Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts
Vasen, Hans F A, Blanco, Ignacio, Aktan-Collan, Katja, Gopie, Jessica P, Alonso, Angel, Aretz, Stefan, Bernstein, Inge, Bertario, Lucio, Burn, John, Capella, Gabriel, Colas, Chrystelle, Engel, Christoph, Frayling, Ian M, Genuardi, Maurizio, Heinimann, Karl, Hes, Frederik J, Hodgson, Shirley V, Karagiannis, John A, Lalloo, Fiona, Lindblom, Annika, Mecklin, Jukka-Pekka, Møller, Pal, Myrhoj, Torben, Nagengast, Fokko M, Parc, Yann, Ponz de Leon, Maurizio, Renkonen-Sinisalo, Laura, Sampson, Julian R, Stormorken, Astrid, Sijmons, Rolf H, Tejpar, Sabine, Thomas, Huw J W, Rahner, Nils, Wijnen, Juul T, Järvinen, Heikki Juhani, Möslein, Gabriela
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Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics
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Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk
ten Broeke, Sanne W, Brohet, Richard M, Tops, Carli M, van der Klift, Heleen M, Velthuizen, Mary E, Bernstein, Inge, Capellá Munar, Gabriel, Gomez Garcia, Encarna, Hoogerbrugge, Nicoline, Letteboer, Tom G W, Menko, Fred H, Lindblom, Annika, Mensenkamp, Arjen R, Moller, Pal, van Os, Theo A, Rahner, Nils, Redeker, Bert J W, Sijmons, Rolf H, Spruijt, Liesbeth, Suerink, Manon, Vos, Yvonne J, Wagner, Anja, Hes, Frederik J, Vasen, Hans F, Nielsen, Maartje, Wijnen, Juul T
Published in Journal of clinical oncology (01.02.2015)
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Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome
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Published in Journal of clinical oncology (10.12.2012)
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GAVIN: Gene-Aware Variant INterpretation for medical sequencing
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Published in Genome Biology (16.01.2017)
Published in Genome Biology (16.01.2017)
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CoNVaDING: Single Exon Variation Detection in Targeted NGS Data
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Published in Human mutation (01.05.2016)
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CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling
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Published in International journal of cancer (15.07.2012)
Published in International journal of cancer (15.07.2012)
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Evaluation of a seven gene mutational profile as a prognostic factor in a population-based study of clear cell renal cell carcinoma
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Published in Scientific reports (20.04.2022)
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NIPTeR: an R package for fast and accurate trisomy prediction in non-invasive prenatal testing
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Published in BMC bioinformatics (17.12.2018)
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Functional Studies on Primary Tubular Epithelial Cells Indicate a Tumor Suppressor Role of SETD2 in Clear Cell Renal Cell Carcinoma
Li, Jun, Kluiver, Joost, Osinga, Jan, Westers, Helga, van Werkhoven, Maaike B, Seelen, Marc A, Sijmons, Rolf H, van den Berg, Anke, Kok, Klaas
Published in Neoplasia (New York, N.Y.) (01.06.2016)
Published in Neoplasia (New York, N.Y.) (01.06.2016)
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Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome
Niessen, Renée C., Hofstra, Robert M. W., Westers, Helga, Ligtenberg, Marjolijn J. L., Kooi, Krista, Jager, Paul O. J., de Groote, Marloes L., Dijkhuizen, Trijnie, Olderode-Berends, Maran J. W., Hollema, Harry, Kleibeuker, Jan H., Sijmons, Rolf H.
Published in Genes chromosomes & cancer (01.08.2009)
Published in Genes chromosomes & cancer (01.08.2009)
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PMS2-associated Lynch syndrome: Past, present and future
Andini, Katarina D, Nielsen, Maartje, Suerink, Manon, Helderman, Noah C, Koornstra, Jan Jacob, Ahadova, Aysel, Kloor, Matthias, Mourits, Marian J E, Kok, Klaas, Sijmons, Rolf H, Bajwa-Ten Broeke, Sanne W
Published in Frontiers in oncology (21.02.2023)
Published in Frontiers in oncology (21.02.2023)
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Systematic Review of the Prognostic Role of the Immune System After Surgery of Colorectal Liver Metastases
Hof, Joost, Kok, Klaas, Sijmons, Rolf H, de Jong, Koert P
Published in Frontiers in oncology (19.03.2019)
Published in Frontiers in oncology (19.03.2019)
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Validation of New Gene Variant Classification Methods: a Field-Test in Diagnostic Cardiogenetics
Alimohamed, Mohamed Z, Westers, Helga, Vos, Yvonne J, Van der Velde, K Joeri, Sijmons, Rolf H, Van der Zwaag, Paul A, Sikkema-Raddatz, Birgit, Jongbloed, Jan D H
Published in Frontiers in genetics (01.03.2022)
Published in Frontiers in genetics (01.03.2022)
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Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization
van der Velde, K. Joeri, Kuiper, Joël, Thompson, Bryony A., Plazzer, John-Paul, van Valkenhoef, Gert, de Haan, Mark, Jongbloed, Jan D.H., Wijmenga, Cisca, de Koning, Tom J., Abbott, Kristin M., Sinke, Richard, Spurdle, Amanda B., Macrae, Finlay, Genuardi, Maurizio, Sijmons, Rolf H., Swertz, Morris A.
Published in Human mutation (01.07.2015)
Published in Human mutation (01.07.2015)
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Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance
Ghorbani, Fatemeh, Alimohamed, Mohamed Z, Vilacha, Juliana F, Van Dijk, Krista K, De Boer-Bergsma, Jelkje, Fokkens, Michiel R, Lemmink, Henny, Sijmons, Rolf H, Sikkema-Raddatz, Birgit, Groves, Matthew R, Verschuuren-Bemelmans, Corien C, Verbeek, Dineke S, Van Diemen, Cleo C, Westers, Helga
Published in Frontiers in genetics (25.03.2022)
Published in Frontiers in genetics (25.03.2022)
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Prevalence and Progression of Pancreatic Cystic Precursor Lesions Differ Between Groups at High Risk of Developing Pancreatic Cancer
Konings, Ingrid C A W, Harinck, Femme, Poley, Jan-Werner, Aalfs, Cora M, van Rens, Anja, Krak, Nanda C, Wagner, Anja, Nio, C Yung, Sijmons, Rolf H, van Dullemen, Hendrik M, Vleggaar, Frank P, Ausems, Margreet G E M, Fockens, Paul, van Hooft, Jeanin E, Bruno, Marco J
Published in Pancreas (01.01.2017)
Published in Pancreas (01.01.2017)
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B Cells as Prognostic Biomarker After Surgery for Colorectal Liver Metastases
Hof, Joost, Visser, Lydia, Höppener, Diederik J, Nierop, Pieter M H, Terpstra, Miente M, Gouw, Annette S H, Grünhagen, Dirk J, Verhoef, Cornelis, Sijmons, Rolf H, de Jong, Koert P, Kok, Klaas
Published in Frontiers in oncology (05.03.2020)
Published in Frontiers in oncology (05.03.2020)
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