-
1
-
-
33748328364
-
Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term
-
Jass JR. Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term. World J Gastroenterol 2006;12:4943-50.
-
(2006)
World J Gastroenterol
, vol.12
, pp. 4943-4950
-
-
Jass, J.R.1
-
2
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos N, Nicolaides NC, Wei YF, Ruben SM, Carter KC, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM, Adams MD, Venter JC, Hamilton SR, Petersen GM, Watson P, Lynch HT, Peltomaki P, Mecklin JP, de La Chapelle A, Kinzler KW, Vogelstein B. 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
Haseltine, W.A.7
Fleischmann, R.D.8
Fraser, C.M.9
Adams, M.D.10
Venter, J.C.11
Hamilton, S.R.12
Petersen, G.M.13
Watson, P.14
Lynch, H.T.15
Peltomaki, P.16
Mecklin, J.P.17
de La Chapelle, A.18
Kinzler, K.W.19
Vogelstein, B.20
more..
-
3
-
-
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, Kane M, Earabino C, Lipford J, Lindblom A, Tannergard P, Bollag RJ, Godwin AR, Ward DC, Nordenskjld M, Fishel R, Kolodner R, Liskay RM. 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
Kane, M.7
Earabino, C.8
Lipford, J.9
Lindblom, A.10
Tannergard, P.11
Bollag, R.J.12
Godwin, A.R.13
Ward, D.C.14
Nordenskjld, M.15
Fishel, R.16
Kolodner, R.17
Liskay, R.M.18
-
4
-
-
0027145633
-
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
-
Leach FS, Nicolaides NC, Papadopoulos N, Liu B, Jen J, Parsons R, Peltomäki P, Sistonen P, Aaltonen LA, Nyström-Lahti M, Guan XY, Zhang J, Meltzer PS, Yu J-W, Kao F-T, Chen DJ, Cerosaletti KM, Fournier REK, Todd S, Lewis T, Leach RJ, Naylor SL, Weissenbach J, Mecklin J-P, Järvinen H, Petersen GM, Hamilton SR, Green J, Jass J, Watson P, Lynch HT, Trent JM, de la Chapelle A, Kinzler KW, Vogelstein B. 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
Peltomäki, P.7
Sistonen, P.8
Aaltonen, L.A.9
Nyström-Lahti, M.10
Guan, X.Y.11
Zhang, J.12
Meltzer, P.S.13
Yu, J.-W.14
Kao, F.-T.15
Chen, D.J.16
Cerosaletti, K.M.17
Fournier, R.E.K.18
Todd, S.19
Lewis, T.20
Leach, R.J.21
Naylor, S.L.22
Weissenbach, J.23
Mecklin, J.-P.24
Järvinen, H.25
Petersen, G.M.26
Hamilton, S.R.27
Green, J.28
Jass, J.29
Watson, P.30
Lynch, H.T.31
Trent, J.M.32
de la Chapelle, A.33
Kinzler, K.W.34
Vogelstein, B.35
more..
-
5
-
-
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, Igari T, Koike M, Chiba M, Mori T. 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
Igari, T.7
Koike, M.8
Chiba, M.9
Mori, T.10
-
6
-
-
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, Yuasa Y. 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
Yuasa, Y.7
-
7
-
-
0027933070
-
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
-
Nicolaides NC, Papadopoulos N, Liu B, Weit Y-F, Carter KC, Ruben SM, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM, Adams MD, Venter JC, Dunlop MG, Hamilton SR, Petersen GM, de la Chapelle A, Vogelstein B, Kinzler KW. 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
Rosen, C.A.7
Haseltine, W.A.8
Fleischmann, R.D.9
Fraser, C.M.10
Adams, M.D.11
Venter, J.C.12
Dunlop, M.G.13
Hamilton, S.R.14
Petersen, G.M.15
de la Chapelle, A.16
Vogelstein, B.17
Kinzler, K.W.18
-
8
-
-
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, van Os T, Wagner A, Ausems MG, Gomez E, Breuning MH, Brocker-Vriends AH, Vasen HF, Wijnen JT. 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
van Os, T.7
Wagner, A.8
Ausems, M.G.9
Gomez, E.10
Breuning, M.H.11
Brocker-Vriends, A.H.12
Vasen, H.F.13
Wijnen, J.T.14
-
9
-
-
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, Lee TY, Bodmer D, Hoenselaar E, Hendriks-Cornelissen SJ, Tsui WY, Kong CK, Brunner HG, van Kessel AG, Yuen ST, van Krieken JH, Leung SY, Hoogerbrugge N. Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 30 exons of TACSTD1. Nat Genet 2009;41:112-17.
-
(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
Lee, T.Y.7
Bodmer, D.8
Hoenselaar, E.9
Hendriks-Cornelissen, S.J.10
Tsui, W.Y.11
Kong, C.K.12
Brunner, H.G.13
van Kessel, A.G.14
Yuen, S.T.15
van Krieken, J.H.16
Leung, S.Y.17
Hoogerbrugge, N.18
-
10
-
-
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
-
11
-
-
0027966880
-
A novel approach to estimate the proportion of hereditary nonpolyposis colorectal cancer of total colorectal cancer burden
-
Aaltonen LA, Sankila R, Mecklin JP, Jarvinen H, Pukkala E, Peltomaki P, de la Chapelle A. A novel approach to estimate the proportion of hereditary nonpolyposis colorectal cancer of total colorectal cancer burden. Cancer Detect Prev 1994;18:57-63.
-
(1994)
Cancer Detect Prev
, vol.18
, pp. 57-63
-
-
Aaltonen, L.A.1
Sankila, R.2
Mecklin, J.P.3
Jarvinen, H.4
Pukkala, E.5
Peltomaki, P.6
de la Chapelle, A.7
-
12
-
-
0028954237
-
Genetics of colon cancer: impact of inheritance on colon cancer risk
-
Burt RW, DiSario JA, Cannon-Albright L. Genetics of colon cancer: impact of inheritance on colon cancer risk. Annu Rev Med 1995;46:371-9.
-
(1995)
Annu Rev Med
, vol.46
, pp. 371-379
-
-
Burt, R.W.1
DiSario, J.A.2
Cannon-Albright, L.3
-
13
-
-
57449097359
-
Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer
-
Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Clendenning M, Sotamaa K, Prior T, Westman JA, Panescu J, Fix D, Lockman J, LaJeunesse J, Comeras I, de la Chapelle A. Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer. J Clin Oncol 2008;26:5783-8.
-
(2008)
J Clin Oncol
, vol.26
, pp. 5783-5788
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
Arnold, M.4
Khanduja, K.5
Kuebler, P.6
Clendenning, M.7
Sotamaa, K.8
Prior, T.9
Westman, J.A.10
Panescu, J.11
Fix, D.12
Lockman, J.13
LaJeunesse, J.14
Comeras, I.15
de la Chapelle, A.16
-
14
-
-
17944362664
-
Screening for the Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)
-
Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A. Screening for the Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer). N Engl J Med 2005;352:1851-60.
