-
1
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
Hall JM, Lee MK, Newman B et al. Linkage of early-onset familial breast cancer to chromosome 17q21. Science 1990: 250 (4988): 1684-1689.
-
(1990)
Science
, vol.250
, Issue.4988
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
-
2
-
-
0027433563
-
Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families. The Breast Cancer Linkage Consortium
-
Easton DF, Bishop DT, Ford D, Crockford GP. Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families. The Breast Cancer Linkage Consortium. Am J Hum Genet 1993: 52 (4): 678-701.
-
(1993)
Am J Hum Genet
, vol.52
, Issue.4
, pp. 678-701
-
-
Easton, D.F.1
Bishop, D.T.2
Ford, D.3
Crockford, G.P.4
-
3
-
-
0028843102
-
Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium
-
Easton DF, Ford D, Bishop DT. Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium. Am J Hum Genet 1995: 56 (1): 265-271.
-
(1995)
Am J Hum Genet
, vol.56
, Issue.1
, pp. 265-271
-
-
Easton, D.F.1
Ford, D.2
Bishop, D.T.3
-
4
-
-
0028885339
-
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium
-
Narod SA, Ford D, Devilee P et al. An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Breast Cancer Linkage Consortium. Am J Hum Genet 1995: 56 (1): 254-264.
-
(1995)
Am J Hum Genet
, vol.56
, Issue.1
, pp. 254-264
-
-
Narod, S.A.1
Ford, D.2
Devilee, P.3
-
5
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
-
Ford D, Easton D, Stratton M et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am J Hum Genet 1998: 2: 676-689.
-
(1998)
Am J Hum Genet
, vol.2
, pp. 676-689
-
-
Ford, D.1
Easton, D.2
Stratton, M.3
-
6
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck Eidens D et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994: 266: 66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck Eidens, D.3
-
7
-
-
0029121898
-
Genetic testing in breast/ovarian cancer (BRCA1) families
-
Watson M, Murday V, Lloyd S et al. Genetic testing in breast/ovarian cancer (BRCA1) families. Lancet 1995: 346: 583.
-
(1995)
Lancet
, vol.346
, pp. 583
-
-
Watson, M.1
Murday, V.2
Lloyd, S.3
-
8
-
-
15844404355
-
BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes
-
Lerman C, Narod S, Schulman K et al. BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes. JAMA 1996: 275: 1885-1892.
-
(1996)
JAMA
, vol.275
, pp. 1885-1892
-
-
Lerman, C.1
Narod, S.2
Schulman, K.3
-
9
-
-
0030638330
-
Psychological responses to BRCA1 mutation testing: Preliminary findings
-
Croyle RT, Smith KR, Botkin JR, Baty B, Nash J. Psychological responses to BRCA1 mutation testing: Preliminary findings. Health Psychol 1997: 16: 63-72.
-
(1997)
Health Psychol 63-72.
, vol.16
, pp. 63-72
-
-
Croyle, R.T.1
Smith, K.R.2
Botkin, J.R.3
Baty, B.4
Nash, J.5
-
10
-
-
0034528209
-
Uptake of hereditary breast ovarian cancer genetic testing in a French national sample of BRCA1 families
-
Julian-Reynier C, Sobol H, Sévilla C et al. Uptake of hereditary breast ovarian cancer genetic testing in a French national sample of BRCA1 families. Psychooncology 2000: 9: 504-510.
-
(2000)
Psychooncology
, vol.9
, pp. 504-510
-
-
Julian-Reynier, C.1
Sobol, H.2
Sévilla, C.3
-
11
-
-
0042322237
-
Genetic testing for a BRCA1 mutation: Prophylactic surgery and screening behavior in women 2 years post testing
-
Botkin JR, Smith KR, Croyle RT et al. Genetic testing for a BRCA1 mutation: Prophylactic surgery and screening behavior in women 2 years post testing. Am J Med Genet 2003: 118A (3): 201-209.
