-
1
-
-
0034793635
-
A systematic review and meta-analysis of familial colorectal cancer risk
-
DOI 10.1016/S0002-9270(01)03239-7, PII S0002927001032397
-
Johns LE, Houlston RS: A systematic review and meta-analysis of familial colorectal cancer risk. Am J Gastroenterol 2001; 96: 2992-3003. (Pubitemid 32959544)
-
(2001)
American Journal of Gastroenterology
, vol.96
, Issue.10
, pp. 2992-3003
-
-
Johns, L.E.1
Houlston, R.S.2
-
2
-
-
16644378293
-
Refining the Amsterdam criteria and Bethesda guidelines: Testing algorithms for the prediction of mismatch repair mutation status in the familial cancer clinic
-
DOI 10.1200/JCO.2004.11.084
-
Lipton LR, Johnson V, Cummings C et al: 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: 4934-4943. (Pubitemid 46638618)
-
(2004)
Journal of Clinical Oncology
, vol.22
, Issue.24
, 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
-
3
-
-
0033200024
-
Genetic testing in hereditary colorectal cancer: Indications and procedures
-
DOI 10.1111/j.1572-0241.1999.01356.x, PII S0002927099004128
-
Terdiman JP, Conrad PG, Sleisenger MH: Genetic testing in hereditary colorectal cancer: indications and procedures. Am J Gastroenterol 1999; 94: 2344-2356. (Pubitemid 29420655)
-
(1999)
American Journal of Gastroenterology
, vol.94
, Issue.9
, pp. 2344-2356
-
-
Terdiman, J.P.1
Conrad, P.G.2
Sleisenger, M.H.3
-
4
-
-
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: 424-425.
-
(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
-
5
-
-
20244386256
-
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X
-
DOI 10.1001/jama.293.16.1979
-
Lindor NM, Rabe K, Petersen GM et al: Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X. JAMA 2005; 293: 1979-1985. (Pubitemid 40570891)
-
(2005)
Journal of the American Medical Association
, vol.293
, Issue.16
, pp. 1979-1985
-
-
Lindor, N.M.1
Rabe, K.2
Petersen, G.M.3
Haile, R.4
Casey, G.5
Baron, J.6
Gallinger, S.7
Bapat, B.8
Aronson, M.9
Hopper, J.10
Jass, J.11
LeMarchand, L.12
Grove, J.13
Potter, J.14
Newcomb, P.15
Terdiman, J.P.16
Conrad, P.17
Moslein, G.18
Goldberg, R.19
Ziogas, A.20
Anton-Culver, H.21
De Andrade, M.22
Siegmund, K.23
Thibodeau, S.N.24
Boardman, L.A.25
Seminara, D.26
more..
-
6
-
-
34848836040
-
Familial Colorectal Cancer Syndrome X
-
DOI 10.1053/j.seminoncol.2007.07.008, PII S0093775407001479, Breast and Colorectal Cancer Genetics for Practicing Oncologists
-
Lipkin SM, Afrasiabi K: Familial colorectal cancer syndrome X. Semin Oncol 2007; 34: 425-427. (Pubitemid 47503277)
-
(2007)
Seminars in Oncology
, vol.34
, Issue.5
, pp. 425-427
-
-
Lipkin, S.M.1
Afrasiabi, K.2
-
7
-
-
56749180189
-
Deciphering the genetics of hereditary non-syndromic colorectal cancer
-
Papaemmanuil E, Carvajal-Carmona L, Sellick GS et al: Deciphering the genetics of hereditary non-syndromic colorectal cancer. Eur J Hum Genet 2008; 16: 1477-1486.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 1477-1486
-
-
Papaemmanuil, E.1
Carvajal-Carmona, L.2
Sellick, G.S.3
-
8
-
-
0242363139
-
A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2
-
DOI 10.1073/pnas.2132286100
-
Wiesner GL, Daley D, Lewis S et al: A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2. Proc Natl Acad Sci USA 2003; 100: 12961-12965. (Pubitemid 37340008)