-
(2005)
N Engl J Med
, vol.352
, pp. 1851-1860
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
Arnold, M.4
Khanduja, K.5
Kuebler, P.6
Nakagawa, H.7
Sotamaa, K.8
Prior, T.W.9
Westman, J.10
Panescu, J.11
Fix, D.12
Lockman, J.13
Comeras, I.14
de la Chapelle, A.15
-
15
-
-
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
-
16
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer
-
Salovaara R, Loukola A, Kristo P, Kaariainen H, Ahtola H, Eskelinen M, Harkonen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, Jarvinen H, Mecklin J-P, Aaltonen LA, de la Chapelle A. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol 2000;18:2193-200.
-
(2000)
J Clin Oncol
, vol.18
, 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 Chapelle, A.16
-
17
-
-
13744255043
-
Application of genetics to the prevention of colorectal cancer
-
Hopper JL. Application of genetics to the prevention of colorectal cancer. Recent Results Cancer Res 2005;166:17-33.
-
(2005)
Recent Results Cancer Res
, vol.166
, pp. 17-33
-
-
Hopper, J.L.1
-
18
-
-
33846332027
-
Explaining the familial colorectal cancer risk associated with Mismatch Repair (MMR)-deficient and MMR-stable tumors
-
Aaltonen L, Johns L, Jarvinen H, Mecklin J-P, Houlston R. Explaining the familial colorectal cancer risk associated with Mismatch Repair (MMR)-deficient and MMR-stable tumors. Clin Cancer Res 2007;13:356-61.
-
(2007)
Clin Cancer Res
, vol.13
, pp. 356-361
-
-
Aaltonen, L.1
Johns, L.2
Jarvinen, H.3
Mecklin, J.-P.4
Houlston, R.5
-
19
-
-
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
-
20
-
-
0034538160
-
Population carrier frequency of hMSH2 and hMLH1 mutations
-
Dunlop MG, Farrington SM, Nicholl I, Aaltonen L, Petersen G, Porteous M, Carothers A. Population carrier frequency of hMSH2 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
Carothers, A.7
-
21
-
-
0034788374
-
HNPCC: an uncommon but important diagnosis
-
Terdiman JP. HNPCC: an uncommon but important diagnosis. Gastroenterology 2001;121:1005-8.
-
(2001)
Gastroenterology
, vol.121
, pp. 1005-1008
-
-
Terdiman, J.P.1
-
22
-
-
77955480648
-
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 2010;139:2197 e1-7.
-
(2010)
Gastroenterology
, vol.139
, Issue.2197
-
-
Boland, C.R.1
Shike, M.2
-
23
-
-
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, Fishel R, Lindor NM, Burgart LJ, Hamelin R, Hamilton SR, Hiatt RA, Jass J, Lindblom A, Lynch HT, Peltomaki P, Ramsey SD, Rodriguez-Bigas MA, Vasen HFA, Hawk ET, Barrett JC, Freedman AN, Srivastava S. 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
Chapelle, A.D.L.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..
-
24
-
-
70350733425
-
Risk of pancreatic cancer in families with Lynch syndrome
-
Kastrinos F, Mukherjee B, Tayob N, Wang F, Sparr J, Raymond VM, Bandipalliam P, Stoffel EM, Gruber SB, Syngal S. Risk of pancreatic cancer in families with Lynch syndrome. JAMA 2009;302:1790-5.
-
(2009)
JAMA
, vol.302
, pp. 1790-1795
-
-
Kastrinos, F.1
Mukherjee, B.2
Tayob, N.3
Wang, F.4
Sparr, J.5
Raymond, V.M.6
Bandipalliam, P.7
Stoffel, E.M.8
Gruber, S.B.9
Syngal, S.10
-
25
-
-
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, Buchanan D, Clendenning M, Giles G, Winship I, Macrae F, Goldblatt J, Southey M, Arnold J, Thibodeau SN, Gunawardena SR, Bapat B, Baron JA, Casey G, Le Marchand L, Newcomb P, Haile R, Hopper JL, Jenkins MA. 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
Buchanan, D.7
Clendenning, M.8
Giles, G.9
Winship, I.10
Macrae, F.11
Goldblatt, J.12
Southey, M.13
Arnold, J.14
Thibodeau, S.N.15
Gunawardena, S.R.16
Bapat, B.17
Baron, J.A.18
Casey, G.19
Le Marchand, L.20
Newcomb, P.21
Haile, R.22
Hopper, J.L.23
Jenkins, M.A.24
more..
-
26
-
-
84879468424
-
Elevated risk of prostate cancer among men with lynch syndrome
-
Raymond VM, Mukherjee B, Wang F, Huang SC, Stoffel EM, Kastrinos F, Syngal S, Cooney KA, Gruber SB. Elevated risk of prostate cancer among men with lynch syndrome. J Clin Oncol 2013;31:1713-18.
-
(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
Syngal, S.7
Cooney, K.A.8
Gruber, S.B.9
-
27
-
-
84866658167
-
Risks of primary extracolonic cancers following colorectal cancer in Lynch syndrome
-
Win AK, Lindor NM, Young JP, Macrae FA, Young GP, Williamson E, Parry S, Goldblatt J, Lipton L, Winship I, Leggett B, Tucker K, Giles G, Buchanan D, Clendenning M, Rosty C, Arnold J, Levine AJ, Haile RW, Gallinger S, Le Marchand L, Newcomb PA, Hopper JL, Jenkins MA. 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
Parry, S.7
Goldblatt, J.8
Lipton, L.9
Winship, I.10
Leggett, B.11
Tucker, K.12
Giles, G.13
Buchanan, D.14
Clendenning, M.15
Rosty, C.16
Arnold, J.17
Levine, A.J.18
Haile, R.W.19
Gallinger, S.20
Le Marchand, L.21
Newcomb, P.A.22
Hopper, J.L.23
Jenkins, M.A.24
more..
-
28
-
-
84875036048
-
Risks of colorectal and other cancers after endometrial cancer for women with lynch syndrome
-
Win AK, Lindor NM, Winship I, Tucker KM, Buchanan DD, Young JP, Rosty C, Leggett B, Giles GG, Goldblatt J, Macrae FA, Parry S, Kalady MF, Baron JA, Ahnen DJ, Marchand LL, Gallinger S, Haile RW, Newcomb PA, Hopper JL, Jenkins MA. Risks of colorectal and other cancers after endometrial cancer for women with lynch syndrome. J Natl Cancer Inst 2013;105:274-9.
-
(2013)
J Natl Cancer Inst
, vol.105
, pp. 274-279
-
-
Win, A.K.1
Lindor, N.M.2
Winship, I.3
Tucker, K.M.4
Buchanan, D.D.5
Young, J.P.6
Rosty, C.7
Leggett, B.8
Giles, G.G.9
Goldblatt, J.10
Macrae, F.A.11
Parry, S.12
Kalady, M.F.13
Baron, J.A.14
Ahnen, D.J.15
Marchand, L.L.16
Gallinger, S.17
Haile, R.W.18
Newcomb, P.A.19
Hopper, J.L.20
Jenkins, M.A.21
more..
-
29
-
-
84875017487
-
Risk of breast cancer in Lynch syndrome: a systematic review
-
Win AK, Lindor N, Jenkins M. Risk of breast cancer in Lynch syndrome: a systematic review. Breast Cancer Res 2013;15:R27.
