173 related articles for article (PubMed ID: 33930674)
1. An intronic variant in the CELF4 gene is associated with risk for colorectal cancer.
Teerlink CC; Stevens J; Hernandez R; Facelli JC; Cannon-Albright LA
Cancer Epidemiol; 2021 Jun; 72():101941. PubMed ID: 33930674
[TBL] [Abstract][Full Text] [Related]
2. FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor.
Cannon-Albright LA; Teerlink CC; Stevens J; Snow AK; Thompson BA; Bell R; Nguyen KN; Sargent NR; Kohlmann WK; Neklason DW; Tavtigian SV
Mol Genet Genomic Med; 2020 Dec; 8(12):e1532. PubMed ID: 33118316
[TBL] [Abstract][Full Text] [Related]
3. Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer.
Bellido F; Sowada N; Mur P; Lázaro C; Pons T; Valdés-Mas R; Pineda M; Aiza G; Iglesias S; Soto JL; Urioste M; Caldés T; Balbín M; Blay P; Rueda D; Durán M; Valencia A; Moreno V; Brunet J; Blanco I; Navarro M; Calin GA; Borck G; Puente XS; Capellá G; Valle L
Gastroenterology; 2018 Jan; 154(1):181-194.e20. PubMed ID: 28912018
[TBL] [Abstract][Full Text] [Related]
4. Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer.
Toma C; Díaz-Gay M; Franch-Expósito S; Arnau-Collell C; Overs B; Muñoz J; Bonjoch L; Soares de Lima Y; Ocaña T; Cuatrecasas M; Castells A; Bujanda L; Balaguer F; Cubiella J; Caldés T; Fullerton JM; Castellví-Bel S
Int J Cancer; 2020 Mar; 146(6):1568-1577. PubMed ID: 31525256
[TBL] [Abstract][Full Text] [Related]
5. Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases.
Zhang JX; Fu L; de Voer RM; Hahn MM; Jin P; Lv CX; Verwiel ET; Ligtenberg MJ; Hoogerbrugge N; Kuiper RP; Sheng JQ; Geurts van Kessel A
World J Gastroenterol; 2015 Apr; 21(14):4136-49. PubMed ID: 25892863
[TBL] [Abstract][Full Text] [Related]
6. A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer.
Cannon-Albright LA; Teerlink CC; Stevens J; Facelli JC; Carr SR; Allen-Brady K; Puri S; Bailey-Wilson JE; Musolf AM; ; Akerley W
Int J Cancer; 2023 Jul; 153(2):364-372. PubMed ID: 36916144
[TBL] [Abstract][Full Text] [Related]
7. Germline Genetic Features of Young Individuals With Colorectal Cancer.
Stoffel EM; Koeppe E; Everett J; Ulintz P; Kiel M; Osborne J; Williams L; Hanson K; Gruber SB; Rozek LS
Gastroenterology; 2018 Mar; 154(4):897-905.e1. PubMed ID: 29146522
[TBL] [Abstract][Full Text] [Related]
8. Little evidence for association between the TGFBR1*6A variant and colorectal cancer: a family-based association study on non-syndromic family members from Australia and Spain.
Ross JP; Lockett LJ; Tabor B; Saunders IW; Young GP; Macrae F; Blanco I; Capella G; Brown GS; Lockett TJ; Hannan GN
BMC Cancer; 2014 Jul; 14():475. PubMed ID: 24981199
[TBL] [Abstract][Full Text] [Related]
9. Role of MYH polymorphisms in sporadic colorectal cancer in China: a case-control, population-based study.
Yang L; Huang XE; Xu L; Zhou JN; Yu DS; Zhou X; Li DZ; Guan X
Asian Pac J Cancer Prev; 2013; 14(11):6403-9. PubMed ID: 24377541
[TBL] [Abstract][Full Text] [Related]
10. The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer.
Esteban-Jurado C; Franch-Expósito S; Muñoz J; Ocaña T; Carballal S; López-Cerón M; Cuatrecasas M; Vila-Casadesús M; Lozano JJ; Serra E; Beltran S; Brea-Fernández A; Ruiz-Ponte C; Castells A; Bujanda L; Garre P; Caldés T; Cubiella J; Balaguer F; Castellví-Bel S
Eur J Hum Genet; 2016 Oct; 24(10):1501-5. PubMed ID: 27165003
[TBL] [Abstract][Full Text] [Related]
11.
