-
1
-
-
0032941343
-
Cancer risks in mutation carriers of DNA-mismatch-repair genes
-
10.1002/(SICI)1097-0215(19990412)81:2<214: AID-IJC8>3.0.CO;2-L 1:STN:280:DyaK1M3gt1Kjtg%3D%3D
-
Aarnio, M., Sankila, R., Pukkala, E., Salovaara, R., Aaltonen, L. A., de la Chapelle, A., et al. (1999). Cancer risks in mutation carriers of DNA-mismatch-repair genes. International Journal of Cancer, 81(2), 214-218.
-
(1999)
International Journal of Cancer
, vol.81
, Issue.2
, pp. 214-218
-
-
Aarnio, M.1
Sankila, R.2
Pukkala, E.3
Salovaara, R.4
Aaltonen, L.A.5
De La Chapelle, A.6
-
2
-
-
0038501057
-
Statement of the American Society of Clinical Oncology policy statement update: Genetic Testing for Cancer susceptibility
-
American Society of Clinical Oncology 10.1200/JCO.2003.03.189
-
American Society of Clinical Oncology. (2003). Statement of the American Society of Clinical Oncology policy statement update: Genetic Testing for Cancer susceptibility. Journal of Clinical Oncology, 21(12), 2397-2406.
-
(2003)
Journal of Clinical Oncology
, vol.21
, Issue.12
, pp. 2397-2406
-
-
-
3
-
-
0033748806
-
Factors associated with decisions about clinical BRCA1/2 testing
-
11097234 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 and Prevention, 9(11), 1251-1254.
-
(2000)
Cancer Epidemiology, Biomarkers and 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
-
4
-
-
79955050956
-
A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families
-
21306348 10.1111/j.1600-0412.2011.01091.x
-
Auranen, A., & Joutsiniemi, T. (2011). A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families. ACTA Obstetricia et Gynecologica Scandinavica, 90(5), 437-444.
-
(2011)
ACTA Obstetricia et Gynecologica Scandinavica
, vol.90
, Issue.5
, pp. 437-444
-
-
Auranen, A.1
Joutsiniemi, T.2
-
5
-
-
70449527475
-
Are prediction models for Lynch syndrome valid for probands with endometrial cancer?
-
19642020 10.1007/s10689-009-9273-5 1:CAS:528:DC%2BD1MXhtlKhtL7F
-
Backes, F. J., Hampel, H., Backes, K. A., Vaccarello, L., Lewandowski, G., Bell, J. A., et al. (2009). Are prediction models for Lynch syndrome valid for probands with endometrial cancer? Familial Cancer, 8(4), 483-487.
-
(2009)
Familial Cancer
, vol.8
, Issue.4
, pp. 483-487
-
-
Backes, F.J.1
Hampel, H.2
Backes, K.A.3
Vaccarello, L.4
Lewandowski, G.5
Bell, J.A.6
-
6
-
-
81155155620
-
Endometrial cancer patients and compliance with genetic counseling: Room for improvement
-
21968342 10.1016/j.ygyno.2011.09.002
-
Backes, F. J., Mitchell, E., Hampel, H., & Cohn, D. E. (2011). Endometrial cancer patients and compliance with genetic counseling: room for improvement. Gynecologic Oncology, 123(3), 532-536.
-
(2011)
Gynecologic Oncology
, vol.123
, Issue.3
, pp. 532-536
-
-
Backes, F.J.1
Mitchell, E.2
Hampel, H.3
Cohn, D.E.4
-
7
-
-
77954387572
-
Familial risk of cancer and knowledge and use of genetic testing
-
20361271 10.1007/s11606-010-1334-9
-
Baer, H. J., Brawarsky, P., Murray, M. F., & Haas, J. S. (2010). Familial risk of cancer and knowledge and use of genetic testing. Journal of General Internal Medicine, 25(7), 717-724.
-
(2010)
Journal of General Internal Medicine
, vol.25
, Issue.7
, pp. 717-724
-
-
Baer, H.J.1
Brawarsky, P.2
Murray, M.F.3
Haas, J.S.4
-
8
-
-
77954326667
-
BRCA in breast cancer: ESMO Clinical Practice Guidelines
-
ESMO Guidelines Working Group 20555082 10.1093/annonc/mdq161
-
Balmaña, J., Diez, O., Rubio, I., Castiglione, M., & ESMO Guidelines Working Group. (2010). BRCA in breast cancer: ESMO Clinical Practice Guidelines. Annals of Oncology, 21(Suppl 5), v20-22.
-
(2010)
Annals of Oncology
, vol.21
, Issue.SUPPL. 5
, pp. 20-22
-
-
Balmaña, J.1
Diez, O.2
Rubio, I.3
Castiglione, M.4
-
9
-
-
4644262947
-
Association of HNPCC and endometrial cancers
-
15375702 10.1007/s10147-004-0402-8 1:CAS:528:DC%2BD2cXnsFejt70%3D
-
Banno, K., Susumu, N., Yanokura, M., Hirao, T., Iwata, T., Hirasawa, A., et al. (2004). Association of HNPCC and endometrial cancers. International Journal of Clinical Oncology, 9(4), 262-269.
-
(2004)
International Journal of Clinical Oncology
, vol.9
, Issue.4
, pp. 262-269
-
-
Banno, K.1
Susumu, N.2
Yanokura, M.3
Hirao, T.4
Iwata, T.5
Hirasawa, A.6
-
10
-
-
79958071334
-
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome
-
21642682 10.1001/jama.2011.743 1:CAS:528:DC%2BC3MXntlyksLk%3D
-
Bonadona, V., Bonaïti, B., Olschwang, S., Grandjouan, S., Huiart, L., Longy, M., et al. (2011). Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. Journal of the American Medical Association, 305(22), 2304-2310.
