-
1
-
-
0032730774
-
Genetic susceptibility to nonpolyposis colorectal cancer
-
Lynch,H.T. and de la Chapelle,A. (1999) Genetic susceptibility to nonpolyposis colorectal cancer. J. Med. Genet., 36, 801-818.
-
(1999)
J. Med. Genet.
, vol.36
, pp. 801-818
-
-
Lynch, H.T.1
de la Chapelle, A.2
-
2
-
-
4944240144
-
Genetic predisposition to colorectal cancer
-
de la Chapelle,A. (2004) Genetic predisposition to colorectal cancer. Nat. Rev. Cancer, 10, 769-780.
-
(2004)
Nat. Rev. Cancer
, vol.10
, pp. 769-780
-
-
de la Chapelle, A.1
-
3
-
-
0027518250
-
Surveillance in hereditary nonpolyposis colorectal cancer: An international cooperative study of 165 families
-
The International Collaborative Group on HNPCC
-
Vasen,H.F., Mecklin,J.P., Watson,P. et al. (1993) Surveillance in hereditary nonpolyposis colorectal cancer: An international cooperative study of 165 families. The International Collaborative Group on HNPCC. Dis. Colon Rectum, 36, 1-4.
-
(1993)
Dis. Colon Rectum
, vol.36
, pp. 1-4
-
-
Vasen, H.F.1
Mecklin, J.P.2
Watson, P.3
-
4
-
-
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. and Lynch,H.T. (1999) New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology, 116, 1453-1456.
-
(1999)
Gastroenterology
, vol.116
, pp. 1453-1456
-
-
Vasen, H.F.1
Watson, P.2
Mecklin, J.P.3
Lynch, H.T.4
-
5
-
-
10144250305
-
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer
-
Moslein,G., Tester,D.J., Lindor,N.M., Honchel,R., Cunningham,J.M., French,A.J., Halling,K.C., Schwab,M., Goretzki,P. and Thibodeau,S.N. (1996) Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. Hum. Mol. Genet., 5, 1245-1252.
-
(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
-
6
-
-
16944364360
-
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations
-
Wijnen,J., Khan,P.M., Vasen,H., van der Klift,H., Mulder,A., van Leeuwen-Cornelisse,I., Bakker,B., Losekoot,M., Moller,P. and Fodde,R. (1997) Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. Am. J. Hum. Genet., 61, 329-335.
-
(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
-
7
-
-
4444272418
-
The search for low-penetrance cancer susceptibility alleles
-
Houlston,R.S. and Peto,J. (2004) The search for low-penetrance cancer susceptibility alleles. Oncogene, 23, 6471-6476.
-
(2004)
Oncogene
, vol.23
, pp. 6471-6476
-
-
Houlston, R.S.1
Peto, J.2
-
8
-
-
0036578764
-
Polygenic susceptibility to breast cancer and implications for prevention
-
Pharoah,P.D., Antoniou,A., Bobrow,M., Zimmern,R.L., Easton,D.F. and Ponder,B.A. (2004) Polygenic susceptibility to breast cancer and implications for prevention. Nat. Genet., 31, 33-36.
-
(2004)
Nat. Genet.
, vol.31
, pp. 33-36
-
-
Pharoah, P.D.1
Antoniou, A.2
Bobrow, M.3
Zimmern, R.L.4
Easton, D.F.5
Ponder, B.A.6
-
9
-
-
16944365288
-
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC
-
Laken,S.J., Petersen,G.M., Gruber,S.B. et al. (1997) Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC. Nat. Genet., 17, 79-83.
-
(1997)
Nat. Genet.
, vol.17
, pp. 79-83
-
-
Laken, S.J.1
Petersen, G.M.2
Gruber, S.B.3
-
10
-
-
18544389716
-
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
-
Meijers-Heijboer,H., van den Ouweland,A., Klijn,J. et al. (2002) Low-penetrance susceptibility to breast cancer due to CHEK2(* 1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat. Genet., 31, 55-59.
-
(2002)
Nat. Genet.
, vol.31
, pp. 55-59
-
-
Meijers-Heijboer, H.1
van den Ouweland, A.2
Klijn, J.3
-
11
-
-
8544264617
-
Genetic factors and colorectal cancer in Ashkenazi Jews
-
Locker,G.Y. and Lynch,H.T. (2004) Genetic factors and colorectal cancer in Ashkenazi Jews. Fam. Cancer, 3, 215-221.
