-
1
-
-
33747385762
-
Genetic testing, genetic information and the role of maternal-child nurses
-
Barnoy, S., et al., 2006. Genetic testing, genetic information and the role of maternal-child nurses. Journal of Nursing Scholarship, 38, 219-224.
-
(2006)
Journal of Nursing Scholarship
, vol.38
, pp. 219-224
-
-
Barnoy, S.1
-
2
-
-
43849109799
-
Intention to communicate BRCA1/BRCA2 genetic test results to the family
-
Barsevick, A., et al., 2008. Intention to communicate BRCA1/BRCA2 genetic test results to the family. Journal of Family Psychology, 22, 303-312.
-
(2008)
Journal of Family Psychology
, vol.22
, pp. 303-312
-
-
Barsevick, A.1
-
4
-
-
0013196755
-
Genetic secrets and the family
-
Bell, D. and Bennett, B., 2001. Genetic secrets and the family. Medical Law Review, 9, 130-161.
-
(2001)
Medical Law Review
, vol.9
, pp. 130-161
-
-
Bell, D.1
Bennett, B.2
-
5
-
-
0029785139
-
Respecting the autonomy of cancer patients when talking with their families: Qualitative analysis of semistructured interviews with patients
-
Benson, J. and Britten, N., 2006. Respecting the autonomy of cancer patients when talking with their families: qualitative analysis of semistructured interviews with patients. British Medical Journal, 313, 729-731.
-
(2006)
British Medical Journal
, vol.313
, pp. 729-731
-
-
Benson, J.1
Britten, N.2
-
6
-
-
79960618962
-
-
Oxford: Berghahn Books
-
Birenbaum-Carmeli, D. and Carmeli, Y., 2010. Kin, gene, community: reproductive technologies among Jewish Israelis. Oxford: Berghahn Books, 1-50.
-
(2010)
Kin, Gene, Community: Reproductive Technologies among Jewish Israelis
, pp. 1-50
-
-
Birenbaum-Carmeli, D.1
Carmeli, Y.2
-
7
-
-
34548511568
-
How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults
-
Bradbury, A., et al., 2007. How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults. Journal of Clinical Oncology, 25 (24), 3705-3711.
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.24
, pp. 3705-3711
-
-
Bradbury, A.1
-
8
-
-
50649086584
-
Colorectal cancer cases and relatives of cases indicate similar willingness to receive and disclose genetic information
-
Ceballos, R., et al., 2008. Colorectal cancer cases and relatives of cases indicate similar willingness to receive and disclose genetic information. Genetic Testing, 12, 415-420.
-
(2008)
Genetic Testing
, vol.12
, pp. 415-420
-
-
Ceballos, R.1
-
9
-
-
0037216727
-
Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients
-
Claes, E., et al., 2003. Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients. American Journal of Medical Genetics, 116A, 11-19.
-
(2003)
American Journal of Medical Genetics
, vol.116 A
, pp. 11-19
-
-
Claes, E.1
-
10
-
-
34447556871
-
Should families own genetic information?
-
Clarke, A., 2007. Should families own genetic information? No. British Medical Journal, 335, 23.
-
(2007)
No. British Medical Journal
, vol.335
, pp. 23
-
-
Clarke, A.1
-
11
-
-
21044456586
-
Genetic professionals' reports of nondisclosure of genetic risk information within families
-
Clarke, A., et al., 2005. Genetic professionals' reports of nondisclosure of genetic risk information within families. European Journal of Human Genetics, 13, 556-562.
-
(2005)
European Journal of Human Genetics
, vol.13
, pp. 556-562
-
-
Clarke, A.1
-
12
-
-
30344445067
-
Genetic testing for hereditary breast and ovarian cancer: Responsibility and choice
-
D'Agincourt-Cannong, L., 2006. Genetic testing for hereditary breast and ovarian cancer: responsibility and choice. Qualitative Health Research, 16, 97-118.
-
(2006)
Qualitative Health Research
, vol.16
, pp. 97-118
-
-
D'agincourt-Cannong, L.1
-
13
-
-
0002929890
-
Autonomy and interdependence: Quandaries in genetic decision-making
-
C. Mackenzie and N. Stoljar. New York: Oxford University Press
-
Donchin, A., 2000. Autonomy and interdependence: quandaries in genetic decision-making. In: C. Mackenzie and N. Stoljar, eds. Relational autonomy: feminist perspectives on autonomy, agency and the social self. New York: Oxford University Press, 236-258.