-
(2013)
Breast Cancer Res
, vol.15
-
-
Win, A.K.1
Lindor, N.2
Jenkins, M.3
-
30
-
-
84873942317
-
Cancer risks for MLH1 and MSH2 mutation carriers
-
Dowty JG, Win AK, Buchanan DD, Lindor NM, Macrae FA, Clendenning M, Antill YC, Thibodeau SN, Casey G, Gallinger S, Marchand LL, Newcomb PA, Haile RW, Young GP, James PA, Giles GG, Gunawardena SR, Leggett BA, Gattas M, Boussioutas A, Ahnen DJ, Baron JA, Parry S, Goldblatt J, Young JP, Hopper JL, Jenkins MA. Cancer risks for MLH1 and MSH2 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
Antill, Y.C.7
Thibodeau, S.N.8
Casey, G.9
Gallinger, S.10
Marchand, L.L.11
Newcomb, P.A.12
Haile, R.W.13
Young, G.P.14
James, P.A.15
Giles, G.G.16
Gunawardena, S.R.17
Leggett, B.A.18
Gattas, M.19
Boussioutas, A.20
Ahnen, D.J.21
Baron, J.A.22
Parry, S.23
Goldblatt, J.24
Young, J.P.25
Hopper, J.L.26
Jenkins, M.A.27
more..
-
31
-
-
0034011564
-
Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer
-
Jarvinen HJ, Aarnio M, Mustonen H, Aktan-Collan K, Aaltonen LA, Peltomaki P, De La Chapelle A, Mecklin JP. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology 2000;118:829-34.
-
(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
De La Chapelle, A.7
Mecklin, J.P.8
-
32
-
-
33644864321
-
Decrease in mortality in lynch syndrome families because of surveillance
-
de Jong AE, Hendriks YMC, Kleibeuker JH, de Boer SY, Cats A, Griffioen G, Nagengast FM, Nelis FG, Rookus MA, Vasen HFA. Decrease in mortality in lynch syndrome families because of surveillance. Gastroenterology 2006;130:665-71.
-
(2006)
Gastroenterology
, vol.130
, pp. 665-671
-
-
de Jong, A.E.1
Hendriks, Y.M.C.2
Kleibeuker, J.H.3
de Boer, S.Y.4
Cats, A.5
Griffioen, G.6
Nagengast, F.M.7
Nelis, F.G.8
Rookus, M.A.9
Vasen, H.F.A.10
-
33
-
-
30944457531
-
Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome
-
Schmeler KM, Lynch HT, Chen LM, Munsell MF, Soliman PT, Clark MB, Daniels MS, White KG, Boyd-Rogers SG, Conrad PG, Yang KY, Rubin MM, Sun CC, Slomovitz BM, Gershenson DM, Lu KH. Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome. N Engl J Med 2006;354:261-9.
-
(2006)
N Engl J Med
, vol.354
, pp. 261-269
-
-
Schmeler, K.M.1
Lynch, H.T.2
Chen, L.M.3
Munsell, M.F.4
Soliman, P.T.5
Clark, M.B.6
Daniels, M.S.7
White, K.G.8
Boyd-Rogers, S.G.9
Conrad, P.G.10
Yang, K.Y.11
Rubin, M.M.12
Sun, C.C.13
Slomovitz, B.M.14
Gershenson, D.M.15
Lu, K.H.16
-
34
-
-
83955161674
-
Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial
-
Burn J, Gerdes AM, Macrae F, Mecklin JP, Moeslein G, Olschwang S, Eccles D, Evans DG, Maher ER, Bertario L, Bisgaard ML, Dunlop MG, Ho JW, Hodgson SV, Lindblom A, Lubinski J, Morrison PJ, Murday V, Ramesar R, Side L, Scott RJ, Thomas HJ, Vasen HF, Barker G, Crawford G, Elliott F, Movahedi M, Pylvanainen K, Wijnen JT, Fodde R, Lynch HT, Mathers JC, Bishop DT. Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial. Lancet 2011;9809:2081-7.
-
(2011)
Lancet
, vol.9809
, pp. 2081-2087
-
-
Burn, J.1
Gerdes, A.M.2
Macrae, F.3
Mecklin, J.P.4
Moeslein, G.5
Olschwang, S.6
Eccles, D.7
Evans, D.G.8
Maher, E.R.9
Bertario, L.10
Bisgaard, M.L.11
Dunlop, M.G.12
Ho, J.W.13
Hodgson, S.V.14
Lindblom, A.15
Lubinski, J.16
Morrison, P.J.17
Murday, V.18
Ramesar, R.19
Side, L.20
Scott, R.J.21
Thomas, H.J.22
Vasen, H.F.23
Barker, G.24
Crawford, G.25
Elliott, F.26
Movahedi, M.27
Pylvanainen, K.28
Wijnen, J.T.29
Fodde, R.30
Lynch, H.T.31
Mathers, J.C.32
Bishop, D.T.33
more..
-
35
-
-
0025848680
-
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
-
Vasen HF, Mecklin JP, Khan PM, Lynch HT. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). 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
-
36
-
-
0028808828
-
The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer
-
Percesepe A, Anti M, Roncucci L, Armelao F, Marra G, Pahor M, Coco C, Gasbarrini G, Ponz de Leon M. The effect of family size on estimates of the frequency of hereditary non-polyposis colorectal cancer. Br J Cancer 1995;72:1320-3.
-
(1995)
Br J Cancer
, vol.72
, pp. 1320-1323
-
-
Percesepe, A.1
Anti, M.2
Roncucci, L.3
Armelao, F.4
Marra, G.5
Pahor, M.6
Coco, C.7
Gasbarrini, G.8
Ponz de Leon, M.9
-
37
-
-
0036304830
-
Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation
-
Bisgaard ML, Jager AC, Myrhoj T, Bernstein I, Nielsen FC. Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation. Hum Mutat 2002;20:20-7.
-
(2002)
Hum Mutat
, vol.20
, pp. 20-27
-
-
Bisgaard, M.L.1
Jager, A.C.2
Myrhoj, T.3
Bernstein, I.4
Nielsen, F.C.5
-
38
-
-
0033825587
-
Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1
-
Syngal S, Fox EA, Eng C, Kolodner RD, Garber JE. Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1. J Med Genet 2000;37:641-5.
-
(2000)
J Med Genet
, vol.37
, pp. 641-645
-
-
Syngal, S.1
Fox, E.A.2
Eng, C.3
Kolodner, R.D.4
Garber, J.E.5
-
39
-
-
16944364360
-
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations
-
Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, Losekoot M, Moller P, Fodde R. Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. Am J Hum Genet 1997;61:329-35.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 329-335
-
-
Wijnen, J.1
Khan, P.M.2
Vasen, H.3
van der Klift, H.4
Mulder, A.5
van Leeuwen-Cornelisse, I.6
Bakker, B.7
Losekoot, M.8
Moller, P.9
Fodde, R.10
-
40
-
-
10144250305
-
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer
-
Moslein G, Tester DJ, Lindor NM, Honchel R, Cunningham JM, French AJ, Halling KC, Schwab M, Goretzki P, Thibodeau SN. Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. Hum Mol Genet 1996;5:1245-52.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1245-1252
-
-
Moslein, G.1
Tester, D.J.2
Lindor, N.M.3
Honchel, R.4
Cunningham, J.M.5
French, A.J.6
Halling, K.C.7
Schwab, M.8
Goretzki, P.9
Thibodeau, S.N.10
-
41
-
-
0032796919
-
Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer
-
Wang Q, Lasset C, Desseigne F, Saurin JC, Maugard C, Navarro C, Ruano E, Descos L, Trillet-Lenoir V, Bosset JF, Puisieux A. Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer. Hum Genet 1999;105:79-85.