-
(2003)
Proceedings of the National Academy of Sciences of the United States of America
, vol.100
, Issue.22
, pp. 12961-12965
-
-
Wiesner, G.L.1
Daley, D.2
Lewis, S.3
Ticknor, C.4
Platzer, P.5
Lutterbaugh, J.6
MacMillen, M.7
Baliner, B.8
Willis, J.9
Elston, R.C.10
Markowitz, S.D.11
-
9
-
-
41149124434
-
Identification of susceptibility genes for cancer in a genome-wide scan: Results from the colon neoplasia sibling study
-
Daley D, Lewis S, Platzer P et al: Identification of susceptibility genes for cancer in a genome-wide scan: results from the colon neoplasia sibling study. Am J Hum Genet 2008; 82: 723-736.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 723-736
-
-
Daley, D.1
Lewis, S.2
Platzer, P.3
-
10
-
-
33749065163
-
Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan
-
DOI 10.1093/hmg/ddl231
-
Kemp Z, Carvajal-Carmona L, Spain S et al: Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan. Hum Mol Genet 2006; 15: 2903-2910. (Pubitemid 44458121)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.19
, pp. 2903-2910
-
-
Kemp, Z.1
Carvajal-Carmona, L.2
Spain, S.3
Barclay, E.4
Gorman, M.5
Martin, L.6
Jaeger, E.7
Brooks, N.8
Bishop, D.T.9
Thomas, H.10
Tomlinson, I.11
Papaemmanuil, E.12
Webb, E.13
Sellick, G.S.14
Wood, W.15
Evans, G.16
Lucassen, A.17
Maher, E.R.18
Houlston, R.S.19
-
11
-
-
33744907495
-
Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom
-
DOI 10.1158/0008-5472.CAN-05-4074
-
Kemp ZE, Carvajal-Carmona LG, Barclay E et al: Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom. Cancer Res 2006; 66: 5003-5006. (Pubitemid 43844919)
-
(2006)
Cancer Research
, vol.66
, Issue.10
, pp. 5003-5006
-
-
Kemp, Z.E.1
Carvajal-Carmona, L.G.2
Barclay, E.3
Gorman, M.4
Martin, L.5
Wood, W.6
Rowan, A.7
Donohue, C.8
Spain, S.9
Jaeger, E.10
Evans, D.G.11
Maher, E.R.12
Bishop, T.13
Thomas, H.14
Houlston, R.15
Tomlinson, I.16
-
12
-
-
43549105874
-
Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q
-
Picelli S, Vandrovcova J, Jones S et al: Genome-wide linkage scan for colorectal cancer susceptibility genes supports linkage to chromosome 3q. BMC Cancer 2008; 8: 87.
-
(2008)
BMC Cancer
, vol.8
, pp. 87
-
-
Picelli, S.1
Vandrovcova, J.2
Jones, S.3
-
13
-
-
33144458558
-
A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer
-
DOI 10.1136/gut.2005.075333
-
Djureinovic T, Skoglund J, Vandrovcova J et al: A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer. Gut 2006; 55: 362-366. (Pubitemid 43268274)
-
(2006)
Gut
, vol.55
, Issue.3
, pp. 362-366
-
-
Djureinovic, T.1
Skoglund, J.2
Vandrovcova, J.3
Zhou, X.-L.4
Kalushkova, A.5
Iselius, L.6
Lindblom, A.7
-
14
-
-
55349101975
-
Common familial colorectal cancer linked to chromosome 7q31: A genome-wide analysis
-
Neklason DW, Kerber RA, Nilson DB et al: Common familial colorectal cancer linked to chromosome 7q31: a genome-wide analysis. Cancer Res 2008; 68: 8993-8997.
-
(2008)
Cancer Res
, vol.68
, pp. 8993-8997
-
-
Neklason, D.W.1
Kerber, R.A.2
Nilson, D.B.3
-
15
-
-
77954382262
-
Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22
-
Gray-McGuire C, Guda K, Adrianto I et al: Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. Cancer Res 2010; 70: 5409-5418.
