-
1
-
-
65649113258
-
Colorectal cancer incidence in the United States, 1999-2004: an updated analysis of data from the National Program of Cancer Registries and the Surveillance, Epidemiology and End Results Program
-
Rim S.H., Seeff L., Ahmed F., et al. Colorectal cancer incidence in the United States, 1999-2004: an updated analysis of data from the National Program of Cancer Registries and the Surveillance, Epidemiology and End Results Program. Cancer 2009, 115:1967-1976.
-
(2009)
Cancer
, vol.115
, pp. 1967-1976
-
-
Rim, S.H.1
Seeff, L.2
Ahmed, F.3
-
2
-
-
53049087129
-
Young-onset colorectal cancer in patients with no known genetic predisposition: can we increase early recognition and improve outcome?
-
Dozois E.J., Boardman L.A., Suwanthanma W., et al. Young-onset colorectal cancer in patients with no known genetic predisposition: can we increase early recognition and improve outcome?. Medicine (Baltimore) 2008, 87:259-263.
-
(2008)
Medicine (Baltimore)
, vol.87
, pp. 259-263
-
-
Dozois, E.J.1
Boardman, L.A.2
Suwanthanma, W.3
-
3
-
-
58049202257
-
Estimates and projections of value of life lost from cancer deaths in the United States
-
Yabroff K.R., Bradley C.J., Mariotto A.B., et al. Estimates and projections of value of life lost from cancer deaths in the United States. J Natl Cancer Inst 2008, 100:1755-1762.
-
(2008)
J Natl Cancer Inst
, vol.100
, pp. 1755-1762
-
-
Yabroff, K.R.1
Bradley, C.J.2
Mariotto, A.B.3
-
4
-
-
67449084400
-
Increase in incidence of colorectal cancer among young men and women in the United States
-
Siegel R.L., Jemal A., Ward E.M. Increase in incidence of colorectal cancer among young men and women in the United States. Cancer Epidemiol Biomarkers Prev 2009, 18:1695-1698.
-
(2009)
Cancer Epidemiol Biomarkers Prev
, vol.18
, pp. 1695-1698
-
-
Siegel, R.L.1
Jemal, A.2
Ward, E.M.3
-
5
-
-
51449120932
-
Concise handbook of familial cancer susceptibility syndromes: second edition
-
Lindor N.M., McMaster M.L., Lindor C.J., et al. Concise handbook of familial cancer susceptibility syndromes: second edition. J Natl Cancer Inst Monogr 2008, 38:1-93.
-
(2008)
J Natl Cancer Inst Monogr
, vol.38
, pp. 1-93
-
-
Lindor, N.M.1
McMaster, M.L.2
Lindor, C.J.3
-
6
-
-
0032552239
-
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer
-
Wijnen J.T., Vasen H.F., Khan P.M., et al. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer. N Engl J Med 1998, 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
-
8
-
-
34447264031
-
A new variant database for mismatch repair genes associated with Lynch syndrome
-
Woods M.O., Williams P., Careen A., et al. A new variant database for mismatch repair genes associated with Lynch syndrome. Hum Mutat 2007, 28:669-673.
-
(2007)
Hum Mutat
, vol.28
, pp. 669-673
-
-
Woods, M.O.1
Williams, P.2
Careen, A.3
-
9
-
-
0037083484
-
Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors
-
Lindor N.M., Burgart L.J., Leontovich O., et al. Immunohistochemistry versus microsatellite instability testing in phenotyping colorectal tumors. J Clin Oncol 2002, 20:1043-1048.
-
(2002)
J Clin Oncol
, vol.20
, pp. 1043-1048
-
-
Lindor, N.M.1
Burgart, L.J.2
Leontovich, O.3
-
10
-
-
13844251880
-
Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer
-
Casey G., Lindor N.M., Papadopoulos N., et al. Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer. JAMA 2005, 293:799-809.
-
(2005)
JAMA
, vol.293
, pp. 799-809
-
-
Casey, G.1
Lindor, N.M.2
Papadopoulos, N.3
-
11
-
-
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., et al. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology 1999, 116:1453-1456.
