75(4): 424-425.
34. Lisker R, Carnevale A, Villa JA, Armendares S, Wertz DC. Mexican geneticists' opinions on disclosure issues. Clinical Genetics. 54:321-329.
Articles, 1997
35. Wertz DC. Is There a "Women's Ethic" in Genetics?: A 37-Nation Survey of Providers. Journal of the American Medical Women's Association 52 (1): 33-38.
36. Wertz DC. International Perspectives on Privacy and Access to Genetic Information. Microbial and Comparative Genomics 2(1): 33-41.
37. Wertz DC. Society and the Not-So-New Genetics: What Are We Afraid Of? Journal of Contemporary Health Law and Policy 13 (2): 299-346.
38. Cohen P, Wertz DC. Genetic Counseling Practices in Germany: A Comparison Between East German and West German Geneticists. Journal of Genetic Counseling 6(1): 61-80.
39. Wertz DC, Reilly PR, Laboratory Policies and Practices for the Genetic Testing of Children: A Survey of the Helix Network. American Journal of Human Genetics 61: 1163-1168.
40. Mao X, Wertz DC. China's Genetics Services Providers' Attitudes Towards Several Ethical Issues: A Cross-Cultural Survey. Clinical Genetics 52: 100-109.
Articles, 1996:
41. Wertz DC. Opinions des généticiens de 37 pays sur la présélection du sexe. Sociologie et Sociéties. 28 (2): 77-92.
42. Wertz DC. Ethical and social issues in preimplantation genetic diagnosis. The Genetic Resource 10(1): 17-26.
43. Wertz DC. Ethics: A primer for non-ethicists. The Genetic Resource 10(1): 5-8.
Articles, 1995:
44. Wertz DC. Professional Perspectives: A Survey of Canadian Providers. Health Law Journal; 3, special edition on "Professional Norms in the Practice of Human Genetics," 1995: pp. 59-130.
Articles, 1994:
45. Wertz DC, Fanos JH, Reilly PR. Genetic testing for children and adolescents: who decides? JAMA 272(11); Sept. 21, 1994: 875-881.
46. Wertz DC, Fanos JH, Reilly PR. Testing healthy children and adolescents: recommendations for avoiding harm. The Genetic Resource 8(2); 1994: 16-20.
47. Wertz DC. Provider gender and moral reasoning: the politics of an "ethics of care". Journal of Genetic Counseling 3(2); 1994: 95-112.
48. Wertz DC. Leave the door open to research. Symposium on human germ-line gene therapy. Politics and the Life Sciences 13(2); 1994: 235-236.
Articles, 1993:
49. Wertz DC. Providers' Gender and Moral Reasoning. In: Evans MI (ed) Reproductive Genetic Testing: Impact Upon Women. Fetal Diagnosis and Therapy 8 [Suppl. 1]; 1993: 81-89. Farmington, CT: Karger.
50. Wertz DC. Fletcher JC. A critique of some feminist challenges to prenatal diagnosis. Journal of Women's Health 2(2); 1993: 1-16.
51. Wertz DC, Fletcher JC. Geneticists Approach Ethics: An International Survey. Clinical Genetics 43; 1993: 104-110.
52. Wertz DC, Fletcher JC. Proposed: An International Code of Ethics for Medical Genetics. Clinical Genetics 44; 1993: 37-43.
53. Wertz DC, International perspectives on ethics and human genetics. Suffolk University Law Review 27 (4); Winter, 1993: 1411-1455.
54. Wertz DC, Fletcher JC. Prenatal diagnosis and sex selection in 19 nations. Social Science and Medicine 37(11); 1993: 1359-1366.
55. Wertz DC, Fletcher JC. Feminist criticism of prenatal diagnosis: A response. In: Evans MI (ed) The New Reproductive Genetics: Implications for Women and Their Physicians. Clinical Obstetrics and Gynecology 36(3); 1993: 541-567. Philadelphia: Lippincott.
56. Wertz DC. Provider Biases and Choices: The Role of Gender. In: Evans MI (ed) The New Reproductive Genetics: Implications for Women and Their Physicians. In: Pitkin R, Scott J (series eds) Clinical Obstetrics and Gynecology 36(3); 1993: 521-531. Philadelphia: Lippincott.
Articles, 1992:
57. Wertz DC, Janes SR, Rosenfield JM, Erbe RW. Attitudes toward the prenatal diagnosis of cystic fibrosis: factors in decision making among affected families. American Journal of Human Genetics 50; 1992: 222-235.
