162 related articles for article (PubMed ID: 20862326)
1. Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3H.
Pittman AM; Naranjo S; Jalava SE; Twiss P; Ma Y; Olver B; Lloyd A; Vijayakrishnan J; Qureshi M; Broderick P; van Wezel T; Morreau H; Tuupanen S; Aaltonen LA; Alonso ME; Manzanares M; Gavilán A; Visakorpi T; Gómez-Skarmeta JL; Houlston RS
PLoS Genet; 2010 Sep; 6(9):e1001126. PubMed ID: 20862326
[TBL] [Abstract][Full Text] [Related]
2. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.
Tomlinson IP; Webb E; Carvajal-Carmona L; Broderick P; Howarth K; Pittman AM; Spain S; Lubbe S; Walther A; Sullivan K; Jaeger E; Fielding S; Rowan A; Vijayakrishnan J; Domingo E; Chandler I; Kemp Z; Qureshi M; Farrington SM; Tenesa A; Prendergast JG; Barnetson RA; Penegar S; Barclay E; Wood W; Martin L; Gorman M; Thomas H; Peto J; Bishop DT; Gray R; Maher ER; Lucassen A; Kerr D; Evans DG; ; Schafmayer C; Buch S; Völzke H; Hampe J; Schreiber S; John U; Koessler T; Pharoah P; van Wezel T; Morreau H; Wijnen JT; Hopper JL; Southey MC; Giles GG; Severi G; Castellví-Bel S; Ruiz-Ponte C; Carracedo A; Castells A; ; Försti A; Hemminki K; Vodicka P; Naccarati A; Lipton L; Ho JW; Cheng KK; Sham PC; Luk J; Agúndez JA; Ladero JM; de la Hoya M; Caldés T; Niittymäki I; Tuupanen S; Karhu A; Aaltonen L; Cazier JB; Campbell H; Dunlop MG; Houlston RS
Nat Genet; 2008 May; 40(5):623-30. PubMed ID: 18372905
[TBL] [Abstract][Full Text] [Related]
3. Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk.
Zeng C; Matsuda K; Jia WH; Chang J; Kweon SS; Xiang YB; Shin A; Jee SH; Kim DH; Zhang B; Cai Q; Guo X; Long J; Wang N; Courtney R; Pan ZZ; Wu C; Takahashi A; Shin MH; Matsuo K; Matsuda F; Gao YT; Oh JH; Kim S; Jung KJ; Ahn YO; Ren Z; Li HL; Wu J; Shi J; Wen W; Yang G; Li B; Ji BT; ; Brenner H; Schoen RE; Küry S; ; Gruber SB; Schumacher FR; Stenzel SL; ; Casey G; Hopper JL; Jenkins MA; Kim HR; Jeong JY; Park JW; Tajima K; Cho SH; Kubo M; Shu XO; Lin D; Zeng YX; Zheng W
Gastroenterology; 2016 Jun; 150(7):1633-1645. PubMed ID: 26965516
[TBL] [Abstract][Full Text] [Related]
4. Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes.
Carvajal-Carmona LG; Cazier JB; Jones AM; Howarth K; Broderick P; Pittman A; Dobbins S; Tenesa A; Farrington S; Prendergast J; Theodoratou E; Barnetson R; Conti D; Newcomb P; Hopper JL; Jenkins MA; Gallinger S; Duggan DJ; Campbell H; Kerr D; Casey G; Houlston R; Dunlop M; Tomlinson I
Hum Mol Genet; 2011 Jul; 20(14):2879-88. PubMed ID: 21531788
[TBL] [Abstract][Full Text] [Related]
5. The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expression.
Pittman AM; Naranjo S; Webb E; Broderick P; Lips EH; van Wezel T; Morreau H; Sullivan K; Fielding S; Twiss P; Vijayakrishnan J; Casares F; Qureshi M; Gómez-Skarmeta JL; Houlston RS
Genome Res; 2009 Jun; 19(6):987-93. PubMed ID: 19395656
[TBL] [Abstract][Full Text] [Related]
6. Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome.
