-
1
-
-
0028350601
-
Mutation of a mutl homolog in hereditary colon cancer
-
Papadopoulos N, Nicolaides NC, Wei YF, Ruben SM, Carter KC, Rosen CA, et al. Mutation of a mutL homolog in hereditary colon cancer. Science 1994;263:1625-9.
-
(1994)
Science
, vol.263
, pp. 1625-1629
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Wei, Y.F.3
Ruben, S.M.4
Carter, K.C.5
Rosen, C.A.6
-
2
-
-
0028221943
-
Mutation in the dna mismatch repair gene homologue hmlh 1 is associated with hereditary non-polyposis colon cancer
-
Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, et al. Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer. Nature 1994;368:258-61.
-
(1994)
Nature
, vol.368
, pp. 258-261
-
-
Bronner, C.E.1
Baker, S.M.2
Morrison, P.T.3
Warren, G.4
Smith, L.G.5
Lescoe, M.K.6
-
3
-
-
0027145633
-
Mutations of a muts homolog in hereditary nonpolyposis colorectal cancer
-
Leach FS, Nicolaides NC, Papadopoulos N, Liu B, Jen J, Parsons R, et al. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell 1993;75:1215-25.
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
Nicolaides, N.C.2
Papadopoulos, N.3
Liu, B.4
Jen, J.5
Parsons, R.6
-
4
-
-
0031278322
-
Germline mutation of msh6 as the cause of hereditary nonpolyposis colorectal cancer
-
Miyaki M, Konishi M, Tanaka K, Kikuchi-Yanoshita R, Muraoka M, Yasuno M, et al. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. Nat Genet 1997;17:271-2.
-
(1997)
Nat Genet
, vol.17
, pp. 271-272
-
-
Miyaki, M.1
Konishi, M.2
Tanaka, K.3
Kikuchi-Yanoshita, R.4
Muraoka, M.5
Yasuno, M.6
-
5
-
-
0030870631
-
Germ-line mutation of the hmsh6/gtbp gene in an atypical hereditary nonpolyposis colorectal cancer kindred
-
Akiyama Y, Sato H, Yamada T, Nagasaki H, Tsuchiya A, Abe R, et al. Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred. Cancer Res 1997;57:3920-3.
-
(1997)
Cancer Res
, vol.57
, pp. 3920-3923
-
-
Akiyama, Y.1
Sato, H.2
Yamada, T.3
Nagasaki, H.4
Tsuchiya, A.5
Abe, R.6
-
6
-
-
0027933070
-
Mutations of two pms homologues in hereditary nonpolyposis colon cancer
-
Nicolaides NC, Papadopoulos N, Liu B, Weit Y-F, Carter KC, Ruben SM, et al. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature 1994;371:75-80.
-
(1994)
Nature
, vol.371
, pp. 75-80
-
-
Nicolaides, N.C.1
Papadopoulos, N.2
Liu, B.3
Weit, Y.-F.4
Carter, K.C.5
Ruben, S.M.6
-
7
-
-
32044450030
-
Heterozygous mutations in pms2 cause hereditary nonpolyposis colorectal carcinoma (lynch syndrome)
-
Hendriks YM, Jagmohan-Changur S, van der Klift HM, Morreau H, van Puijenbroek M, Tops C, et al. Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome). Gastroenterology 2006;130:312-22.
-
(2006)
Gastroenterology
, vol.130
, pp. 312-322
-
-
Hendriks, Y.M.1
Jagmohan-Changur, S.2
Van Der Klift, H.M.3
Morreau, H.4
Van Puijenbroek, M.5
Tops, C.6
-
8
-
-
58149144567
-
Heritable somatic methylation and inactivation of msh2 in families with lynch syndrome due to deletion of the 30 exons of tacstd1
-
Ligtenberg MJ, Kuiper RP, Chan TL, Goossens M, Hebeda KM, Voorendt M, et al. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 30 exons of TACSTD1. Nat Genet 2009;41:112-7.
