-
1
-
-
79960565912
-
Qualitative thematic analysis of consent forms used in cancer genome sequencing
-
3170865 21771309 10.1186/1472-6939-12-14
-
Allen, C.; Foulkes, W. D. (2011). Qualitative thematic analysis of consent forms used in cancer genome sequencing. BMC Medical Ethics, 12, 14.
-
(2011)
BMC Medical Ethics
, vol.12
, pp. 14
-
-
Allen, C.1
Foulkes, W.D.2
-
2
-
-
33847346789
-
The genomic era and serious mental illness: A potential application for psychiatric genetic counseling
-
17287384 10.1176/appi.ps.58.2.254
-
Austin, J. C.; Honer, W. G. (2007). The genomic era and serious mental illness: a potential application for psychiatric genetic counseling. Psychiatric Services, 58(2), 254-261.
-
(2007)
Psychiatric Services
, vol.58
, Issue.2
, pp. 254-261
-
-
Austin, J.C.1
Honer, W.G.2
-
3
-
-
80054820783
-
Opinions and intentions of parents of an autistic child toward genetic research results: Two typical profiles
-
3198138 21673746 10.1038/ejhg.2011.106
-
Baret, L.; Godard, B. (2011). Opinions and intentions of parents of an autistic child toward genetic research results: two typical profiles. European Journal of Human Genetics, 19(11), 1127-1132.
-
(2011)
European Journal of Human Genetics
, vol.19
, Issue.11
, pp. 1127-1132
-
-
Baret, L.1
Godard, B.2
-
4
-
-
0035188689
-
Goals of genetic counseling
-
1:STN:280:DC%2BD387ptVOhtw%3D%3D 11903329 10.1034/j.1399-0004.2001. 600501.x
-
Biesecker, B. B. (2001). Goals of genetic counseling. Clinical Genetics, 60, 323-330.
-
(2001)
Clinical Genetics
, vol.60
, pp. 323-330
-
-
Biesecker, B.B.1
-
5
-
-
1642496976
-
Ethical issues in psychiatric genetics research: Points to consider
-
1:CAS:528:DC%2BD3sXpsVGisbs%3D 13680086 10.1007/s00213-003-1502-2
-
Biesecker, B. B.; Peay, H. L. (2003). Ethical issues in psychiatric genetics research: points to consider. Psychopharmacology, 171(1), 27-35.
-
(2003)
Psychopharmacology
, vol.171
, Issue.1
, pp. 27-35
-
-
Biesecker, B.B.1
Peay, H.L.2
-
6
-
-
84880900798
-
Lessons from next-generation sequencing analysis in hematological malignancies
-
1:STN:280:DC%2BC3sfis12gtA%3D%3D 3730204 23872706 10.1038/bcj.2013.26
-
Braggio, E.; Egan, J. B.; Fonseca, R.; Stewart, A. K. (2013). Lessons from next-generation sequencing analysis in hematological malignancies. Blood Cancer Journal, 3, e127.
-
(2013)
Blood Cancer Journal
, vol.3
, pp. 127
-
-
Braggio, E.1
Egan, J.B.2
Fonseca, R.3
Stewart, A.K.4
-
7
-
-
84862605504
-
Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease
-
1:CAS:528:DC%2BC38XovVagtrs%3D 10.1038/nrn3271
-
Bras, J.; Guerreiro, R.; Hardy, J. (2012). Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease. Nature Review Neuroscience, 13(7), 453-464.
-
(2012)
Nature Review Neuroscience
, vol.13
, Issue.7
, pp. 453-464
-
-
Bras, J.1
Guerreiro, R.2
Hardy, J.3
-
8
-
-
79151476271
-
Disclosure of individual genetic data to research participants: The debate reconsidered
-
1:CAS:528:DC%2BC3MXhtlams78%3D 21190750 10.1016/j.tig.2010.11.004
-
Bredenoord, A. L.; Kroes, H. Y.; Cuppen, E.; Parker, M.; van Delden, J. J. (2011). Disclosure of individual genetic data to research participants: the debate reconsidered. Trends in Genetics, 27(2), 41-47.