Talseth-Palmer BA; Brenne IS; Ashton KA; Evans TJ; McPhillips M; Groombridge C; Suchy J; Kurzawski G; Spigelman A; Lubinski J; Scott RJ
J Med Genet; 2011 Apr; 48(4):279-84. PubMed ID: 21097774
[TBL] [Abstract][Full Text] [Related]
7. A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
Meyer KB; Maia AT; O'Reilly M; Ghoussaini M; Prathalingam R; Porter-Gill P; Ambs S; Prokunina-Olsson L; Carroll J; Ponder BA
PLoS Genet; 2011 Jul; 7(7):e1002165. PubMed ID: 21814516
[TBL] [Abstract][Full Text] [Related]
8. Quantitative assessment of the influence of common variation rs16892766 at 8q23.3 with colorectal adenoma and cancer susceptibility.
Li M; Gu Y
Mol Genet Genomics; 2015 Apr; 290(2):461-9. PubMed ID: 25293934
[TBL] [Abstract][Full Text] [Related]
9. Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk.
Baert-Desurmont S; Charbonnier F; Houivet E; Ippolito L; Mauillon J; Bougeard M; Abadie C; Malka D; Duffour J; Desseigne F; Colas C; Pujol P; Lejeune S; Dugast C; Buecher B; Faivre L; Leroux D; Gesta P; Coupier I; Guimbaud R; Berthet P; Manouvrier S; Cauchin E; Prieur F; Laurent-Puig P; Lebrun M; Jonveaux P; Chiesa J; Caron O; Morin-Meschin ME; Polycarpe-Osaer F; Giraud S; Zaanan A; Bonnet D; Mansuy L; Bonadona V; El Chehadeh S; Duhoux F; Gauthier-Villars M; Saurin JC; Collonge-Rame MA; Brugières L; Wang Q; Bressac-de Paillerets B; Rey JM; Toulas C; Buisine MP; Bronner M; Sokolowska J; Hardouin A; Cailleux AF; Sebaoui H; Blot J; Tinat J; Benichou J; Frebourg T
Eur J Hum Genet; 2016 Jan; 24(1):99-105. PubMed ID: 25873010
[TBL] [Abstract][Full Text] [Related]
10. The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer.
Pomerantz MM; Ahmadiyeh N; Jia L; Herman P; Verzi MP; Doddapaneni H; Beckwith CA; Chan JA; Hills A; Davis M; Yao K; Kehoe SM; Lenz HJ; Haiman CA; Yan C; Henderson BE; Frenkel B; Barretina J; Bass A; Tabernero J; Baselga J; Regan MM; Manak JR; Shivdasani R; Coetzee GA; Freedman ML
Nat Genet; 2009 Aug; 41(8):882-4. PubMed ID: 19561607
[TBL] [Abstract][Full Text] [Related]
11. Susceptibility genetic variants associated with colorectal cancer risk correlate with cancer phenotype.
Abulí A; Bessa X; González JR; Ruiz-Ponte C; Cáceres A; Muñoz J; Gonzalo V; Balaguer F; Fernández-Rozadilla C; González D; de Castro L; Clofent J; Bujanda L; Cubiella J; Reñé JM; Morillas JD; Lanas A; Rigau J; García AM; Latorre M; Saló J; Fernández Bañares F; Argüello L; Peña E; Vilella A; Riestra S; Carreño R; Paya A; Alenda C; Xicola RM; Doyle BJ; Jover R; Llor X; Carracedo A; Castells A; Castellví-Bel S; Andreu M;
Gastroenterology; 2010 Sep; 139(3):788-96, 796.e1-6. PubMed ID: 20638935
[TBL] [Abstract][Full Text] [Related]
12. Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.