-
(2010)
Cancer Res
, vol.70
, pp. 5409-5418
-
-
Gray-Mcguire, C.1
Guda, K.2
Adrianto, I.3
-
16
-
-
60549092759
-
Population characteristics related to colorectal cancer testing in New South Wales, Australia: Results from the 45 and Up Study cohort
-
Weber MF, Banks E, Ward R, Sitas F: Population characteristics related to colorectal cancer testing in New South Wales, Australia: results from the 45 and Up Study cohort. J Med Screen 2008; 15: 137-142.
-
(2008)
J Med Screen
, vol.15
, pp. 137-142
-
-
Weber, M.F.1
Banks, E.2
Ward, R.3
Sitas, F.4
-
17
-
-
58149260360
-
Colorectal cancer mortality in Spain: Trends and projections for 1985-2019
-
Ribes J, Navarro M, Cleries R et al: Colorectal cancer mortality in Spain: trends and projections for 1985-2019. Eur J Gastroenterol Hepatol 2009; 21: 92-100.
-
(2009)
Eur J Gastroenterol Hepatol
, vol.21
, pp. 92-100
-
-
Ribes, J.1
Navarro, M.2
Cleries, R.3
-
18
-
-
34547472163
-
A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker data
-
DOI 10.1002/gepi.20229
-
Saunders IW, Hannan GN, Brohede J et al: A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker data. Genet Epidemiol 2007; 31: 565-576. (Pubitemid 350246542)
-
(2007)
Genetic Epidemiology
, vol.31
, Issue.6
, pp. 565-576
-
-
Saunders, I.W.1
Hannan, G.N.2
Brohede, J.3
Giles, G.G.4
Jenkins, M.A.5
Hopper, J.L.6
Southey, M.C.7
-
19
-
-
33646243226
-
An evaluation of the replicate pool method: Quick estimation of genome-wide linkage peak p-values
-
Wigginton JE, Abecasis GR: An evaluation of the replicate pool method: quick estimation of genome-wide linkage peak p-values. Genet Epidemiol 2006; 30: 320-332.
-
(2006)
Genet Epidemiol
, vol.30
, pp. 320-332
-
-
Wigginton, J.E.1
Abecasis, G.R.2
-
20
-
-
0000353178
-
A maximization technique occuring in the statistical analysis of probabilistic functions of Markov Chains
-
Baum L, Petrie T, Soules G, Weiss N: A maximization technique occuring in the statistical analysis of probabilistic functions of Markov Chains. Ann Math Statist 1970; 41: 164-171.
-
(1970)
Ann Math Statist
, vol.41
, pp. 164-171
-
-
Baum, L.1
Petrie, T.2
Soules, G.3
Weiss, N.4
-
21
-
-
34547425321
-
Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference
-
DOI 10.1016/j.ygeno.2007.05.011, PII S088875430700136X
-
Saunders IW, Brohede J, Hannan GN: Estimating genotyping error rates from Mendelian errors in SNP array genotypes and their impact on inference. Genomics 2007; 90: 291-296. (Pubitemid 47176339)
-
(2007)
Genomics
, vol.90
, Issue.3
, pp. 291-296
-
-
Saunders, I.W.1
Brohede, J.2
Hannan, G.N.3
-
22
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR: Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002; 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
23
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
DOI 10.1086/301592
-
Kong A, Cox NJ: Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet 1997; 61: 1179-1188. (Pubitemid 27492328)
-
(1997)
American Journal of Human Genetics
, vol.61
, Issue.5
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
24
-
-
0028301661
-
A class of tests for linkage using affected pedigree members
-
Whittemore AS, Halpern J: A class of tests for linkage using affected pedigree members. Biometrics 1994; 50: 118-127. (Pubitemid 24138579)
-
(1994)
Biometrics
, vol.50
, Issue.1
