-
1
-
-
0028226295
-
Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients
-
Aaltonen, L. A., Peltomaki, P., Mecklin, J. P., Jarvinen, H., Jass, J. R., Green, J. S., et al. (1994). Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients. Cancer Res, 54, 1645-1648.
-
(1994)
Cancer Res
, vol.54
, pp. 1645-1648
-
-
Aaltonen, L.A.1
Peltomaki, P.2
Mecklin, J.P.3
Jarvinen, H.4
Jass, J.R.5
Green, J.S.6
-
2
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
Aaltonen, L. A., Salovaara, R., Kristo, P., Canzian, F., Hemminki, A., Peltomaki, P., et al. (1998). Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med, 338, 1481-1487.
-
(1998)
N Engl J Med
, vol.338
, pp. 1481-1487
-
-
Aaltonen, L.A.1
Salovaara, R.2
Kristo, P.3
Canzian, F.4
Hemminki, A.5
Peltomaki, P.6
-
3
-
-
0032941343
-
Cancer risk in mutation carriers of DNA-mismatch-repair genes
-
Aarnio, M., Sankila, R., Pukkala, E., Salovaara, R., Aaltonen, L. A., de la Chapelle, A., et al. (1999). Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer, 81, 214-218.
-
(1999)
Int J Cancer
, vol.81
, pp. 214-218
-
-
Aarnio, M.1
Sankila, R.2
Pukkala, E.3
Salovaara, R.4
Aaltonen, L.A.5
De La Chapelle, A.6
-
4
-
-
33750008530
-
-
A cancer predisposition risk assessment program from Dr. David Euhus. Retrieved September 2004 from
-
CancerGene (v. 4.0). A cancer predisposition risk assessment program from Dr. David Euhus. University of Texas SouthWestern. Retrieved September 2004 from http://www3.utsouthwestern.edu/cancergene
-
CancerGene (V. 4.0)
-
-
-
5
-
-
9144237543
-
The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC
-
De Jong, A. E., Morreau, H., Van Puijenbroek, M., Eilers, P. H., Wijnen, J., Nagengast, F. M., et al. (2004). The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC. Gastroenterology, 126, 42-48.
-
(2004)
Gastroenterology
, vol.126
, pp. 42-48
-
-
De Jong, A.E.1
Morreau, H.2
Van Puijenbroek, M.3
Eilers, P.H.4
Wijnen, J.5
Nagengast, F.M.6
-
6
-
-
27944464473
-
Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer
-
Engel, C., Forberg, J., Holinski-Feder, E., Pagenstecher, C., Plaschke, J., Kloor, M., et al. (2006). Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer. Int J Cancer, 118, 115-122.
-
(2006)
Int J Cancer
, vol.118
, pp. 115-122
-
-
Engel, C.1
Forberg, J.2
Holinski-Feder, E.3
Pagenstecher, C.4
Plaschke, J.5
Kloor, M.6
-
7
-
-
0034955851
-
AGA technical review on hereditary colorectal cancer and genetic testing
-
Giardiello, F. M., Brensinger, J. D., & Petersen, G. M. (2001). AGA technical review on hereditary colorectal cancer and genetic testing. Gastroenterology, 121, 198-213.
-
(2001)
Gastroenterology
, vol.121
, pp. 198-213
-
-
Giardiello, F.M.1
Brensinger, J.D.2
Petersen, G.M.3
-
8
-
-
21044452350
-
Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families
-
Grabowski, M., Mueller-Koch, Y., Grasbon-Frodl, E., Koehler, U., Keller, G., Vogelsang, H., et al. (2005). Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families. Genet Test, 9(2), 138-146.
-
(2005)
Genet Test
, vol.9
, Issue.2
, pp. 138-146
-
-
Grabowski, M.1
Mueller-Koch, Y.2
Grasbon-Frodl, E.3
Koehler, U.4
Keller, G.5
Vogelsang, H.6
-
9
-
-
0027285475
-
Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
-
Ionov, Y., Peinado, M. A., Malkhosyan, S., Shibata, D., & Perucho, M. (1993). Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis. Nature, 363, 558-561.
-
(1993)
Nature
, vol.363
, pp. 558-561
-
-
Ionov, Y.1
Peinado, M.A.2
Malkhosyan, S.3
Shibata, D.4
Perucho, M.5
-
10
-
-
0034011564
-
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
-
Jarvinen, H. J., Aarnio, M., Mustonen, H., Aktan-Collan, K., Aaltonen, L. A., Peltomaki, P., et al. (2000). Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology, 118, 829-834.