-
(2011)
Trends in Genetics
, vol.27
, Issue.2
, pp. 41-47
-
-
Bredenoord, A.L.1
Kroes, H.Y.2
Cuppen, E.3
Parker, M.4
Van Delden, J.J.5
-
9
-
-
0034130561
-
Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays
-
10.1038/76469 1:CAS:528:DC%2BD3cXkt12gur8%3D 10835600 10.1038/76469
-
Brenner, S.; Johnson, M.; Bridgham, J.; Golda, G.; Lloyd, D. H.; Johnson, D.; et al. (2000). Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays. Nature Biotechnology, 18(6), 630-634. doi: 10.1038/76469.
-
(2000)
Nature Biotechnology
, vol.18
, Issue.6
, pp. 630-634
-
-
Brenner, S.1
Johnson, M.2
Bridgham, J.3
Golda, G.4
Lloyd, D.H.5
Johnson, D.6
-
11
-
-
84859517950
-
-
Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada, & Social Sciences and Humanities Research Council of Canada Accessed 22 Oct 2012
-
Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada, & Social Sciences and Humanities Research Council of Canada. (2010). Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (TCPS 2). Retrieved from http://www.pre.ethics.gc.ca/ pdf/eng/tcps2/TCPS-2-FINAL-Web.pdf. Accessed 22 Oct 2012.
-
(2010)
Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (TCPS 2)
-
-
-
13
-
-
44449088050
-
Genetic testing and genetic counseling in cardiovascular genetic medicine: Overview and preliminary recommendations
-
18401220 10.1111/j.1751-7133.2008.08217.x
-
Cowan, J.; Morales, A.; Dagua, J.; Hershberger, R. E. (2008). Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations. Congestive Heart Failure, 14(2), 97-105.
-
(2008)
Congestive Heart Failure
, vol.14
, Issue.2
, pp. 97-105
-
-
Cowan, J.1
Morales, A.2
Dagua, J.3
Hershberger, R.E.4
-
14
-
-
84868686559
-
Diagnostic exome sequencing in persons with severe intellectual disability
-
23033978 10.1056/NEJMoa1206524
-
de Ligt, J.; Willemsen, M. H.; van Bon, B. W.; Kleefstra, T.; Yntema, H. G.; Kroes, T.; et al. (2012). Diagnostic exome sequencing in persons with severe intellectual disability. New England Journal of Medicine, 367(20), 1921-1929.
-
(2012)
New England Journal of Medicine
, vol.367
, Issue.20
, pp. 1921-1929
-
-
De Ligt, J.1
Willemsen, M.H.2
Van Bon, B.W.3
Kleefstra, T.4
Yntema, H.G.5
Kroes, T.6
-
15
-
-
84873025492
-
Emerging issues in paediatric health research consent forms in Canada: Working towards best practices
-
3571865 23363554 10.1186/1472-6939-14-5
-
Dove, E. S.; Avard, D.; Black, L.; Knoppers, B. M. (2013). Emerging issues in paediatric health research consent forms in Canada: working towards best practices. BMC Medical Ethics, 14, 5.
-
(2013)
BMC Medical Ethics
, vol.14
, pp. 5
-
-
Dove, E.S.1
Avard, D.2
Black, L.3
Knoppers, B.M.4
-
16
-
-
33645760482
-
Genetic counseling in psychiatry
-
16603476 10.1080/10673220600655723
-
Finn, C. T.; Smoller, J. W. (2006). Genetic counseling in psychiatry. Harvard Review of Psychiatry, 14(2), 109-121.
-
(2006)
Harvard Review of Psychiatry
, vol.14
, Issue.2
, pp. 109-121
-
-
Finn, C.T.1
Smoller, J.W.2
-
17
-
-
84874592689
-
Risk counselling for family members in bipolar disorder and schizophrenia
-
23137787 10.1017/S1461145712001150
-
Gershon, E. S. (2013). Risk counselling for family members in bipolar disorder and schizophrenia. International Journal of Neuropsychopharmacology, 16(3), 713-714.