-
(2011)
Journal of the American Medical Association
, vol.305
, Issue.22
, pp. 2304-2310
-
-
Bonadona, V.1
Bonaïti, B.2
Olschwang, S.3
Grandjouan, S.4
Huiart, L.5
Longy, M.6
-
11
-
-
38649137993
-
High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland
-
17997147 10.1016/j.ygyno.2007.09.035 1:CAS:528:DC%2BD1cXhtlOqtbg%3D
-
Brozek, I., Ochman, K., Debniak, J., Morzuch, L., Ratajska, M., Stepnowska, M., et al. (2008). High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland. Gynecologic Oncology, 108(2), 433-437.
-
(2008)
Gynecologic Oncology
, vol.108
, Issue.2
, pp. 433-437
-
-
Brozek, I.1
Ochman, K.2
Debniak, J.3
Morzuch, L.4
Ratajska, M.5
Stepnowska, M.6
-
12
-
-
38549165615
-
Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts
-
18269114
-
Devlin, L., Graham, C. A., Price, J. H., & Morrison, P. J. (2008). Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts. Ulster Medical Journal, 77(1), 25-30.
-
(2008)
Ulster Medical Journal
, vol.77
, Issue.1
, pp. 25-30
-
-
Devlin, L.1
Graham, C.A.2
Price, J.H.3
Morrison, P.J.4
-
13
-
-
65349177304
-
Knowledge about hereditary non-polyposis colorectal cancer; Mutation carriers and physicians at equal levels
-
19323816 10.1186/1471-2350-10-30
-
Domanska, K., Carlsson, C., Bendahl, P. O., & Nilbert, M. (2009). Knowledge about hereditary non-polyposis colorectal cancer; mutation carriers and physicians at equal levels. BMC Medical Genetics, 10, 30.
-
(2009)
BMC Medical Genetics
, vol.10
, pp. 30
-
-
Domanska, K.1
Carlsson, C.2
Bendahl, P.O.3
Nilbert, M.4
-
14
-
-
27744477699
-
Prevention of colorectal cancer by colonoscopic surveillance in individuals with a family history of colorectal cancer: 16 year, prospective, follow-up study
-
16243849 10.1136/bmj.38606.794560.EB
-
Dove-Edwin, I., Sasieni, P., Adams, J., & Thomas, H. J. (2005). Prevention of colorectal cancer by colonoscopic surveillance in individuals with a family history of colorectal cancer: 16 year, prospective, follow-up study. British Medical Journal, 331(7524), 1047.
-
(2005)
British Medical Journal
, vol.331
, Issue.7524
, pp. 1047
-
-
Dove-Edwin, I.1
Sasieni, P.2
Adams, J.3
Thomas, H.J.4
-
15
-
-
53149147473
-
The potential of PARP inhibitors in genetic breast and ovarian cancers
-
18837894 10.1196/annals.1414.020 1:CAS:528:DC%2BD1cXhtlemsLnF
-
Drew, Y., & Calvert, H. (2008). The potential of PARP inhibitors in genetic breast and ovarian cancers. Annals of the New York Academy of Sciences, 1138, 136-145.
-
(2008)
Annals of the New York Academy of Sciences
, vol.1138
, pp. 136-145
-
-
Drew, Y.1
Calvert, H.2
-
16
-
-
84875661358
-
-
Dutch Society for Clinical Genetics (VKGN) Oisterwijk: Van den Boogaard Print- &Mediamanagement
-
Dutch Society for Clinical Genetics (VKGN). (2008). Guideline hereditary colorectal cancer. Oisterwijk: Van den Boogaard Print- &Mediamanagement. http://www.oncoline.nl.
-
(2008)
Guideline Hereditary Colorectal Cancer
-
-
-
17
-
-
84877925479
-
-
Dutch Society for Clinical Genetics (VKGN)
-
Dutch Society for Clinical Genetics (VKGN). (2012). Guideline breast cancer 2012. http://www.oncoline.nl.
-
(2012)
Guideline Breast Cancer 2012
-
-
-
18
-
-
0037087536
-
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: Analysis of 10,000 individuals
-
11896095 10.1200/JCO.20.6.1480 1:CAS:528:DC%2BD38XivFeisbY%3D
-
Frank, T. S., Deffenbaugh, A. M., Reid, J. E., Hulick, M., Ward, B. E., Lingenfelter, B., et al. (2002). Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals. Journal of Clinical Oncology, 20(6), 1480-1490.
-
(2002)
Journal of Clinical Oncology
, vol.20
, Issue.6
, pp. 1480-1490
-
-
Frank, T.S.1
Deffenbaugh, A.M.2
Reid, J.E.3
Hulick, M.4
Ward, B.E.5
Lingenfelter, B.6
-
19
-
-
68149165810
-
Lynch syndrome (hereditary non-polyposis colorectal cancer) and endometrial carcinoma
-
19638537 10.1136/jcp.2009.064949 1:STN:280:DC%2BD1Mrhsl2nsQ%3D%3D
-
Garg, K., & Soslow, R. A. (2009). Lynch syndrome (hereditary non-polyposis colorectal cancer) and endometrial carcinoma. Journal of Clinical Pathology, 62(8), 679-684.
-
(2009)
Journal of Clinical Pathology
, vol.62
, Issue.8
, pp. 679-684
-
-
Garg, K.1
Soslow, R.A.2
-
20
-
-
0035258280
-
Factors influencing patients' decisions to decline cancer genetic counseling services
-
11767799 10.1023/A:1009451213035 1:STN:280:DC%2BD38%2FksVWgtA%3D%3D
-
Geer, K. P., Ropka, M. E., Cohn, W. F., Jones, S. M., & Miesfeldt, S. (2001). Factors influencing patients' decisions to decline cancer genetic counseling services. Journal of Genetic Counseling, 10(1), 25-40.
-
(2001)
Journal of Genetic Counseling
, vol.10
, Issue.1
, pp. 25-40
-
-
Geer, K.P.1
Ropka, M.E.2
Cohn, W.F.3
Jones, S.M.4
Miesfeldt, S.5
-
21
-
-
34147149098
-
Factors associated with an individual's decision to withdraw from genetic testing for breast and ovarian cancer susceptibility: Implications for counseling
-
17394392 10.1089/gte.2006.9998
-
Godard, B., Pratte, A., Dumont, M., Simard-Lebrun, A., & Simard, J. (2007). Factors associated with an individual's decision to withdraw from genetic testing for breast and ovarian cancer susceptibility: implications for counseling. Genetic Testing, 11(1), 45-54.