, pp. 118-127
-
-
Whittemore, A.S.1
Halpern, J.2
-
25
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995; 11: 241-247.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
26
-
-
34247115114
-
Difference in the role of loss of heterozygosity at 10p15 (KLF6 locus) in colorectal carcinogenesis between sporadic and familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer patients
-
DOI 10.1159/000100523
-
Miyaki M, Yamaguchi T, Iijima T, Funata N, Mori T: Difference in the role of loss of heterozygosity at 10p15 (KLF6 locus) in colorectal carcinogenesis between sporadic and familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer patients. Oncology 2006; 71: 131-135. (Pubitemid 46588172)
-
(2007)
Oncology
, vol.71
, Issue.1-2
, pp. 131-135
-
-
Miyaki, M.1
Yamaguchi, T.2
Iijima, T.3
Funata, N.4
Mori, T.5
-
27
-
-
33846057724
-
NCBI reference sequences (RefSeq): A curated non-redundant sequence database of genomes, transcripts and proteins
-
DOI 10.1093/nar/gkl842
-
Pruitt KD, Tatusova T, Maglott DR: NCBI reference sequences (RefSeq): a curated nonredundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res 2007; 35: D61-D65. (Pubitemid 46056171)
-
(2007)
Nucleic Acids Research
, vol.35
, Issue.SUPPL. 1
-
-
Pruitt, K.D.1
Tatusova, T.2
Maglott, D.R.3
-
28
-
-
18244389734
-
KLF6, a candidate tumor suppressor gene mutated in prostate cancer
-
DOI 10.1126/science.1066326
-
Narla G, Heath KE, Reeves HL et al: KLF6, a candidate tumor suppressor gene mutated in prostate cancer. Science 2001; 294: 2563-2566. (Pubitemid 34027299)
-
(2001)
Science
, vol.294
, Issue.5551
, pp. 2563-2566
-
-
Narla, G.1
Heath, K.E.2
Reeves, H.L.3
Li, D.4
Giono, L.E.5
Kimmelman, A.C.6
Glucksman, M.J.7
Narla, J.8
Eng, F.J.9
Chan, A.M.10
Ferrari, A.C.11
Martignetti, J.A.12
Friedman, S.L.13
-
29
-
-
11144357280
-
Kruppel-Like Factor 6 (KLF6) Is a Tumor-Suppressor Gene Frequently Inactivated in Colorectal Cancer
-
DOI 10.1053/j.gastro.2004.01.005
-
Reeves HL, Narla G, Ogunbiyi O et al: Kruppel-like factor 6 (KLF6) is a tumorsuppressor gene frequently inactivated in colorectal cancer. Gastroenterology 2004; 126: 1090-1103. (Pubitemid 38451180)
-
(2004)
Gastroenterology
, vol.126
, Issue.4
, pp. 1090-1103
-
-
Reeves, H.L.1
Narla, G.2
Ogunbiyi, O.3
Haq, A.I.4
Katz, A.5
Benzeno, S.6
Hod, E.7
Harpaz, N.8
Goldberg, S.9
Tal-Kremer, S.10
Eng, F.J.11
Arthur, M.J.P.12
Martignetti, J.A.13
Friedman, S.L.14
-
30
-
-
0037255084
-
Human gene-centric databases at the Weizmann Institute of science: GeneCards, UDB, CroW 21 and HORDE
-
DOI 10.1093/nar/gkg050
-
Safran M, Chalifa-Caspi V, Shmueli O et al: Human gene-centric databases at the Weizmann institute of science: GeneCards, UDB, CroW 21 and HORDE. Nucleic Acids Res 2003; 31: 142-146. (Pubitemid 36157280)
-
(2003)
Nucleic Acids Research
, vol.31
, Issue.1
, pp. 142-146
-
-
Safran, M.1
Chalifa-Caspi, V.2
Shmueli, O.3
Olender, T.4
Lapidot, M.5
Rosen, N.6
Shmoish, M.7
Peter, Y.8
Glusman, G.9
Feldmesser, E.10
Adato, A.11
Peter, I.12
Khen, M.13
Atarot, T.14
Groner, Y.15
Lancet, D.16
-
31
-
-
56849112856
-
Low-penetrance alleles predisposing to sporadic colorectal cancers: A French case-controlled genetic association study
-
Kury S, Buecher B, Robiou-du-Pont S et al: Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study. BMC Cancer 2008; 8: 326.