-
(1999)
Hum Genet
, vol.105
, pp. 79-85
-
-
Wang, Q.1
Lasset, C.2
Desseigne, F.3
Saurin, J.C.4
Maugard, C.5
Navarro, C.6
Ruano, E.7
Descos, L.8
Trillet-Lenoir, V.9
Bosset, J.F.10
Puisieux, A.11
-
42
-
-
1842477266
-
Current clinical selection strategies for identification of hereditary non-polyposis colorectal cancer families are inadequate: a meta-analysis
-
Kievit W, de Bruin JH, Adang EM, Ligtenberg MJ, Nagengast FM, van Krieken JH, Hoogerbrugge N. Current clinical selection strategies for identification of hereditary non-polyposis colorectal cancer families are inadequate: a meta-analysis. Clin Genet 2004;65:308-16.
-
(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
Hoogerbrugge, N.7
-
43
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu B, Parsons R, Papadopoulos N, Nicolaides NC, Lynch HT, Watson P, Jass JR, Dunlop M, Wyllie A, Peltomaki P, de la Chapelle A, Hamilton SR, Vogelstein B, Kinzler KW. Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med 1996;2:169-74.
-
(1996)
Nat Med
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.2
Papadopoulos, N.3
Nicolaides, N.C.4
Lynch, H.T.5
Watson, P.6
Jass, J.R.7
Dunlop, M.8
Wyllie, A.9
Peltomaki, P.10
de la Chapelle, A.11
Hamilton, S.R.12
Vogelstein, B.13
Kinzler, K.W.14
-
44
-
-
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
-
45
-
-
0036136726
-
Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients
-
Katballe N, Christensen M, Wikman FP, Orntoft TF, Laurberg S. Frequency of hereditary non-polyposis colorectal cancer in Danish colorectal cancer patients. Gut 2002;50:43-51.
-
(2002)
Gut
, vol.50
, pp. 43-51
-
-
Katballe, N.1
Christensen, M.2
Wikman, F.P.3
Orntoft, T.F.4
Laurberg, S.5
-
46
-
-
0036935179
-
Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study
-
Park JG, Vasen HF, Park YJ, Park KJ, Peltomaki P, de Leon MP, Rodriguez-Bigas MA, Lubinski J, Beck NE, Bisgaard ML, Miyaki M, Wijnen JT, Baba S, Lindblom A, Madlensky L, Lynch HT. Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study. Int J Colorectal Dis 2002;17:109-14.
-
(2002)
Int J Colorectal Dis
, vol.17
, pp. 109-114
-
-
Park, J.G.1
Vasen, H.F.2
Park, Y.J.3
Park, K.J.4
Peltomaki, P.5
de Leon, M.P.6
Rodriguez-Bigas, M.A.7
Lubinski, J.8
Beck, N.E.9
Bisgaard, M.L.10
Miyaki, M.11
Wijnen, J.T.12
Baba, S.13
Lindblom, A.14
Madlensky, L.15
Lynch, H.T.16
-
47
-
-
0027177167
-
Identification of hereditary nonpolyposis colorectal cancer in the general population The 6-year experience of a population-based registry
-
Ponz de Leon M, Sassatelli R, Benatti P, Roncucci L. Identification of hereditary nonpolyposis colorectal cancer in the general population. The 6-year experience of a population-based registry. Cancer 1993;71:3493-501.
-
(1993)
Cancer
, vol.71
, pp. 3493-3501
-
-
Ponz de Leon, M.1
Sassatelli, R.2
Benatti, P.3
Roncucci, L.4
-
48
-
-
0027276469
-
Tumour spectrum in hereditary non-polyposis colorectal cancer (HNPCC) and in families with "suspected HNPCC"
-
A population-based study in northern Italy. Colorectal Cancer Study Group
-
Benatti P, Sassatelli R, Roncucci L, Pedroni M, Fante R, Di Gregorio C, Losi L, Gelmini R, Ponz de Leon M. Tumour spectrum in hereditary non-polyposis colorectal cancer (HNPCC) and in families with "suspected HNPCC". A population-based study in northern Italy. Colorectal Cancer Study Group. Int J Cancer 1993;54:371-7.
-
(1993)
Int J Cancer
, vol.54
, pp. 371-377
-
-
Benatti, P.1
Sassatelli, R.2
Roncucci, L.3
Pedroni, M.4
Fante, R.5
Di Gregorio, C.6
Losi, L.7
Gelmini, R.8
Ponz de Leon, M.9
-
49
-
-
0029329835
-
A preventive registry for hereditary nonpolyposis colorectal cancer
-
Madlensky L, Berk TC, Bapat BV, McLeod RS, Couture J, Baron D, Hiruki T, Redston M, Cohen Z, Gallinger S. A preventive registry for hereditary nonpolyposis colorectal cancer. Can J Oncol 1995;5:355-60.
-
(1995)
Can J Oncol
, vol.5
, pp. 355-360
-
-
Madlensky, L.1
Berk, T.C.2
Bapat, B.V.3
McLeod, R.S.4
Couture, J.5
Baron, D.6
Hiruki, T.7
Redston, M.8
Cohen, Z.9
Gallinger, S.10
-
50
-
-
0030266652
-
Prognosis of hereditary nonpolyposis colorectal cancer (HNPCC) and the role of Japanese criteria for HNPCC
-
Fujita S, Moriya Y, Sugihara K, Akasu T, Ushio K. Prognosis of hereditary nonpolyposis colorectal cancer (HNPCC) and the role of Japanese criteria for HNPCC. Jpn J Clin Oncol 1996;26:351-5.
-
(1996)
Jpn J Clin Oncol
, vol.26
, pp. 351-355
-
-
Fujita, S.1
Moriya, Y.2
Sugihara, K.3
Akasu, T.4
Ushio, K.5
-
51
-
-
9544241423
-
Germline mutations of hMLH1 and hMSH2 genes in Korean hereditary nonpolyposis colorectal cancer
-
Han HJ, Yuan Y, Ku JL, Oh JH, Won YJ, Kang KJ, Kim KY, Kim S, Kim CY, Kim JP, Oh NG, Lee KH, Choe KJ, Nakamura Y, Park JG. Germline mutations of hMLH1 and hMSH2 genes in Korean hereditary nonpolyposis colorectal cancer. J Natl Cancer Inst 1996;88:1317-9.