-
(2009)
Nat Genet
, vol.41
, 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
-
9
-
-
59749085710
-
Deletions removing the last exon of tacstd1 constitute a distinct class of mutations predisposing to lynch syndrome
-
Kovacs ME, Papp J, Szentirmay Z, Otto S, Olah E. Deletions removing the last exon of TACSTD1 constitute a distinct class of mutations predisposing to Lynch syndrome. Hum Mutat 2009; 30:197-203.
-
(2009)
Hum Mutat
, vol.30
, pp. 197-203
-
-
Kovacs, M.E.1
Papp, J.2
Szentirmay, Z.3
Otto, S.4
Olah, E.5
-
10
-
-
24144484905
-
The incidence of lynch syndrome
-
de la Chapelle A. The incidence of Lynch syndrome. Fam Cancer 2005;4:233-7.
-
(2005)
Fam Cancer
, vol.4
, pp. 233-237
-
-
De La Chapelle, A.1
-
11
-
-
0034538160
-
Population carrier frequency ofhmsh2 and hmlh1 mutations
-
Dunlop MG, FarringtonSM, Nicholl I, Aaltonen L, Petersen G, Porteous M, et al. Population carrier frequency ofhMSH2 and hMLH1 mutations. Br J Cancer 2000;83:1643-5.
-
(2000)
Br J Cancer
, vol.83
, pp. 1643-1645
-
-
Dunlop, M.G.1
Farrington, S.M.2
Nicholl, I.3
Aaltonen, L.4
Petersen, G.5
Porteous, M.6
-
12
-
-
78650844345
-
The search for unaffected individuals with lynch syndrome: Do the ends justify the means?
-
Hampel H, de la Chapelle A. The search for unaffected individuals with Lynch syndrome: do the ends justify the means? Cancer Prev Res 2011;4:1-5.
-
(2011)
Cancer Prev Res
, vol.4
, pp. 1-5
-
-
Hampel, H.1
De La Chapelle, A.2
-
13
-
-
79958071334
-
Cancer risks associated with germline mutations in mlh1, msh2, and msh6 genes in lynch syndrome
-
Bonadona V, Bonaiti B, Olschwang S, Grandjouan S, Huiart L, Longy M, et al. Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. JAMA 2011;305: 2304-10.
-
(2011)
JAMA
, vol.305
, pp. 2304-2310
-
-
Bonadona, V.1
Bonaiti, B.2
Olschwang, S.3
Grandjouan, S.4
Huiart, L.5
Longy, M.6
-
14
-
-
84860605783
-
Colorectal and other cancer risks for carriers and noncarriers from families with a dna mismatch repair gene mutation: A prospective cohort study
-
Win AK, Young JP, Lindor NM, Tucker K, Ahnen D, Young GP, et al. Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study. J Clin Oncol 2012;30:958-64.
-
(2012)
J Clin Oncol
, vol.30
, pp. 958-964
-
-
Win, A.K.1
Young, J.P.2
Lindor, N.M.3
Tucker, K.4
Ahnen, D.5
Young, G.P.6
-
15
-
-
84873942317
-
Cancer risks for mlh1 andmsh2 mutation carriers
-
Dowty JG, Win AK, Buchanan DD, Lindor NM, Macrae FA, Clendenning M, et al. Cancer risks for MLH1 andMSH2 mutation carriers. Hum Mutat 2013;34:490-7.
-
(2013)
Hum Mutat
, vol.34
, pp. 490-497
-
-
Dowty, J.G.1
Win, A.K.2
Buchanan, D.D.3
Lindor, N.M.4
Macrae, F.A.5
Clendenning, M.6
-
16
-
-
0043195893
-
Prostate cancer is part of the hereditary non-polyposis colorectal cancer (hnpcc) tumor spectrum
-
SoraviaC, van derKliftH,BrundlerMA,Blouin JL,Wijnen J,HutterP, et al. Prostate cancer is part of the hereditary non-polyposis colorectal cancer (HNPCC) tumor spectrum. Am J Med Genet A 2003;121A:159-62.