-
(2008)
BMC Cancer
, vol.8
, pp. 326
-
-
Kury, S.1
Buecher, B.2
Robiou-Du-Pont, S.3
-
32
-
-
67649083644
-
Microsomal prostaglandin e synthase protein levels correlate with prognosis in colorectal cancer patients
-
Seo T, Tatsuguchi A, Shinji S et al: Microsomal prostaglandin E synthase protein levels correlate with prognosis in colorectal cancer patients. Virchows Arch 2009; 454: 667-676.
-
(2009)
Virchows Arch
, vol.454
, pp. 667-676
-
-
Seo, T.1
Tatsuguchi, A.2
Shinji, S.3
-
33
-
-
64849092309
-
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene
-
Jones S, Hruban RH, Kamiyama M et al: Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. Science 2009; 324: 217.
-
(2009)
Science
, vol.324
, pp. 217
-
-
Jones, S.1
Hruban, R.H.2
Kamiyama, M.3
-
34
-
-
33746381505
-
EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis
-
Kokko A, Laiho P, Lehtonen R et al: EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis. BMC Cancer 2006; 6: 145.
-
(2006)
BMC Cancer
, vol.6
, pp. 145
-
-
Kokko, A.1
Laiho, P.2
Lehtonen, R.3
-
35
-
-
33745920193
-
Association of MUTYH and colorectal cancer
-
DOI 10.1038/sj.bjc.6603239, PII 6603239
-
Tenesa A, Campbell H, Barnetson R, Porteous M, Dunlop M, Farrington SM: Association of MUTYH and colorectal cancer. Br J Cancer 2006; 95: 239-242. (Pubitemid 44050924)
-
(2006)
British Journal of Cancer
, vol.95
, Issue.2
, pp. 239-242
-
-
Tenesa, A.1
Campbell, H.2
Barnetson, R.3
Porteous, M.4
Dunlop, M.5
Farrington, S.M.6
-
36
-
-
12844266901
-
Identification of HNPCC by molecular analysis of colorectal and endometrial tumors
-
Lynch Syndrome (HNPCC) and Microsatellite Instability
-
Vasen HF, Hendriks Y, de Jong AE et al: Identification of HNPCC by molecular analysis of colorectal and endometrial tumors. Dis Markers 2004; 20: 207-213. (Pubitemid 40164093)
-
(2004)
Disease Markers
, vol.20
, Issue.4-5
, pp. 207-213
-
-
Vasen, H.F.A.1
Hendriks, Y.2
De Jong, A.E.3
Van Puijenbroek, M.4
Tops, C.5
Brocker-Vriends, A.H.J.T.6
Wijnen, J.Th.7
Morreau, H.8
-
37
-
-
0032829265
-
Familial adenomatous polyposis (FAP) and its gene, APC
-
Bodmer W: Familial adenomatous polyposis (FAP) and its gene, APC. Cytogenet Cell Genet 1999; 86: 99-104. (Pubitemid 29488300)
-
(1999)
Cytogenetics and Cell Genetics
, vol.86
, Issue.2
, pp. 99-104
-
-
Bodmer, W.1
-
38
-
-
42649124305
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
-
DOI 10.1038/ng.133, PII NG133
-
Tenesa A, Farrington SM, Prendergast JG et al: Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Nat Genet 2008; 40: 631-637. (Pubitemid 351601219)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 631-637
-
-
Tenesa, A.1
Farrington, S.M.2
Prendergast, J.G.D.3
Porteous, M.E.4
Walker, M.5
Haq, N.6
Barnetson, R.A.7
Theodoratou, E.8
Cetnarskyj, R.9
Cartwright, N.10
Semple, C.11
Clark, A.J.12
Reid, F.J.L.13
Smith, L.A.14
Kavoussanakis, K.15