-
(1996)
J Natl Cancer Inst
, vol.88
, pp. 1317-1319
-
-
Han, H.J.1
Yuan, Y.2
Ku, J.L.3
Oh, J.H.4
Won, Y.J.5
Kang, K.J.6
Kim, K.Y.7
Kim, S.8
Kim, C.Y.9
Kim, J.P.10
Oh, N.G.11
Lee, K.H.12
Choe, K.J.13
Nakamura, Y.14
Park, J.G.15
-
53
-
-
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, Khan P, Lynch H, Smyrk T, Perucho M. 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
Khan, P.7
Lynch, H.8
Smyrk, T.9
Perucho, M.10
-
54
-
-
26644441586
-
Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer
-
Southey MC, Jenkins MA, Mead L, Whitty J, Trivett M, Tesoriero AA, Smith LD, Jennings K, Grubb G, Royce SG, Walsh MD, Barker MA, Young JP, Jass JR, St John DJB, Macrae FA, Giles GG, Hopper JL. Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer. J Clin Oncol 2005;23:6524-32.
-
(2005)
J Clin Oncol
, vol.23
, pp. 6524-6532
-
-
Southey, M.C.1
Jenkins, M.A.2
Mead, L.3
Whitty, J.4
Trivett, M.5
Tesoriero, A.A.6
Smith, L.D.7
Jennings, K.8
Grubb, G.9
Royce, S.G.10
Walsh, M.D.11
Barker, M.A.12
Young, J.P.13
Jass, J.R.14
St John, D.J.B.15
Macrae, F.A.16
Giles, G.G.17
Hopper, J.L.18
-
55
-
-
58749110893
-
Molecular screening of all colorectal tumors diagnosed before age 50 years followed by genetic testing efficiently identifies Lynch syndrome cases
-
Jenkins MA, Dowty JG, Hopper JL, Southey MC. Molecular screening of all colorectal tumors diagnosed before age 50 years followed by genetic testing efficiently identifies Lynch syndrome cases. Int J Cancer 2009;124:x-xi.
-
(2009)
Int J Cancer
, vol.124
-
-
Jenkins, M.A.1
Dowty, J.G.2
Hopper, J.L.3
Southey, M.C.4
-
56
-
-
58749101712
-
Population-based detection of Lynch syndrome in young colorectal cancer patients using microsatellite instability as the initial test
-
Schofield L, Watson N, Grieu F, Li WQ, Zeps N, Harvey J, Stewart C, Abdo M, Goldblatt J, Iacopetta B. Population-based detection of Lynch syndrome in young colorectal cancer patients using microsatellite instability as the initial test. Int J Cancer 2009;124:1097-102.
-
(2009)
Int J Cancer
, vol.124
, pp. 1097-1102
-
-
Schofield, L.1
Watson, N.2
Grieu, F.3
Li, W.Q.4
Zeps, N.5
Harvey, J.6
Stewart, C.7
Abdo, M.8
Goldblatt, J.9
Iacopetta, B.10
-
57
-
-
84858297003
-
A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours
-
Schofield L, Grieu F, Goldblatt J, Amanuel B, Iacopetta B. A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours. Fam Cancer 2012;11:1-6.
-
(2012)
Fam Cancer
, vol.11
, pp. 1-6
-
-
Schofield, L.1
Grieu, F.2
Goldblatt, J.3
Amanuel, B.4
Iacopetta, B.5
-
58
-
-
20244386395
-
Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer
-
Pinol V, Castells A, Andreu M, Castellvi-Bel S, Alenda C, Llor X, Xicola RM, Rodriguez-Moranta F, Paya A, Jover R, Bessa X. Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer. JAMA 2005;293:1986-94.
-
(2005)
JAMA
, vol.293
, pp. 1986-1994
-
-
Pinol, V.1
Castells, A.2
Andreu, M.3
Castellvi-Bel, S.4
Alenda, C.5
Llor, X.6
Xicola, R.M.7
Rodriguez-Moranta, F.8
Paya, A.9
Jover, R.10
Bessa, X.11
-
59
-
-
33747871345
-
Screening for lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients
-
Hampel H, Frankel W, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, La Jeunesse J, Nakagawa H, Westman JA, Prior TW, Clendenning M, Penzone P, Lombardi J, Dunn P, Cohn DE, Copeland L, Eaton L, Fowler J, Lewandowski G, Vaccarello L, Bell J, Reid G, de la Chapelle A. Screening for lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 2006;66:7810-17.
-
(2006)
Cancer Res
, vol.66
, pp. 7810-7817
-
-
Hampel, H.1
Frankel, W.2
Panescu, J.3
Lockman, J.4
Sotamaa, K.5
Fix, D.6
Comeras, I.7
La Jeunesse, J.8
Nakagawa, H.9
Westman, J.A.10
Prior, T.W.11
Clendenning, M.12
Penzone, P.13
Lombardi, J.14
Dunn, P.15
Cohn, D.E.16
Copeland, L.17
Eaton, L.18
Fowler, J.19
Lewandowski, G.20
Vaccarello, L.21
Bell, J.22
Reid, G.23
de la Chapelle, A.24
more..
-
60
-
-
84867499525
-
Identification of Lynch syndrome among patients with colorectal cancer
-
Moreira L, Balaguer F, Lindor N, de la Chapelle A, Hampel H, Aaltonen LA, Hopper JL, Le Marchand L, Gallinger S, Newcomb PA, Haile R, Thibodeau SN, Gunawardena S, Jenkins MA, Buchanan DD, Potter JD, Baron JA, Ahnen DJ, Moreno V, Andreu M, Ponz de Leon M, Rustgi AK, Castells A. Identification of Lynch syndrome among patients with colorectal cancer. JAMA 2012;308:1555-65.
-
(2012)
JAMA
, vol.308
, pp. 1555-1565
-
-
Moreira, L.1
Balaguer, F.2
Lindor, N.3
de la Chapelle, A.4
Hampel, H.5
Aaltonen, L.A.6
Hopper, J.L.7
Le Marchand, L.8
Gallinger, S.9
Newcomb, P.A.10
Haile, R.11
Thibodeau, S.N.12
Gunawardena, S.13
Jenkins, M.A.14
Buchanan, D.D.15
Potter, J.D.16
Baron, J.A.17
Ahnen, D.J.18
Moreno, V.19
Andreu, M.20
Ponz de Leon, M.21
Rustgi, A.K.22
Castells, A.23
more..
-
61
-
-
59849108362
-
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
-
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 2009;11:35-41.
-
(2009)
Genet Med
, vol.11
, pp. 35-41
-
-
-
62
-
-
1642535480
-
BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer
-
Deng G, Bell I, Crawley S, Gum J, Terdiman JP, Allen BA, Truta B, Sleisenger MH, Kim YS. BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer. Clin Cancer Res 2004;10(1 Pt 1):191-5.
-
(2004)
Clin Cancer Res
, vol.10
, Issue.1 PART 1
, pp. 191-195
-
-
Deng, G.1
Bell, I.2
Crawley, S.3
Gum, J.4
Terdiman, J.P.5
Allen, B.A.6
Truta, B.7
Sleisenger, M.H.8
Kim, Y.S.9
-
63
-
-
4444311092
-
BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing
-
Domingo E, Laiho P, Ollikainen M, Pinto M, Wang L, French AJ, Westra J, Frebourg T, Espin E, Armengol M, Hamelin R, Yamamoto H, Hofstra RM, Seruca R, Lindblom A, Peltomaki P, Thibodeau SN, Aaltonen LA, Schwartz S Jr. BRAF screening as a low-cost effective strategy for simplifying HNPCC genetic testing. J Med Genet 2004;41:664-8.