-
(2013)
International Journal of Neuropsychopharmacology
, vol.16
, Issue.3
, pp. 713-714
-
-
Gershon, E.S.1
-
18
-
-
84859916597
-
Disease gene identification strategies for exome sequencing
-
1:CAS:528:DC%2BC38XlvV2kur8%3D 3330229 22258526 10.1038/ejhg.2011.258
-
Gilissen, C.; Hoischen, A.; Brunner, H. G.; Veltman, J. A. (2012). Disease gene identification strategies for exome sequencing. European Journal of Human Genetics, 20(5), 490-497.
-
(2012)
European Journal of Human Genetics
, vol.20
, Issue.5
, pp. 490-497
-
-
Gilissen, C.1
Hoischen, A.2
Brunner, H.G.3
Veltman, J.A.4
-
19
-
-
84880535720
-
ACMG Recommendations for reporting of incidental findings in clinical exome and genome sequencing
-
Green, R. C.; Berg, J. S.; Grody, W. W.; Kalia, S. S.; Korf, B. R.; Martin, C. L.; et al. (2013). ACMG Recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genetics in Medicine, 15(7), 565-574.
-
(2013)
Genetics in Medicine
, vol.15
, Issue.7
, pp. 565-574
-
-
Green, R.C.1
Berg, J.S.2
Grody, W.W.3
Kalia, S.S.4
Korf, B.R.5
Martin, C.L.6
-
20
-
-
84872165516
-
Use of next generation sequencing technologies in research and beyond: Are participants with mental health disorders fully protected?
-
3537639 23256847 10.1186/1472-6939-13-36
-
Groisman, I. J.; Mathieu, G.; Godard, B. (2012). Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? BMC Medical Ethics, 13(1), 36.
-
(2012)
BMC Medical Ethics
, vol.13
, Issue.1
, pp. 36
-
-
Groisman, I.J.1
Mathieu, G.2
Godard, B.3
-
21
-
-
84863625960
-
Genetic counseling and the ethical issues around direct to consumer genetic testing
-
22290190 10.1007/s10897-012-9488-8
-
Hawkins, A. K.; Ho, A. (2012). Genetic counseling and the ethical issues around direct to consumer genetic testing. Journal of Genetic Counseling, 21(3), 367-373.
-
(2012)
Journal of Genetic Counseling
, vol.21
, Issue.3
, pp. 367-373
-
-
Hawkins, A.K.1
Ho, A.2
-
23
-
-
57649112541
-
Ethical considerations in psychiatric genetics
-
19085387 10.1080/10673220802576859
-
Hoop, J. G. (2008). Ethical considerations in psychiatric genetics. Harvard Review of Psychiatry, 16(6), 322-338.
-
(2008)
Harvard Review of Psychiatry
, vol.16
, Issue.6
, pp. 322-338
-
-
Hoop, J.G.1
-
24
-
-
78649941297
-
Exome sequencing reveals VCP mutations as a cause of familial ALS
-
1:CAS:528:DC%2BC3cXhsFGhu73J 3032425 21145000 10.1016/j.neuron.2010.11. 036
-
Johnson, J. O.; Mandrioli, J.; Benatar, M.; Abramzon, Y.; Van Deerlin, V. M.; Trojanowski, J. Q.; et al. (2010). Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron, 68(5), 857-864.
-
(2010)
Neuron
, vol.68
, Issue.5
, pp. 857-864
-
-
Johnson, J.O.1
Mandrioli, J.2
Benatar, M.3
Abramzon, Y.4
Van Deerlin, V.M.5
Trojanowski, J.Q.6
-
25
-
-
77949653046
-
Ethical implications of the use of whole genome methods in medical research
-
1:CAS:528:DC%2BC3cXjsFCrsrc%3D 2879322 19888293 10.1038/ejhg.2009.191
-
Kaye, J.; Boddington, P.; de Vries, J.; Hawkins, N.; Melham, K. (2010). Ethical implications of the use of whole genome methods in medical research. European Journal of Human Genetics, 18(4), 398-403.