Koessler, T.16
Pharoah, P.D.P.17
Buch, S.18
Schafmayer, C.19
Tepel, J.20
Schreiber, S.21
Volzke, H.22
Schmidt, C.O.23
Hampe, J.24
Chang-Claude, J.25
Hoffmeister, M.26
Brenner, H.27
Wilkening, S.28
Canzian, F.29
Capella, G.30
Moreno, V.31
Deary, I.J.32
Starr, J.M.33
Tomlinson, I.P.M.34
Kemp, Z.35
Howarth, K.36
Carvajal-Carmona, L.37
Webb, E.38
Broderick, P.39
Vijayakrishnan, J.40
Houlston, R.S.41
Rennert, G.42
Ballinger, D.43
Rozek, L.44
Gruber, S.B.45
Matsuda, K.46
Kidokoro, T.47
Nakamura, Y.48
Zanke, B.W.49
Greenwood, C.M.T.50
Rangrej, J.51
Kustra, R.52
Montpetit, A.53
Hudson, T.J.54
Gallinger, S.55
Campbell, H.56
Dunlop, M.G.57
more..
-
39
-
-
68149170044
-
The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling
-
Tuupanen S, Turunen M, Lehtonen R et al: The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling. Nat Genet 2009; 41: 885-890.
-
(2009)
Nat Genet
, vol.41
, pp. 885-890
-
-
Tuupanen, S.1
Turunen, M.2
Lehtonen, R.3
-
40
-
-
67349205051
-
TGFBR1 variants TGFBR1(*)6A and Int7G24A are not associated with an increased familial colorectal cancer risk
-
Skoglund Lundin J, Vandrovcova J, Song B et al: TGFBR1 variants TGFBR1(*)6A and Int7G24A are not associated with an increased familial colorectal cancer risk. Br J Cancer 2009; 100: 1674-1679.
-
(2009)
Br J Cancer
, vol.100
, pp. 1674-1679
-
-
Skoglund Lundin, J.1
Vandrovcova, J.2
Song, B.3
-
41
-
-
34250330252
-
Is TGFBR1*6A a susceptibility allele for nonsyndromic familial colorectal neoplasia?
-
DOI 10.1158/1055-9965.EPI-06-0965
-
Daley D, Morgan W, Lewis S et al: Is TGFBR1*6A a susceptibility allele for nonsyndromic familial colorectal neoplasia? Cancer Epidemiol Biomarkers Prev 2007; 16: 892-894. (Pubitemid 46910087)
-
(2007)
Cancer Epidemiology Biomarkers and Prevention
, vol.16
, Issue.5
, pp. 892-894
-
-
Daley, D.1
Morgan, W.2
Lewis, S.3
Willis, J.4
Elston, R.C.5
Markowitz, S.D.6
Wiesner, G.L.7
-
42
-
-
78049451452
-
Hereditary mixed polyposis syndrome due to a Bmpr1a mutation
-
O'Riordan J, O'Donoghue D, Green A et al: Hereditary mixed polyposis syndrome due to a Bmpr1a mutation. Colorectal Dis 2010; 12: 570-573.
-
(2010)
Colorectal Dis
, vol.12
, pp. 570-573
-
-
O'Riordan, J.1
O'Donoghue, D.2
Green, A.3
-
43
-
-
0842308265
-
PTEN mutations are common in sporadic microsatellite stable colorectal cancer
-
DOI 10.1038/sj.onc.1207059
-
Nassif NT, Lobo GP, Wu X et al: PTEN mutations are common in sporadic microsatellite stable colorectal cancer. Oncogene 2004; 23: 617-628. (Pubitemid 38175018)
-
(2004)
Oncogene
, vol.23
, Issue.2
, pp. 617-628
-
-
Nassif, N.T.1
Lobo, G.P.2
Wu, X.3
Henderson, C.J.A.4
Morrison, C.D.5
Eng, C.6
Jalaludin, B.7
Segelov, E.8
-
44
-
-
37549072226
-
Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk
-
Jaeger E, Webb E, Howarth K et al: Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk. Nat Genet 2008; 40: 26-28.