-
(2004)
J Med Genet
, vol.41
, pp. 664-668
-
-
Domingo, E.1
Laiho, P.2
Ollikainen, M.3
Pinto, M.4
Wang, L.5
French, A.J.6
Westra, J.7
Frebourg, T.8
Espin, E.9
Armengol, M.10
Hamelin, R.11
Yamamoto, H.12
Hofstra, R.M.13
Seruca, R.14
Lindblom, A.15
Peltomaki, P.16
Thibodeau, S.N.17
Aaltonen, L.A.18
Schwartz Jr, S.19
-
64
-
-
79960604164
-
Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis
-
Ladabaum U, Wang G, Terdiman J, Blanco A, Kuppermann M, Boland CR, Ford J, Elkin E, Phillips KA. Strategies to identify the Lynch syndrome among patients with colorectal cancer: a cost-effectiveness analysis. Ann Intern Med 2011;155:69-79.
-
(2011)
Ann Intern Med
, vol.155
, pp. 69-79
-
-
Ladabaum, U.1
Wang, G.2
Terdiman, J.3
Blanco, A.4
Kuppermann, M.5
Boland, C.R.6
Ford, J.7
Elkin, E.8
Phillips, K.A.9
-
65
-
-
77149122082
-
The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer
-
Mvundura M, Grosse SD, Hampel H, Palomaki GE. The cost-effectiveness of genetic testing strategies for Lynch syndrome among newly diagnosed patients with colorectal cancer. Genet Med 2010;12:93-104.
-
(2010)
Genet Med
, vol.12
, pp. 93-104
-
-
Mvundura, M.1
Grosse, S.D.2
Hampel, H.3
Palomaki, G.E.4
-
66
-
-
0030823368
-
Hereditary nonpolyposis colorectal cancer: an update
-
Baba S. Hereditary nonpolyposis colorectal cancer: an update. Dis Colon Rectum 1997;40:S86-95.
-
(1997)
Dis Colon Rectum
, vol.40
-
-
Baba, S.1
-
67
-
-
0035899935
-
Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer
-
Ramsey S, Clarke L, Etzioni R, Higashi M, Berry K, Urban N. Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer. Ann Intern Med 2001;135(8 Part 1):577.
-
(2001)
Ann Intern Med
, vol.135
, Issue.8 PART 1
, pp. 577
-
-
Ramsey, S.1
Clarke, L.2
Etzioni, R.3
Higashi, M.4
Berry, K.5
Urban, N.6
-
68
-
-
4444328981
-
Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients
-
Grover S, Stoffel E, Bussone L, Tschoegl E, Syngal S. Physician assessment of family cancer history and referral for genetic evaluation in colorectal cancer patients. Clin Gastroenterol Hepatol 2004;2:813-19.
-
(2004)
Clin Gastroenterol Hepatol
, vol.2
, pp. 813-819
-
-
Grover, S.1
Stoffel, E.2
Bussone, L.3
Tschoegl, E.4
Syngal, S.5
-
69
-
-
0032552239
-
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer
-
Wijnen JT, Vasen HFA, Khan PM, Zwinderman AH, van der Klift H, Mulder A, Tops C, Møller P, Fodde R, Menko F, Taal B, Nagengast F, Brunner H, Kleibeuker J, Sijmons R, Griffioen G, Bröcker-Vriends A, Bakker E, van Leeuwen-Cornelisse I, Meijers-Heijboer A, Lindhout D, Breuning M, Post J, Schaap C, Apold J, Heimdal K, Bertario L, Bisgaard ML, Goetz P. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer. N Engl J Med 1998;339:511-18.
-
(1998)
N Engl J Med
, vol.339
, pp. 511-518
-
-
Wijnen, J.T.1
Vasen, H.F.A.2
Khan, P.M.3
Zwinderman, A.H.4
van der Klift, H.5
Mulder, A.6
Tops, C.7
Møller, P.8
Fodde, R.9
Menko, F.10
Taal, B.11
Nagengast, F.12
Brunner, H.13
Kleibeuker, J.14
Sijmons, R.15
Griffioen, G.16
Bröcker-Vriends, A.17
Bakker, E.18
van Leeuwen-Cornelisse, I.19
Meijers-Heijboer, A.20
Lindhout, D.21
Breuning, M.22
Post, J.23
Schaap, C.24
Apold, J.25
Heimdal, K.26
Bertario, L.27
Bisgaard, M.L.28
Goetz, P.29
more..
-
70
-
-
16644378293
-
Refining the Amsterdam Criteria and Bethesda Guidelines: testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic
-
Lipton LR, Johnson V, Cummings C, Fisher S, Risby P, Eftekhar Sadat AT, Cranston T, Izatt L, Sasieni P, Hodgson SV, Thomas HJW, Tomlinson IPM. 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 2004;22:4934-43.
-
(2004)
J Clin Oncol
, vol.22
, pp. 4934-4943
-
-
Lipton, L.R.1
Johnson, V.2
Cummings, C.3
Fisher, S.4
Risby, P.5
Eftekhar Sadat, A.T.6
Cranston, T.7
Izatt, L.8
Sasieni, P.9
Hodgson, S.V.10
Thomas, H.J.W.11
Tomlinson, I.P.M.12
-
71
-
-
33749066191
-
Prediction of germline mutations and cancer risk in the Lynch syndrome
-
Chen S, Wang W, Lee S, Nafa K, Lee J, Romans K, Watson P, Gruber SB, Euhus D, Kinzler KW. Prediction of germline mutations and cancer risk in the Lynch syndrome. JAMA 2006;296:1479-87.
-
(2006)
JAMA
, vol.296
, 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
-
72
-
-
33749040947
-
Prediction of MLH1 and MSH2 mutations in lynch syndrome
-
Balmaña J, Stockwell DH, Steyerberg EW, Stoffel EM, Deffenbaugh AM, Reid JE, Ward B, Scholl T, Hendrickson B, Tazelaar J, Burbidge LA, Syngal S. Prediction of MLH1 and MSH2 mutations in lynch syndrome. JAMA 2006;296:1469-78.
-
(2006)
JAMA
, vol.296
, pp. 1469-1478
-
-
Balmaña, 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
-
73
-
-
78650513224
-
The PREMM 1 2,6 model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history
-
Kastrinos F, Steyerberg EW, Mercado R, Balmaña J, Holter S, Gallinger S, Siegmund KD, Church JM, Jenkins MA, Lindor NM, Thibodeau SN, Burbidge LA, Wenstrup RJ, Syngal S. The PREMM 1,2,6 model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history. Gastroenterology 2011;140:73-81.
-
(2011)
Gastroenterology
, vol.140
, pp. 73-81
-
-
Kastrinos, F.1
Steyerberg, E.W.2
Mercado, R.3
Balmaña, J.4
Holter, S.5
Gallinger, S.6
Siegmund, K.D.7
Church, J.M.8
Jenkins, M.A.9
Lindor, N.M.10
Thibodeau, S.N.11
Burbidge, L.A.12
Wenstrup, R.J.13
Syngal, S.14
-
74
-
-
33745658837
-
Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer
-
Barnetson RA, Tenesa A, Farrington SM, Nicholl ID, Cetnarskyj R, Porteous ME, Campbell H, Dunlop MG. Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. N Engl J Med 2006;354:2751-63.