-
(2007)
Genetic Testing
, vol.11
, Issue.1
, pp. 45-54
-
-
Godard, B.1
Pratte, A.2
Dumont, M.3
Simard-Lebrun, A.4
Simard, J.5
-
22
-
-
0037609660
-
Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers
-
10.1073/pnas.1030231100 1:CAS:528:DC%2BD3sXjvFOltr4%3D
-
Goodfellow, P. J., Buttin, B. M., Herzog, T. J., Rader, J. S., Gibb, R. K., Swisher, E., et al. (2003). Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers. Proceedings of the National Academy of the Sciences, 100(10), 5908-5913.
-
(2003)
Proceedings of the National Academy of the Sciences
, vol.100
, Issue.10
, pp. 5908-5913
-
-
Goodfellow, P.J.1
Buttin, B.M.2
Herzog, T.J.3
Rader, J.S.4
Gibb, R.K.5
Swisher, E.6
-
23
-
-
33747871345
-
Screening for Lynch syndrome (Hereditary Nonpolyposis Colorectal Cancer) among endometrial cancer patients
-
16885385 10.1158/0008-5472.CAN-06-1114 1:CAS:528:DC%2BD28XnsFyqs70%3D
-
Hampel, H., Frankel, W., Panescu, J., Lockman, J., Sotamaa, K., Fix, D., et al. (2006). Screening for Lynch syndrome (Hereditary Nonpolyposis Colorectal Cancer) among endometrial cancer patients. Cancer Research, 66(15), 7810-7817.
-
(2006)
Cancer Research
, vol.66
, Issue.15
, pp. 7810-7817
-
-
Hampel, H.1
Frankel, W.2
Panescu, J.3
Lockman, J.4
Sotamaa, K.5
Fix, D.6
-
24
-
-
40649093839
-
Lynch syndrome: Still not a familiar picture
-
18284705 10.1186/1477-7819-6-21
-
Hes, F. J. (2008). Lynch syndrome: still not a familiar picture. World Journal of Surgical Oncology, 6, 21.
-
(2008)
World Journal of Surgical Oncology
, vol.6
, pp. 21
-
-
Hes, F.J.1
-
25
-
-
84877926355
-
Recognizing hereditary cancer: New simple referral criteria for solid cancers
-
Hoogerbrugge, N. (2010). Recognizing hereditary cancer: new simple referral criteria for solid cancers. Netherlands Journal of Oncology, 7, 330-337.
-
(2010)
Netherlands Journal of Oncology
, vol.7
, pp. 330-337
-
-
Hoogerbrugge, N.1
-
26
-
-
34247138331
-
Prediction of BRCA1/2 mutation status in patients with ovarian cancer from a hospital-based cohort
-
17413421 10.1097/GIM.0b013e318032e4ab
-
Jacobi, C. E., Van Ierland, Y., Van Asperen, C. J., Hallensleben, E., Devilee, P., et al. (2007). Prediction of BRCA1/2 mutation status in patients with ovarian cancer from a hospital-based cohort. Genetics in Medicine, 9(3), 173-179.
-
(2007)
Genetics in Medicine
, vol.9
, Issue.3
, pp. 173-179
-
-
Jacobi, C.E.1
Van Ierland, Y.2
Van Asperen, C.J.3
Hallensleben, E.4
Devilee, P.5
-
27
-
-
0034011564
-
Controlled 15-year trial on screening for colorectal cancer in families with hereditary non-polyposis colorectal cancer
-
10784581 10.1016/S0016-5085(00)70168-5
-
Järvinen, H. J., Aarnio, M., Mustonen, H., Aktan-Collan, K., Aaltonen, L. A., Peltomäki, P., et al. (2000). Controlled 15-year trial on screening for colorectal cancer in families with hereditary non-polyposis colorectal cancer. Gastroenterology, 118(5), 829-834.
-
(2000)
Gastroenterology
, vol.118
, Issue.5
, pp. 829-834
-
-
Järvinen, H.J.1
Aarnio, M.2
Mustonen, H.3
Aktan-Collan, K.4
Aaltonen, L.A.5
Peltomäki, P.6
-
28
-
-
0032169911
-
Cancer genetic clinics: Why do women who already have cancer attend?
-
9893626 10.1016/S0959-8049(98)00164-6 1:STN:280:DyaK1M7gvFGjtg%3D%3D
-
Julian-Reynier, C., Eisinger, F., Chabal, F., Aurran, Y., Bignon, Y. J., Noguès, C., et al. (1998). Cancer genetic clinics: why do women who already have cancer attend? European Journal of Cancer, 34(10), 1549-1553.
-
(1998)
European Journal of Cancer
, vol.34
, Issue.10
, pp. 1549-1553
-
-
Julian-Reynier, C.1
Eisinger, F.2
Chabal, F.3
Aurran, Y.4
Bignon, Y.J.5
Noguès, C.6
-
29
-
-
0034221277
-
Mutational analysis of BRCA1 and BRCA2 genes in Chinese ovarian cancer identifies 6 novel germline mutations
-
10874312 10.1002/1098-1004(200007)16:1<88: AID-HUMU16>3.0.CO;2-G 1:STN:280:DC%2BD3cvhtFSruw%3D%3D
-
Khoo, U. S., Ngan, H. Y., Cheung, A. N., Chan, K. Y., Lu, J., Chan, V. W., et al. (2000). Mutational analysis of BRCA1 and BRCA2 genes in Chinese ovarian cancer identifies 6 novel germline mutations. Human Mutation, 16(1), 88-89.
