-
1
-
-
79960604164
-
Strategies to identify the Lynch syndrome among patients with colorectal cancer: A cost-effectiveness analysis
-
Ladabaum U, Wang G, Terdiman J, at al: Strategies to identify the Lynch syndrome among patients with colorectal cancer: A cost-effectiveness analysis. Ann Intern Med 155:69-79, 2011
-
(2011)
Ann Intern Med
, vol.155
, pp. 69-79
-
-
Ladabaum, U.1
Wang, G.2
Terdiman, J.3
-
2
-
-
38749113701
-
A prospective, multicenter, population-based study of BRAF mutational analysis for Lynch syndrome screening
-
Bessa X, Ballesté B, Andreu M, et al: A prospective, multicenter, population-based study of BRAF mutational analysis for Lynch syndrome screening. Clin Gastroenterol Hepatol 6:206-214, 2008
-
(2008)
Clin Gastroenterol Hepatol
, vol.6
, pp. 206-214
-
-
Bessa, X.1
Ballesté, B.2
Andreu, M.3
-
3
-
-
59849108362
-
Genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives
-
Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group. Recommendations from the EGAPP Working Group
-
Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Working Group. Recommendations from the EGAPP Working Group: Genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives. Genet Med 11:35-41, 2009
-
(2009)
Genet Med
, vol.11
, pp. 35-41
-
-
-
4
-
-
17944362664
-
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
-
Hampel H, Frankel WL, Martin E, et al: Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 352:1851-1860, 2005
-
(2005)
N Engl J Med
, vol.352
, pp. 1851-1860
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
5
-
-
77952965113
-
Point: Justification for Lynch syndrome screening among all patients with newly diagnosed colorectal cancer
-
Hampel H: Point: Justification for Lynch syndrome screening among all patients with newly diagnosed colorectal cancer. J Natl Compr Canc Netw 8:597-601, 2010
-
(2010)
J Natl Compr Canc Netw
, vol.8
, pp. 597-601
-
-
Hampel, H.1
-
6
-
-
77953006470
-
Counterpoint: Implementing population genetic screening for Lynch syndrome among newly diagnosed colorectal cancer patients - Will the ends justify the means?
-
Hall MJ: Counterpoint: Implementing population genetic screening for Lynch syndrome among newly diagnosed colorectal cancer patients - Will the ends justify the means? J Natl Compr Canc Netw 8:606-611, 2010
-
(2010)
J Natl Compr Canc Netw
, vol.8
, pp. 606-611
-
-
Hall, M.J.1
-
7
-
-
0031551963
-
A National Cancer Institute workshop on hereditary nonpolyposis colorectal cancer syndrome: Meeting highlights and Bethesda guidelines
-
Rodriguez-Bigas MA, Boland CR, Hamilton SR, et al: A National Cancer Institute workshop on hereditary nonpolyposis colorectal cancer syndrome: Meeting highlights and Bethesda guidelines. J Natl Cancer Inst 89:1758-1762, 1997
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 1758-1762
-
-
Rodriguez-Bigas, M.A.1
Boland, C.R.2
Hamilton, S.R.3
-
8
-
-
10744233937
-
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, et al: Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 96:261-268, 2004 (Pubitemid 38256271)
-
(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, C.A.5
Ruschoff, J.6
Fishel, R.7
Lindor, N.M.8
Burgart, L.J.9
Hamelin, R.10
Hamilton, S.R.11
Hiatt, R.A.12
Jass, J.13
Lindblom, A.14
Lynch, H.T.15
Peltomaki, P.16
Ramsey, S.D.17
Rodriguez-Bigas, M.A.18
Vasen, H.F.A.19
Hawk, E.T.20
Barrett, J.C.21
Freedman, A.N.22
Srivastava, S.23
more..