-
(2004)
Fam. Cancer
, vol.3
, pp. 215-221
-
-
Locker, G.Y.1
Lynch, H.T.2
-
12
-
-
3042582651
-
CHEK2*1100delC and susceptibility to breast cancer: A collaborative analysis involving 10 860 breast cancer cases and 9065 controls from 10 studies
-
CHEK2 Breast Cancer Case Control Consortium
-
CHEK2 Breast Cancer Case Control Consortium (2004) CHEK2*1100delC and susceptibility to breast cancer: A collaborative analysis involving 10 860 breast cancer cases and 9065 controls from 10 studies. Am. J. Hum. Genet., 74, 1175-1182.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 1175-1182
-
-
-
13
-
-
0036478899
-
Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors
-
Al-Tassan,N., Chmiel,N.H., Maynard,J. et al. (2002) Inherited variants of MYH associated with somatic G:C→T:A mutations in colorectal tumors. Nat. Genet., 30, 227-232.
-
(2002)
Nat. Genet.
, vol.30
, pp. 227-232
-
-
Al-Tassan, N.1
Chmiel, N.H.2
Maynard, J.3
-
14
-
-
0037468517
-
Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH
-
Sieber,O.M., Lipton,L., Crabtree,M. et al. (2003) Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH. N. Engl. J. Med., 348, 791-799.
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 791-799
-
-
Sieber, O.M.1
Lipton, L.2
Crabtree, M.3
-
15
-
-
0041423452
-
Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients
-
Enholm,S., Hienonen,T., Suomalainen,A. et al. (2003) Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients. Am. J. Pathol., 163, 827-832.
-
(2003)
Am. J. Pathol.
, vol.163
, pp. 827-832
-
-
Enholm, S.1
Hienonen, T.2
Suomalainen, A.3
-
16
-
-
1542719919
-
Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer
-
Fleischmann,C., Peto,J., Cheadle,J., Shah,B., Sampson,J. and Houlston,R.S. (2004) Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer. Int. J. Cancer, 109, 554-558.
-
(2004)
Int. J. Cancer
, vol.109
, pp. 554-558
-
-
Fleischmann, C.1
Peto, J.2
Cheadle, J.3
Shah, B.4
Sampson, J.5
Houlston, R.S.6
-
17
-
-
7944225535
-
Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk
-
Croitoru,M.E., Cleary,S.P., Di Nicola,N. et al. (2004) Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk. J. Natl. Cancer Inst., 96, 1631-1634.
-
(2004)
J. Natl. Cancer Inst.
, vol.96
, pp. 1631-1634
-
-
Croitoru, M.E.1
Cleary, S.P.2
Di Nicola, N.3
-
18
-
-
3242689475
-
MYE mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps
-
Wang,L., Baudhuin,L.M., Boardman,L.A. et al. (2004) MYE mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps. Gastroenterology, 127, 9-16.
-
(2004)
Gastroenterology
, vol.127
, pp. 9-16
-
-
Wang, L.1
Baudhuin, L.M.2
Boardman, L.A.3
-
19
-
-
12144289614
-
Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas
-
Gismondi,V., Meta,M., Bonelli,L. et al. (2004) Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas. Int. J. Cancer, 109, 680-684.
-
(2004)
Int. J. Cancer
, vol.109
, pp. 680-684
-
-
Gismondi, V.1
Meta, M.2
Bonelli, L.3
-
20
-
-
14044276307
-
Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH
-
Peterlongo,P., Mitra,M., Chuai,S., Kirchhoff,T., Palmer,C., Huang,H., Nafa,K., Offit,K. and Ellis,N.A. (2005) Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH. Int. J. Cancer, 114, 505-507.
-
(2005)
Int. J. Cancer
, vol.114
, pp. 505-507
-
-
Peterlongo, P.1
Mitra, M.2
Chuai, S.3
Kirchhoff, T.4
Palmer, C.5
Huang, H.6
Nafa, K.7
Offit, K.8
Ellis, N.A.9
-
21
-
-
20544452084
-
Germline susceptibility to colorectal cancer due to base-excision repair gene defects
-
Farrington,S.M., Tenesa,A., Barnetson,R., Wiltshire,A., Prendergast,J., Porteous,M., Campbell,H. and Dunlop,M.G. (2005) Germline susceptibility to colorectal cancer due to base-excision repair gene defects. Am. J. Hum. Genet., 77, 112-119.
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 112-119
-
-
Farrington, S.M.1
Tenesa, A.2
Barnetson, R.3
Wiltshire, A.4
Prendergast, J.5
Porteous, M.6
Campbell, H.7
Dunlop, M.G.8
-
22
-
-
21044458154
-
Germline mutations in the MYH gene in Swedish familial and sporadic colorectal cancer
-
the Swedish Low-Risk Colorectal Cancer Group
-
Zhou,X.L., Djureinovic,T., Werelius,B., Lindmark,G., Sun,X.F. and Lindblom,A. and the Swedish Low-Risk Colorectal Cancer Group (2005) Germline mutations in the MYH gene in Swedish familial and sporadic colorectal cancer. Genet. Test, 9, 147-151.