-
(2003)
Am J Med Genet
, vol.118 A
, Issue.3
, pp. 201-209
-
-
Botkin, J.R.1
Smith, K.R.2
Croyle, R.T.3
-
12
-
-
0034532383
-
Proband family uptake of familial genetic counselling
-
Hagoel L, Dishon S, Almog R, Silman Z, Bisland-Becktell S, Rennert G. Proband family uptake of familial genetic counselling. Psychooncology 2000: 9: 522-527.
-
(2000)
Psychooncology
, vol.9
, pp. 522-527
-
-
Hagoel, L.1
Dishon, S.2
Almog, R.3
Silman, Z.4
Bisland-Becktell, S.5
Rennert, G.6
-
13
-
-
0034648501
-
Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian families
-
Bowles Biesecker B, Ishibe N, Hadley DW et al. Psychosocial factors predicting BRCA1/BRCA2 testing decisions in members of hereditary breast and ovarian families. Am J Med Genet 2000: 93: 257-263.
-
(2000)
Am J Med Genet
, vol.93
, pp. 257-263
-
-
Bowles Biesecker, B.1
Ishibe, N.2
Hadley, D.W.3
-
14
-
-
0032954046
-
Familial context of genetic testing for cancer susceptibility: Moderating effect of siblings' test results on psychological distress one to two weeks after BRCA1 mutation testing
-
Smith KR, West JA, Croyle RT, Botkin JR. Familial context of genetic testing for cancer susceptibility: Moderating effect of siblings' test results on psychological distress one to two weeks after BRCA1 mutation testing. Cancer Epidemiol Biomarkers Prev 1999: 8: 385-392.
-
(1999)
Cancer Epidemiol Biomarkers Prev
, vol.8
, pp. 385-392
-
-
Smith, K.R.1
West, J.A.2
Croyle, R.T.3
Botkin, J.R.4
-
15
-
-
0032752989
-
Uptake of genetic testing and pre-test levels of mental distress in Norwegian families with known BRCA1 mutations
-
Reichelt JG, Dahl AA, Heimdal K, Moller P. Uptake of genetic testing and pre-test levels of mental distress in Norwegian families with known BRCA1 mutations. Dis Markers 1999: 15: 139-143.
-
(1999)
Dis Markers
, vol.15
, pp. 139-143
-
-
Reichelt, J.G.1
Dahl, A.A.2
Heimdal, K.3
Moller, P.4
-
16
-
-
0034631316
-
Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation
-
Meijers-Heijboer EJ, Verhoog LC, Brekelmans CTM et al. Presymptomatic DNA testing and prophylactic surgery in families with a BRCA1 or BRCA2 mutation. Lancet 2000: 355: 2015-2020.
-
(2000)
Lancet
, vol.355
, pp. 2015-2020
-
-
Meijers-Heijboer, E.J.1
Verhoog, L.C.2
Brekelmans, C.T.M.3
-
17
-
-
0042405009
-
Early adoption of BRCA1/2 testing: Who and why
-
Armstrong K, Weiner J, Weber B, Asch DA. Early adoption of BRCA1/2 testing: Who and why. Genet Med 2003: 5 (2): 92-98.
-
(2003)
Genet Med
, vol.5
, Issue.2
, pp. 92-98
-
-
Armstrong, K.1
Weiner, J.2
Weber, B.3
Asch, D.A.4
-
18
-
-
18544376723
-
Predictive testing for BRCA1/2: Attributes, risk perception and management in a multi-centre clinical cohort
-
Foster C, Evans DGR, Eeles R et al. Predictive testing for BRCA1/2: attributes, risk perception and management in a multi-centre clinical cohort. Br J Cancer 2002: 86: 1209-1216.
-
(2002)
Br J Cancer
, vol.86
, pp. 1209-1216
-
-
Foster, C.1
Evans, D.G.R.2
Eeles, R.3
-
19
-
-
10844222436
-
Psychosocial impact of breast/ovarian (BRCA1/2) cancer-predictive genetic testing in a UK multi-centre clinical cohort
-
Watson M, Foster C, Eeles R et al. Psychosocial impact of breast/ovarian (BRCA1/2) cancer-predictive genetic testing in a UK multi-centre clinical cohort. Br J Cancer 2004: 91 (10): 1787-1794.