-
(2000)
Relational Autonomy: Feminist Perspectives on Autonomy, Agency and the Social Self
, pp. 236-258
-
-
Donchin, A.1
-
14
-
-
1042266542
-
Genetics providers and the family covenant: Connecting individuals with their families
-
Doukas, D., 2003. Genetics providers and the family covenant: connecting individuals with their families. Genetic Testing, 7 (4), 315-322.
-
(2003)
Genetic Testing
, vol.7
, Issue.4
, pp. 315-322
-
-
Doukas, D.1
-
15
-
-
0035383268
-
The family covenant and genetic testing
-
Doukas, D. and Berg, J., 2001. The family covenant and genetic testing. American Journal of Bioethics, 1 (3), 2-10.
-
(2001)
American Journal of Bioethics
, vol.1
, Issue.3
, pp. 2-10
-
-
Doukas, D.1
Berg, J.2
-
16
-
-
0043037219
-
Duty to warn at-risk relatives for genetic disease: Genetic counselors' clinical experience
-
Dugan, R.B., et al., 2003. Duty to warn at-risk relatives for genetic disease: genetic counselors' clinical experience. American Journal of Medical Genetics, 119C, 27-34.
-
(2003)
American Journal of Medical Genetics
, vol.119 C
, pp. 27-34
-
-
Dugan, R.B.1
-
18
-
-
21544456087
-
Facilitating family communication about predictive genetic testing: Probands' perceptions
-
Gaff, C., et al., 2005. Facilitating family communication about predictive genetic testing: probands' perceptions. Journal of Genetic Counseling, 14, 133-140.
-
(2005)
Journal of Genetic Counseling
, vol.14
, pp. 133-140
-
-
Gaff, C.1
-
19
-
-
34848813214
-
Process and outcome in communication of genetic information within families: A systematic review
-
Gaff, C., et al., 2007. Process and outcome in communication of genetic information within families: a systematic review. European Journal of Human Genetics, 15, 999-1011.
-
(2007)
European Journal of Human Genetics
, vol.15
, pp. 999-1011
-
-
Gaff, C.1
-
20
-
-
18844421951
-
Medical confidentiality in the family: The doctor's duty reconsidered
-
Gilbar, R., 2004. Medical confidentiality in the family: the doctor's duty reconsidered. International Journal of Law, Policy and the Family, 18, 195-213.
-
(2004)
International Journal of Law, Policy and the Family
, vol.18
, pp. 195-213
-
-
Gilbar, R.1
-
21
-
-
34447508170
-
Communicating genetic information in the family: The familial relationship as the forgotten factor
-
Gilbar, R., 2007a. Communicating genetic information in the family: the familial relationship as the forgotten factor. Journal of Medical Ethics, 33, 390-393.
-
(2007)
Journal of Medical Ethics
, vol.33
, pp. 390-393
-
-
Gilbar, R.1
-
22
-
-
38849117002
-
Patient autonomy and relatives' right to know genetic information
-
Gilbar, R., 2007b. Patient autonomy and relatives' right to know genetic information. Medicine and Law, 26, 677-697.
-
(2007)
Medicine and Law
, vol.26
, pp. 677-697
-
-
Gilbar, R.1
-
23
-
-
77249133885
-
Between unconditional acceptance and responsibility: Should family ethics limit the scope of reproductive autonomy?
-
Gilbar, R., 2009. Between unconditional acceptance and responsibility: should family ethics limit the scope of reproductive autonomy? Child and Family Law Quarterly, 21, 309-334.
-
(2009)
Child and Family Law Quarterly
, vol.21
, pp. 309-334
-
-
Gilbar, R.1
-
24
-
-
0033183718
-
Genetic privacy and the law: An end to genetics exceptionalism
-
Gostin, L. and Hodge, J., 1999. Genetic privacy and the law: an end to genetics exceptionalism. Jurimetrics, 40 (1), 21-58.
-
(1999)
Jurimetrics
, vol.40
, Issue.1
, pp. 21-58
-
-
Gostin, L.1
Hodge, J.2
-
25
-
-
0033158588
-
Autonomy and paternalism in a communitarian society
-
Gross, M., 1999. Autonomy and paternalism in a communitarian society. Hastings Center Report, 29, 13-20.