-
(2003)
Am J Med Genet A
, vol.121
, Issue.A
, pp. 159-162
-
-
Soravia, C.1
Van DerKlift, H.2
Brundler, M.A.3
Blouin, J.L.4
Wijnen, J.5
Hutter, P.6
-
17
-
-
78649249282
-
Neuroendocrine-type prostatic adenocarcinoma with microsatellite instability in a patient with lynch syndrome
-
Wagner DG, Gatalica Z, Lynch HT, Kohl S, Johansson SL, Lele SM. Neuroendocrine-type prostatic adenocarcinoma with microsatellite instability in a patient with lynch syndrome. Int J Surg Pathol 2010;18:550-3.
-
(2010)
Int J Surg Pathol
, vol.18
, pp. 550-553
-
-
Wagner, D.G.1
Gatalica, Z.2
Lynch, H.T.3
Kohl, S.4
Johansson, S.L.5
Lele, S.M.6
-
18
-
-
2442708840
-
Penetrance and expressivity of msh6 germline mutations in seven kindreds not ascertained by family history
-
Buttin BM, Powell MA, Mutch DG, Babb SA, Huettner PC, Edmonston TB, et al. Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history. Am J Hum Genet 2004;74:1262-9.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1262-1269
-
-
Buttin, B.M.1
Powell, M.A.2
Mutch, D.G.3
Babb, S.A.4
Huettner, P.C.5
Edmonston, T.B.6
-
19
-
-
70349321608
-
Germ-line mutations in mismatch repair genes associated with prostate cancer
-
Grindedal EM, Moller P, Eeles R, Stormorken AT, Bowitz-Lothe IM, Landro SM, et al. Germ-line mutations in mismatch repair genes associated with prostate cancer. Cancer Epidemiol Biomarkers Prev 2009;18:2460-7.
-
(2009)
Cancer Epidemiol Biomarkers Prev
, vol.18
, pp. 2460-2467
-
-
Grindedal, E.M.1
Moller, P.2
Eeles, R.3
Stormorken, A.T.4
Bowitz-Lothe, I.M.5
Landro, S.M.6
-
20
-
-
84896538013
-
-
submitted
-
Rosty C, Walsh MD, Lindor NM, Thibodeau S, Mundt E, Gallinger S, et al. High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the Colon Cancer Family Registry. submitted 2013.
-
(2013)
High prevalence of mismatch repair deficiency in prostate cancers diagnosed in mismatch repair gene mutation carriers from the Colon Cancer Family Registry
-
-
Rosty, C.1
Walsh, M.D.2
Lindor, N.M.3
Thibodeau, S.4
Mundt, E.5
Gallinger, S.6
-
21
-
-
79951858605
-
Hereditary prostate cancer as a feature of lynch syndrome
-
Bauer C, Ray A, Halstead-Nussloch B, Dekker R, Raymond V, Gruber S, et al. Hereditary prostate cancer as a feature of Lynch Syndrome. Fam Cancer 2011;10:37-42.
-
(2011)
Fam Cancer
, vol.10
, pp. 37-42
-
-
Bauer, C.1
Ray, A.2
Halstead-Nussloch, B.3
Dekker, R.4
Raymond, V.5
Gruber, S.6
-
22
-
-
0032941343
-
Cancer risk in mutation carriers of dna-mismatch-repair genes
-
Aarnio M, Sankila R, Pukkala E, Salovaara R, Aaltonen LA, de la Chapelle A, et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer 1999;81:214-8.
-
(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
-
23
-
-
0034922346
-
Second primary cancers after sporadic and familial colorectal cancer
-
Hemminki K, Li X, Dong C. Second primary cancers after sporadic and familial colorectal cancer. Cancer Epidemiol Biomarkers Prev 2001; 10:793-8.
-
(2001)
Cancer Epidemiol Biomarkers Prev
, vol.10
, pp. 793-798
-
-
Hemminki, K.1
Li, X.2
Dong, C.3
-
24
-
-
0035162347
-
Hereditary nonpolyposis colorectal cancer in 95 families: Differences and similarities between mutation-positive and mutationnegative kindreds
-
Scott RJ, McPhillips M, Meldrum CJ, Fitzgerald PE, Adams K, Spigelman AD, et al. Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutationnegative kindreds. Am J Hum Genet 2001;68:118-27.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 118-127
-
-
Scott, R.J.1
McPhillips, M.2
Meldrum, C.J.3
Fitzgerald, P.E.4
Adams, K.5
Spigelman, A.D.6
-
25
-
-
16344388386
-
Clinical phenotype and prevalence of hereditary nonpolyposis colorectal cancer syndrome in chinese population
-
Zhang YZ, Sheng JQ, Li SR, Zhang H. Clinical phenotype and prevalence of hereditary nonpolyposis colorectal cancer syndrome in Chinese population. World J Gastroenterol 2005;11:1481-8.
