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.
155 related articles for article (PubMed ID: 29987844)
1. Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes. Kayser K; Degenhardt F; Holzapfel S; Horpaopan S; Peters S; Spier I; Morak M; Vangala D; Rahner N; von Knebel-Doeberitz M; Schackert HK; Engel C; Büttner R; Wijnen J; Doerks T; Bork P; Moebus S; Herms S; Fischer S; Hoffmann P; Aretz S; Steinke-Lange V Int J Cancer; 2018 Dec; 143(11):2800-2813. PubMed ID: 29987844 [TBL] [Abstract][Full Text] [Related]
2. Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics. Morak M; Steinke-Lange V; Massdorf T; Benet-Pages A; Locher M; Laner A; Kayser K; Aretz S; Holinski-Feder E Fam Cancer; 2020 Apr; 19(2):161-167. PubMed ID: 32002723 [TBL] [Abstract][Full Text] [Related]
3. Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing. Soares BL; Brant AC; Gomes R; Pastor T; Schneider NB; Ribeiro-Dos-Santos Â; de Assumpção PP; Achatz MIW; Ashton-Prolla P; Moreira MAM Fam Cancer; 2018 Jul; 17(3):387-394. PubMed ID: 28932927 [TBL] [Abstract][Full Text] [Related]
4. Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes. Villacis RA; Miranda PM; Gomy I; Santos EM; Carraro DM; Achatz MI; Rossi BM; Rogatto SR Int J Cancer; 2016 Apr; 138(8):1928-35. PubMed ID: 26620301 [TBL] [Abstract][Full Text] [Related]
6. Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome. Carneiro da Silva F; Ferreira JR; Torrezan GT; Figueiredo MC; Santos ÉM; Nakagawa WT; Brianese RC; Petrolini de Oliveira L; Begnani MD; Aguiar-Junior S; Rossi BM; Ferreira Fde O; Carraro DM PLoS One; 2015; 10(10):e0139753. PubMed ID: 26437257 [TBL] [Abstract][Full Text] [Related]
7. Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome. Ferrer-Avargues R; Castillejo MI; Dámaso E; Díez-Obrero V; Garrigos N; Molina T; Codoñer-Alejos A; Segura Á; Sánchez-Heras AB; Castillejo A; Soto JL Cancer Commun (Lond); 2021 Mar; 41(3):218-228. PubMed ID: 33630411 [TBL] [Abstract][Full Text] [Related]
8. Next Generation Sequencing Reveals Novel Mutations in Mismatch Repair Genes and Other Cancer Predisposition Genes in Asian Patients with Suspected Lynch Syndrome. Ow SGW; Tan KT; Yang H; Yap HL; Sapari NSB; Ong PY; Soong R; Lee SC Clin Colorectal Cancer; 2019 Dec; 18(4):e324-e334. PubMed ID: 31350202 [TBL] [Abstract][Full Text] [Related]
9. Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients. Jansen AM; Geilenkirchen MA; van Wezel T; Jagmohan-Changur SC; Ruano D; van der Klift HM; van den Akker BE; Laros JF; van Galen M; Wagner A; Letteboer TG; Gómez-García EB; Tops CM; Vasen HF; Devilee P; Hes FJ; Morreau H; Wijnen JT PLoS One; 2016; 11(6):e0157381. PubMed ID: 27300758 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome. Arnold AM; Morak M; Benet-Pagès A; Laner A; Frishman D; Holinski-Feder E Eur J Hum Genet; 2020 May; 28(5):597-608. PubMed ID: 31822864 [TBL] [Abstract][Full Text] [Related]
12. Copy Number Variants Captured by the Array Comparative Genomic Hybridization in a Cohort of Patients Affected with Hereditary Colorectal Cancer in Sri Lanka: The First CNV Analysis Study of the Hereditary Colorectal Cancer in the Sri Lankan Population. Wijesiriwardhana P; Wettasinghe K; Dissanayeke VHW Asian Pac J Cancer Prev; 2021 Jun; 22(6):1957-1966. PubMed ID: 34181357 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients. Talseth-Palmer BA; Holliday EG; Evans TJ; McEvoy M; Attia J; Grice DM; Masson AL; Meldrum C; Spigelman A; Scott RJ BMC Med Genomics; 2013 Mar; 6():10. PubMed ID: 23531357 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome. Ziada-Bouchaar H; Sifi K; Filali T; Hammada T; Satta D; Abadi N Fam Cancer; 2017 Jan; 16(1):57-66. PubMed ID: 27468915 [TBL] [Abstract][Full Text] [Related]
18. Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development. Villacis RAR; Basso TR; Canto LM; Pinheiro M; Santiago KM; Giacomazzi J; de Paula CAA; Carraro DM; Ashton-Prolla P; Achatz MI; Rogatto SR J Mol Med (Berl); 2017 May; 95(5):523-533. PubMed ID: 28093616 [TBL] [Abstract][Full Text] [Related]