-
(1999)
Hastings Center Report
, vol.29
, pp. 13-20
-
-
Gross, M.1
-
26
-
-
0033181470
-
Doing the right thing: Genetic risk and responsibility
-
Hallowell, N., 1999. Doing the right thing: genetic risk and responsibility. Sociology of Health & Illness, 21 (5), 597-621.
-
(1999)
Sociology of Health & Illness
, vol.21
, Issue.5
, pp. 597-621
-
-
Hallowell, N.1
-
27
-
-
0037398070
-
Balancing autonomy and responsibility: The ethics of generating and disclosing genetic information
-
Hallowell, N., et al., 2003. Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information. Journal of Medical Ethics, 29, 74-83.
-
(2003)
Journal of Medical Ethics
, vol.29
, pp. 74-83
-
-
Hallowell, N.1
-
28
-
-
18344381796
-
Communication about genetic testing in families of male BRCA1/2 carriers and non-carriers: Patterns, priorities and problems
-
Hallowell, N., et al., 2005. Communication about genetic testing in families of male BRCA1/2 carriers and non-carriers: patterns, priorities and problems. Clinical Genetics, 67, 492-502.
-
(2005)
Clinical Genetics
, vol.67
, pp. 492-502
-
-
Hallowell, N.1
-
30
-
-
85050175310
-
Between mothers, fetuses and society: Reproductive genetics in the israeli jewish context
-
Hashiloni-Dolev, Y., 2006. Between mothers, fetuses and society: reproductive genetics in the Israeli Jewish context. Nashim: A Journal of Jewish Women's Studies & Gender, 12, 129-150.
-
(2006)
Nashim: A Journal of Jewish Women's Studies & Gender
, vol.12
, pp. 129-150
-
-
Hashiloni-Dolev, Y.1
-
32
-
-
18244374810
-
All in the family: Evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results
-
Hughes, C., et al., 2002. All in the family: evaluation of the process and content of sisters' communication about BRCA1 and BRCA2 genetic test results. American Journal of Medical Genetics, 107, 143-150.
-
(2002)
American Journal of Medical Genetics
, vol.107
, pp. 143-150
-
-
Hughes, C.1
-
33
-
-
0036468106
-
Genetic information and the family: Are we our brother's keeper?
-
Knoppers, B., 2002. Genetic information and the family: are we our brother's keeper? Trends in Biotechnology, 20, 85-86.
-
(2002)
Trends in Biotechnology
, vol.20
, pp. 85-86
-
-
Knoppers, B.1
-
34
-
-
34250750776
-
Should healthcare providers have a duty to warn family members of individuals with an HNPCC-causing mutation? A survey of patients from the ontario familial colon cancer registry
-
Kohut, K., et al., 2007. Should healthcare providers have a duty to warn family members of individuals with an HNPCC-causing mutation? A survey of patients from the Ontario familial colon cancer registry. Journal of Medical Genetics, 4, 404-407.
-
(2007)
Journal of Medical Genetics
, vol.4
, pp. 404-407
-
-
Kohut, K.1
-
36
-
-
0001146181
-
Family disclosure in genetic testing for cancer susceptibility: Determinants and consequences
-
Lerman, C., et al., 1998. Family disclosure in genetic testing for cancer susceptibility: determinants and consequences. Journal of Health Care, Law & Policy, 1, 353-372.
-
(1998)
Journal of Health Care, Law & Policy
, vol.1
, pp. 353-372
-
-
Lerman, C.1
-
38
-
-
77951630613
-
Confidentiality and sharing genetic information with relatives
-
Lucassen, A. and Parker, M., 2010. Confidentiality and sharing genetic information with relatives. The Lancet, 375, 1507-1509.
-
(2010)
The Lancet
, vol.375
, pp. 1507-1509
-
-
Lucassen, A.1
Parker, M.2
-
40
-
-
0033755522
-
Prenatal genetic testing in Japan
-
Matsuda, I. and Suzumori, K., 2000. Prenatal genetic testing in Japan. Community Genetics, 3, 12-16.