-
(2000)
Human Mutation
, vol.16
, Issue.1
, pp. 88-89
-
-
Khoo, U.S.1
Ngan, H.Y.2
Cheung, A.N.3
Chan, K.Y.4
Lu, J.5
Chan, V.W.6
-
30
-
-
0036512383
-
Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: A founder mutation of BRCA1 identified in the Chinese population
-
11857749 10.1002/humu.9015
-
Khoo, U. S., Chan, K. Y., Cheung, A. N., Xue, W. C., Shen, D. H., Fung, K. Y., et al. (2002). Recurrent BRCA1 and BRCA2 germline mutations in ovarian cancer: a founder mutation of BRCA1 identified in the Chinese population. Human Mutation, 19(3), 307-308.
-
(2002)
Human Mutation
, vol.19
, Issue.3
, pp. 307-308
-
-
Khoo, U.S.1
Chan, K.Y.2
Cheung, A.N.3
Xue, W.C.4
Shen, D.H.5
Fung, K.Y.6
-
31
-
-
52049087559
-
What women with ovarian cancer think and know about genetic testing
-
18684498 10.1016/j.ygyno.2008.06.016
-
Lacour, R. A., Daniels, M. S., Westin, S. N., Meyer, L. A., Burke, C. C., Burns, K. A., et al. (2008). What women with ovarian cancer think and know about genetic testing. Gynecologic Oncology, 111(1), 132-136.
-
(2008)
Gynecologic Oncology
, vol.111
, Issue.1
, pp. 132-136
-
-
Lacour, R.A.1
Daniels, M.S.2
Westin, S.N.3
Meyer, L.A.4
Burke, C.C.5
Burns, K.A.6
-
32
-
-
84859566031
-
Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤ 70 years
-
22306203 10.1016/j.ygyno.2012.01.049 1:CAS:528:DC%2BC38XlslSgtrY%3D
-
Leenen, C. H., Van Lier, M. G., Van Doorn, H. C., Van Leerdam, M. E., Kooi, S. G., De Waard, J., et al. (2012). Prospective evaluation of molecular screening for Lynch syndrome in patients with endometrial cancer ≤ 70 years. Gynecologic Oncology, 125(2), 414-420.
-
(2012)
Gynecologic Oncology
, vol.125
, Issue.2
, pp. 414-420
-
-
Leenen, C.H.1
Van Lier, M.G.2
Van Doorn, H.C.3
Van Leerdam, M.E.4
Kooi, S.G.5
De Waard, J.6
-
33
-
-
0036724556
-
Contribution of BRCA1 and BRCA2 mutations to breast and ovarian cancer in Pakistan
-
12181777 10.1086/342506 1:CAS:528:DC%2BD38XmvFOhtbo%3D
-
Liede, A., Malik, I. A., Aziz, Z., De los Rios, P., Kwan, E., & Narod, S. A. (2002). Contribution of BRCA1 and BRCA2 mutations to breast and ovarian cancer in Pakistan. American Journal of Human Genetics, 71(3), 595-606.
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.3
, pp. 595-606
-
-
Liede, A.1
Malik, I.A.2
Aziz, Z.3
De Los Rios, P.4
Kwan, E.5
Narod, S.A.6
-
34
-
-
58149144567
-
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1
-
19098912 10.1038/ng.283 1:CAS:528:DC%2BD1cXhsFajtbnN
-
Ligtenberg, M. J., Kuiper, R. P., Chan, T. L., Goossens, M., Hebeda, K. M., Voorendt, M., et al. (2009). Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1. Nature Genetics, 41(1), 112-117.
-
(2009)
Nature Genetics
, vol.41
, Issue.1
, pp. 112-117
-
-
Ligtenberg, M.J.1
Kuiper, R.P.2
Chan, T.L.3
Goossens, M.4
Hebeda, K.M.5
Voorendt, M.6
-
35
-
-
78649536905
-
Hereditary non-polyposis colorectal cancer/Lynch syndrome in Korean patients with endometrial cancer
-
20965939 10.1093/jjco/hyq144
-
Lim, M. C., Seo, S. S., Kang, S., Seong, M. W., Lee, B. Y., & Park, S. Y. (2010). Hereditary non-polyposis colorectal cancer/Lynch syndrome in Korean patients with endometrial cancer. Japanese Journal of Clinical Oncology, 40(12), 1121-1127.
-
(2010)
Japanese Journal of Clinical Oncology
, vol.40
, Issue.12
, pp. 1121-1127
-
-
Lim, M.C.1
Seo, S.S.2
Kang, S.3
Seong, M.W.4
Lee, B.Y.5
Park, S.Y.6
-
36
-
-
80052031064
-
Hereditary ovarian cancer: Recent molecular insights and their impact on screening strategies
-
21734577 10.1097/CCO.0b013e3283499da9
-
Long, K. C., & Kauff, N. D. (2011). Hereditary ovarian cancer: recent molecular insights and their impact on screening strategies. Current Opinion in Oncology, 23(5), 526-530.
-
(2011)
Current Opinion in Oncology
, vol.23
, Issue.5
, pp. 526-530
-
-
Long, K.C.1
Kauff, N.D.2
-
37
-
-
0032988715
-
An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer
-
10.1016/S0165-4608(98)00165-4 1:CAS:528:DyaK1MXitVWqu78%3D
-
Lynch, H. T., Watson, P., Tinley, S., Snyder, C., Durham, C., Lynch, J., et al. (1999). An update on DNA-based BRCA1/BRCA2 genetic counseling in hereditary breast cancer. Cancer Genetica and Cytogenetics, 109(2), 91-98.
-
(1999)
Cancer Genetica and Cytogenetics
, vol.109
, Issue.2
, pp. 91-98
-
-
Lynch, H.T.1
Watson, P.2
Tinley, S.3
Snyder, C.4
Durham, C.5
Lynch, J.6
-
38
-
-
19944422091
-
Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases - Preliminary report
-
15617999 10.1016/j.ejca.2004.10.011 1:CAS:528:DC%2BD2MXhtVGitQ%3D%3D
-
Majdak, E. J., De Bock, G. H., Brozek, I., Perkowska, M., Ochman, K., Debniak, J., et al. (2005). Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases - preliminary report. European Journal of Cancer, 41(1), 143-150.