-
(2004)
Br J Cancer
, vol.91
, Issue.10
, pp. 1787-1794
-
-
Watson, M.1
Foster, C.2
Eeles, R.3
-
20
-
-
33847765415
-
Predictive genetic testing for BRCA1/2 in a UK clinical cohort: Three-year follow-up
-
Foster C, Watson M, Eeles R et al. Predictive genetic testing for BRCA1/ 2 in a UK clinical cohort: Three-year follow-up. Br J Cancer 2007: 96 (5): 718-724.
-
(2007)
Br J Cancer
, vol.96
, Issue.5
, pp. 718-724
-
-
Foster, C.1
Watson, M.2
Eeles, R.3
-
21
-
-
0142119267
-
Long-term psychological impact of carrying a BRCA1/2 mutation and prophylactic surgery: A 5-year follow-up study
-
van Oostrom I, Meijers-Heijboer H, Ladder LN et al. Long-term psychological impact of carrying a BRCA1/2 mutation and prophylactic surgery: A 5-year follow-up study. J Clin Oncol 2003: 21: 3867-3874.
-
(2003)
J Clin Oncol
, vol.21
, pp. 3867-3874
-
-
van Oostrom, I.1
Meijers-Heijboer, H.2
Ladder, L.N.3
-
22
-
-
0028330276
-
Risks of cancer in BRCA1 mutation carriers
-
Ford D, Easton D, Bishop DT, Narod S, Goldgar D, BCLC Consortium. Risks of cancer in BRCA1 mutation carriers. Lancet 1994: 343: 692-695.
-
(1994)
Lancet
, vol.343
, pp. 692-695
-
-
Ford, D.1
Easton, D.2
Bishop, D.T.3
Narod, S.4
Goldgar, D.5
-
23
-
-
0037130887
-
Cancer incidence in BRCA1 mutation carriers
-
Thompson D, Easton DF; Breast Cancer Linkage Consortium. Cancer incidence in BRCA1 mutation carriers. J Natl Cancer Inst 2002: 94 (18): 1358-1365.
-
(2002)
J Natl Cancer Inst
, vol.94
, Issue.18
, pp. 1358-1365
-
-
Thompson, D.1
Easton, D.F.2
-
24
-
-
4444316405
-
BRCA1/2 predictive testing: A study of uptake in two centres
-
Brooks L, Lennard F, Shenton A et al. BRCA1/2 predictive testing: A study of uptake in two centres. Eur J Hum Genet 2004: 12 (8): 654-662.
-
(2004)
Eur J Hum Genet
, vol.12
, Issue.8
, pp. 654-662
-
-
Brooks, L.1
Lennard, F.2
Shenton, A.3
-
25
-
-
0031847821
-
Men in breast cancer families: A preliminary study on awareness and perception
-
McAllister M, Evans DGR, Ormiston W et al. Men in breast cancer families: A preliminary study on awareness and perception. J Med Genet 1998: 35: 739-744.
-
(1998)
J Med Genet
, vol.35
, pp. 739-744
-
-
McAllister, M.1
Evans, D.G.R.2
Ormiston, W.3
-
26
-
-
33644848688
-
Sharing BRCA1/2 test results with first-degree relatives: Factors predicting who women tell
-
Patenaude AF, Dorval M, DiGianni LS, Schneider KA, Chittenden A, Garber JE. Sharing BRCA1/2 test results with first-degree relatives: Factors predicting who women tell. J Clin Oncol 2006: 24 (4): 700-706.
