356 related articles for article (PubMed ID: 25822476)
1. Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.
Rosner G; Bercovich D; Daniel YE; Strul H; Fliss-Isakov N; Ben-Yehoiada M; Santo E; Halpern Z; Kariv R
Fam Cancer; 2015 Sep; 14(3):427-36. PubMed ID: 25822476
[TBL] [Abstract][Full Text] [Related]
2. Common MUTYH mutations and colorectal cancer risk in multiethnic populations.
Lejbkowicz F; Cohen I; Barnett-Griness O; Pinchev M; Poynter J; Gruber SB; Rennert G
Fam Cancer; 2012 Sep; 11(3):329-35. PubMed ID: 22371070
[TBL] [Abstract][Full Text] [Related]
3. MutYH mutation carriers have increased breast cancer risk.
Rennert G; Lejbkowicz F; Cohen I; Pinchev M; Rennert HS; Barnett-Griness O
Cancer; 2012 Apr; 118(8):1989-93. PubMed ID: 21952991
[TBL] [Abstract][Full Text] [Related]
4. Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature review.
Knopperts AP; Nielsen M; Niessen RC; Tops CM; Jorritsma B; Varkevisser J; Wijnen J; Siezen CL; Heine-Bröring RC; van Kranen HJ; Vos YJ; Westers H; Kampman E; Sijmons RH; Hes FJ
Fam Cancer; 2013 Mar; 12(1):43-50. PubMed ID: 23007840
[TBL] [Abstract][Full Text] [Related]
5. MUTYH hotspot mutations in unselected colonoscopy patients.
Casper M; Plotz G; Juengling B; Zeuzem S; Lammert F; Raedle J
Colorectal Dis; 2012 May; 14(5):e238-44. PubMed ID: 22469480
[TBL] [Abstract][Full Text] [Related]
6. Simplifying the detection of MUTYH mutations by high resolution melting analysis.
López-Villar I; Ayala R; Wesselink J; Morillas JD; López E; Marín JC; Díaz-Tasende J; González S; Robles L; Martínez-López J
BMC Cancer; 2010 Aug; 10():408. PubMed ID: 20687945
[TBL] [Abstract][Full Text] [Related]
7. A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants.
Theodoratou E; Campbell H; Tenesa A; Houlston R; Webb E; Lubbe S; Broderick P; Gallinger S; Croitoru EM; Jenkins MA; Win AK; Cleary SP; Koessler T; Pharoah PD; Küry S; Bézieau S; Buecher B; Ellis NA; Peterlongo P; Offit K; Aaltonen LA; Enholm S; Lindblom A; Zhou XL; Tomlinson IP; Moreno V; Blanco I; Capellà G; Barnetson R; Porteous ME; Dunlop MG; Farrington SM
Br J Cancer; 2010 Dec; 103(12):1875-84. PubMed ID: 21063410
[TBL] [Abstract][Full Text] [Related]
8. Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.
Grover S; Kastrinos F; Steyerberg EW; Cook EF; Dewanwala A; Burbidge LA; Wenstrup RJ; Syngal S
JAMA; 2012 Aug; 308(5):485-492. PubMed ID: 22851115
[TBL] [Abstract][Full Text] [Related]
9. APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
Filipe B; Baltazar C; Albuquerque C; Fragoso S; Lage P; Vitoriano I; Mão de Ferro S; Claro I; Rodrigues P; Fidalgo P; Chaves P; Cravo M; Nobre Leitão C
Clin Genet; 2009 Sep; 76(3):242-55. PubMed ID: 19793053
[TBL] [Abstract][Full Text] [Related]
10. Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer.
Elsaid A; Elshazli R; El-Tarapely F; Darwish H; Abdel-Malak C
Fam Cancer; 2017 Jan; 16(1):83-90. PubMed ID: 27631816
[TBL] [Abstract][Full Text] [Related]
11. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
Lejeune S; Guillemot F; Triboulet JP; Cattan S; Mouton C; ; Porchet N; Manouvrier S; Buisine MP
Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
[TBL] [Abstract][Full Text] [Related]
12. Characterizing germline APC and MUTYH variants in Ashkenazi Jews compared to other individuals.
Ukaegbu C; Levi Z; Fehlmann TD; Uno H; Chittenden A; Inra JA; Grover S; Kastrinos F; Syngal S; Yurgelun MB
Fam Cancer; 2021 Apr; 20(2):111-116. PubMed ID: 32743790
[TBL] [Abstract][Full Text] [Related]
13. Spectrum of APC and MUTYH germ-line mutations in Russian patients with colorectal malignancies.
Yanus GA; Akhapkina TA; Ivantsov AO; Preobrazhenskaya EV; Aleksakhina SN; Bizin IV; Sokolenko AP; Mitiushkina NV; Kuligina ES; Suspitsin EN; Venina AR; Holmatov MM; Zaitseva OA; Yatsuk OS; Pashkov DV; Belyaev AM; Togo AV; Imyanitov EN; Iyevleva AG
Clin Genet; 2018 May; 93(5):1015-1021. PubMed ID: 29406563
[TBL] [Abstract][Full Text] [Related]
14. Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
Nielsen M; Hes FJ; Nagengast FM; Weiss MM; Mathus-Vliegen EM; Morreau H; Breuning MH; Wijnen JT; Tops CM; Vasen HF
Clin Genet; 2007 May; 71(5):427-33. PubMed ID: 17489848
[TBL] [Abstract][Full Text] [Related]
15. MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations.
Morak M; Laner A; Bacher U; Keiling C; Holinski-Feder E
Clin Genet; 2010 Oct; 78(4):353-63. PubMed ID: 20618354
[TBL] [Abstract][Full Text] [Related]
16. Somatic c.34G>T KRAS mutation: a new prescreening test for MUTYH-associated polyposis?
Aimé A; Coulet F; Lefevre JH; Colas C; Cervera P; Flejou JF; Lascols O; Soubrier F; Parc Y
Cancer Genet; 2015; 208(7-8):390-5. PubMed ID: 26056087
[TBL] [Abstract][Full Text] [Related]
17. Endoscopic Phenotype of Monoallelic Carriers of MUTYH Gene Mutations in the Family of Polyposis Patients: A Prospective Study.
El Hachem N; Abadie C; Longy M; Colas C; Fert-Ferrer S; Leroux D; Grandval P; Prieur F; Collonge-Rame M; Faivre L; Fricker JP; Zerbib F; Coupier I; Cauchin E; Pinson S; Saurin JC
Dis Colon Rectum; 2019 Apr; 62(4):470-475. PubMed ID: 30640315
[TBL] [Abstract][Full Text] [Related]
18. Frequency of the common germline MUTYH mutations p.G396D and p.Y179C in patients diagnosed with colorectal cancer in Southern Brazil.
Pitroski CE; Cossio SL; Koehler-Santos P; Graudenz M; Prolla JC; Ashton-Prolla P
Int J Colorectal Dis; 2011 Jul; 26(7):841-6. PubMed ID: 21424714
[TBL] [Abstract][Full Text] [Related]
19. Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP.
Cheng TH; Gorman M; Martin L; Barclay E; Casey G; ; ; Saunders B; Thomas H; Clark S; Tomlinson I
Eur J Hum Genet; 2015 Feb; 23(2):260-3. PubMed ID: 24801760
[TBL] [Abstract][Full Text] [Related]
20. First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
Morak M; Massdorf T; Sykora H; Kerscher M; Holinski-Feder E
Eur J Cancer; 2011 May; 47(7):1046-55. PubMed ID: 21195604
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