-
(2005)
European Journal of Cancer
, vol.41
, Issue.1
, pp. 143-150
-
-
Majdak, E.J.1
De Bock, G.H.2
Brozek, I.3
Perkowska, M.4
Ochman, K.5
Debniak, J.6
-
39
-
-
1642554820
-
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: Results of a prospective study in Southern Sweden
-
14746861 10.1016/j.ejca.2003.09.016 1:CAS:528:DC%2BD2cXmvFGjsw%3D%3D
-
Malander, S., Ridderheim, M., Måsbäck, A., Loman, N., Kristoffersson, U., Olsson, H., et al. (2004). One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden. European Journal of Cancer, 40(3), 422-428.
-
(2004)
European Journal of Cancer
, vol.40
, Issue.3
, pp. 422-428
-
-
Malander, S.1
Ridderheim, M.2
Måsbäck, A.3
Loman, N.4
Kristoffersson, U.5
Olsson, H.6
-
40
-
-
79957554816
-
Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome
-
21273057 10.1016/j.ejca.2010.12.024 1:STN:280:DC%2BC3Mrlt1ertg%3D%3D
-
Manders, P., Spruijt, L., Kets, C. M., Willems, H. W., Bodmer, D., Hebeda, K. M., et al. (2011). Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome. European Journal of Cancer, 47(9), 1407-1413.
-
(2011)
European Journal of Cancer
, vol.47
, Issue.9
, pp. 1407-1413
-
-
Manders, P.1
Spruijt, L.2
Kets, C.M.3
Willems, H.W.4
Bodmer, D.5
Hebeda, K.M.6
-
41
-
-
77951521419
-
Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: Missed opportunities
-
20410767 10.1097/AOG.0b013e3181da08d7
-
Meyer, L. A., Anderson, M. E., Lacour, R. A., Suri, A., Daniels, M. S., Urbauer, D. L., et al. (2010). Evaluating women with ovarian cancer for BRCA1 and BRCA2 mutations: missed opportunities. Obstetrics and Gynecology, 115(5), 945-952.
-
(2010)
Obstetrics and Gynecology
, vol.115
, Issue.5
, pp. 945-952
-
-
Meyer, L.A.1
Anderson, M.E.2
Lacour, R.A.3
Suri, A.4
Daniels, M.S.5
Urbauer, D.L.6
-
42
-
-
80052035210
-
Frequency of mismatch repair deficiency in ovarian cancer: A systematic review
-
10.1002/ijc.25835 1:CAS:528:DC%2BC3MXhtVKlsr3L
-
Murphy, M. A., & Wentzensen, N. (2011). Frequency of mismatch repair deficiency in ovarian cancer: a systematic review. International Journal of Cancer, 129, 1914-1922.
-
(2011)
International Journal of Cancer
, vol.129
, pp. 1914-1922
-
-
Murphy, M.A.1
Wentzensen, N.2
-
43
-
-
84877922217
-
-
Netherlands Foundation for the Detection of Hereditary Tumours (STOET) and Dutch Society for Clinical Genetics (VKGN) 3rd edition, 2005 and 4th edition
-
Netherlands Foundation for the Detection of Hereditary Tumours (STOET) and Dutch Society for Clinical Genetics (VKGN). (2005, 2010). Hereditary Tumours: guidelines for diagnostics and prevention. 3rd edition, 2005 and 4th edition
-
(2005)
Hereditary Tumours: Guidelines for Diagnostics and Prevention
-
-
-
44
-
-
29144509766
-
BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases
-
16284991 10.1002/cncr.21536 1:CAS:528:DC%2BD28XptlSrsA%3D%3D
-
Pal, T., Permuth-Wey, J., Betts, J. A., Krischer, J. P., Fiorica, J., Arango, H., et al. (2005). BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases. Cancer, 104(12), 2807-2816.
-
(2005)
Cancer
, vol.104
, Issue.12
, pp. 2807-2816
-
-
Pal, T.1
Permuth-Wey, J.2
Betts, J.A.3
Krischer, J.P.4
Fiorica, J.5
Arango, H.6
-
45
-
-
14644396669
-
Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: The German hereditary nonpolyposis colorectal cancer consortium
-
15483016 10.1200/JCO.2004.02.033 1:CAS:528:DC%2BD2cXhtFWqt7%2FM
-
Plaschke, J., Engel, C., Krüger, S., Holinski-Feder, E., Pagenstecher, C., Mangold, E., et al. (2004). Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German hereditary nonpolyposis colorectal cancer consortium. Journal of Clinical Oncology, 22(22), 4486-4494.
-
(2004)
Journal of Clinical Oncology
, vol.22
, Issue.22
, pp. 4486-4494
-
-
Plaschke, J.1
Engel, C.2
Krüger, S.3
Holinski-Feder, E.4
Pagenstecher, C.5
Mangold, E.6
-
46
-
-
78650078754
-
Identification and management of women with BRCA mutations or hereditary predisposition for breast and ovarian cancer
-
21123638 10.4065/mcp.2010.0414
-
Pruthi, S., Gostout, B. S., & Lindor, N. M. (2010). Identification and management of women with BRCA mutations or hereditary predisposition for breast and ovarian cancer. Mayo Clinic Proceedings, 85(12), 1111-1120.
-
(2010)
Mayo Clinic Proceedings
, vol.85
, Issue.12
, pp. 1111-1120
-
-
Pruthi, S.1
Gostout, B.S.2
Lindor, N.M.3
-
47
-
-
54349109188
-
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting
-
18625694 10.1136/gut.2008.156695 1:CAS:528:DC%2BD1cXhtl2gtr7F
-
Ramsoekh, D., Wagner, A., Van Leerdam, M. E., Dinjens, W. N., Steyerberg, E. W., Halley, D. J., et al. (2008). A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting. Gut, 57(11), 1539-1544.