58. Wertz DC. Ethical and legal implications of the new genetics: Issues for discussion. Social Science and Medicine, 35(4); 1992: 495-505.
Articles, 1991
59. Wertz DC, Rosenfield JM, Janes SR, Erbe RW. Attitudes toward abortion among parents of children with cystic fibrosis. American Journal of Public Health 81 (8); 1991: 992-996.
60. Wertz DC, Fletcher JC. Privacy and disclosure in medical genetics examined in an ethics of care. Bioethics 5 (3); 1991: 212-232.
61. Wertz DC. Lives in the balance: Assessing the risks of waiting for perfectly accurate tests. The Scientist, January 21, 1991: 9-11.
Articles, 1990
62. Wertz DC, Fletcher JC, Mulvihill JJ. Medical geneticists confront ethical dilemmas: Cross-Cultural Comparisons among 18 Nations. American Journal of Human Genetics 46; 1990: 1200-1213.
63. Fletcher JC, Wertz DC. Ethics, Law, and Medical Genetics: After the Human Genome is Mapped. Emory Law Journal 39 (3); Summer 1990: 747-809.
64. Janes SR, Rosenfield JM, Wertz DC, Erbe RW. DNA diagnosis of cystic fibrosis: Utilization of genetic counseling. In: Fine BA, Gettig E, Greendale K, Leopold B, Paul NW, eds. Strategies in Genetic Counseling: Reproductive Genetics and New Technologies. Birth defects: Original Articles Series 1990; 26: 254-257.
Articles, 1989:
65. Wertz DC, Fletcher JC. Fatal Knowledge? Prenatal Diagnosis and Sex Selection. Hastings Center Report 19: 3; (May/June, 1989): 21-27.
66. Wertz, DC. Fletcher JC. Ethical Problems in Prenatal Diagnosis: A Cross-Cultural Survey of Medical Geneticists in 18 Nations. Prenatal Diagnosis 9 (3); 1989: 145-157.
67. Wertz DC, Fletcher JC. An International; Survey of Attitudes of Medical Geneticists Toward Mass Screening and Access to Results. Public Health Reports 4 (1); January/February 1989: 34-44.
68. Wertz DC, Fletcher JC. Disclosing Genetic Information: Who Should Know? Technology Review 92 (5); July, 1989: 22-23.
69. Wertz DC, Fletcher JC. Ethics and Genetics: An International Survey. Hastings Center Report 19 (Special Supplement); (July/August, 1989): 20-24.
70. Wertz DC, Fletcher JC. Ethical Issues in Prenatal Diagnosis. Pediatric Annals 18 (11); 1989: 739-749.
71. Wertz DC, Fletcher JC. Moral Reasoning Among Medical Geneticists in 18 Nations. Theoretical Medicine 10; 1989: 123-138.
72. Wertz DC, Silvia AM, Dreyer J, Sandison G, LaCharite C. The AIDS Action Committee SafetyNet Program; Small Group Parties for Safer Sex Education. American Journal of Public Health 79 (9); 1989: 1305-1306.
Articles, 1988:
73. Wertz DC, Fletcher JC. Ethics and Medical Genetics in the United States: A National Survey. American Journal of Medical Genetics 29; April, 1988: 815-827.
74. Wertz DC, Fletcher JC. Attitudes of Genetic Counselors: A Multi-National Survey. American Journal of Human Genetics 42 (4); April, 1988: 592-600.
75. Wertz DC, Sorenson JR, Heeren TC. Communication in health professional-lay encounters: How often does each party know what the other wants to discuss? In: Ruben BD, ed. Information and Behavior. Vol. 2. New Brunswick, NJ: Transaction Books, 1988, pp. 329-342.
76. Wertz DC, Sorenson JR, Heeren TC. 'Can't Get No (dis)Satisfaction': Professional Satisfaction with Professional-Client Encounters. Work and Occupations. 12 (1); 1988: 36-54.
77. Wertz DC, Sorenson JR, Liebling L, Kessler L, Heeren TC. Caring for persons with AIDS: Knowledge and attitudes of 1,047 health care workers attending AIDS Action Committee educational programs. Journal of Primary Prevention, 8 (3); Spring, 1988: 109-124.
Articles, 1987:
78. Wertz DC, Fletcher JC. Communicating Genetic Risks. Science, Technology, and Human Values 12 (3.4); 1987: 60-66.... This is page 11 of 56 of this resume. There is no room to display any more.
Obituary
DR. DOROTHY CORBETT WERTZ
Author: Laura Levis, Globe Correspondent
Date: August 10, 2003
Publication: Boston Globe, The (MA)
Page: A30
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