Talseth-Palmer BA; Wijnen JT; Brenne IS; Jagmohan-Changur S; Barker D; Ashton KA; Tops CM; Evans TJ; McPhillips M; Groombridge C; Suchy J; Kurzawski G; ; Spigelman A; Møller P; Morreau HM; Van Wezel T; Lubinski J; Vasen HF; Scott RJ
Int J Cancer; 2013 Apr; 132(7):1556-64. PubMed ID: 22987364
[TBL] [Abstract][Full Text] [Related]
13. The 14q22.2 colorectal cancer variant rs4444235 shows cis-acting regulation of BMP4.
Lubbe SJ; Pittman AM; Olver B; Lloyd A; Vijayakrishnan J; Naranjo S; Dobbins S; Broderick P; Gómez-Skarmeta JL; Houlston RS
Oncogene; 2012 Aug; 31(33):3777-84. PubMed ID: 22158048
[TBL] [Abstract][Full Text] [Related]
14. MAGI2-AS3 rs7783388 polymorphism contributes to colorectal cancer risk through altering the binding affinity of the transcription factor GR to the MAGI2-AS3 promoter.
Yang X; Wu S; Li X; Yin Y; Chen R
J Clin Lab Anal; 2020 Oct; 34(10):e23431. PubMed ID: 32533587
[TBL] [Abstract][Full Text] [Related]
15. Systematic search for enhancer elements and somatic allelic imbalance at seven low-penetrance colorectal cancer predisposition loci.
Niittymäki I; Tuupanen S; Li Y; Järvinen H; Mecklin JP; Tomlinson IP; Houlston RS; Karhu A; Aaltonen LA
BMC Med Genet; 2011 Feb; 12():23. PubMed ID: 21314996
[TBL] [Abstract][Full Text] [Related]
16. Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort.
Middeldorp A; Jagmohan-Changur S; van Eijk R; Tops C; Devilee P; Vasen HF; Hes FJ; Houlston R; Tomlinson I; Houwing-Duistermaat JJ; Wijnen JT; Morreau H; van Wezel T
Cancer Epidemiol Biomarkers Prev; 2009 Nov; 18(11):3062-7. PubMed ID: 19843678
[TBL] [Abstract][Full Text] [Related]
17. Functional analyses of a low-penetrance risk variant rs6702619/1p21.2 associating with colorectal cancer in Polish population.
Statkiewicz M; Maryan N; Kulecka M; Kuklinska U; Ostrowski J; Mikula M
Acta Biochim Pol; 2019 Sep; 66(3):329-336. PubMed ID: 31531420
[TBL] [Abstract][Full Text] [Related]
18. Identification and characterization of functional risk variants for colorectal cancer mapping to chromosome 11q23.1.
Biancolella M; Fortini BK; Tring S; Plummer SJ; Mendoza-Fandino GA; Hartiala J; Hitchler MJ; Yan C; Schumacher FR; Conti DV; Edlund CK; Noushmehr H; Coetzee SG; Bresalier RS; Ahnen DJ; Barry EL; Berman BP; Rice JC; Coetzee GA; Casey G
Hum Mol Genet; 2014 Apr; 23(8):2198-209. PubMed ID: 24256810
[TBL] [Abstract][Full Text] [Related]
19. Chromosome 8q23.3 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome.
Wijnen JT; Brohet RM; van Eijk R; Jagmohan-Changur S; Middeldorp A; Tops CM; van Puijenbroek M; Ausems MG; Gómez García E; Hes FJ; Hoogerbrugge N; Menko FH; van Os TA; Sijmons RH; Verhoef S; Wagner A; Nagengast FM; Kleibeuker JH; Devilee P; Morreau H; Goldgar D; Tomlinson IP; Houlston RS; van Wezel T; Vasen HF
Gastroenterology; 2009 Jan; 136(1):131-7. PubMed ID: 19010329
[TBL] [Abstract][Full Text] [Related]
20. Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility.
Arnau-Collell C; Soares de Lima Y; Díaz-Gay M; Muñoz J; Carballal S; Bonjoch L; Moreira L; Lozano JJ; Ocaña T; Cuatrecasas M; Díaz de Bustamante A; Castells A; Capellà G; Bujanda L; Cubiella J; Rodríguez-Alcalde D; Balaguer F; Ruiz-Ponte C; Valle L; Moreno V; Castellvi-Bel S
J Med Genet; 2020 Oct; 57(10):677-682. PubMed ID: 32170005
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