-
(2008)
Gut
, vol.57
, Issue.11
, pp. 1539-1544
-
-
Ramsoekh, D.1
Wagner, A.2
Van Leerdam, M.E.3
Dinjens, W.N.4
Steyerberg, E.W.5
Halley, D.J.6
-
48
-
-
77957888649
-
Obstetrics/gynecology residents' knowledge of hereditary breast and ovarian cancer and Lynch syndrome
-
20186516 10.1007/s13187-010-0063-4
-
Ready, K. J., Daniels, M. S., Sun, C. C., Peterson, S. K., Northrup, H., & Lu, K. H. (2010). Obstetrics/gynecology residents' knowledge of hereditary breast and ovarian cancer and Lynch syndrome. Journal of Cancer Education, 25(3), 401-404.
-
(2010)
Journal of Cancer Education
, vol.25
, Issue.3
, pp. 401-404
-
-
Ready, K.J.1
Daniels, M.S.2
Sun, C.C.3
Peterson, S.K.4
Northrup, H.5
Lu, K.H.6
-
49
-
-
33846619639
-
Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome
-
10.1002/ijc.22446
-
Renkonen-Sinisalo, L., Bützow, R., Leminen, A., Lehtovirta, P., Mecklin, J. P., & Järvinen, H. J. (2006). Surveillance for endometrial cancer in hereditary nonpolyposis colorectal cancer syndrome. International Journal of Cancer, 120(4), 821-824.
-
(2006)
International Journal of Cancer
, vol.120
, Issue.4
, pp. 821-824
-
-
Renkonen-Sinisalo, L.1
Bützow, R.2
Leminen, A.3
Lehtovirta, P.4
Mecklin, J.P.5
Järvinen, H.J.6
-
50
-
-
69549110049
-
Lynch syndrome screening strategies among newly diagnosed endometrial cancer patients
-
19701031 10.1097/AOG.0b013e3181b11ecc
-
Resnick, K., Straughn, J. M., Jr., Backes, F., Hampel, H., Matthews, K. S., & Cohn, D. E. (2009). Lynch syndrome screening strategies among newly diagnosed endometrial cancer patients. Obstetrics and Gynecology, 114(3), 530-536.
-
(2009)
Obstetrics and Gynecology
, vol.114
, Issue.3
, pp. 530-536
-
-
Resnick, K.1
Straughn, Jr.J.M.2
Backes, F.3
Hampel, H.4
Matthews, K.S.5
Cohn, D.E.6
-
51
-
-
33845654907
-
Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: A kin-cohort study in Ontario, Canada
-
17148771 10.1093/jnci/djj465 1:CAS:528:DC%2BD28XhtlCru7nJ
-
Risch, H. A., McLaughlin, J. R., Cole, D. E., Rosen, B., Bradley, L., Fan, I., et al. (2006). Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada. Journal of the National Cancer Institute, 98(23), 1694-1706.
-
(2006)
Journal of the National Cancer Institute
, vol.98
, Issue.23
, pp. 1694-1706
-
-
Risch, H.A.1
McLaughlin, J.R.2
Cole, D.E.3
Rosen, B.4
Bradley, L.5
Fan, I.6
-
52
-
-
0031958466
-
BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: Relationship to family history and implications for genetic testing
-
9579428 10.1016/S0002-9378(98)70476-4 1:STN:280:DyaK1c3jvFSgsw%3D%3D
-
Rubin, S. C., Blackwood, M. A., Bandera, C., Behbakht, K., Benjamin, I., et al. (1998). BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: relationship to family history and implications for genetic testing. American Journal of Obstetrics and Gynecology, 178(4), 670-677.
-
(1998)
American Journal of Obstetrics and Gynecology
, vol.178
, Issue.4
, pp. 670-677
-
-
Rubin, S.C.1
Blackwood, M.A.2
Bandera, C.3
Behbakht, K.4
Benjamin, I.5
-
53
-
-
0034948376
-
BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients
-
11436123 10.1038/sj.ejhg.5200652 1:CAS:528:DC%2BD3MXlt12nsLs%3D
-
Sarantaus, L., Vahteristo, P., Bloom, E., Tamminen, A., Unkila-Kallio, L., et al. (2001). BRCA1 and BRCA2 mutations among 233 unselected Finnish ovarian carcinoma patients. European Journal of Human Genetics, 9(6), 424-430.
-
(2001)
European Journal of Human Genetics
, vol.9
, Issue.6
, pp. 424-430
-
-
Sarantaus, L.1
Vahteristo, P.2
Bloom, E.3
Tamminen, A.4
Unkila-Kallio, L.5
-
54
-
-
36248965183
-
Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer
-
18007146 10.1097/GIM.0b013e318159a318
-
Schlich-Bakker, K. J., Ten Kroode, H. F., Wárlám-Rodenhuis, C. C., Van den Bout, J., & Ausems, M. G. (2007). Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer. Genetics in Medicine, 9(11), 766-777.
-
(2007)
Genetics in Medicine
, vol.9
, Issue.11
, pp. 766-777
-
-
Schlich-Bakker, K.J.1
Ten Kroode, H.F.2
Wárlám-Rodenhuis, C.C.3
Van Den Bout, J.4
Ausems, M.G.5
-
55
-
-
0034077306
-
Accuracy of family history of cancer: Clinical genetic implications
-
10780783 10.1038/sj.ejhg.5200441 1:STN:280:DC%2BD3c3ktFKqtw%3D%3D
-
Sijmons, R. H., Boonstra, A. E., Reefhuis, J., Hordijk-Hos, J. M., De Walle, H. E., et al. (2000). Accuracy of family history of cancer: clinical genetic implications. European Journal of Human Genetics, 8(3), 181-186.
-
(2000)
European Journal of Human Genetics
, vol.8
, Issue.3
, pp. 181-186
-
-
Sijmons, R.H.1
Boonstra, A.E.2
Reefhuis, J.3
Hordijk-Hos, J.M.4
De Walle, H.E.5
-
56
-
-
52449114074
-
BRCA1 and BRCA2 mutation prevalence and clinical characteristics of a population-based series of ovarian cancer cases from Denmark
-
18559594 10.1158/1078-0432.CCR-07-4806 1:CAS:528:DC%2BD1cXntlWrsL8%3D
-
Soegaard, M., Kjaer, S. K., Cox, M., Wozniak, E., Høgdall, E., Høgdall, C., et al. (2008). BRCA1 and BRCA2 mutation prevalence and clinical characteristics of a population-based series of ovarian cancer cases from Denmark. Clinical Cancer Research, 14(12), 3761-3767.