-
(2000)
Gastroenterology
, vol.118
, pp. 829-834
-
-
Jarvinen, H.J.1
Aarnio, M.2
Mustonen, H.3
Aktan-Collan, K.4
Aaltonen, L.A.5
Peltomaki, P.6
-
11
-
-
5444242604
-
An update on the genetics of colorectal cancer
-
Kemp, Z., Thirlwell, C., Sieber, O., Silver, A., & Tomlinson, I. (2004). An update on the genetics of colorectal cancer. Hum Mol Genet, 13, R177-R185.
-
(2004)
Hum Mol Genet
, vol.13
-
-
Kemp, Z.1
Thirlwell, C.2
Sieber, O.3
Silver, A.4
Tomlinson, I.5
-
12
-
-
1842477266
-
Current clinical selection strategies for identification of hereditary nonpolyposis colorectal cancer families are inadequate: A meta-analysis
-
Kievit, W., de Bruin, J. H., Adang, E. M., Ligtenberg, M. J., Nagengast, F. M., van Krieken, J. H., et al. (2004). Current clinical selection strategies for identification of hereditary nonpolyposis colorectal cancer families are inadequate: A meta-analysis. Clin Genet, 65, 308-316.
-
(2004)
Clin Genet
, vol.65
, pp. 308-316
-
-
Kievit, W.1
De Bruin, J.H.2
Adang, E.M.3
Ligtenberg, M.J.4
Nagengast, F.M.5
Van Krieken, J.H.6
-
13
-
-
0037083484
-
Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors
-
Lindor, N. M., Burgart, L. J., Leontovich, O., Goldberg, R. M., Cunningham, J. M., Sargent, D. J., et al. (2002). Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. J Clin Oncol, 15, 20(4):1043-1048.
-
(2002)
J Clin Oncol
, vol.20
, Issue.4
, pp. 1043-1048
-
-
Lindor, N.M.1
Burgart, L.J.2
Leontovich, O.3
Goldberg, R.M.4
Cunningham, J.M.5
Sargent, D.J.6
-
14
-
-
16644378293
-
Refining the Amsterdam Criteria and Bethesda Guidelines: Testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic
-
Lipton, L. R., Johnson, V., Cummings, C., Fisher, S., Risby, P., Eftekhar Sadat, A. T., et al. (2004). Refining the Amsterdam Criteria and Bethesda Guidelines: Testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic. J Clin Oncol, 22(24), 4934-4943.
-
(2004)
J Clin Oncol
, vol.22
, Issue.24
, pp. 4934-4943
-
-
Lipton, L.R.1
Johnson, V.2
Cummings, C.3
Fisher, S.4
Risby, P.5
Eftekhar Sadat, A.T.6
-
15
-
-
33645609504
-
History of the International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer
-
Lynch, H. T., Cristofaro, G., Rozen, P., Vasen, H., Lynch, P., Mecklin, J. P., et al. (2003). History of the International Collaborative Group on Hereditary Non Polyposis Colorectal Cancer. Fam Cancer, 2, 3-5.
-
(2003)
Fam Cancer
, vol.2
, pp. 3-5
-
-
Lynch, H.T.1
Cristofaro, G.2
Rozen, P.3
Vasen, H.4
Lynch, P.5
Mecklin, J.P.6
-
16
-
-
0032730774
-
Genetic susceptibility to non-polyposis colorectal cancer
-
Lynch, H. T., & de la Chapelle, A. (1999). Genetic susceptibility to non-polyposis colorectal cancer. J Med Genet, 36, 801-818.
-
(1999)
J Med Genet
, vol.36
, pp. 801-818
-
-
Lynch, H.T.1
De La Chapelle, A.2
-
17
-
-
0042281959
-
Clinical implications of molecular diagnosis in hereditary nonpolyposis colorectal cancer
-
Moslein, G. (2003). Clinical implications of molecular diagnosis in hereditary nonpolyposis colorectal cancer. Recent Results Cancer Res, 162, 73-78.
-
(2003)
Recent Results Cancer Res
, vol.162
, pp. 73-78
-
-
Moslein, G.1
-
19
-
-
17444372361
-
Evaluating the impact of genetic counseling and testing with signal detection methods
-
Palmer, C. G. S., & Hadley, D. W. (2005). Evaluating the impact of genetic counseling and testing with signal detection methods. J Genet Couns, 14(1), 17-27.
-
(2005)
J Genet Couns
, vol.14
, Issue.1
, pp. 17-27
-
-
Palmer, C.G.S.1
Hadley, D.W.2
-
20
-
-
4544310802
-
Mutations associated with HNPCC predisposition - Update of ICG-HNPCC/INSiGHT mutation database
-
Peltomaki, P., & Vasen, H. (2004). Mutations associated with HNPCC predisposition - Update of ICG-HNPCC/INSiGHT mutation database. Dis Markers, 20, 269-276.
