-
1
-
-
84873567975
-
-
Informed consent. Accessed November 8, 2013
-
American Medical Association. Informed consent. http://www.ama-assn.org/ama/pub/physician-resources/medical-ethics/code-medical-ethics/opinion808.page. Accessed November 8, 2013.
-
American Medical Association
-
-
-
2
-
-
53949123575
-
Living with long QT syndrome: a qualitative study of coping with increased risk of sudden cardiac death
-
PID: 18719982
-
Andersen, J., Oyen, N., Bjorvatn, C., & Gjengdal, E. (2008). Living with long QT syndrome: a qualitative study of coping with increased risk of sudden cardiac death. Journal of Genetic Counseling, 17, 489–498.
-
(2008)
Journal of Genetic Counseling
, vol.17
, pp. 489-498
-
-
Andersen, J.1
Oyen, N.2
Bjorvatn, C.3
Gjengdal, E.4
-
3
-
-
0033748806
-
Factors associated with decisions about clinical BRCA1/2 testing
-
COI: 1:STN:280:DC%2BD3M7jsFCrtw%3D%3D
-
Armstrong, K., Calzone, K., Stopfer, J., Fitzgerald, G., Coyne, J., & Weber, B. (2000). Factors associated with decisions about clinical BRCA1/2 testing. Cancer Epidemiology, Biomarkers & Prevention, 9(11), 1251–1254.
-
(2000)
Cancer Epidemiology, Biomarkers & Prevention
, vol.9
, Issue.11
, pp. 1251-1254
-
-
Armstrong, K.1
Calzone, K.2
Stopfer, J.3
Fitzgerald, G.4
Coyne, J.5
Weber, B.6
-
5
-
-
2342518843
-
Comparison of motivations and concerns for genetic testing in hereditary colorectal and breast cancer syndromes
-
COI: 1:STN:280:DC%2BD2c7ms1aktg%3D%3D, PID: 15060120
-
Balmana, J., Stoffel, E. M., Emmons, K. M., Garber, J. E., & Syngal, S. (2004). Comparison of motivations and concerns for genetic testing in hereditary colorectal and breast cancer syndromes. Journal of Medical Genetics, 41(4), e44.
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.4
, pp. e44
-
-
Balmana, J.1
Stoffel, E.M.2
Emmons, K.M.3
Garber, J.E.4
Syngal, S.5
-
6
-
-
77955600300
-
Deaf adults’ reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study
-
PID: 20488870
-
Boudreault, P., Baldwin, E. E., Fox, M., Dutton, L., Tullis, L., Linden, J., et al. (2010). Deaf adults’ reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study. Journal of Deaf Studies and Deaf Education, 15(3), 209–227.
-
(2010)
Journal of Deaf Studies and Deaf Education
, vol.15
, Issue.3
, pp. 209-227
-
-
Boudreault, P.1
Baldwin, E.E.2
Fox, M.3
Dutton, L.4
Tullis, L.5
Linden, J.6
-
7
-
-
18644374087
-
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience
-
COI: 1:STN:280:DC%2BD38nhsVCrsw%3D%3D, PID: 12362031
-
Charron, P., Heron, D., Gargiulo, M., Richard, P., Dubourg, O., Desnos, M., et al. (2002). Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience. Journal of Medical Genetics, 39, 741–746.
-
(2002)
Journal of Medical Genetics
, vol.39
, pp. 741-746
-
-
Charron, P.1
Heron, D.2
Gargiulo, M.3
Richard, P.4
Dubourg, O.5
Desnos, M.6
-
8
-
-
7644224776
-
Predictive testing for hereditary non-polyposis colorectal cancer: motivation, illness representations and short-term psychological impact
-
PID: 15530764
-
Claes, E., Denayer, L., Evers-Kiebooms, G., Boogaerts, A., & Legius, E. (2004). Predictive testing for hereditary non-polyposis colorectal cancer: motivation, illness representations and short-term psychological impact. Patient Education and Counseling, 55(2), 265–274.