-
(2008)
Clinical Cancer Research
, vol.14
, Issue.12
, pp. 3761-3767
-
-
Soegaard, M.1
Kjaer, S.K.2
Cox, M.3
Wozniak, E.4
Høgdall, E.5
Høgdall, C.6
-
58
-
-
0033028701
-
Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history
-
10422801 10.1034/j.1399-0004.1999.550504.x 1:STN:280:DyaK1MzkvFKlsQ%3D%3D
-
Tonin, P. N., Mes-Masson, A. M., Narod, S. A., Ghadirian, P., & Provencher, D. (1999). Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history. Clinical Genetics, 55(5), 318-324.
-
(1999)
Clinical Genetics
, vol.55
, Issue.5
, pp. 318-324
-
-
Tonin, P.N.1
Mes-Masson, A.M.2
Narod, S.A.3
Ghadirian, P.4
Provencher, D.5
-
59
-
-
35448938065
-
A review of histopathological subtypes of ovarian cancer in BRCA-related French Canadian cancer families
-
17636423 10.1007/s10689-007-9152-x 1:CAS:528:DC%2BD2sXhtF2htb3K
-
Tonin, P. N., Maugard, C. M., Perret, C., Mes-Masson, A. M., & Provencher, D. M. (2007). A review of histopathological subtypes of ovarian cancer in BRCA-related French Canadian cancer families. Familial Cancer, 6(4), 491-497.
-
(2007)
Familial Cancer
, vol.6
, Issue.4
, pp. 491-497
-
-
Tonin, P.N.1
Maugard, C.M.2
Perret, C.3
Mes-Masson, A.M.4
Provencher, D.M.5
-
60
-
-
77956858334
-
Moving toward personalized medicine: Treatment-focused genetic testing of women newly diagnosed with ovarian cancer
-
20973257 10.1111/IGC.0b013e3181dbd1a5
-
Trainer, A. H., Meiser, B., Watts, K., Mitchell, G., Tucker, K., & Friedlander, M. (2010). Moving toward personalized medicine: treatment-focused genetic testing of women newly diagnosed with ovarian cancer. International Journal of Gynecological Cancer, 20(5), 704-716.
-
(2010)
International Journal of Gynecological Cancer
, vol.20
, Issue.5
, pp. 704-716
-
-
Trainer, A.H.1
Meiser, B.2
Watts, K.3
Mitchell, G.4
Tucker, K.5
Friedlander, M.6
-
61
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
14970275 10.1093/jnci/djh034 1:CAS:528:DC%2BD2cXhsV2qtLk%3D
-
Umar, A., Boland, C. R., Terdiman, J. P., Syngal, S., De la Chapelle, A., Rüschoff, J., et al. (2004). Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. Journal of the National Cancer Institute, 96(4), 261-268.
-
(2004)
Journal of the National Cancer Institute
, vol.96
, Issue.4
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
Syngal, S.4
De La Chapelle, A.5
Rüschoff, J.6
-
62
-
-
18444417396
-
What do women really want to know? Motives for attending familial breast cancer clinics
-
12070250 10.1136/jmg.39.6.410
-
Van Asperen, C. J., Van Dijk, S., Zoeteweij, M. W., Timmermans, D. R., De Bock, G. H., Meijers-Heijboer, E. J., et al. (2002). What do women really want to know? Motives for attending familial breast cancer clinics. Journal of Medical Genetics, 39(6), 410-414.
-
(2002)
Journal of Medical Genetics
, vol.39
, Issue.6
, pp. 410-414
-
-
Van Asperen, C.J.1
Van Dijk, S.2
Zoeteweij, M.W.3
Timmermans, D.R.4
De Bock, G.H.5
Meijers-Heijboer, E.J.6
-
63
-
-
78649322429
-
Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: High cancer incidence at older age
-
20204502 10.1007/s10549-010-0805-3 1:CAS:528:DC%2BC3cXhtlyrsrjO
-
Van der Kolk, D. M., de Bock, G. H., Leegte, B. K., Schaapveld, M., Mourits, M. J., de Vries, J., et al. (2010). Penetrance of breast cancer, ovarian cancer and contralateral breast cancer in BRCA1 and BRCA2 families: high cancer incidence at older age. Breast Cancer Research and Treatment, 124(3), 643-651.
-
(2010)
Breast Cancer Research and Treatment
, vol.124
, Issue.3
, pp. 643-651
-
-
Van Der Kolk, D.M.1
De Bock, G.H.2
Leegte, B.K.3
Schaapveld, M.4
Mourits, M.J.5
De Vries, J.6
-
64
-
-
77953151348
-
BRCA testing of breast cancer patients: Medical specialists' referral patterns, knowledge and attitudes to genetic testing
-
19659662 10.1111/j.1365-2354.2008.01065.x
-
Van Riel, E., Wárlám-Rodenhuis, C. C., Verhoef, S., Rutgers, E. J., & Ausems, M. G. (2010). BRCA testing of breast cancer patients: medical specialists' referral patterns, knowledge and attitudes to genetic testing. European Journal of Cancer Care, 19(3), 369-376.
-
(2010)
European Journal of Cancer Care
, vol.19
, Issue.3
, pp. 369-376
-
-
Van Riel, E.1
Wárlám-Rodenhuis, C.C.2
Verhoef, S.3
Rutgers, E.J.4
Ausems, M.G.5
-
65
-
-
24144432339
-
Clinical description of the Lynch syndrome [hereditary nonpolyposis colorectal cancer (HNPCC)]
-
16136381 10.1007/s10689-004-3906-5 1:STN:280:DC%2BD2MvmslKrsA%3D%3D
-
Vasen, H. F. (2005). Clinical description of the Lynch syndrome [hereditary nonpolyposis colorectal cancer (HNPCC)]. Familial Cancer, 4(3), 219-225.