-
(2005)
Genet. Test
, vol.9
, pp. 147-151
-
-
Zhou, X.L.1
Djureinovic, T.2
Werelius, B.3
Lindmark, G.4
Sun, X.F.5
Lindblom, A.6
-
23
-
-
0142053924
-
MSH6 germline mutations are rare in colorectal cancer families
-
Peterlongo,P., Nafa,K., Lerman,G.S. et al. (2003) MSH6 germline mutations are rare in colorectal cancer families. Int. J. Cancer, 107, 571-579.
-
(2003)
Int. J. Cancer
, vol.107
, pp. 571-579
-
-
Peterlongo, P.1
Nafa, K.2
Lerman, G.S.3
-
24
-
-
11144279281
-
Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms
-
Shia,J., Klimstra,D.S., Nafa,K., Offit,K., Guillem,J.G., Markowitz,A.J., Gerald,W.L. and Ellis,N.A. (2005) Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms. Am. J. Surg. Pathol., 291, 96-104.
-
(2005)
Am. J. Surg. Pathol.
, vol.291
, pp. 96-104
-
-
Shia, J.1
Klimstra, D.S.2
Nafa, K.3
Offit, K.4
Guillem, J.G.5
Markowitz, A.J.6
Gerald, W.L.7
Ellis, N.A.8
-
25
-
-
33644747476
-
Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: A population-based case-family study
-
Jenkins,M.A., Croitoru,M.E., Monga,N., Cleary,S.P., Cotterchio,M., Hopper,J.L. and Gallinger,S. (2006) Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: A population-based case-family study. Cancer Epidemiol. Biomarkers Prev., 15, 312-314.
-
(2006)
Cancer Epidemiol. Biomarkers Prev.
, vol.15
, pp. 312-314
-
-
Jenkins, M.A.1
Croitoru, M.E.2
Monga, N.3
Cleary, S.P.4
Cotterchio, M.5
Hopper, J.L.6
Gallinger, S.7
-
26
-
-
26244444771
-
Correlation of polyp number and family history of colon cancer with germline MYH mutations
-
Jo,W.S., Bandipalliam,P., Shannon,K.M., Niendorf,K.B., Chan-Smutko, G., Hur,C., Syngal,S. and Chung,D.C. (2005) Correlation of polyp number and family history of colon cancer with germline MYH mutations. Clin. Gastroenterol. Hepatol., 3, 1022-1028.
-
(2005)
Clin. Gastroenterol. Hepatol.
, vol.3
, pp. 1022-1028
-
-
Jo, W.S.1
Bandipalliam, P.2
Shannon, K.M.3
Niendorf, K.B.4
Chan-Smutko, G.5
Hur, C.6
Syngal, S.7
Chung, D.C.8
-
27
-
-
22144488788
-
Frequency of the common MYH mutations (G382D and Y165C) in MMR mutation positive and negative HNPCC patients
-
Ashton,K.A., Meldrum,C.J., McPhillips,M.L., Kairupan,C.F. and Scott,R.J. (2005) Frequency of the common MYH mutations (G382D and Y165C) in MMR mutation positive and negative HNPCC patients. Hereditary Cancer Clin. Pract., 3, 65-70.
-
(2005)
Hereditary Cancer Clin. Pract.
, vol.3
, pp. 65-70
-
-
Ashton, K.A.1
Meldrum, C.J.2
McPhillips, M.L.3
Kairupan, C.F.4
Scott, R.J.5
-
28
-
-
0033570376
-
ThetaR-I(6A) is a candidate tumor susceptibility allele
-
Pasche,B., Kolachana,P., Nafa,K. et al. (1999) ThetaR-I(6A) is a candidate tumor susceptibility allele. Cancer. Res., 59, 5678-5682.
-
(1999)
Cancer. Res.
, vol.59
, pp. 5678-5682
-
-
Pasche, B.1
Kolachana, P.2
Nafa, K.3
-
29
-
-
21144448326
-
TGFBR1*6A may contribute to hereditary colorectal cancer
-
Bian,Y., Caldes,T., Wijnen,J. et al. (2005) TGFBR1*6A may contribute to hereditary colorectal cancer. J. Clin. Oncol., 23, 3074-3078.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 3074-3078
-
-
Bian, Y.1
Caldes, T.2
Wijnen, J.3
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