-
(2008)
Nat Genet
, vol.40
, pp. 26-28
-
-
Jaeger, E.1
Webb, E.2
Howarth, K.3
-
45
-
-
11144356056
-
A TP53 polymorphism is associated with increased risk of colorectal cancer and with reduced levels of TP53 mRNA
-
DOI 10.1038/sj.onc.1207305
-
Gemignani F, Moreno V, Landi S et al: A TP53 polymorphism is associated with increased risk of colorectal cancer and with reduced levels of TP53 mRNA. Oncogene 2004; 23: 1954-1956. (Pubitemid 38445422)
-
(2004)
Oncogene
, vol.23
, Issue.10
, pp. 1954-1956
-
-
Gemignani, F.1
Moreno, V.2
Landi, S.3
Moullan, N.4
Chabrier, A.5
Gutierrez-Enriquez, S.6
Hall, J.7
Guino, E.8
Peinado, M.A.9
Capella, G.10
Canzian, F.11
-
46
-
-
32544444419
-
The TP53 colorectal cancer international collaborative study on the prognostic and predictive significance of p53 mutation: Influence of tumor site, type of mutation, and adjuvant treatment
-
DOI 10.1200/JCO.2005.00.471
-
Russo A, Bazan V, Iacopetta B, Kerr D, Soussi T, Gebbia N: The TP53 colorectal cancer international collaborative study on the prognostic and predictive significance of p53 mutation: influence of tumor site, type of mutation, and adjuvant treatment. J Clin Oncol 2005; 23: 7518-7528. (Pubitemid 46291815)
-
(2005)
Journal of Clinical Oncology
, vol.23
, Issue.30
, pp. 7518-7528
-
-
Russo, A.1
Bazan, V.2
Iacopetta, B.3
Kerr, D.4
Soussi, T.5
Gebbia, N.6
-
47
-
-
0037220169
-
TP53 mutation in colorectal cancer
-
DOI 10.1002/humu.10175
-
Iacopetta B: TP53 mutation in colorectal cancer. Hum Mutat 2003; 21: 271-276. (Pubitemid 36292968)
-
(2003)
Human Mutation
, vol.21
, Issue.3
, pp. 271-276
-
-
Iacopetta, B.1
-
48
-
-
66449107196
-
The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression
-
Pittman AM, Naranjo S, Webb E et al: The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression. Genome Res 2009; 19: 987-993.
-
(2009)
Genome Res
, vol.19
, pp. 987-993
-
-
Pittman, A.M.1
Naranjo, S.2
Webb, E.3
-
49
-
-
77954351635
-
The role of SMAD4 in early onset colorectal cancer
-
Royce SG, Alsop K, Haydon A et al: The role of SMAD4 in early onset colorectal cancer. Colorectal Dis 2010; 12: 213-219.
-
(2010)
Colorectal Dis
, vol.12
, pp. 213-219
-
-
Royce, S.G.1
Alsop, K.2
Haydon, A.3
-
50
-
-
14444272759
-
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer
-
Resta N, Simone C, Mareni C et al: STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer. Cancer Res 1998; 58: 4799-4801. (Pubitemid 28503671)
-
(1998)
Cancer Research
, vol.58
, Issue.21
, pp. 4799-4801
-
-
Resta, N.1
Simone, C.2
Mareni, C.3
Montera, M.4
Gentile, M.5
Susca, F.6
Gristina, R.7
Pozzi, S.8
Bertario, L.9
Bufo, P.10
Carlomagno, N.11
Ingrosso, M.12
Rossini, F.P.13
Tenconi, R.14
Guanti, G.15
|