-
(2005)
Familial Cancer
, vol.4
, Issue.3
, pp. 219-225
-
-
Vasen, H.F.1
-
66
-
-
0033063711
-
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch Syndrome) proposed by the international collaborative group on HNPCC
-
10348829 10.1016/S0016-5085(99)70510-X 1:STN:280:DyaK1M3nvVamuw%3D%3D
-
Vasen, H. F., Watson, P., Mecklin, J. P., & Lynch, H. T. (1999). New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch Syndrome) proposed by the international collaborative group on HNPCC. Gastroenterology, 116(6), 1453-1456.
-
(1999)
Gastroenterology
, vol.116
, Issue.6
, pp. 1453-1456
-
-
Vasen, H.F.1
Watson, P.2
Mecklin, J.P.3
Lynch, H.T.4
-
67
-
-
84863609627
-
Identification of individuals at risk for lynch syndrome using targeted evaluations and genetic testing: National society of genetic counselors and the collaborative group of the Americas on inherited colorectal cancer joint practice guideline
-
22167527 10.1007/s10897-011-9465-7
-
Weissman, S. M., Burt, R., Church, J., Erdman, S., Hampel, H., Holter, S., et al. (2012). Identification of individuals at risk for lynch syndrome using targeted evaluations and genetic testing: national society of genetic counselors and the collaborative group of the Americas on inherited colorectal cancer joint practice guideline. Journal of Genetic Counseling, 21(4), 484-493.
-
(2012)
Journal of Genetic Counseling
, vol.21
, Issue.4
, pp. 484-493
-
-
Weissman, S.M.1
Burt, R.2
Church, J.3
Erdman, S.4
Hampel, H.5
Holter, S.6
-
68
-
-
84866620449
-
Breast cancer genetic counseling after diagnosis but before treatment: A pilot study on treatment consequences and psychological impact
-
in press
-
Wevers, M. R., Hahn, D. E., Verhoef, S., Bolhaar, M. D., Ausems, M. G., Aaronson, N. K., et al. (2012). Breast cancer genetic counseling after diagnosis but before treatment: A pilot study on treatment consequences and psychological impact. Patient Education and Counseling; in press
-
(2012)
Patient Education and Counseling
-
-
Wevers, M.R.1
Hahn, D.E.2
Verhoef, S.3
Bolhaar, M.D.4
Ausems, M.G.5
Aaronson, N.K.6
-
69
-
-
26944439058
-
Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians
-
15784723 10.1136/jmg.2004.030296 1:CAS:528:DC%2BD2MXhtFyhu7bE
-
Wideroff, L., Vadaparampil, S. T., Greene, M. H., Taplin, S., Olson, L., & Freedman, A. N. (2005). Hereditary breast/ovarian and colorectal cancer genetics knowledge in a national sample of US physicians. Journal of Medical Genetics, 42(10), 749-755.
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.10
, pp. 749-755
-
-
Wideroff, L.1
Vadaparampil, S.T.2
Greene, M.H.3
Taplin, S.4
Olson, L.5
Freedman, A.N.6
-
70
-
-
0001628596
-
Familial endometrial cancer in female carriers of MSH6 germline mutations
-
10508506 10.1038/13773 1:CAS:528:DyaK1MXmtlOhtLg%3D
-
Wijnen, J., De Leeuw, W., Vasen, H., Van der Klift, H., Møller, P., Stormorken, A., et al. (1999). Familial endometrial cancer in female carriers of MSH6 germline mutations. Nature Genetics, 23(2), 142-144.
-
(1999)
Nature Genetics
, vol.23
, Issue.2
, pp. 142-144
-
-
Wijnen, J.1
De Leeuw, W.2
Vasen, H.3
Van Der Klift, H.4
Møller, P.5
Stormorken, A.6
-
71
-
-
18444414286
-
BRCA1 and BRCA2 mutations in Turkish familial and non-familial ovarian cancer patients: A high incidence of mutations in non-familial cases
-
12112655 10.1002/humu.10090 1:CAS:528:DC%2BD38XlslKrtrs%3D
-
Yazici, H., Glendon, G., Yazici, H., Burnie, S. J., Saip, P., Buyru, F., et al. (2002). BRCA1 and BRCA2 mutations in Turkish familial and non-familial ovarian cancer patients: a high incidence of mutations in non-familial cases. Human Mutation, 20(1), 28-34.
-
(2002)
Human Mutation
, vol.20
, Issue.1
, pp. 28-34
-
-
Yazici, H.1
Glendon, G.2
Yazici, H.3
Burnie, S.J.4
Saip, P.5
Buyru, F.6
-
72
-
-
0037262071
-
The importance of paternal family history in hereditary breast cancer is underappreciated by health care professionals
-
12697961 10.1159/000069309
-
Yong, M. C., Zhou, X. J., & Lee, S. C. (2003). The importance of paternal family history in hereditary breast cancer is underappreciated by health care professionals. Oncology, 64(3), 220-226.
-
(2003)
Oncology
, vol.64
, Issue.3
, pp. 220-226
-
-
Yong, M.C.1
Zhou, X.J.2
Lee, S.C.3
-
73
-
-
84868453539
-
Are we being overly cautious? A qualitative inquiry into the experiences and perceptions of treatment-focused germline BRCA genetic testing amongst women recently diagnosed with breast cancer
-
in press
-
Zilliacus, E., Meiser, B., Gleeson, M., Watts, K., Tucker, K., Lobb, E. A., et al. (2012) Are we being overly cautious? A qualitative inquiry into the experiences and perceptions of treatment-focused germline BRCA genetic testing amongst women recently diagnosed with breast cancer. Supportive Care in Cancer; in press.
-
(2012)
Supportive Care in Cancer
-
-
Zilliacus, E.1
Meiser, B.2
Gleeson, M.3
Watts, K.4
Tucker, K.5
Lobb, E.A.6
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