-
(2004)
Patient Education and Counseling
, vol.55
, Issue.2
, pp. 265-274
-
-
Claes, E.1
Denayer, L.2
Evers-Kiebooms, G.3
Boogaerts, A.4
Legius, E.5
-
9
-
-
0033922967
-
Patient motivation, satisfaction, and coping in genetic counseling and testing for BRCA1 and BRCA2
-
Clark, S., Bluman, L. G., Borstelmann, N., Regan, K., Winer, E. P., Rimer, B. K., et al. (2000). Patient motivation, satisfaction, and coping in genetic counseling and testing for BRCA1 and BRCA2. Journal of Genetic Counseling, 9(3), 219–235.
-
(2000)
Journal of Genetic Counseling
, vol.9
, Issue.3
, pp. 219-235
-
-
Clark, S.1
Bluman, L.G.2
Borstelmann, N.3
Regan, K.4
Winer, E.P.5
Rimer, B.K.6
-
10
-
-
84860469422
-
Challenges of genetic testing in adolescents with cardiac arrhythmia syndromes
-
PID: 21955955
-
Cohen, L. L., Stolerman, M., Walsh, C., Wasserman, D., & Dolan, S. M. (2012). Challenges of genetic testing in adolescents with cardiac arrhythmia syndromes. Journal of Medical Ethics, 38(3), 163–167.
-
(2012)
Journal of Medical Ethics
, vol.38
, Issue.3
, pp. 163-167
-
-
Cohen, L.L.1
Stolerman, M.2
Walsh, C.3
Wasserman, D.4
Dolan, S.M.5
-
11
-
-
33645764457
-
Sense-making, grief, and the experience of violent loss: toward a mediational model
-
PID: 16610156
-
Currier, J. M., Holland, J. M., & Neimeyer, R. A. (2006). Sense-making, grief, and the experience of violent loss: toward a mediational model. Death Studies, 30(5), 403–428.
-
(2006)
Death Studies
, vol.30
, Issue.5
, pp. 403-428
-
-
Currier, J.M.1
Holland, J.M.2
Neimeyer, R.A.3
-
12
-
-
0033818392
-
Searching for meaning in loss: are clinical assumptions correct
-
COI: 1:STN:280:DC%2BD3MvmtFOmtA%3D%3D, PID: 11503666
-
Davis, C. G., Wortman, C. B., Lehman, D. R., & Silver, R. C. (2000). Searching for meaning in loss: are clinical assumptions correct. Death Studies, 24(6), 497–540.
-
(2000)
Death Studies
, vol.24
, Issue.6
, pp. 497-540
-
-
Davis, C.G.1
Wortman, C.B.2
Lehman, D.R.3
Silver, R.C.4
-
13
-
-
79952631004
-
Experience over fifteen years with a protocol for predictive testing for huntington disease
-
COI: 1:CAS:528:DC%2BC3MXjtFGqsLY%3D, PID: 21220204
-
Dufrasne, S., Roy, M., Galvez, M., & Rosenblatt, D. S. (2011). Experience over fifteen years with a protocol for predictive testing for huntington disease. Molecular Genetics and Metabolism, 102(4), 494–504.
-
(2011)
Molecular Genetics and Metabolism
, vol.102
, Issue.4
, pp. 494-504
-
-
Dufrasne, S.1
Roy, M.2
Galvez, M.3
Rosenblatt, D.S.4
-
14
-
-
84871405506
-
An interdisciplinary approach to personalized medicine: case studies from a cardiogenetics clinic
-
COI: 1:CAS:528:DC%2BC38XhvVGmtrfL
-
Erskine, K., Griffith, E., DeGroat, N., Stolerman, M., Silverstein, L. B., Hidayatallah, N., et al. (2013). An interdisciplinary approach to personalized medicine: case studies from a cardiogenetics clinic. Future Medicine, 10(1), 73–80.
-
(2013)
Future Medicine
, vol.10
, Issue.1
, pp. 73-80
-
-
Erskine, K.1
Griffith, E.2
DeGroat, N.3
Stolerman, M.4
Silverstein, L.B.5
Hidayatallah, N.6
-
15
-
-
35348853843
-
Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: Motivational factors and psychosocial functioning
-
COI: 1:STN:280:DC%2BD2snmtleitQ%3D%3D, PID: 17892499
-
Esplen, M. J., Madlensky, L., Aronson, M., Rothenmund, H., Gallinger, S., Butler, K., et al. (2007). Colorectal cancer survivors undergoing genetic testing for hereditary non-polyposis colorectal cancer: Motivational factors and psychosocial functioning. Clinical Genetics, 72(5), 394–401.
