-
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
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer: Analyses of cohorts of twins from Sweden, Denmark, and Finland
-
DOI 10.1056/NEJM200007133430201
-
Lichtenstein P, Holm NV, Verkasalo PK, et al. Environmental and heritable factors in the causation of cancer - analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 2000;343:78-85. (Pubitemid 30451850)
-
(2000)
New England Journal of Medicine
, vol.343
, Issue.2
, pp. 78-85
-
-
Lichtenstein, P.1
Holm, N.V.2
Verkasalo, P.K.3
Iliadou, A.4
Kaprio, J.5
Koskenvuo, M.6
Pukkala, E.7
Skytthe, A.8
Hemminki, K.9
-
3
-
-
33846332027
-
Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors
-
DOI 10.1158/1078-0432.CCR-06-1256
-
Aaltonen L, Johns L, Jarvinen H, Mecklin JP, 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. (Pubitemid 46121890)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.1
, pp. 356-361
-
-
Aaltonen, L.1
Johns, L.2
Jarvinen, H.3
Mecklin, J.-P.4
Houlston, R.5
-
4
-
-
34547498546
-
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
-
Tomlinson I, Webb E, Carvajal-Carmona L, et al. A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Nat Genet 2007;39:984-8.
-
(2007)
Nat Genet
, vol.39
, pp. 984-988
-
-
Tomlinson, I.1
Webb, E.2
Carvajal-Carmona, L.3
-
5
-
-
34547092701
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
-
Zanke BW, Greenwood CM, Rangrej J, et al. Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Nat Genet 2007;39:989-94.
-
(2007)
Nat Genet
, vol.39
, pp. 989-994
-
-
Zanke, B.W.1
Greenwood, C.M.2
Rangrej, J.3
-
6
-
-
34547121725
-
A common genetic risk factor for colorectal and prostate cancer
-
DOI 10.1038/ng2098, PII NG2098
-
Haiman CA, Le Marchand L, Yamamato J, et al. A common genetic risk factor for colorectal and prostate cancer. Nat Genet 2007;39: 954-6. (Pubitemid 47185184)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 954-956
-
-
Haiman, C.A.1
Le Marchand, L.2
Yamamato, J.3
Stram, D.O.4
Sheng, X.5
Kolonel, L.N.6
Wu, A.H.7
Reich, D.8
Henderson, B.E.9
-
7
-
-
35648937584
-
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk
-
Broderick P, Carvajal-Carmona L, Pittman AM, et al. A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Nat Genet 2007;39:1315-7.
-
(2007)
Nat Genet
, vol.39
, pp. 1315-1317
-
-
Broderick, P.1
Carvajal-Carmona, L.2
Pittman, A.M.3
-
8
-
-
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;40:26-8.
-
(2008)
Nat Genet
, vol.40
, pp. 26-28
-
-
Jaeger, E.1
Webb, E.2
Howarth, K.3
-
9
-
-
42649136554
-
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
-
Tomlinson IP, Webb E, Carvajal-Carmona L, et al. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet 2008;40:623-30.
-
(2008)
Nat Genet
, vol.40
, pp. 623-630
-
-
Tomlinson, I.P.1
Webb, E.2
Carvajal-Carmona, L.3
-
10
-
-
42649124305
-
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21
-
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;40:631-7.
-
(2008)
Nat Genet
, vol.40
, pp. 631-637
-
-
Tenesa, A.1
Farrington, S.M.2
Prendergast, J.G.3
-
11
-
-
56049119387
-
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer
-
Pittman AM, Webb E, Carvajal-Carmona L, et al. Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer. Hum Mol Genet 2008;17:3720-7.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 3720-3727
-
-
Pittman, A.M.1
Webb, E.2
Carvajal-Carmona, L.3
-
12
-
-
56749176944
-
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
-
Houlston RS, Webb E, Broderick P, et al. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet 2008;40:1426-35.
-
(2008)
Nat Genet
, vol.40
, pp. 1426-1435
-
-
Houlston, R.S.1
Webb, E.2
Broderick, P.3
-
13
-
-
67349245787
-
New insights into the aetiology of colorectal cancer from genome-wide association studies
-
Tenesa A, Dunlop MG. New insights into the aetiology of colorectal cancer from genome-wide association studies. Nat Rev Genet 2009; 10:353-8.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 353-358
-
-
Tenesa, A.1
Dunlop, M.G.2
-
14
-
-
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: 885-90.
-
(2009)
Nat Genet
, vol.41
, pp. 885-890
-
-
Tuupanen, S.1
Turunen, M.2
Lehtonen, R.3
-
15
-
-
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;19:987-93.
-
(2009)
Genome Res
, vol.19
, pp. 987-993
-
-
Pittman, A.M.1
Naranjo, S.2
Webb, E.3
-
16
-
-
72749099050
-
Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort
-
Middeldorp A, Jagmohan-Changur S, van Eijk R, et al. Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort. Cancer Epidemiol Biomarkers Prev 2009;18:3062-7.
-
(2009)
Cancer Epidemiol Biomarkers Prev
, vol.18
, pp. 3062-3067
-
-
Middeldorp, A.1
Jagmohan-Changur, S.2
Van Eijk, R.3
-
17
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
Aaltonen LA, Salovaara R, Kristo P, et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med 1998;338:1481-7.
-
(1998)
N Engl J Med
, vol.338
, pp. 1481-1487
-
-
Aaltonen, L.A.1
Salovaara, R.2
Kristo, P.3
-
18
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer
-
Salovaara R, Loukola A, Kristo P, et al. 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
-
19
-
-
39149131045
-
Allelic imbalance at rs6983267 suggests selection of the risk allele in somatic colorectal tumor evolution
-
Tuupanen S, Niittymaki I, Nousiainen K, et al. Allelic imbalance at rs6983267 suggests selection of the risk allele in somatic colorectal tumor evolution. Cancer Res 2008;68:14-7.
-
(2008)
Cancer Res
, vol.68
, pp. 14-17
-
-
Tuupanen, S.1
Niittymaki, I.2
Nousiainen, K.3
-
20
-
-
84903896407
-
-
Primer3 software: http://frodo.wi.mit.edu/primer3/.
-
Primer3 Software
-
-
-
21
-
-
85069138519
-
-
database
-
Ensembl database: www.ensembl.org.
-
-
-
-
23
-
-
46849098205
-
Multiple loci with different cancer specificities within the 8q24 gene desert
-
Ghoussaini M, Song H, Koessler T, et al. Multiple loci with different cancer specificities within the 8q24 gene desert. J Natl Cancer Inst 2008;100:962-6.
-
(2008)
J Natl Cancer Inst
, vol.100
, pp. 962-966
-
-
Ghoussaini, M.1
Song, H.2
Koessler, T.3
-
24
-
-
75549083862
-
COGENT (COlorectal cancer GENeTics): An international consortium to study the role of polymorphic variation on the risk of colorectal cancer
-
Tomlinson IP, Dunlop M, Campbell H, et al. COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer. Br J Cancer 2010;102:447-54.
-
(2010)
Br J Cancer
, vol.102
, pp. 447-454
-
-
Tomlinson, I.P.1
Dunlop, M.2
Campbell, H.3
-
25
-
-
49449100346
-
The 'common disease-common variant' hypothesis and familial risks
-
Hemminki K, Forsti A, Bermejo JL. The 'common disease-common variant' hypothesis and familial risks. PLoS ONE 2008;3:e2504.
-
(2008)
PLoS ONE
, vol.3
-
-
Hemminki, K.1
Forsti, A.2
Bermejo, J.L.3
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