-
(2010)
European Journal of Human Genetics
, vol.18
, Issue.4
, pp. 398-403
-
-
Kaye, J.1
Boddington, P.2
De Vries, J.3
Hawkins, N.4
Melham, K.5
-
26
-
-
84861618864
-
Exome sequencing and the genetic basis of complex traits
-
1:CAS:528:DC%2BC38XnsFKgsL0%3D 3727622 22641211 10.1038/ng.2303
-
Kiezun, A.; Garimella, K.; Do, R.; Stitziel, N. O.; Neale, B. M.; McLaren, P. J.; et al. (2012). Exome sequencing and the genetic basis of complex traits. Nature Genetics, 44(6), 623-630.
-
(2012)
Nature Genetics
, vol.44
, Issue.6
, pp. 623-630
-
-
Kiezun, A.1
Garimella, K.2
Do, R.3
Stitziel, N.O.4
Neale, B.M.5
McLaren, P.J.6
-
27
-
-
33750388916
-
The emergence of an ethical duty to disclose genetic research results: International perspectives
-
16868560 10.1038/sj.ejhg.5201690
-
Knoppers, B. M.; Joly, Y.; Simard, J.; Durocher, F. (2006). The emergence of an ethical duty to disclose genetic research results: international perspectives. European Journal of Human Genetics, 14(11), 1170-1178.
-
(2006)
European Journal of Human Genetics
, vol.14
, Issue.11
, pp. 1170-1178
-
-
Knoppers, B.M.1
Joly, Y.2
Simard, J.3
Durocher, F.4
-
28
-
-
84878787520
-
Management of incidental findings in clinical genomic sequencing
-
Krier, J. B.; Green, R. C. (2013). Management of incidental findings in clinical genomic sequencing. Current Protocols in Human Genetics, 77, 9.23.1-9.23.13.
-
(2013)
Current Protocols in Human Genetics
, vol.77
, pp. 9231-92313
-
-
Krier, J.B.1
Green, R.C.2
-
29
-
-
84862833585
-
Exome sequencing and unrelated findings in the context of complex disease research: Ethical and clinical implications
-
3544941 21794208
-
Lyon, G.; Jiang, T.; Van Wijk, R.; Wang, W.; Bodily, P.; Xing, J.; et al. (2011). Exome sequencing and unrelated findings in the context of complex disease research: ethical and clinical implications. Discovery Medicine, 12(62), 41-55.
-
(2011)
Discovery Medicine
, vol.12
, Issue.62
, pp. 41-55
-
-
Lyon, G.1
Jiang, T.2
Van Wijk, R.3
Wang, W.4
Bodily, P.5
Xing, J.6
-
30
-
-
16644374629
-
The interface between the practice of medical genetics and human genetic research: What every genetic counselor needs to know
-
15604636 10.1023/B:JOGC.0000044198.19298.e2
-
Markel, D. S.; Yashar, B. M. (2004). The interface between the practice of medical genetics and human genetic research: what every genetic counselor needs to know. Journal of Genetic Counseling, 13(5), 351-368.
-
(2004)
Journal of Genetic Counseling
, vol.13
, Issue.5
, pp. 351-368
-
-
Markel, D.S.1
Yashar, B.M.2
-
31
-
-
84883341950
-
Next generation sequencing in psychiatric research: What study participants need to know about research findings
-
23725748 10.1017/S1461145713000527
-
Mathieu, G.; Groisman, I. J.; Godard, B. (2013). Next generation sequencing in psychiatric research: what study participants need to know about research findings. The International Journal of Neuropsychopharmacology, 16(9), 2119-2127.