-
(2005)
World J Gastroenterol
, vol.11
, pp. 1481-1488
-
-
Zhang, Y.Z.1
Sheng, J.Q.2
Li, S.R.3
Zhang, H.4
-
26
-
-
33749029656
-
Genotype-phenotype comparison of german mlh1 and msh2 mutation carriers clinically affected with lynch syndrome: A report by the german hnpcc consortium
-
Goecke T, Schulmann K, Engel C, Holinski-Feder E, Pagenstecher C, Schackert HK, et al. Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium. J Clin Oncol 2006;24:4285-92.
-
(2006)
J Clin Oncol
, vol.24
, pp. 4285-4292
-
-
Goecke, T.1
Schulmann, K.2
Engel, C.3
Holinski-Feder, E.4
Pagenstecher, C.5
Schackert, H.K.6
-
27
-
-
33745566715
-
Extracolonic cancers associated with hereditary nonpolyposis colorectal cancer in the utah population database
-
Maul JS, Warner NR, Kuwada SK, Burt RW, Cannon-Albright LA. Extracolonic cancers associated with hereditary nonpolyposis colorectal cancer in the Utah Population Database. Am J Gastroenterol 2006;101:1591-6.
-
(2006)
Am J Gastroenterol
, vol.101
, pp. 1591-1596
-
-
Maul, J.S.1
Warner, N.R.2
Kuwada, S.K.3
Burt, R.W.4
Cannon-Albright, L.A.5
-
28
-
-
58849130663
-
Cumulative lifetime incidence of extracolonic cancers in lynch syndrome: A report of 121 families with proven mutations
-
Barrow E, Robinson L, Alduaij W, Shenton A, Clancy T, Lalloo F, et al. Cumulative lifetime incidence of extracolonic cancers in Lynch syndrome: a report of 121 families with proven mutations. Clin Genet 2009;75:141-9.
-
(2009)
Clin Genet
, vol.75
, pp. 141-149
-
-
Barrow, E.1
Robinson, L.2
Alduaij, W.3
Shenton, A.4
Clancy, T.5
Lalloo, F.6
-
29
-
-
70449524309
-
Cancer risk in a cohort of subjects carrying a single mismatch repair gene mutation
-
Stupart DA, Goldberg PA, Algar U, Ramesar R. Cancer risk in a cohort of subjects carrying a single mismatch repair gene mutation. Fam Cancer 2009;8:519-23.
-
(2009)
Fam Cancer
, vol.8
, pp. 519-523
-
-
Stupart, D.A.1
Goldberg, P.A.2
Algar, U.3
Ramesar, R.4
-
30
-
-
78650212145
-
Frequency of extracolonic tumors in brazilian families with lynch syndrome: Analysis of a hereditary colorectal cancer institutional registry
-
da SilvaFC, de Oliveira LP, Santos EM, Nakagawa WT, Aguiar Junior S, Valentin MD, et al. Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registry. Fam Cancer 2010;9:563-70.
-
(2010)
Fam Cancer
, vol.9
, pp. 563-570
-
-
Da Silva, F.C.1
De Oliveira, L.P.2
Santos, E.M.3
Nakagawa, W.T.4
Aguiar Junior, S.5
Valentin, M.D.6
-
31
-
-
79551563973
-
Msh6 and pms2 mutation positive australian lynch syndrome families: Novel mutations, cancer risk and age of diagnosis of colorectal cancer
-
Talseth-Palmer BA, McPhillips M, Groombridge C, Spigelman A, Scott RJ. MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer. Hered Cancer Clin Pract 2010;8:5.