-
(2007)
Clinical Genetics
, vol.72
, Issue.5
, pp. 394-401
-
-
Esplen, M.J.1
Madlensky, L.2
Aronson, M.3
Rothenmund, H.4
Gallinger, S.5
Butler, K.6
-
16
-
-
44649173167
-
Long QT syndrome
-
PID: 18549912
-
Goldenberg, I., & Moss, A. J. (2008). Long QT syndrome. Journal of the American College of Cardiology, 51(24), 2291–2300.
-
(2008)
Journal of the American College of Cardiology
, vol.51
, Issue.24
, pp. 2291-2300
-
-
Goldenberg, I.1
Moss, A.J.2
-
17
-
-
0037429615
-
Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer
-
Hadley, D. W., Jenkins, J., Dimond, E., Nakahara, K., Grogan, L., Liewehr, D. J., et al. (2003). Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer. Archives of Internal Medicine, 163.
-
(2003)
Archives of Internal Medicine
, pp. 163
-
-
Hadley, D.W.1
Jenkins, J.2
Dimond, E.3
Nakahara, K.4
Grogan, L.5
Liewehr, D.J.6
-
18
-
-
53849095165
-
Predictors of grief following the death of one’s child: the contribution of finding meaning
-
PID: 18698614
-
Keesee, N. J., Currier, J. M., & Neimeyer, R. A. (2008). Predictors of grief following the death of one’s child: the contribution of finding meaning. Journal of Clinical Psychology, 64(10), 1145–1163.
-
(2008)
Journal of Clinical Psychology
, vol.64
, Issue.10
, pp. 1145-1163
-
-
Keesee, N.J.1
Currier, J.M.2
Neimeyer, R.A.3
-
19
-
-
77954572243
-
Genetic testing in li-fraumeni syndrome: uptake and psychosocial consequences
-
PID: 20479422
-
Lammens, C. R., Aaronson, N. K., Wagner, A., Sijmons, R. H., Ausems, M. G., Vriends, A. H., et al. (2010). Genetic testing in li-fraumeni syndrome: uptake and psychosocial consequences. Journal of Clinical Oncology, 28(18), 3008–3014.
-
(2010)
Journal of Clinical Oncology
, vol.28
, Issue.18
, pp. 3008-3014
-
-
Lammens, C.R.1
Aaronson, N.K.2
Wagner, A.3
Sijmons, R.H.4
Ausems, M.G.5
Vriends, A.H.6
-
20
-
-
85019203967
-
-
Accessed November 8, 2013
-
Long QT syndrome | GeneDx. http://www.genedx.com/test-catalog/disorders/long-qt-syndrome-lqts/. Accessed November 8, 2013.
-
Long QT syndrome | GeneDx
-
-
-
22
-
-
77953421580
-
-
NCCN clinical practice guidelines in oncology (NCCN guidelines TM): Genetic/Familial high risk assessment: Breast and ovarian. Accessed April 25, 2012
-
National Comprehensive Cancer Network. NCCN clinical practice guidelines in oncology (NCCN guidelines TM): Genetic/Familial high risk assessment: Breast and ovarian. http://www.nccn.org/professionals/physician_gls/pdf/genetics_screening.pdf. Accessed April 25, 2012.
-
National Comprehensive Cancer Network
-
-
-
24
-
-
38049146378
-
Clinical practice. long-QT syndrome
-
COI: 1:CAS:528:DC%2BD1cXltFantg%3D%3D, PID: 18184962
-
Roden, D. M. (2008). Clinical practice. long-QT syndrome. New England Journal of Medicine, 358(2), 169–176.