-
(2013)
The International Journal of Neuropsychopharmacology
, vol.16
, Issue.9
, pp. 2119-2127
-
-
Mathieu, G.1
Groisman, I.J.2
Godard, B.3
-
32
-
-
38549085235
-
Research ethics and the challenge of whole-genome sequencing
-
1:CAS:528:DC%2BD1cXnt1ensg%3D%3D 2225443 18087293 10.1038/nrg2302
-
McGuire, A. L.; Caulfield, T.; Cho, M. K. (2008). Research ethics and the challenge of whole-genome sequencing. Nature Reviews Genetics, 9, 152-156.
-
(2008)
Nature Reviews Genetics
, vol.9
, pp. 152-156
-
-
McGuire, A.L.1
Caulfield, T.2
Cho, M.K.3
-
33
-
-
32444436499
-
Genetic counseling and ethical issues for autism
-
10.1002/ajmg.c.30082
-
McMahon, W. M.; Baty, B. J.; Botkin, J. (2006). Genetic counseling and ethical issues for autism. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 142C(1), 52-57.
-
(2006)
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
, vol.142
, Issue.1
, pp. 52-57
-
-
McMahon, W.M.1
Baty, B.J.2
Botkin, J.3
-
34
-
-
33750624177
-
Undesirable implications of disclosing individual genetic results to research participants
-
17085401 10.1080/15265160600935811
-
Meltzer, L. A. (2006). Undesirable implications of disclosing individual genetic results to research participants. The American Journal of Bioethics, 6(6), 28-30.
-
(2006)
The American Journal of Bioethics
, vol.6
, Issue.6
, pp. 28-30
-
-
Meltzer, L.A.1
-
35
-
-
72849144434
-
Sequencing technologies - The next generation
-
1:CAS:528:DC%2BD1MXhsFOht7fO 19997069 10.1038/nrg2626
-
Metzker, M. L. (2010). Sequencing technologies - the next generation. Nature Reviews Genetics, 11(1), 31-46.
-
(2010)
Nature Reviews Genetics
, vol.11
, Issue.1
, pp. 31-46
-
-
Metzker, M.L.1
-
36
-
-
33749870193
-
The code of ethics of the National Society of Genetic Counselors
-
National Society of Genetic Counselors 10.1007/s10897-006-9036-5
-
National Society of Genetic Counselors. (2006). The code of ethics of the National Society of Genetic Counselors. Journal of Genetic Counseling, 15(5), 309-311.
-
(2006)
Journal of Genetic Counseling
, vol.15
, Issue.5
, pp. 309-311
-
-
-
37
-
-
73349110071
-
Exome sequencing identifies the cause of a mendelian disorder
-
1:CAS:528:DC%2BD1MXhsVWlsbzE 2847889 19915526 10.1038/ng.499
-
Ng, S. B.; Buckingham, K. J.; Lee, C.; Bigham, A. W.; Tabor, H. K.; Dent, K. M.; et al. (2010). Exome sequencing identifies the cause of a mendelian disorder. Nature Genetics, 42(1), 30-35.
-
(2010)
Nature Genetics
, vol.42
, Issue.1
, pp. 30-35
-
-
Ng, S.B.1
Buckingham, K.J.2
Lee, C.3
Bigham, A.W.4
Tabor, H.K.5
Dent, K.M.6
-
38
-
-
84884769487
-
In search of low-frequency and rare variants affecting complex traits
-
1:CAS:528:DC%2BC3sXhsFegs7rM 3782074 23922232 10.1093/hmg/ddt376
-
Panoutsopoulou, K.; Tachmazidou, I.; Zeggini, E. (2013). In search of low-frequency and rare variants affecting complex traits. Human Molecular Genetics, 22(R1), R16-R21.