Martín-Morales L; Garre P; Lorca V; Cazorla M; Llovet P; Bando I; García-Barberan V; González-Morales ML; Esteban-Jurado C; de la Hoya M; Castellví-Bel S; Caldés T
Cancer Prev Res (Phila); 2021 Feb; 14(2):185-194. PubMed ID: 33115781
[TBL] [Abstract][Full Text] [Related]
12. Update on genetic predisposition to colorectal cancer and polyposis.
Valle L; de Voer RM; Goldberg Y; Sjursen W; Försti A; Ruiz-Ponte C; Caldés T; Garré P; Olsen MF; Nordling M; Castellvi-Bel S; Hemminki K
Mol Aspects Med; 2019 Oct; 69():10-26. PubMed ID: 30862463
[TBL] [Abstract][Full Text] [Related]
13. Germline Mutations in FAF1 Are Associated With Hereditary Colorectal Cancer.
Bonjoch L; Franch-Expósito S; Garre P; Belhadj S; Muñoz J; Arnau-Collell C; Díaz-Gay M; Gratacós-Mulleras A; Raimondi G; Esteban-Jurado C; Soares de Lima Y; Herrera-Pariente C; Cuatrecasas M; Ocaña T; Castells A; Fillat C; Capellá G; Balaguer F; Caldés T; Valle L; Castellví-Bel S
Gastroenterology; 2020 Jul; 159(1):227-240.e7. PubMed ID: 32179092
[TBL] [Abstract][Full Text] [Related]
14. Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer.
Skopelitou D; Srivastava A; Miao B; Kumar A; Dymerska D; Paramasivam N; Schlesner M; Lubinski J; Hemminki K; Försti A; Reddy Bandapalli O
Mol Genet Genomics; 2022 Jul; 297(4):965-979. PubMed ID: 35562597
[TBL] [Abstract][Full Text] [Related]
15. Identification of MYH mutation carriers in colorectal cancer: a multicenter, case-control, population-based study.
Balaguer F; Castellví-Bel S; Castells A; Andreu M; Muñoz J; Gisbert JP; Llor X; Jover R; de Cid R; Gonzalo V; Bessa X; Xicola RM; Pons E; Alenda C; Payá A; Piqué JM;
Clin Gastroenterol Hepatol; 2007 Mar; 5(3):379-87. PubMed ID: 17368238
[TBL] [Abstract][Full Text] [Related]
16. Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
Mur P; Sánchez-Cuartielles E; Aussó S; Aiza G; Valdés-Mas R; Pineda M; Navarro M; Brunet J; Urioste M; Lázaro C; Moreno V; Capellá G; Puente XS; Valle L
Sci Rep; 2016 Feb; 6():20697. PubMed ID: 26852919
[TBL] [Abstract][Full Text] [Related]
17. Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing.
Singh AK; Talseth-Palmer B; Xavier A; Scott RJ; Drabløs F; Sjursen W
BMC Med Genomics; 2023 Jun; 16(1):126. PubMed ID: 37296477
[TBL] [Abstract][Full Text] [Related]
18. Germline mutations in a DNA repair pathway are associated with familial colorectal cancer.
Xu P; Sun D; Gao Y; Jiang Y; Zhong M; Zhao G; Chen J; Wang Z; Liu Q; Hong J; Chen H; Chen YX; Fang JY
JCI Insight; 2021 Sep; 6(18):. PubMed ID: 34549727
[TBL] [Abstract][Full Text] [Related]
19. Activating mutation in MET oncogene in familial colorectal cancer.
Neklason DW; Done MW; Sargent NR; Schwartz AG; Anton-Culver H; Griffin CA; Ahnen DJ; Schildkraut JM; Tomlinson GE; Strong LC; Miller AR; Stopfer JE; Burt RW
BMC Cancer; 2011 Oct; 11():424. PubMed ID: 21970370
[TBL] [Abstract][Full Text] [Related]
20. Variant Characterization of a Representative Large Pedigree Suggests "Variant Risk Clusters" Convey Varying Predisposition of Risk to Lynch Syndrome.
Barbirou M; Miller AA; Mezlini A; Bouhaouala-Zahar B; Tonellato PJ
Cancers (Basel); 2023 Aug; 15(16):. PubMed ID: 37627102
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
