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Cited by in CrossRef
For: Tanyi M, Olasz J, Lukács G, Csuka O, Tóth L, Szentirmay Z, Ress Z, Barta Z, Tanyi JL, Damjanovich L. Pedigree and genetic analysis of a novel mutation carrier patient suffering from hereditary nonpolyposis colorectal cancer. World J Gastroenterol 2006; 12(8): 1192-1197 [PMID: 16534870 DOI: 10.3748/wjg.v12.i8.1192]
URL: https://www.wjgnet.com/1007-9327/full/v12/i8/1192.htm
Number Citing Articles
Ann Demogines, Alex Wong, Charles Aquadro, Eric Alani, Orna Cohen-Fix. Incompatibilities Involving Yeast Mismatch Repair Genes: A Role for Genetic Modifiers and Implications for Disease Penetrance and Variation in Genomic Mutation RatesPLoS Genetics 2008; 4(6): e1000103 doi: 10.1371/journal.pgen.1000103
Semra Demokan, Yusufhan Suoglu, Murat Ulusan, Nejat Dalay. Analysis of the hMSH2 Gene Variants in Head and Neck CancerDNA and Cell Biology 2010; 29(8): 449 doi: 10.1089/dna.2009.1013
M. Tanyi, J. Olasz, J.L. Tanyi, L. Tóth, P. Antal-Szalmás, Z. Ress, T. Bubán, K. Palatka, C. András, H. Urbancsek, Z. Garami, O. Csuka, L. Damjanovich. MLH1 and MSH2 mutation screening in HNPCC families of Hungary – Two new MMR gene mutationsEuropean Journal of Surgical Oncology (EJSO) 2014; 40(11): 1445 doi: 10.1016/j.ejso.2014.07.032
Marietta E. Kovacs, Janos Papp, Zoltan Szentirmay, Szabolcs Otto, Edith Olah. Deletions removing the last exon ofTACSTD1constitute a distinct class of mutations predisposing to Lynch syndromeHuman Mutation 2009; 30(2): 197 doi: 10.1002/humu.20942
Miklós Tanyi, Judit Olasz, Janos L. Tanyi, László Tóth, Péter Antal-Szalmás, Tamás Bubán, Csilla András, Hilda Urbancsek, Zoltán Garami, Orsolya Csuka, László Damjanovich. Q48P mutation in the hMLH1 gene associated with Lynch syndrome in three Hungarian familiesFamilial Cancer 2012; 11(3): 519 doi: 10.1007/s10689-012-9515-9
Juan M. Marqués-Lespier, Yaritza Diaz-Algorri, Maria Gonzalez-Pons, Marcia Cruz-Correa. Report of a Novel Mutation inMLH1Gene in a Hispanic Family from Puerto Rico Fulfilling Classic Amsterdam Criteria for Lynch SyndromeGastroenterology Research and Practice 2014; 2014: 1 doi: 10.1155/2014/527946
Lise Lotte Christensen, Reetta Kariola, Mari K. Korhonen, Friedrik P. Wikman, Lone Sunde, Anne-Marie Gerdes, Henrik Okkels, Carsten A. Brandt, Inge Bernstein, Thomas V. O. Hansen, Rikke Hagemann-Madsen, Claus L. Andersen, Minna Nyström, Torben F. Ørntoft. Functional characterization of rare missense mutations in MLH1 and MSH2 identified in Danish colorectal cancer patientsFamilial Cancer 2009; 8(4): 489 doi: 10.1007/s10689-009-9274-4
Jukka Kantelinen, Minttu Kansikas, Satu Candelin, Heather Hampel, Betsy Smith, Liisa Holm, Reetta Kariola, Minna Nyström. Mismatch repair analysis of inherited MSH2 and/or MSH6 variation pairs found in cancer patientsHuman Mutation 2012; 33(8): 1294 doi: 10.1002/humu.22119
Lise Lotte Christensen, Bo E Madsen, Friedrik P Wikman, Carsten Wiuf, Karen Koed, Anne Tjønneland, Anja Olsen, Ann-Christine Syvänen, Claus L Andersen, Torben F Ørntoft. The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish populationBMC Medical Genetics 2008; 9(1) doi: 10.1186/1471-2350-9-52
M. Tanyi, J. Olasz, E. Kámory, O. Csuka, J.L. Tanyi, Z. Ress, L. Damjanovich. Difficulties in recognizing families with Hereditary Non-polyposis Colorectal Carcinoma. Presentation of 4 families with proven mutationEuropean Journal of Surgical Oncology (EJSO) 2008; 34(12): 1322 doi: 10.1016/j.ejso.2008.01.006
Saara Ollila, Denis Dermadi Bebek, Marc Greenblatt, Minna Nyström. Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classificationInternational Journal of Cancer 2008; 123(3): 720 doi: 10.1002/ijc.23573
Judit Olasz. Significance of genetic instability in development and chemosensitivity of malignant tumorsClinical and Experimental Medical Journal 2009; 3(1): 175 doi: 10.1556/CEMED.3.2009.1.17
Jennifer J. Wanat, Nikhil Singh, Eric Alani. The effect of genetic background on the function of Saccharomyces cerevisiae mlh1 alleles that correspond to HNPCC missense mutationsHuman Molecular Genetics 2007; 16(4): 445 doi: 10.1093/hmg/ddl479