-
(2010)
Hered Cancer Clin Pract
, vol.8
, pp. 5
-
-
Talseth-Palmer, B.A.1
McPhillips, M.2
Groombridge, C.3
Spigelman, A.4
Scott, R.J.5
-
32
-
-
84870747205
-
Risks of less common cancers in proven mutation carriers with lynch syndrome
-
Engel C, Loeffler M, Steinke V, Rahner N, Holinski-Feder E, Dietmaier W, et al. Risks of less common cancers in proven mutation carriers with lynch syndrome. J Clin Oncol 2012;30:4409-15.
-
(2012)
J Clin Oncol
, vol.30
, pp. 4409-4415
-
-
Engel, C.1
Loeffler, M.2
Steinke, V.3
Rahner, N.4
Holinski-Feder, E.5
Dietmaier, W.6
-
33
-
-
84866658167
-
Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome
-
Win AK, Lindor NM, Young JP, Macrae FA, Young GP, Williamson E, et al. Risks of primary extracolonic cancers following colorectal cancer in Lynch syndrome. J Natl Cancer Inst 2012;104:1363-72.
-
(2012)
J Natl Cancer Inst
, vol.104
, pp. 1363-1372
-
-
Win, A.K.1
Lindor, N.M.2
Young, J.P.3
Macrae, F.A.4
Young, G.P.5
Williamson, E.6
-
34
-
-
84870400389
-
Cancer spectrum in dna mismatch repair gene mutation carriers: Results from a hospital based lynch syndrome registry
-
Pande M, Wei C, Chen J, Amos CI, Lynch PM, Lu KH, et al. Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry. Fam Cancer 2012;11: 441-7.
-
(2012)
Fam Cancer
, vol.11
, pp. 441-447
-
-
Pande, M.1
Wei, C.2
Chen, J.3
Amos, C.I.4
Lynch, P.M.5
Lu, K.H.6
-
35
-
-
84873414349
-
The spectrum of urological malignancy in lynch syndrome
-
Barrow PJ, Ingham S, O'Hara C, Green K, McIntyre I, Lalloo F, et al. The spectrum of urological malignancy in Lynch syndrome. Fam Cancer 2013;12:57-63.
-
(2013)
Fam Cancer
, vol.12
, pp. 57-63
-
-
Barrow, P.J.1
Ingham, S.2
O'Hara, C.3
Green, K.4
McIntyre, I.5
Lalloo, F.6
-
36
-
-
84879468424
-
Elevated risk of prostate cancer among men with lynch syndrome
-
Raymond VM, Mukherjee B, Wang F, Huang SC, Stoffel EM, Kastrinos F, et al. Elevated risk of prostate cancer among men with Lynch syndrome. J Clin Oncol 2013;31:1713-8.
-
(2013)
J Clin Oncol
, vol.31
, pp. 1713-1718
-
-
Raymond, V.M.1
Mukherjee, B.2
Wang, F.3
Huang, S.C.4
Stoffel, E.M.5
Kastrinos, F.6
-
37
-
-
84876900933
-
Revised guidelines for the clinical management of lynch syndrome (hnpcc): Recommendations by a group of european experts
-
Vasen HF, Blanco I, Aktan-Collan K, Gopie JP, Alonso A, Aretz S, et al. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts. Gut 2013;62:812-23.
-
(2013)
Gut
, vol.62
, pp. 812-823
-
-
Vasen, H.F.1
Blanco, I.2
Aktan-Collan, K.3
Gopie, J.P.4
Alonso, A.5
Aretz, S.6
-
38
-
-
63249118690
-
Screening and prostate-cancer mortality in a randomized european study
-
Schroder FH, Hugosson J, Roobol MJ, Tammela TL, Ciatto S, Nelen V, et al. Screening and prostate-cancer mortality in a randomized European study. N Engl J Med 2009;360:1320-8.