-
(2006)
N Engl J Med
, vol.354
, 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
-
75
-
-
33644813813
-
A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability
-
Marroni F, Pastrello C, Benatti P, Torrini M, Barana D, Cordisco E, Viel A, Mareni C, Oliani C, Genuardi M, Bailey-Wilson J, Ponz de Leon M, Presciuttini S. A genetic model for determining MSH2 and MLH1 carrier probabilities based on family history and tumor microsatellite instability. Clin Genet 2006;69:254-62.
-
(2006)
Clin Genet
, vol.69
, pp. 254-262
-
-
Marroni, F.1
Pastrello, C.2
Benatti, P.3
Torrini, M.4
Barana, D.5
Cordisco, E.6
Viel, A.7
Mareni, C.8
Oliani, C.9
Genuardi, M.10
Bailey-Wilson, J.11
Ponz de Leon, M.12
Presciuttini, S.13
-
76
-
-
84890246453
-
-
Myriad Genetic Laboratories MLH1 and MSH2 Prevalence Table
-
Myriad Genetic Laboratories. MLH1 and MSH2 Prevalence Table. 2007.
-
(2007)
-
-
-
77
-
-
59849129653
-
EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome
-
Palomaki GE, McClain MR, Melillo S, Hampel HL, Thibodeau SN. EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome. Genet Med 2009;11:42-65.
-
(2009)
Genet Med
, vol.11
, pp. 42-65
-
-
Palomaki, G.E.1
McClain, M.R.2
Melillo, S.3
Hampel, H.L.4
Thibodeau, S.N.5
-
78
-
-
48549099663
-
The clinical phenotype of lynch syndrome due to germ-line PMS2 mutations
-
Senter L, Clendenning M, Sotamaa K, Hampel H, Green J, Potter JD, Lindblom A, Lagerstedt K, Thibodeau SN, Lindor NM, Young J, Winship I, Dowty JG, White DM, Hopper JL, Baglietto L, Jenkins MA, de la Chapelle A. The clinical phenotype of lynch syndrome due to germ-line PMS2 mutations. Gastroenterology 2008;135:419-28.
-
(2008)
Gastroenterology
, vol.135
, pp. 419-428
-
-
Senter, L.1
Clendenning, M.2
Sotamaa, K.3
Hampel, H.4
Green, J.5
Potter, J.D.6
Lindblom, A.7
Lagerstedt, K.8
Thibodeau, S.N.9
Lindor, N.M.10
Young, J.11
Winship, I.12
Dowty, J.G.13
White, D.M.14
Hopper, J.L.15
Baglietto, L.16
Jenkins, M.A.17
de la Chapelle, A.18
-
79
-
-
80051606899
-
Prediction models: revolutionary in principle, but do they do more good than harm?
-
Vickers AJ. Prediction models: revolutionary in principle, but do they do more good than harm? J Clin Oncol 2011;29:2951-2.
-
(2011)
J Clin Oncol
, vol.29
, pp. 2951-2952
-
-
Vickers, A.J.1
-
80
-
-
73849094087
-
Assessing the performance of prediction models: a framework for traditional and novel measures
-
Steyerberg EW, Vickers AJ, Cook NR, Gerds T, Gonen M, Obuchowski N, Pencina MJ, Kattan MW. Assessing the performance of prediction models: a framework for traditional and novel measures. Epidemiology 2010;21:128-38.
-
(2010)
Epidemiology
, vol.21
, pp. 128-138
-
-
Steyerberg, E.W.1
Vickers, A.J.2
Cook, N.R.3
Gerds, T.4
Gonen, M.5
Obuchowski, N.6
Pencina, M.J.7
Kattan, M.W.8
-
81
-
-
84890157512
-
-
StataCorp., Stata Statistical Software: Release, 11., College Station, TX: StataCorp LP
-
StataCorp. Stata Statistical Software: Release 11. College Station, TX: StataCorp LP, 2009.
-
(2009)
-
-
-
82
-
-
37449019456
-
Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients
-
Balaguer F, Balmaña J, Castellví-Bel S, Steyerberg EW, Andreu M, Llor X, Jover R, Syngal S, Castells A. Validation and extension of the PREMM1,2 model in a population-based cohort of colorectal cancer patients. Gastroenterology 2008;134:39-46.
-
(2008)
Gastroenterology
, vol.134
, pp. 39-46
-
-
Balaguer, F.1
Balmaña, J.2
Castellví-Bel, S.3
Steyerberg, E.W.4
Andreu, M.5
Llor, X.6
Jover, R.7
Syngal, S.8
Castells, A.9
-
83
-
-
51849147419
-
Association ftGOGotSG. 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, Steyerberg EW, Andreu M, Llor X, Jover R, Castells A, Syngal S, Association ftGOGotSG. 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 2008;45:557-63.
-
(2008)
J Med Genet
, vol.45
, pp. 557-563
-
-
Balmaña, J.1
Balaguer, F.2
Castellví-Bel, S.3
Steyerberg, E.W.4
Andreu, M.5
Llor, X.6
Jover, R.7
Castells, A.8
Syngal, S.9
-
84
-
-
62349128915
-
Prediction of Lynch syndrome in consecutive patients with colorectal cancer
-
Green R, Parfrey P, Woods M, Younghusband H. Prediction of Lynch syndrome in consecutive patients with colorectal cancer. J Natl Cancer Inst 2009;101:331.
-
(2009)
J Natl Cancer Inst
, vol.101
, pp. 331
-
-
Green, R.1
Parfrey, P.2
Woods, M.3
Younghusband, H.4
-
85
-
-
63549118755
-
A comparison of models used to predict MLH1 MSH2 and MSH6 mutation carriers
-
Pouchet CJ, Wong N, Chong G, Sheehan MJ, Schneider G, Rosen-Sheidley B, Foulkes W, Tischkowitz M. A comparison of models used to predict MLH1, MSH2 and MSH6 mutation carriers. Ann Oncol 2009;20:681-8.
-
(2009)
Ann Oncol
, vol.20
, pp. 681-688
-
-
Pouchet, C.J.1
Wong, N.2
Chong, G.3
Sheehan, M.J.4
Schneider, G.5
Rosen-Sheidley, B.6
Foulkes, W.7
Tischkowitz, M.8
-
86
-
-
72449136819
-
Mutation prediction models in Lynch syndrome: evaluation in a clinical genetic setting
-
Ramsoekh D, van Leerdam ME, Wagner A, Kuipers EJ, Steyerberg EW. Mutation prediction models in Lynch syndrome: evaluation in a clinical genetic setting. J Med Genet 2009;46:745-51.
-
(2009)
J Med Genet
, vol.46
, pp. 745-751
-
-
Ramsoekh, D.1
van Leerdam, M.E.2
Wagner, A.3
Kuipers, E.J.4
Steyerberg, E.W.5
-
87
-
-
70449527475
-
Are prediction models for Lynch syndrome valid for probands with endometrial cancer?