-
(2000)
Community Genetics
, vol.3
, pp. 12-16
-
-
Matsuda, I.1
Suzumori, K.2
-
41
-
-
70449625708
-
Family communication, genetic testing and colonoscopy screening in hereditary non-polyposis colon cancer: A qualitative study
-
McCann, S., et al., 2009. Family communication, genetic testing and colonoscopy screening in hereditary non-polyposis colon cancer: a qualitative study. Psycho-Oncology, 18, 1208-1215.
-
(2009)
Psycho-Oncology
, vol.18
, pp. 1208-1215
-
-
McCann, S.1
-
42
-
-
9644310312
-
Family communication about positive BRCA1 and BRCA2 genetic test results
-
McGivern, B., et al., 2004. Family communication about positive BRCA1 and BRCA2 genetic test results. Genetics in Medicine, 6, 503-509.
-
(2004)
Genetics in Medicine
, vol.6
, pp. 503-509
-
-
McGivern, B.1
-
43
-
-
84871272820
-
-
Accessed 15 September 2011
-
Ministry of Health, 2004. Genetic testing- BRCA1 and BRCA2 testing [in Hebrew] [online]. Available from: http://www.health.gov.il/pages/default.asp? PageId=1696&catId=217&maincat=42 [Accessed 15 September 2011].
-
(2004)
Genetic Testing- BRCA1 and BRCA2 Testing [In Hebrew] [Online]
-
-
-
46
-
-
67649240271
-
Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information
-
Nycum, G., Avard, D., and Knoppers, B.M., 2009. Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information. European Journal of Human Genetics, 17, 872-880.
-
(2009)
European Journal of Human Genetics
, vol.17
, pp. 872-880
-
-
Nycum, G.1
Avard, D.2
Knoppers, B.M.3
-
47
-
-
3242732814
-
Genetic information: A joint account
-
Parker, M. and Lucassen, A., 2004. Genetic information: a joint account. British Medical Journal, 329, 165-167.
-
(2004)
British Medical Journal
, vol.329
, pp. 165-167
-
-
Parker, M.1
Lucassen, A.2
-
48
-
-
33644848688
-
Sharing BRCA1/2 test results with first-degree relatives: Factors predicting who women tell
-
Patenaude, A., et al., 2006. Sharing BRCA1/2 test results with first-degree relatives: factors predicting who women tell. Journal of Clinical Oncology, 24, 700-706.
-
(2006)
Journal of Clinical Oncology
, vol.24
, pp. 700-706
-
-
Patenaude, A.1
-
49
-
-
27144478922
-
Hereditary nonpolyposis colorectal cancer family members' perceptions about the duty to inform and health professionals' role in disseminating genetic information
-
Pentz, R., et al., 2005. Hereditary nonpolyposis colorectal cancer family members' perceptions about the duty to inform and health professionals' role in disseminating genetic information. Genetic Testing, 9, 261-269.
-
(2005)
Genetic Testing
, vol.9
, pp. 261-269
-
-
Pentz, R.1
-
50
-
-
0041818178
-
How families communicate about HNPCC genetic testing: Findings from a qualitative study
-
Peterson, S., et al., 2003. How families communicate about HNPCC genetic testing: findings from a qualitative study. American Journal of Medical Genetics, 119C, 78-86.
-
(2003)
American Journal of Medical Genetics
, vol.119 C
, pp. 78-86
-
-
Peterson, S.1
-
51
-
-
4143137555
-
"Important to test, important to support": Attitudes toward disability rights and prenatal diagnosis among leaders of support groups for genetic disorders in Israel
-
Raz, A., 2004. "Important to test, important to support": attitudes toward disability rights and prenatal diagnosis among leaders of support groups for genetic disorders in Israel. Social Science & Medicine, 59, 1857-1866.
-
(2004)
Social Science & Medicine
, vol.59
, pp. 1857-1866
-
-
Raz, A.1
-
52
-
-
77952968031
-
Diversity and uniformity in genetic responsibility: Moral attitudes of patients, relatives and lay people in Germany and Israel
-
Raz, A. and Schicktanz, S., 2009a. Diversity and uniformity in genetic responsibility: moral attitudes of patients, relatives and lay people in Germany and Israel. Medicine, Health Care and Philosophy: A European Journal, 12 (4), 433-442.