-
(2006)
J Clin Oncol
, vol.24
, Issue.4
, pp. 700-706
-
-
Patenaude, A.F.1
Dorval, M.2
DiGianni, L.S.3
Schneider, K.A.4
Chittenden, A.5
Garber, J.E.6
-
27
-
-
0037216727
-
Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients
-
Claes E, Evers-Kiebooms G, Boogaerts A, Decruyenaere M, Denayer L, Legius E. Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients. Am J Med Genet A 2003: 116 (1): 11-19.
-
(2003)
Am J Med Genet A
, vol.116
, Issue.1
, pp. 11-19
-
-
Claes, E.1
Evers-Kiebooms, G.2
Boogaerts, A.3
Decruyenaere, M.4
Denayer, L.5
Legius, E.6
-
28
-
-
0035104727
-
Risk perception and cancer worry: An exploratory study of the impact of genetic risk counselling and bereavement in women with a family history of breast cancer
-
Hopwood P, Shenton A, Lalloo F, Evans DGR, Howell A. Risk perception and cancer worry: An exploratory study of the impact of genetic risk counselling and bereavement in women with a family history of breast cancer. J Med Genet 2001: 38: 139-142.
-
(2001)
J Med Genet
, vol.38
, pp. 139-142
-
-
Hopwood, P.1
Shenton, A.2
Lalloo, F.3
Evans, D.G.R.4
Howell, A.5
-
29
-
-
21244473319
-
Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients
-
Landsbergen K, Verhaak C, Kraaimaat F, Hoogerbrugge N. Genetic uptake in BRCA-mutation families is related to emotional and behavioral communication characteristics of index patients. Fam Cancer 2005: 4 (2): 115-119.
-
(2005)
Fam Cancer
, vol.4
, Issue.2
, pp. 115-119
-
-
Landsbergen, K.1
Verhaak, C.2
Kraaimaat, F.3
Hoogerbrugge, N.4
-
30
-
-
33747057716
-
Letting the family know: Balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder
-
Suthers GK, Armstrong J, McCormack J, Trott D. Letting the family know: balancing ethics and effectiveness when notifying relatives about genetic testing for a familial disorder. J Med Genet 2006: 43 (8): 665-670.
-
(2006)
J Med Genet
, vol.43
, Issue.8
, pp. 665-670
-
-
Suthers, G.K.1
Armstrong, J.2
McCormack, J.3
Trott, D.4
-
31
-
-
36349002802
-
Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing
-
Aktan-Collan K, Haukkala A, Pylvänäinen K et al. Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing. J Med Genet 2007: 44 (11): 732-738.
-
(2007)
J Med Genet
, vol.44
, Issue.11
, pp. 732-738
-
-
Aktan-Collan, K.1
Haukkala, A.2
Pylvänäinen, K.3
-
32
-
-
0027000793
-
The use of information (autonomy and confidentiality)
-
Harris J. The use of information (autonomy and confidentiality). Dis Markers 1992: 10: 195-198.
-
(1992)
Dis Markers
, vol.10
, pp. 195-198
-
-
Harris, J.1
-
33
-
-
0031448740
-
Breast cancer, the genetic "quick fix"and the Jewish community
-
Rothenberg KH. Breast cancer, the genetic "quick fix"and the Jewish community. Health Matrix Clevel 1997: 7: 97-124.
-
(1997)
Health Matrix Clevel
, vol.7
, pp. 97-124
-
-
Rothenberg, K.H.1
-
34
-
-
4544245238
-
The "duty to warn"a patient's family members about hereditary disease risks
-
Offit K, Groeger E, Turner S, Wadsworth EA, Weiser MA. The "duty to warn"a patient's family members about hereditary disease risks. JAMA 2004: 292 (12): 1469-1473.
-
(2004)
JAMA
, vol.292
, Issue.12
, pp. 1469-1473
-
-
Offit, K.1
Groeger, E.2
Turner, S.3
Wadsworth, E.A.4
Weiser, M.A.5
-
35
-
-
0031991614
-
ASHG statement: Professional disclosure of familial genetic information
-
ASHG statement: Professional disclosure of familial genetic information. Am J Hum Genet 1998: 62: 474-483.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 474-483
-
-
|