-
(1999)
Gastroenterology
, vol.116
, pp. 1453-1456
-
-
Vasen, H.F.1
Watson, P.2
Mecklin, J.P.3
-
12
-
-
33745658837
-
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer
-
Barnetson R.A., Tenesa A., Farrington S.M., et al. Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. N Engl J Med 2006, 354:2751-2763.
-
(2006)
N Engl J Med
, vol.354
, pp. 2751-2763
-
-
Barnetson, R.A.1
Tenesa, A.2
Farrington, S.M.3
-
13
-
-
17944362664
-
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer)
-
Hampel H., Frankel W.L., Martin E., et al. Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). N Engl J Med 2005, 352:1851-1860.
-
(2005)
N Engl J Med
, vol.352
, pp. 1851-1860
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
14
-
-
0034011564
-
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
-
Jarvinen H.J., Aarnio M., Mustonen H., et al. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology 2000, 118:829-834.
-
(2000)
Gastroenterology
, vol.118
, pp. 829-834
-
-
Jarvinen, H.J.1
Aarnio, M.2
Mustonen, H.3
-
15
-
-
29144505362
-
Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures
-
Wagner A., van Kessel I., Kriege M.G., et al. Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures. Fam Cancer 2005, 4:295-300.
-
(2005)
Fam Cancer
, vol.4
, pp. 295-300
-
-
Wagner, A.1
van Kessel, I.2
Kriege, M.G.3
-
16
-
-
33644864321
-
Decrease in mortality in Lynch syndrome families because of surveillance
-
de Jong A.E., Hendriks Y.M., Kleibeuker J.H., et al. Decrease in mortality in Lynch syndrome families because of surveillance. Gastroenterology 2006, 130:665-671.
-
(2006)
Gastroenterology
, vol.130
, pp. 665-671
-
-
de Jong, A.E.1
Hendriks, Y.M.2
Kleibeuker, J.H.3
-
17
-
-
1842477266
-
Current clinical selection strategies for identification of hereditary non-polyposis colorectal cancer families are inadequate: a meta-analysis
-
Kievit W., de Bruin J.H., Adang E.M., et al. Current clinical selection strategies for identification of hereditary non-polyposis colorectal cancer families are inadequate: a meta-analysis. Clin Genet 2004, 65:308-316.
-
(2004)
Clin Genet
, vol.65
, pp. 308-316
-
-
Kievit, W.1
de Bruin, J.H.2
Adang, E.M.3
-
18
-
-
38849170356
-
Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer
-
Newcomb P.A., Baron J., Cotterchio M., et al. Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. Cancer Epidemiol Biomarkers Prev 2007, 16:2331-2343.
-
(2007)
Cancer Epidemiol Biomarkers Prev
, vol.16
, pp. 2331-2343
-
-
Newcomb, P.A.1
Baron, J.2
Cotterchio, M.3
-
19
-
-
55349099844
-
Identification in daily practice of patients with Lynch syndrome (hereditary nonpolyposis colorectal cancer): revised Bethesda guidelines-based approach versus molecular screening
-
quiz 2836
-
Julie C., Tresallet C., Brouquet A., et al. Identification in daily practice of patients with Lynch syndrome (hereditary nonpolyposis colorectal cancer): revised Bethesda guidelines-based approach versus molecular screening. Am J Gastroenterol 2008, 103:2825-2835. quiz 2836.
-
(2008)
Am J Gastroenterol
, vol.103
, pp. 2825-2835
-
-
Julie, C.1
Tresallet, C.2
Brouquet, A.3
-
20
-
-
57449097359
-
Feasibility of screening for Lynch syndrome among patients with colorectal cancer
-
Hampel H., Frankel W.L., Martin E., et al. Feasibility of screening for Lynch syndrome among patients with colorectal cancer. J Clin Oncol 2008, 26:5783-5788.
-
(2008)
J Clin Oncol
, vol.26
, pp. 5783-5788
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
-
21
-
-
58149144567
-
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1
-
Ligtenberg M.J., Kuiper R.P., Chan T.L., et al. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1. Nat Genet 2009, 41:112-117.