-
(2013)
Human Molecular Genetics
, vol.22
, Issue.R1
-
-
Panoutsopoulou, K.1
Tachmazidou, I.2
Zeggini, E.3
-
39
-
-
0036264294
-
Ethical issues in bipolar disorders pedigree research: Privacy concerns, informed consent, and grounds for waiver
-
12047491 10.1034/j.1399-5618.2002.01155.x
-
Parker, L. S. (2002). Ethical issues in bipolar disorders pedigree research: privacy concerns, informed consent, and grounds for waiver. Bipolar Disorders, 4(1), 1-16.
-
(2002)
Bipolar Disorders
, vol.4
, Issue.1
, pp. 1-16
-
-
Parker, L.S.1
-
40
-
-
77956396559
-
Tailoring the process of informed consent in genetic and genomic research
-
2873798 20346094 10.1186/gm141
-
Rotimi, C.; Marshall, P. (2010). Tailoring the process of informed consent in genetic and genomic research. Genome Medicine, 2(3), 20.
-
(2010)
Genome Medicine
, vol.2
, Issue.3
, pp. 20
-
-
Rotimi, C.1
Marshall, P.2
-
41
-
-
79956103957
-
A clinical perspective on ethical issues in genetic testing
-
1:STN:280:DC%2BC3MrhtlOhtw%3D%3D 21574071 10.1080/08989621.2011.575033
-
Sijmons, R. H.; Van Langen, I. M.; Sijmons, J. G. (2011). A clinical perspective on ethical issues in genetic testing. Accountability in Research, 18(3), 148-162.
-
(2011)
Accountability in Research
, vol.18
, Issue.3
, pp. 148-162
-
-
Sijmons, R.H.1
Van Langen, I.M.2
Sijmons, J.G.3
-
42
-
-
84862911210
-
Informed consent and genomic incidental findings: IRB chair perspectives
-
3616513 22228060 10.1525/jer.2011.6.4.53
-
Simon, C. M.; Williams, J. K.; Shinkunas, L.; Brandt, D.; Daack-Hirsch, S.; Driessnack, M. (2011). Informed consent and genomic incidental findings: IRB chair perspectives. Journal of Empirical Research on Human Research Ethics, 6(4), 53-67.
-
(2011)
Journal of Empirical Research on Human Research Ethics
, vol.6
, Issue.4
, pp. 53-67
-
-
Simon, C.M.1
Williams, J.K.2
Shinkunas, L.3
Brandt, D.4
Daack-Hirsch, S.5
Driessnack, M.6
-
43
-
-
81955167410
-
Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research
-
22038764 10.1002/ajmg.a.34357
-
Tabor, H. K.; Berkman, B. E.; Hull, S. C.; Bamshad, M. J. (2011). Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research. American Journal of Medical Genetics Part A, 155A(12), 2916-2924.
-
(2011)
American Journal of Medical Genetics Part A
, vol.155
, Issue.12
, pp. 2916-2924
-
-
Tabor, H.K.1
Berkman, B.E.2
Hull, S.C.3
Bamshad, M.J.4
-
44
-
-
84861225247
-
Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms
-
3426313 22532433 10.1002/ajmg.a.35328
-
Tabor, H. K.; Stock, J.; Brazg, T.; McMillin, M. J.; Dent, K. M.; Yu, J. H.; et al. (2012). Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms. American Journal of Medical Genetics Part A, 158A(6), 1310-1319.
-
(2012)
American Journal of Medical Genetics Part A
, vol.158
, Issue.6
, pp. 1310-1319
-
-
Tabor, H.K.1
Stock, J.2
Brazg, T.3
McMillin, M.J.4
Dent, K.M.5
Yu, J.H.6
-
45
-
-
84883800683
-
Content analysis and thematic analysis: Implications for conducting a qualitative descriptive study
-
10.1111/nhs.12048
-
Vaismoradi, M.; Turunen, H.; Bondas, T. (2013). Content analysis and thematic analysis: Implications for conducting a qualitative descriptive study. Nursing & Health Sciences, 15(3), 398-405.
-
(2013)
Nursing & Health Sciences
, vol.15
, Issue.3
, pp. 398-405
-
-
Vaismoradi, M.1
Turunen, H.2
Bondas, T.3
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