-
9
-
-
57449097359
-
Feasibility of screening for Lynch syndrome among patients with colorectal cancer
-
Hampel H, Frankel WL, Martin E, et al: Feasibility of screening for Lynch syndrome among patients with colorectal cancer. J Clin Oncol 26:5783-5788, 2008
-
(2008)
J Clin Oncol
, vol.26
, pp. 5783-5788
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
10
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer
-
Salovaara R, Loukola A, Kristo P, et al: Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol 18:2193-2200, 2000 (Pubitemid 30350210)
-
(2000)
Journal of Clinical Oncology
, vol.18
, Issue.11
, pp. 2193-2200
-
-
Salovaara, R.1
Loukola, A.2
Kristo, P.3
Kaariainen, H.4
Ahtola, H.5
Eskelinen, M.6
Harkonen, N.7
Julkunen, R.8
Kangas, E.9
Ojala, S.10
Tulikoura, J.11
Valkamo, E.12
Jarvinen, H.13
Mecklin, J.-P.14
Aaltonen, L.A.15
De La, C.A.16
-
12
-
-
84862530392
-
Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results
-
Beamer LC, Grant ML, Espendschied CR, et al: Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results. J Clin Oncol 30:1058-1063, 2012
-
(2012)
J Clin Oncol
, vol.30
, pp. 1058-1063
-
-
Beamer, L.C.1
Grant, M.L.2
Espendschied, C.R.3
-
13
-
-
33749040947
-
Prediction of MLH1 and MSH2 mutations in lynch syndrome
-
DOI 10.1001/jama.296.12.1469
-
Balmaña J, Stockwell DH, Steyerberg EW, et al: Prediction of MLH1 and MSH2 mutations in Lynch syndrome. JAMA 296:1469-1478, 2006 (Pubitemid 44465511)
-
(2006)
Journal of the American Medical Association
, vol.296
, Issue.12
, pp. 1469-1478
-
-
Balmana, J.1
Stockwell, D.H.2
Steyerberg, E.W.3
Stoffel, E.M.4
Deffenbaugh, A.M.5
Reid, J.E.6
Ward, B.7
Scholl, T.8
Hendrickson, B.9
Tazelaar, J.10
Burbidge, L.A.11
Syngal, S.12
-
14
-
-
33745658837
-
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer
-
DOI 10.1056/NEJMoa053493
-
Barnetson RA, Tenesa A, Farrington SM, et al: Identification and survival of carriers of mutations in DNA mismatch repair genes in colon cancers. N Engl J Med 354:2751-2763, 2006 (Pubitemid 43974193)
-
(2006)
New England Journal of Medicine
, vol.354
, Issue.26
, pp. 2751-2763
-
-
Barnetson, R.A.1
Tenesa, A.2
Farrington, S.M.3
Nicholl, I.D.4
Cetnarskyj, R.5
Porteous, M.E.6
Campbell, H.7
Dunlop, M.G.8
-
15
-
-
33749066191
-
Prediction of germline mutations and cancer risk in the lynch syndrome
-
DOI 10.1001/jama.296.12.1479
-
Chen S, Wang W, Lee S, et al: Prediction of germline mutations and cancer risk in the Lynch syndrome. JAMA 296:1479-1487, 2006 (Pubitemid 44465512)
-
(2006)
Journal of the American Medical Association
, vol.296
, Issue.12
, pp. 1479-1487
-
-
Chen, S.1
Wang, W.2
Lee, S.3
Nafa, K.4
Lee, J.5
Romans, K.6
Watson, P.7
Gruber, S.B.8
Euhus, D.9
Kinzler, K.W.10
Jass, J.11
Gallinger, S.12
Lindor, N.M.13
Casey, G.14
Ellis, N.15
Giardiello, F.M.16
Offit, K.17
Parmigiani, G.18
-
16
-
-
51849147419
-
Comparison of predictive models, clinical criteria and molecular tumour screening for the identification of patients with Lynch syndrome in a population-based cohort of colorectal cancer patients
-
Balmaña J, Balaguer F, Castellví-Bel S, et al: Comparison of predictive models, clinical criteria and molecular tumour screening for the identification of patients with Lynch syndrome in a population-based cohort of colorectal cancer patients. J Med Genet 45:557-563, 2008
-
(2008)
J Med Genet
, vol.45
, pp. 557-563
-
-
Balmaña, J.1
Balaguer, F.2
Castellví-Bel, S.3
-
17
-
-
62349128915
-
Prediction of Lynch syndrome in consecutive patients with colorectal cancer
-
Green RC, Parfrey PS, Woods MO, et al: Prediction of Lynch syndrome in consecutive patients with colorectal cancer. J Natl Cancer Inst 101:331-340, 2009
-
(2009)
J Natl Cancer Inst
, vol.101
, pp. 331-340
-
-
Green, R.C.1
Parfrey, P.S.2
Woods, M.O.3
-
18
-
-
74049157657
-
Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer
-
Monzon JG, Cremin C, Armstrong L, et al: Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer. Int J Cancer 126:930-939, 2010
-
(2010)
Int J Cancer
, vol.126
, pp. 930-939
-
-
Monzon, J.G.1
Cremin, C.2
Armstrong, L.3
-
19
-
-
77952681872
-
Report from the Jerusalem Workshop on Lynch Syndrome-Hereditary nonpolyposis colorectal cancer
-
Boland CR, Shike M: Report from the Jerusalem Workshop on Lynch Syndrome-Hereditary nonpolyposis colorectal cancer. Gastroenterology 138: 2197-2201, 2010
-
(2010)
Gastroenterology
, vol.138
, pp. 2197-2201
-
-
Boland, C.R.1
Shike, M.2
-
20
-
-
20244386256
-
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X
-
DOI 10.1001/jama.293.16.1979
-
Lindor NM, Rabe K, Petersen GM, et al: Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X. JAMA 293:1979-1985, 2005 (Pubitemid 40570891)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.16
, pp. 1979-1985
-
-
Lindor, N.M.1
Rabe, K.2
Petersen, G.M.3
Haile, R.4
Casey, G.5
Baron, J.6
Gallinger, S.7
Bapat, B.8
Aronson, M.9
Hopper, J.10
Jass, J.11
LeMarchand, L.12
Grove, J.13
Potter, J.14
Newcomb, P.15
Terdiman, J.P.16
Conrad, P.17
Moslein, G.18
Goldberg, R.19
Ziogas, A.20
Anton-Culver, H.21
De Andrade, M.22
Siegmund, K.23
Thibodeau, S.N.24
Boardman, L.A.25
Seminara, D.26
more..
|