-
(2009)
N Engl J Med
, vol.360
, pp. 1320-1328
-
-
Schroder, F.H.1
Hugosson, J.2
Roobol, M.J.3
Tammela, T.L.4
Ciatto, S.5
Nelen, V.6
-
39
-
-
84896525879
-
-
PubMed. Available from
-
PubMed. Available from: http://www.ncbi.nlm.nih.gov/pubmed
-
-
-
-
40
-
-
0025848680
-
The international collaborative group on hereditary non-polyposis colorectal cancer (icghnpcc)
-
Vasen HF, Mecklin JP, Khan PM, Lynch HT. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICGHNPCC). Dis Colon Rectum 1991;34:424-5.
-
(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
-
41
-
-
0033063711
-
New clinical criteria for hereditary nonpolyposis colorectal cancer (hnpcc, lynch syndrome) proposed by the international collaborative group on hnpcc
-
Vasen HFA, Watson P, Mecklin JP, Lynch HT. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC. Gastroenterology 1999;116:1453-6.
-
(1999)
Gastroenterology
, vol.116
, pp. 1453-1456
-
-
Vasen, H.F.A.1
Watson, P.2
Mecklin, J.P.3
Lynch, H.T.4
-
42
-
-
10744233937
-
Revised bethesda guidelines for hereditary nonpolyposis colorectal cancer (lynch syndrome) and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, Syngal S, Chapelle Adl, Ruschoff J, et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 2004;96:261-8.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
Syngal, S.4
Adl, C.5
Ruschoff, J.6
-
43
-
-
84896496472
-
-
StataCorp College Station, TX: StataCorp LP
-
StataCorp. Stata Statistical Software: Release 12. College Station, TX: StataCorp LP; 2011.
-
Stata Statistical Software: Release 12
, vol.2011
-
-
-
44
-
-
17644421000
-
-
Bethesda, MD: National Cancer Institute
-
Ries L, Eisner M, Kosary C, Hankey B, Miller B, Clegg L, et al. SEER Cancer Statistics Review, 1975-2000. Bethesda, MD: National Cancer Institute; 2003.
-
SEER Cancer Statistics Review, 1975-2000
, vol.2003
-
-
Ries, L.1
Eisner, M.2
Kosary, C.3
Hankey, B.4
Miller, B.5
Clegg, L.6
-
45
-
-
0142232032
-
Value of histopathology in predicting microsatellite instability in hereditary nonpolyposis colorectal cancer and sporadic colorectal cancer
-
Shia J, Ellis NA, Paty PB, Nash GM, Qin J, Offit K, et al. Value of histopathology in predicting microsatellite instability in hereditary nonpolyposis colorectal cancer and sporadic colorectal cancer. Am J Surg Pathol 2003;27:1407-17.
-
(2003)
Am J Surg Pathol
, vol.27
, pp. 1407-1417
-
-
Shia, J.1
Ellis, N.A.2
Paty, P.B.3
Nash, G.M.4
Qin, J.5
Offit, K.6
-
46
-
-
34447251079
-
Pathology features in bethesda guidelines predict colorectal cancer microsatellite instability: A population-based study
-
Jenkins MA, Hayashi S, O'Shea AM, Burgart LJ, Smyrk TC, Shimizu D, et al. Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study. Gastroenterology 2007;133:48-56.
-
(2007)
Gastroenterology
, vol.133
, pp. 48-56
-
-
Jenkins, M.A.1
Hayashi, S.2
O'Shea, A.M.3
Burgart, L.J.4
Smyrk, T.C.5
Shimizu, D.6
-
47
-
-
0036096514
-
Hereditary nonpolyposis colorectal cancer: Current risks of colorectal cancer largely overestimated
-
Carayol J, Khlat M, Maccario J, Bonaiti-Pellie C. Hereditary nonpolyposis colorectal cancer: current risks of colorectal cancer largely overestimated. J Med Genet 2002;39:335-9.
-
(2002)
J Med Genet
, vol.39
, pp. 335-339
-
-
Carayol, J.1
Khlat, M.2
Maccario, J.3
Bonaiti-Pellie, C.4
-
48
-
-
0028873796
-
Inherent intractability of the ascertainment problem for pedigree data: A general likelihood framework
-
Vieland VJ, Hodge SE. Inherent intractability of the ascertainment problem for pedigree data: a general likelihood framework. Am J Hum Genet 1995;56:33-43.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 33-43
-
-
Vieland, V.J.1
Hodge, S.E.2
-
49
-
-
84883475375
-
Is prostate cancer a lynch syndrome cancer?