-
(2009)
Medicine, Health Care and Philosophy: A European Journal
, vol.12
, Issue.4
, pp. 433-442
-
-
Raz, A.1
Schicktanz, S.2
-
53
-
-
85050648302
-
Lay perceptions of genetic testing in Germany and Israel: The interplay of national culture and individual experience
-
Raz, A. and Schicktanz, S., 2009b. Lay perceptions of genetic testing in Germany and Israel: the interplay of national culture and individual experience. New Genetics and Society, 28 (4), 401-414.
-
(2009)
New Genetics and Society
, vol.28
, Issue.4
, pp. 401-414
-
-
Raz, A.1
Schicktanz, S.2
-
54
-
-
33644699330
-
The quest after the perfect baby: Why do Israeli women seek prenatal genetic testing?
-
Remennick, L., 2006. The quest after the perfect baby: why do Israeli women seek prenatal genetic testing? Sociology of Health & Illness, 28, 21-53.
-
(2006)
Sociology of Health & Illness
, vol.28
, pp. 21-53
-
-
Remennick, L.1
-
55
-
-
0031994762
-
Genetic links, family ties and social bonds: Rights and responsibilities in the face of genetic knowledge
-
Rhodes, R., 1998. Genetic links, family ties and social bonds: rights and responsibilities in the face of genetic knowledge. Journal of Medicine & Philosophy, 23 (1), 10-30.
-
(1998)
Journal of Medicine & Philosophy
, vol.23
, Issue.1
, pp. 10-30
-
-
Rhodes, R.1
-
56
-
-
84856967482
-
The Israeli abortion committees' process of decision making: An ethical analysis
-
Rimon-Zarfaty, N. and Jotkowitz, A., 2012. The Israeli abortion committees' process of decision making: an ethical analysis. Journal of Medical Ethics, 38 (1), 26-30.
-
(2012)
Journal of Medical Ethics
, vol.38
, Issue.1
, pp. 26-30
-
-
Rimon-Zarfaty, N.1
Jotkowitz, A.2
-
57
-
-
70350236490
-
Genetic testing in Israel: An overview
-
Rosner, G., Rosner, R., and Orr-Urtreger, A., 2009. Genetic testing in Israel: an overview. Annual Review of Human Genetics, 10, 175-192.
-
(2009)
Annual Review of Human Genetics
, vol.10
, pp. 175-192
-
-
Rosner, G.1
Rosner, R.2
Orr-Urtreger, A.3
-
58
-
-
0042324045
-
Factors affecting performance of prenatal genetic testing by Israeli Jewish women
-
Sher, C., et al., 2003. Factors affecting performance of prenatal genetic testing by Israeli Jewish women. American Journal of Medical Genetics, 120A, 418-422.
-
(2003)
American Journal of Medical Genetics
, vol.120 A
, pp. 418-422
-
-
Sher, C.1
-
59
-
-
0032009804
-
Patients' rights or family responsibilities
-
Skene, L., 1998. Patients' rights or family responsibilities. Medical Law Review, 6, 1-41.
-
(1998)
Medical Law Review
, vol.6
, pp. 1-41
-
-
Skene, L.1
-
61
-
-
39949085409
-
Sharing genetic test results in Lynch Syndrome: Communication with close and distant relatives
-
Stoffel, E., et al., 2008. Sharing genetic test results in Lynch Syndrome: communication with close and distant relatives. Clinical Gastroenterology and Hepatology, 6, 333-338.
-
(2008)
Clinical Gastroenterology and Hepatology
, vol.6
, pp. 333-338
-
-
Stoffel, E.1
-
63
-
-
33845986771
-
Confidentiality versus duty to inform - An empirical study on attitudes towards the handling of genetic information
-
Wolff, K., et al., 2007. Confidentiality versus duty to inform - an empirical study on attitudes towards the handling of genetic information. American Journal of Medical Genetics, 134A, 142-148.
-
(2007)
American Journal of Medical Genetics
, vol.134 A
, pp. 142-148
-
-
Wolff, K.1
-
64
-
-
0033818681
-
Screening for genetic disorders among Jews: How should the Tay-Sachs screening program be continued?
-
Zlotogora, J. and Leventhal, A., 2000. Screening for genetic disorders among Jews: how should the Tay-Sachs screening program be continued? Israeli Medical Association Journal, 2, 665-7.
-
(2000)
Israeli Medical Association Journal
, vol.2
, pp. 665-667
-
-
Zlotogora, J.1
Leventhal, A.2
|