-
Backes FJ, Hampel H, Backes KA, Vaccarello L, Lewandowski G, Bell JA, Reid GC, Copeland LJ, Fowler JM, Cohn DE. Are prediction models for Lynch syndrome valid for probands with endometrial cancer? Fam Cancer 2009;8:483-7.
-
(2009)
Fam Cancer
, vol.8
, pp. 483-487
-
-
Backes, F.J.1
Hampel, H.2
Backes, K.A.3
Vaccarello, L.4
Lewandowski, G.5
Bell, J.A.6
Reid, G.C.7
Copeland, L.J.8
Fowler, J.M.9
Cohn, D.E.10
-
88
-
-
74049157657
-
Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer
-
Monzon JG, Cremin C, Armstrong L, Nuk J, Young S, Horsman DE, Garbutt K, Bajdik CD, Gill S. Validation of predictive models for germline mutations in DNA mismatch repair genes in colorectal cancer. Int J Cancer 2010;126:930-9.
-
(2010)
Int J Cancer
, vol.126
, pp. 930-939
-
-
Monzon, J.G.1
Cremin, C.2
Armstrong, L.3
Nuk, J.4
Young, S.5
Horsman, D.E.6
Garbutt, K.7
Bajdik, C.D.8
Gill, S.9
-
89
-
-
80053916307
-
Performance of lynch syndrome predictive models in a multi-center US referral population
-
Khan O, Blanco A, Conrad P, Gulden C, Moss TZ, Olopade OI, Kupfer SS, Terdiman J. Performance of lynch syndrome predictive models in a multi-center US referral population. Am J Gastroenterol 2011;106:1822-7.
-
(2011)
Am J Gastroenterol
, vol.106
, pp. 1822-1827
-
-
Khan, O.1
Blanco, A.2
Conrad, P.3
Gulden, C.4
Moss, T.Z.5
Olopade, O.I.6
Kupfer, S.S.7
Terdiman, J.8
-
90
-
-
84858148591
-
Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries
-
Monteiro Santos EM, Valentin MD, Carneiro F, de Oliveira LP, de Oliveira Ferreira F, Junior SA, Nakagawa WT, Gomy I, de Faria Ferraz VE, da Silva Junior WA, Carraro DM, Rossi BM. Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries. BMC Cancer 2012;12:64.
-
(2012)
BMC Cancer
, vol.12
, pp. 64
-
-
Monteiro Santos, E.M.1
Valentin, M.D.2
Carneiro, F.3
de Oliveira, L.P.4
de Oliveira Ferreira, F.5
Junior, S.A.6
Nakagawa, W.T.7
Gomy, I.8
de Faria Ferraz, V.E.9
da Silva Junior, W.A.10
Carraro, D.M.11
Rossi, B.M.12
-
91
-
-
84856117692
-
Evaluation of predictive models for the identification in daily practice of patients with lynch syndrome
-
Tresallet C, Brouquet A, Julie C, Beauchet A, Vallot C, Menegaux F, Mitry E, Radvanyi F, Malafosse R, Rougier P, Nordlinger B, Laurent-Puig P, Boileau C, Emile JF, Muti C, Penna C, Hofmann-Radvanyi H. Evaluation of predictive models for the identification in daily practice of patients with lynch syndrome. Int J Cancer 2012;130:1367-77.
-
(2012)
Int J Cancer
, vol.130
, pp. 1367-1377
-
-
Tresallet, C.1
Brouquet, A.2
Julie, C.3
Beauchet, A.4
Vallot, C.5
Menegaux, F.6
Mitry, E.7
Radvanyi, F.8
Malafosse, R.9
Rougier, P.10
Nordlinger, B.11
Laurent-Puig, P.12
Boileau, C.13
Emile, J.F.14
Muti, C.15
Penna, C.16
Hofmann-Radvanyi, H.17
-
92
-
-
84872071989
-
Comparison of the clinical prediction model PREMM1,2 6 and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer
-
Kastrinos F, Steyerberg EW, Balmana J, Mercado R, Gallinger S, Haile R, Casey G, Hopper JL, Lemarchand L, Lindor NM, Newcomb PA, Thibodeau SN, Syngal S. Comparison of the clinical prediction model PREMM1,2,6 and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer. Gut 2013;62:272-9.
-
(2013)
Gut
, vol.62
, pp. 272-279
-
-
Kastrinos, F.1
Steyerberg, E.W.2
Balmana, J.3
Mercado, R.4
Gallinger, S.5
Haile, R.6
Casey, G.7
Hopper, J.L.8
Lemarchand, L.9
Lindor, N.M.10
Newcomb, P.A.11
Thibodeau, S.N.12
Syngal, S.13
-
93
-
-
84863636958
-
Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases
-
Mercado RC, Hampel H, Kastrinos F, Steyerberg E, Balmana J, Stoffel E, Cohn DE, Backes FJ, Hopper JL, Jenkins MA, Lindor NM, Casey G, Haile R, Madhavan S, de la Chapelle A, Syngal S. Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases. Genet Med 2012;14:670-80.
-
(2012)
Genet Med
, vol.14
, pp. 670-680
-
-
Mercado, R.C.1
Hampel, H.2
Kastrinos, F.3
Steyerberg, E.4
Balmana, J.5
Stoffel, E.6
Cohn, D.E.7
Backes, F.J.8
Hopper, J.L.9
Jenkins, M.A.10
Lindor, N.M.11
Casey, G.12
Haile, R.13
Madhavan, S.14
de la Chapelle, A.15
Syngal, S.16
-
94
-
-
84864856743
-
Diagnosing Lynch syndrome: more light at the end of the tunnel
-
Burt RW. Diagnosing Lynch syndrome: more light at the end of the tunnel. Cancer Prev Res (Phila) 2012;5:507-10.
-
(2012)
Cancer Prev Res (Phila)
, vol.5
, pp. 507-510
-
-
Burt, R.W.1
-
95
-
-
78650801916
-
Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population
-
Dinh TA, Rosner BI, Atwood JC, Boland CR, Syngal S, Vasen HF, Gruber SB, Burt RW. Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population. Cancer Prev Res (Phila) 2011;4:9-22.
-
(2011)
Cancer Prev Res (Phila)
, vol.4
, pp. 9-22
-
-
Dinh, T.A.1
Rosner, B.I.2
Atwood, J.C.3
Boland, C.R.4
Syngal, S.5
Vasen, H.F.6
Gruber, S.B.7
Burt, R.W.8
-
96
-
-
84890231687
-
-
National Comprehensive Cancer, Network., NCCN., Clinical Practice Guidelines in Oncology Version, 1.2013., Colorectal Cancer, Screening., 2013., National Comprehensive Cancer Network
-
National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology Version 1.2013. Colorectal Cancer Screening. 2013. National Comprehensive Cancer Network, 2013.
-
(2013)
-
-
-
97
-
-
84863903548
-
Screening patients with colorectal cancer for lynch syndrome: what are we waiting for?
-
Kastrinos F, Syngal S. Screening patients with colorectal cancer for lynch syndrome: what are we waiting for? J Clin Oncol 2012;30:1024-7.
-
(2012)
J Clin Oncol
, vol.30
, pp. 1024-1027
-
-
Kastrinos, F.1
Syngal, S.2
|