These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. BRAF mutation analysis is a valid tool to implement in Lynch syndrome diagnosis in patients classified according to the Bethesda guidelines. Molinari F; Signoroni S; Lampis A; Bertan C; Perrone F; Sala P; Mondini P; Crippa S; Bertario L; Frattini M Tumori; 2014; 100(3):315-20. PubMed ID: 25076244 [TBL] [Abstract][Full Text] [Related]
4. Lynch-like syndrome: characterization and comparison with EPCAM deletion carriers. Kang SY; Park CK; Chang DK; Kim JW; Son HJ; Cho YB; Yun SH; Kim HC; Kwon M; Kim KM Int J Cancer; 2015 Apr; 136(7):1568-78. PubMed ID: 25110875 [TBL] [Abstract][Full Text] [Related]
5. Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer. Pérez-Carbonell L; Ruiz-Ponte C; Guarinos C; Alenda C; Payá A; Brea A; Egoavil CM; Castillejo A; Barberá VM; Bessa X; Xicola RM; Rodríguez-Soler M; Sánchez-Fortún C; Acame N; Castellví-Bel S; Piñol V; Balaguer F; Bujanda L; De-Castro ML; Llor X; Andreu M; Carracedo A; Soto JL; Castells A; Jover R Gut; 2012 Jun; 61(6):865-72. PubMed ID: 21868491 [TBL] [Abstract][Full Text] [Related]
6. The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational Prevalence. Moufid FZ; Bouguenouch L; El Bouchikhi I; Chbani L; Iraqui Houssaini M; Sekal M; Belhassan K; Bennani B; Ouldim K Genet Test Mol Biomarkers; 2018 Aug; 22(8):492-497. PubMed ID: 30044143 [TBL] [Abstract][Full Text] [Related]
7. Tumor Testing and Genetic Analysis to Identify Lynch Syndrome Patients in an Italian Colorectal Cancer Cohort. Pantaleo A; Forte G; Cariola F; Valentini AM; Fasano C; Sanese P; Grossi V; Buonadonna AL; De Marco K; Lepore Signorile M; Guglielmi AF; Manghisi A; Gigante G; Armentano R; Disciglio V; Simone C Cancers (Basel); 2023 Oct; 15(20):. PubMed ID: 37894428 [TBL] [Abstract][Full Text] [Related]
8. Comparison of screening strategies for Lynch syndrome in patients with newly diagnosed endometrial cancer: a prospective cohort study in China. Chao X; Li L; Wu M; Ma S; Tan X; Zhong S; Bi Y; Lang J Cancer Commun (Lond); 2019 Jul; 39(1):42. PubMed ID: 31307542 [TBL] [Abstract][Full Text] [Related]
9. Identification of Lynch syndrome among patients with colorectal cancer. Moreira L; Balaguer F; Lindor N; de la Chapelle A; Hampel H; Aaltonen LA; Hopper JL; Le Marchand L; Gallinger S; Newcomb PA; Haile R; Thibodeau SN; Gunawardena S; Jenkins MA; Buchanan DD; Potter JD; Baron JA; Ahnen DJ; Moreno V; Andreu M; Ponz de Leon M; Rustgi AK; Castells A; JAMA; 2012 Oct; 308(15):1555-65. PubMed ID: 23073952 [TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular characterisation of hereditary and sporadic metastatic colorectal cancers harbouring microsatellite instability/DNA mismatch repair deficiency. Cohen R; Buhard O; Cervera P; Hain E; Dumont S; Bardier A; Bachet JB; Gornet JM; Lopez-Trabada D; Dumont S; Kaci R; Bertheau P; Renaud F; Bibeau F; Parc Y; Vernerey D; Duval A; Svrcek M; André T Eur J Cancer; 2017 Nov; 86():266-274. PubMed ID: 29055842 [TBL] [Abstract][Full Text] [Related]
11. Prevalence of Lynch syndrome in a Middle Eastern population with colorectal cancer. Siraj AK; Prabhakaran S; Bavi P; Bu R; Beg S; Hazmi MA; Al-Rasheed M; Al-Assiri M; Sairafi R; Al-Dayel F; Al-Sanea N; Uddin S; Al-Kuraya KS Cancer; 2015 Jun; 121(11):1762-71. PubMed ID: 25712738 [TBL] [Abstract][Full Text] [Related]
12. Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer. Piñol V; Castells A; Andreu M; Castellví-Bel S; Alenda C; Llor X; Xicola RM; Rodríguez-Moranta F; Payá A; Jover R; Bessa X; JAMA; 2005 Apr; 293(16):1986-94. PubMed ID: 15855432 [TBL] [Abstract][Full Text] [Related]
13. DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer. Ricker CN; Hanna DL; Peng C; Nguyen NT; Stern MC; Schmit SL; Idos GE; Patel R; Tsai S; Ramirez V; Lin S; Shamasunadara V; Barzi A; Lenz HJ; Figueiredo JC Cancer; 2017 Oct; 123(19):3732-3743. PubMed ID: 28640387 [TBL] [Abstract][Full Text] [Related]
14. Identification of Germline Mutations in Upper Tract Urothelial Carcinoma With Suspected Lynch Syndrome. Guan B; Wang J; Li X; Lin L; Fang D; Kong W; Tian C; Li J; Yang K; Han G; Wu Y; He Y; Peng Y; Yu Y; He Q; He S; Gong Y; Zhou L; Tang Q Front Oncol; 2022; 12():774202. PubMed ID: 35372080 [TBL] [Abstract][Full Text] [Related]
15. Prognostic impact of mismatch repair genes germline defects in colorectal cancer patients: are all mutations equal? Maccaroni E; Bracci R; Giampieri R; Bianchi F; Belvederesi L; Brugiati C; Pagliaretta S; Del Prete M; Scartozzi M; Cascinu S Oncotarget; 2015 Nov; 6(36):38737-48. PubMed ID: 26485756 [TBL] [Abstract][Full Text] [Related]
16. Taiwan hospital-based detection of Lynch syndrome distinguishes 2 types of microsatellite instabilities in colorectal cancers. Chang SC; Lin PC; Yang SH; Wang HS; Liang WY; Lin JK Surgery; 2010 May; 147(5):720-8. PubMed ID: 20045164 [TBL] [Abstract][Full Text] [Related]
17. Screening for Lynch syndrome in young Saudi colorectal cancer patients using microsatellite instability testing and next generation sequencing. Alqahtani M; Edwards C; Buzzacott N; Carpenter K; Alsaleh K; Alsheikh A; Abozeed W; Mashhour M; Almousa A; Housawi Y; Al Hawwaj S; Iacopetta B Fam Cancer; 2018 Apr; 17(2):197-203. PubMed ID: 28643016 [TBL] [Abstract][Full Text] [Related]
18. Performance of tumor testing for Lynch syndrome identification in patients with colorectal cancer: A retrospective single-center study. Signoroni S; Tibiletti MG; Ricci MT; Milione M; Perrone F; Pensotti V; Chiaravalli AM; Carnevali I; Morabito A; Bertario L; Vitellaro M Tumori; 2019 Feb; 105(1):76-83. PubMed ID: 30117378 [TBL] [Abstract][Full Text] [Related]
19. Clinical and Molecular Assessment of Patients with Lynch Syndrome and Sarcomas Underpinning the Association with de Angelis de Carvalho N; Niitsuma BN; Kozak VN; Costa FD; de Macedo MP; Kupper BEC; Silva MLG; Formiga MN; Volc SM; Aguiar Junior S; Palmero EI; Casali-da-Rocha JC; Carraro DM; Torrezan GT Cancers (Basel); 2020 Jul; 12(7):. PubMed ID: 32659967 [TBL] [Abstract][Full Text] [Related]
20. Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis. Vargas-Parra GM; González-Acosta M; Thompson BA; Gómez C; Fernández A; Dámaso E; Pons T; Morak M; Del Valle J; Iglesias S; Velasco À; Solanes A; Sanjuan X; Padilla N; de la Cruz X; Valencia A; Holinski-Feder E; Brunet J; Feliubadaló L; Lázaro C; Navarro M; Pineda M; Capellá G Int J Cancer; 2017 Oct; 141(7):1365-1380. PubMed ID: 28577310 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]