247 related articles for article (PubMed ID: 33673279)
1. Whole Exome Sequencing Identifies
Skopelitou D; Miao B; Srivastava A; Kumar A; Kuswick M; Dymerska D; Paramasivam N; Schlesner M; Lubinski J; Hemminki K; Försti A; Bandapalli OR
Int J Mol Sci; 2021 Feb; 22(4):. PubMed ID: 33673279
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Whole-Exome Sequencing Identifies a Novel Germline Variant in
Miao B; Skopelitou D; Srivastava A; Giangiobbe S; Dymerska D; Paramasivam N; Kumar A; Kuświk M; Kluźniak W; Paszkowska-Szczur K; Schlesner M; Lubinski J; Hemminki K; Försti A; Bandapalli OR
Int J Mol Sci; 2022 Jan; 23(3):. PubMed ID: 35163215
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Identification of known and novel familial cancer genes in Swedish colorectal cancer families.
Helgadottir HT; Thutkawkorapin J; Rohlin A; Nordling M; Lagerstedt-Robinson K; Lindblom A
Int J Cancer; 2021 Aug; 149(3):627-634. PubMed ID: 33729574
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Novel candidates in early-onset familial colorectal cancer.
Jansen AML; Ghosh P; Dakal TC; Slavin TP; Boland CR; Goel A
Fam Cancer; 2020 Jan; 19(1):1-10. PubMed ID: 31555933
[TBL] [Abstract][Full Text] [Related]
10. NRAS germline variant G138R and multiple rare somatic mutations on APC in colorectal cancer patients in Taiwan by next generation sequencing.
Chang PY; Chen JS; Chang NC; Chang SC; Wang MC; Tsai SH; Wen YH; Tsai WS; Chan EC; Lu JJ
Oncotarget; 2016 Jun; 7(25):37566-37580. PubMed ID: 27121310
[TBL] [Abstract][Full Text] [Related]
11. Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer.
Esteban-Jurado C; Vila-Casadesús M; Garre P; Lozano JJ; Pristoupilova A; Beltran S; Muñoz J; Ocaña T; Balaguer F; López-Cerón M; Cuatrecasas M; Franch-Expósito S; Piqué JM; Castells A; Carracedo A; Ruiz-Ponte C; Abulí A; Bessa X; Andreu M; Bujanda L; Caldés T; Castellví-Bel S
Genet Med; 2015 Feb; 17(2):131-42. PubMed ID: 25058500
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Whole exome sequencing identifies MAP3K1, MSH2, and MLH1 as potential cancer-predisposing genes in familial early-onset colorectal cancer.
Fatemi N; Tu SJ; Chung CC; Moghadam PK; Mojarad EN; Sadeghi A; Totonchi M; Aghdaei HA; Chang JG
Kaohsiung J Med Sci; 2023 Sep; 39(9):896-903. PubMed ID: 37314251
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Exome sequencing in 51 early onset non-familial CRC cases.
Thutkawkorapin J; Lindblom A; Tham E
Mol Genet Genomic Med; 2019 May; 7(5):e605. PubMed ID: 30809968
[TBL] [Abstract][Full Text] [Related]
17. Germline Mutations for Novel Candidate Predisposition Genes in Sporadic Schwannomatosis.
Min BJ; Kang YK; Chung YG; Seo ME; Chang KB; Joo MW
Clin Orthop Relat Res; 2020 Nov; 478(11):2442-2450. PubMed ID: 32281771
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome identifies RXRG and TH germline variants in familial isolated prolactinoma.
Melo FM; Couto PP; Bale AE; Bastos-Rodrigues L; Passos FM; Lisboa RG; Ng JM; Curran T; Dias EP; Friedman E; De Marco L
Cancer Genet; 2016 Jun; 209(6):251-7. PubMed ID: 27245436
[TBL] [Abstract][Full Text] [Related]
19. 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]
20.
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]
[Next] [New Search]