-
(2008)
New England Journal of Medicine
, vol.358
, Issue.2
, pp. 169-176
-
-
Roden, D.M.1
-
26
-
-
0034721235
-
A molecular link between the sudden infant death syndrome and the long-QT syndrome
-
COI: 1:CAS:528:DC%2BD3cXlvVSmtLk%3D, PID: 10911008
-
Schwartz, P. J., Priori, S. G., Dumaine, R., Napolitano, C., Antzelevitch, C., Stramba-Badiale, M., et al. (2000). A molecular link between the sudden infant death syndrome and the long-QT syndrome. New England Journal of Medicine, 343(4), 262–267.
-
(2000)
New England Journal of Medicine
, vol.343
, Issue.4
, pp. 262-267
-
-
Schwartz, P.J.1
Priori, S.G.2
Dumaine, R.3
Napolitano, C.4
Antzelevitch, C.5
Stramba-Badiale, M.6
-
27
-
-
0035830365
-
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life- threatening arrhythmias
-
COI: 1:STN:280:DC%2BD3M%2FovVSitg%3D%3D, PID: 11136691
-
Schwartz, P. J., Priori, S. G., Spazzolini, C., Moss, A. J., Vincent, G. M., Napolitano, C., et al. (2001). Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life- threatening arrhythmias. Circulation, 103(1), 89–95.
-
(2001)
Circulation
, vol.103
, Issue.1
, pp. 89-95
-
-
Schwartz, P.J.1
Priori, S.G.2
Spazzolini, C.3
Moss, A.J.4
Vincent, G.M.5
Napolitano, C.6
-
28
-
-
78650169725
-
Inpediments to DNA testing and cascade screening for hypertrophic cardiomyopathy and long QT syndrome: a qualitative study of patient experiences
-
PID: 20680418
-
Smart, A. (2010). Inpediments to DNA testing and cascade screening for hypertrophic cardiomyopathy and long QT syndrome: a qualitative study of patient experiences. Journal of Genetic Counseling, 19, 630–639.
-
(2010)
Journal of Genetic Counseling
, vol.19
, pp. 630-639
-
-
Smart, A.1
-
30
-
-
33846425740
-
Cardiac sodium channel dysfunction in sudden infant death syndrome
-
COI: 1:CAS:528:DC%2BD2sXlt1yrtg%3D%3D, PID: 17210841
-
Wang, D. W., Desai, R. R., Crotti, L., Arnestad, M., Insolia, R., Pedrazzini, M., et al. (2007). Cardiac sodium channel dysfunction in sudden infant death syndrome. Circulation, 115(3), 368–376.
-
(2007)
Circulation
, vol.115
, Issue.3
, pp. 368-376
-
-
Wang, D.W.1
Desai, R.R.2
Crotti, L.3
Arnestad, M.4
Insolia, R.5
Pedrazzini, M.6
-
31
-
-
0035185345
-
Parental bereavement: the crisis of meaning
-
COI: 1:STN:280:DC%2BD3MvmtFymsA%3D%3D, PID: 11503762
-
Wheeler, I. (2001). Parental bereavement: the crisis of meaning. Death Studies, 25(1), 51–66.
-
(2001)
Death Studies
, vol.25
, Issue.1
, pp. 51-66
-
-
Wheeler, I.1
-
32
-
-
25144503454
-
Genetics of cardiac arrhythmias
-
COI: 1:CAS:528:DC%2BD2MXhtFGiu7rL, PID: 16162633
-
Wilde, A. A., & Bezzina, C. R. (2005). Genetics of cardiac arrhythmias. Heart, 91(10), 1352–1358.
-
(2005)
Heart
, vol.91
, Issue.10
, pp. 1352-1358
-
-
Wilde, A.A.1
Bezzina, C.R.2
-
33
-
-
44949119539
-
Consumer motivations for pursuing genetic testing and their preferences for the provision of genetic services for hearing loss
-
PID: 18247107
-
Withrow, K. A., Burton, S., Arnos, K. S., Kalfoglou, A., & Pandya, A. (2008). Consumer motivations for pursuing genetic testing and their preferences for the provision of genetic services for hearing loss. Journal of Genetic Counseling, 17(3), 252–260.
-
(2008)
Journal of Genetic Counseling
, vol.17
, Issue.3
, pp. 252-260
-
-
Withrow, K.A.1
Burton, S.2
Arnos, K.S.3
Kalfoglou, A.4
Pandya, A.5
|