-
(2004)
Dis Markers
, vol.20
, pp. 269-276
-
-
Peltomaki, P.1
Vasen, H.2
-
21
-
-
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
-
Plaschke, J., Engel, C., Kruger, 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. J Clin Oncol, 22, 4486-4494.
-
(2004)
J Clin Oncol
, vol.22
, pp. 4486-4494
-
-
Plaschke, J.1
Engel, C.2
Kruger, S.3
Holinski-Feder, E.4
Pagenstecher, C.5
Mangold, E.6
-
22
-
-
0031551963
-
A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting highlights and Bethesda guidelines
-
Rodriguez-Bigas, M. A., Boland, C. R., Hamilton, S. R., Henson, D. E., Jass, J. R., Khan, P. M., et al. (1997). A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines. J Natl Cancer Inst, 89, 1758-1762.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 1758-1762
-
-
Rodriguez-Bigas, M.A.1
Boland, C.R.2
Hamilton, S.R.3
Henson, D.E.4
Jass, J.R.5
Khan, P.M.6
-
23
-
-
23044453645
-
Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer
-
Stormorken, A. T., Bowitz-Lothe, I. M., Noren, T., Kure, E., Aase, S., Wijnen, J., et al. (2005). Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer. J Clin Oncol, 23, 4705-4712.
-
(2005)
J Clin Oncol
, vol.23
, pp. 4705-4712
-
-
Stormorken, A.T.1
Bowitz-Lothe, I.M.2
Noren, T.3
Kure, E.4
Aase, S.5
Wijnen, J.6
-
24
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar, A., Boland, C. R., Terdiman, J. P., Syngal, S., de la Chapelle, A., Ruschoff, J., et al. (2004). Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst, 96, 261-268.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
Syngal, S.4
De La Chapelle, A.5
Ruschoff, J.6
-
25
-
-
0025848680
-
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
-
Vasen, H. F., Mecklin, J. P., Khan, P. M., & Lynch, H. T. (1991). The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum, 34, 424-425.
-
(1991)
Dis Colon Rectum
, vol.34
, pp. 424-425
-
-
Vasen, H.F.1
Mecklin, J.P.2
Khan, P.M.3
Lynch, H.T.4
-
26
-
-
0033063711
-
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC
-
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, 1453-1456.
-
(1999)
Gastroenterology
, vol.116
, pp. 1453-1456
-
-
Vasen, H.F.1
Watson, P.2
Mecklin, J.P.3
Lynch, H.T.4
-
27
-
-
0000151696
-
Hereditary Nonpolyposis Colorectal Cancer: An Approach to the Selection of Candidates to Genetic Testing Based on Clinical and Molecular Characteristics
-
Viel, A., Genuardi, M., Lucci-Cordisco, E., Capozzi, E., Rovella, V., Fornasarig, M., et al. (1998). Hereditary Nonpolyposis Colorectal Cancer: An Approach to the Selection of Candidates to Genetic Testing Based on Clinical and Molecular Characteristics. Community Genet, 1, 229-236.
-
(1998)
Community Genet
, vol.1
, pp. 229-236
-
-
Viel, A.1
Genuardi, M.2
Lucci-Cordisco, E.3
Capozzi, E.4
Rovella, V.5
Fornasarig, M.6
-
28
-
-
0032552239
-
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer
-
Wijnen, J. T., Vasen, H. F., Khan, P. M., Zwinderman, A. H., van der Klift, H., Mulder, A., et al. (1998). Clinical findings with implications for genetic testing in families with clustering of colorectal cancer. N Engl J Med, 339, 511-518.
-
(1998)
N Engl J Med
, vol.339
, pp. 511-518
-
-
Wijnen, J.T.1
Vasen, H.F.2
Khan, P.M.3
Zwinderman, A.H.4
Van Der Klift, H.5
Mulder, A.6
-
29
-
-
0033361894
-
Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations
-
Wu, Y., Berends, M. J., Mensink, R. G., Kempinga, C., Sijmons, R. H., van Der Zee, A. G., et al. (1999). Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. Am J Hum Genet, 65(5), 1291-1298.
-
(1999)
Am J Hum Genet
, vol.65
, Issue.5
, pp. 1291-1298
-
-
Wu, Y.1
Berends, M.J.2
Mensink, R.G.3
Kempinga, C.4
Sijmons, R.H.5
Van Der Zee, A.G.6
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