187 related articles for article (PubMed ID: 35715570)
21. Germline variation in O
Belhadj S; Moutinho C; Mur P; Setien F; Llinàs-Arias P; Pérez-Salvia M; Pons T; Pineda M; Brunet J; Navarro M; Capellá G; Esteller M; Valle L
Cancer Lett; 2019 Apr; 447():86-92. PubMed ID: 30677446
[TBL] [Abstract][Full Text] [Related]
22. Mutation cluster region, association between germline and somatic mutations and genotype-phenotype correlation in upper gastrointestinal familial adenomatous polyposis.
Groves C; Lamlum H; Crabtree M; Williamson J; Taylor C; Bass S; Cuthbert-Heavens D; Hodgson S; Phillips R; Tomlinson I
Am J Pathol; 2002 Jun; 160(6):2055-61. PubMed ID: 12057910
[TBL] [Abstract][Full Text] [Related]
23. Survey of germline variants in cancer-associated genes in young adults with colorectal cancer.
Mikaeel RR; Young JP; Li Y; Smith E; Horsnell M; Uylaki W; Tapia Rico G; Poplawski NK; Hardingham JE; Tomita Y; Townsend AR; Feng J; Zibat A; Kaulfuß S; Müller C; Yigit G; Wollnik B; Price TJ
Genes Chromosomes Cancer; 2022 Feb; 61(2):105-113. PubMed ID: 34761457
[TBL] [Abstract][Full Text] [Related]
24. Genetic analysis and allele-specific expression of SMAD7 3'UTR variants in human colorectal cancer reveal a novel somatic variant exhibiting allelic imbalance.
Rosic J; Miladinov M; Dragicevic S; Eric K; Bogdanovic A; Krivokapic Z; Nikolic A
Gene; 2023 Apr; 859():147217. PubMed ID: 36690223
[TBL] [Abstract][Full Text] [Related]
25. Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas.
Buckley AR; Ideker T; Carter H; Harismendy O; Schork NJ
Genome Med; 2018 Sep; 10(1):69. PubMed ID: 30217226
[TBL] [Abstract][Full Text] [Related]
26. Interaction analysis between germline genetic variants and somatic mutations in head and neck cancer.
Feng G; Feng H; Qi Y; Wang T; Ni N; Wu J; Yuan H
Oral Oncol; 2022 May; 128():105859. PubMed ID: 35428027
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. 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]
31. Whole exome sequencing and single nucleotide polymorphism array analyses to identify germline alterations in genes associated with testosterone metabolism in a patient with androgen insensitivity syndrome and early-onset colorectal cancer.
Disciglio V; Devecchi A; Palumbo O; Carella M; Penso D; Milione M; Valle G; Pierotti MA; Vitellaro M; Bertario L; Canevari S; Signoroni S; De Cecco L
Chin J Cancer; 2016 Jun; 35(1):51. PubMed ID: 27267075
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. Genome-wide association study identifies a new SMAD7 risk variant associated with colorectal cancer risk in East Asians.
Zhang B; Jia WH; Matsuo K; Shin A; Xiang YB; Matsuda K; Jee SH; Kim DH; Cheah PY; Ren Z; Cai Q; Long J; Shi J; Wen W; Yang G; Ji BT; Pan ZZ; Matsuda F; Gao YT; Oh JH; Ahn YO; Kubo M; Thean LF; Park EJ; Li HL; Park JW; Jo J; Jeong JY; Hosono S; Nakamura Y; Shu XO; Zeng YX; Zheng W
Int J Cancer; 2014 Aug; 135(4):948-55. PubMed ID: 24448986
[TBL] [Abstract][Full Text] [Related]
35. Molecular characteristics of young-onset colorectal cancer in Vietnamese patients.
Do MD; Nguyen TH; Le KT; Le LHG; Nguyen BH; Le KT; Doan TPT; Ho CQ; Nguyen HN; Tran TD; Vu HA
Asia Pac J Clin Oncol; 2022 Dec; 18(6):678-685. PubMed ID: 35098669
[TBL] [Abstract][Full Text] [Related]
36. Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data.
Bien SA; Auer PL; Harrison TA; Qu C; Connolly CM; Greenside PG; Chen S; Berndt SI; Bézieau S; Kang HM; Huyghe J; Brenner H; Casey G; Chan AT; Hopper JL; Banbury BL; Chang-Claude J; Chanock SJ; Haile RW; Hoffmeister M; Fuchsberger C; Jenkins MA; Leal SM; Lemire M; Newcomb PA; Gallinger S; Potter JD; Schoen RE; Slattery ML; Smith JD; Le Marchand L; White E; Zanke BW; Abeçasis GR; Carlson CS; Peters U; Nickerson DA; Kundaje A; Hsu L;
PLoS One; 2017; 12(11):e0186518. PubMed ID: 29161273
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Data-adaptive and pathway-based tests for association studies between somatic mutations and germline variations in human cancers.
Chen Z; Liang H; Wei P
Genet Epidemiol; 2023 Dec; 47(8):617-636. PubMed ID: 37822029
[TBL] [Abstract][Full Text] [Related]
39. Association between colorectal cancer susceptibility loci and survival time after diagnosis with colorectal cancer.
Phipps AI; Newcomb PA; Garcia-Albeniz X; Hutter CM; White E; Fuchs CS; Hazra A; Ogino S; Nan H; Ma J; Campbell PT; Figueiredo JC; Peters U; Chan AT
Gastroenterology; 2012 Jul; 143(1):51-4.e4. PubMed ID: 22580541
[TBL] [Abstract][Full Text] [Related]
40. Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
Hansen MF; Johansen J; Sylvander AE; Bjørnevoll I; Talseth-Palmer BA; Lavik LAS; Xavier A; Engebretsen LF; Scott RJ; Drabløs F; Sjursen W
Clin Genet; 2017 Oct; 92(4):405-414. PubMed ID: 28195393
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
