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Oct 7, 2005 (publication date) through Apr 18, 2024
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Publication Name
World Journal of Gastroenterology
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1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Abajo AS, Hoya ML, Tosar A, Godino J, Fernández JM, Asenjo JL, Villamil BP, Segura PP, Diaz-Rubio E, Caldes T. Low prevalence of germline hMSH6 mutations in colorectal cancer families from Spain. World J Gastroenterol 2005; 11(37): 5770-5776 [PMID: 16270383 DOI: 10.3748/wjg.v11.i37.5770] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v11/i37/5770.htm |
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Rebecca A. Barnetson, Nicola Cartwright, Annelot van Vliet, Naila Haq, Kate Drew, Susan Farrington, Nicola Williams, Jon Warner, Harry Campbell, Mary E. Porteous, Malcolm G. Dunlop. Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer. Human Mutation 2008; 29(3): 367 doi: 10.1002/humu.20635
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Pilar Garre, Verónica Briceño, Rosa M. Xicola, Brian J. Doyle, Miguel de la Hoya, Julián Sanz, Patricia Llovet, Paula Pescador, Javier Puente, Eduardo Díaz-Rubio, Xavier Llor, Trinidad Caldés. Analysis of the Oxidative Damage Repair GenesNUDT1,OGG1, andMUTYHin Patients from Mismatch Repair Proficient HNPCC Families (MSS-HNPCC). Clinical Cancer Research 2011; 17(7): 1701 doi: 10.1158/1078-0432.CCR-10-2491
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Lucia Pérez-Cabornero, Mar Infante, Eladio Velasco, Enrique Lastra, Cristina Miner, Mercedes Durán. Evaluating the Effect of Unclassified Variants Identified in MMR Genes Using Phenotypic Features, Bioinformatics Prediction, and RNA Assays. The Journal of Molecular Diagnostics 2013; 15(3): 380 doi: 10.1016/j.jmoldx.2013.02.003
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María Dolores Giráldez, Francesc Balaguer, Trinidad Caldés, Ana Sanchez-de-Abajo, Nuria Gómez-Fernández, Clara Ruiz-Ponte, Jenifer Muñoz, Pilar Garre, Victoria Gonzalo, Leticia Moreira, Teresa Ocaña, Joan Clofent, Angel Carracedo, Montserrat Andreu, Rodrigo Jover, Xavier Llor, Antoni Castells, Sergi Castellví-Bel. Association of MUTYH and MSH6 germline mutations in colorectal cancer patients. Familial Cancer 2009; 8(4): 525 doi: 10.1007/s10689-009-9282-4
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Sanne M Petersen, Mette Dandanell, Lene J Rasmussen, Anne-Marie Gerdes, Lotte N Krogh, Inge Bernstein, Henrik Okkels, Friedrik Wikman, Finn C Nielsen, Thomas v O Hansen. Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients. BMC Medical Genetics 2013; 14(1) doi: 10.1186/1471-2350-14-103
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Christian Adonizio, Michelle Gazzillo, Joseph Knezetic, Carrie Snyder, Henry T. Lynch, Christina Rybak, Michael J. Hall, Kristina Lowstuter, Julie Eggington, Gloria J. Morris. Thirty-Nine-Year-Old With Familial Colon Cancer, and Variant of Undetermined Significance in MSH6. Seminars in Oncology 2012; 39(2): 125 doi: 10.1053/j.seminoncol.2012.01.013
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Gašper Berginc, Matej Bračko, Metka Ravnik-Glavač, Damjan Glavač. Screening for germline mutations of MLH1, MSH2, MSH6 and PMS2 genes in Slovenian colorectal cancer patients: implications for a population specific detection strategy of Lynch syndrome. Familial Cancer 2009; 8(4): 421 doi: 10.1007/s10689-009-9258-4
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Pilar Garre, Pedro Pérez-Segura, Eduardo Díaz-Rubio, Trinidad Caldés, Miguel de la Hoya. Reassessing the TARBP2 mutation rate in hereditary nonpolyposis colorectal cancer. Nature Genetics 2010; 42(10): 817 doi: 10.1038/ng1010-817
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Atocha Romero, Pilar Garre, Olivia Valentin, Julian Sanz, Pedro Pérez-Segura, Patricia Llovet, Eduardo Díaz-Rubio, Miguel de la Hoya, Trinidad Caldés, Paolo Peterlongo. Frequency and Variability of Genomic Rearrangements on MSH2 in Spanish Lynch Syndrome Families. PLoS ONE 2013; 8(9): e72195 doi: 10.1371/journal.pone.0072195
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J Suchy, G Kurzawski, K Jakubowska, ME Rać, K Safranow, J Kładny, I Rzepka‐Górska, M Chosia, B Czeszyńska, O Oszurek, RJ Scott, J Lubiński. Frequency and nature of hMSH6 germline mutations in Polish patients with colorectal, endometrial and ovarian cancers. Clinical Genetics 2006; 70(1): 68 doi: 10.1111/j.1399-0004.2006.00630.x
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| 11 |
Denisa Kacerovska, Katerina Cerna, Petr Martinek, Petr Grossmann, Michal Michal, Jan Ricar, Dmitry V. Kazakov. MSH6 Mutation in a Family Affected by Muir–Torre Syndrome. The American Journal of Dermatopathology 2012; 34(6): 648 doi: 10.1097/DAD.0b013e3182446fe2
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Heather Hampel, Wendy Frankel, Jenny Panescu, Janet Lockman, Kaisa Sotamaa, Daniel Fix, Ilene Comeras, Jennifer La Jeunesse, Hidewaki Nakagawa, Judith A. Westman, Thomas W. Prior, Mark Clendenning, Pamela Penzone, Janet Lombardi, Patti Dunn, David E. Cohn, Larry Copeland, Lynne Eaton, Jeffrey Fowler, George Lewandowski, Luis Vaccarello, Jeffrey Bell, Gary Reid, Albert de la Chapelle. Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients. Cancer Research 2006; 66(15): 7810 doi: 10.1158/0008-5472.CAN-06-1114
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P. Garre, L. Martín, J. Sanz, A. Romero, A. Tosar, I. Bando, P. Llovet, P. Diaque, B. García‐Paredes, E. Díaz‐Rubio, M. de la Hoya, T. Caldés. BRCA2 gene: a candidate for clinical testing in familial colorectal cancer type X. Clinical Genetics 2015; 87(6): 582 doi: 10.1111/cge.12427
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| 15 |
Ana Sánchez-de-Abajo, Miguel de la Hoya, Marjo van Puijenbroek, Alicia Tosar, J.A. López-Asenjo, Eduardo Díaz-Rubio, Hans Morreau, Trinidad Caldes. Molecular Analysis of Colorectal Cancer Tumors from Patients with Mismatch Repair–Proficient Hereditary Nonpolyposis Colorectal Cancer Suggests Novel Carcinogenic Pathways. Clinical Cancer Research 2007; 13(19): 5729 doi: 10.1158/1078-0432.CCR-06-2996
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