-
Win AK. Is prostate cancer a Lynch syndrome cancer? Asian J Androl 2013;15:588-9.
-
(2013)
Asian J Androl
, vol.15
, pp. 588-589
-
-
Win, A.K.1
-
50
-
-
74549203193
-
Population-based study of the association of variants in mismatch repair genes with prostate cancer risk and outcomes
-
Langeberg WJ, Kwon EM, Koopmeiners JS, Ostrander EA, Stanford JL. Population-based study of the association of variants in mismatch repair genes with prostate cancer risk and outcomes. Cancer Epidemiol Biomarkers Prev 2010;19:258-64.
-
(2010)
Cancer Epidemiol Biomarkers Prev
, vol.19
, pp. 258-264
-
-
Langeberg, W.J.1
Kwon, E.M.2
Koopmeiners, J.S.3
Ostrander, E.A.4
Stanford, J.L.5
-
51
-
-
67349189451
-
Polymorphisms of mlh1 in benign prostatic hyperplasia and sporadic prostate cancer
-
Tanaka Y, Zaman MS, Majid S, Liu J, Kawakami K, Shiina H, et al. Polymorphisms of MLH1 in benign prostatic hyperplasia and sporadic prostate cancer. Biochem Biophys Res Commun 2009;383: 440-4.
-
(2009)
Biochem Biophys Res Commun
, vol.383
, pp. 440-444
-
-
Tanaka, Y.1
Zaman, M.S.2
Majid, S.3
Liu, J.4
Kawakami, K.5
Shiina, H.6
-
52
-
-
41949109349
-
Mismatch repair genemsh3polymorphismis associated with the risk of sporadic prostate cancer
-
Hirata H, Hinoda Y, Kawamoto K, Kikuno N, Suehiro Y, Okayama N, et al. Mismatch repair geneMSH3polymorphismis associated with the risk of sporadic prostate cancer. J Urol 2008;179:2020-4.
-
(2008)
J Urol
, vol.179
, pp. 2020-2024
-
-
Hirata, H.1
Hinoda, Y.2
Kawamoto, K.3
Kikuno, N.4
Suehiro, Y.5
Okayama, N.6
-
53
-
-
84877022133
-
Association between mismatch repair gene msh3 codons 1036 and 222 polymorphisms and sporadic prostate cancer in the iranian population
-
Jafary F, Salehi M, Sedghi M, Nouri N, Jafary F, Sadeghi F, et al. Association between mismatch repair gene MSH3 codons 1036 and 222 polymorphisms and sporadic prostate cancer in the Iranian population. Asian Pac J Cancer Prev 2012;13:6055-7.
-
(2012)
Asian Pac J Cancer Prev
, vol.13
, pp. 6055-6057
-
-
Jafary, F.1
Salehi, M.2
Sedghi, M.3
Nouri, N.4
Jafary, F.5
Sadeghi, F.6
-
54
-
-
78049485263
-
Estimates of worldwide burden of cancer in 2008:Globocan2008
-
Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008:GLOBOCAN2008. Int J Cancer 2010;127:2893-917.
-
(2010)
Int J Cancer
, vol.127
, pp. 2893-2917
-
-
Ferlay, J.1
Shin, H.R.2
Bray, F.3
Forman, D.4
Mathers, C.5
Parkin, D.M.6
-
55
-
-
0031551963
-
A national cancer institute workshop on hereditary nonpolyposis colorectal cancer syndrome: Meeting highlights and bethesda guidelines
-
Rodriguez-Bigas M, Boland C, Hamilton S, Henson D, Srivastava S, Jass J, et al. A National Cancer Institute workshop on hereditary nonpolyposis colorectal cancer syndrome: meeting highlights and Bethesda guidelines. J Natl Cancer Inst 1997;89:1758-62.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 1758-1762
-
-
Rodriguez-Bigas, M.1
Boland, C.2
Hamilton, S.3
Henson, D.4
Srivastava, S.5
Jass, J.6
|