-
(2009)
Nat Genet
, vol.41
, pp. 112-117
-
-
Ligtenberg, M.J.1
Kuiper, R.P.2
Chan, T.L.3
-
22
-
-
21344454662
-
Assessing the predictive accuracy of QUICKI as a surrogate index for insulin sensitivity using a calibration model
-
Chen H., Sullivan G., Quon M.J. Assessing the predictive accuracy of QUICKI as a surrogate index for insulin sensitivity using a calibration model. Diabetes 2005, 54:1914-1925.
-
(2005)
Diabetes
, vol.54
, pp. 1914-1925
-
-
Chen, H.1
Sullivan, G.2
Quon, M.J.3
-
23
-
-
33749040947
-
Prediction of MLH1 and MSH2 mutations in Lynch syndrome
-
Balmana J., Stockwell D.H., Steyerberg E.W., et al. Prediction of MLH1 and MSH2 mutations in Lynch syndrome. JAMA 2006, 296:1469-1478.
-
(2006)
JAMA
, vol.296
, pp. 1469-1478
-
-
Balmana, J.1
Stockwell, D.H.2
Steyerberg, E.W.3
-
24
-
-
79952195445
-
Quantitative models for predicting mutations in Lynch syndrome genes
-
Chen S., Euhus D.M., Parmigiani G. Quantitative models for predicting mutations in Lynch syndrome genes. Curr Colorectal Cancer Reports 2007, 3:206-211.
-
(2007)
Curr Colorectal Cancer Reports
, vol.3
, pp. 206-211
-
-
Chen, S.1
Euhus, D.M.2
Parmigiani, G.3
-
25
-
-
62349128915
-
Prediction of Lynch syndrome in consecutive patients with colorectal cancer
-
Green R.C., Parfrey P.S., Woods M.O., et al. Prediction of Lynch syndrome in consecutive patients with colorectal cancer. J Natl Cancer Inst 2009, 101:331-340.
-
(2009)
J Natl Cancer Inst
, vol.101
, pp. 331-340
-
-
Green, R.C.1
Parfrey, P.S.2
Woods, M.O.3
-
26
-
-
45249083654
-
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome
-
Clendenning M., Senter L., Hampel H., et al. A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome. J Med Genet 2008, 45:340-345.
-
(2008)
J Med Genet
, vol.45
, pp. 340-345
-
-
Clendenning, M.1
Senter, L.2
Hampel, H.3
-
27
-
-
73849097853
-
Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer
-
South C.D., Yearsley M., Martin E., et al. Immunohistochemistry staining for the mismatch repair proteins in the clinical care of patients with colorectal cancer. Genet Med 2009, 11:812-817.
-
(2009)
Genet Med
, vol.11
, pp. 812-817
-
-
South, C.D.1
Yearsley, M.2
Martin, E.3
-
28
-
-
70149086692
-
Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch syndrome (hereditary nonpolyposis colorectal cancer) cases
-
Mueller J., Gazzoli I., Bandipalliam P., et al. Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch syndrome (hereditary nonpolyposis colorectal cancer) cases. Cancer Res 2009, 69:7053-7061.
-
(2009)
Cancer Res
, vol.69
, pp. 7053-7061
-
-
Mueller, J.1
Gazzoli, I.2
Bandipalliam, P.3
-
30
-
-
51649092608
-
The counsellees' view of an unclassified variant in BRCA1/2: recall, interpretation, and impact on life
-
Vos J., Otten W., van Asperen C., et al. The counsellees' view of an unclassified variant in BRCA1/2: recall, interpretation, and impact on life. Psychooncology 2008, 17:822-830.
-
(2008)
Psychooncology
, vol.17
, pp. 822-830
-
-
Vos, J.1
Otten, W.2
van Asperen, C.3
-
31
-
-
69849099009
-
Colorectal cancer risk perception on the basis of genetic test results in individuals at risk for Lynch syndrome
-
Grover S., Stoffel E.M., Mercado R.C., et al. Colorectal cancer risk perception on the basis of genetic test results in individuals at risk for Lynch syndrome. J Clin Oncol 2009, 27:3981-3986.
-
(2009)
J Clin Oncol
, vol.27
, pp. 3981-3986
-
-
Grover, S.1
Stoffel, E.M.2
Mercado, R.C.3
|