Papers authored by Niessen RC

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Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patients.
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Ferreira AM, Westers H, Sousa S, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, Reuvekamp PT, Seruca R, Kleibeuker JH, Hollema H, Sijmons RH, and Hofstra RM
The Journal of pathology 219(1):96-102, 2009 Sep - Who cited this? | PubMed ID: 19521971 | Fulltext
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Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.
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Niessen RC, Hofstra RM, Westers H, Ligtenberg MJ, Kooi K, Jager PO, de Groote ML, Dijkhuizen T, Olderode-Berends MJ, Hollema H, Kleibeuker JH, and Sijmons RH
Genes, chromosomes & cancer 48(8):737-44, 2009 Aug - Who cited this? | PubMed ID: 19455606 | Fulltext
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Do microsatellite instability profiles really differ between colorectal and endometrial tumors?.
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Ferreira AM, Westers H, Wu Y, Niessen RC, Olderode-Berends M, van der Sluis T, van der Zee AG, Hollema H, Kleibeuker JH, Sijmons RH, and Hofstra RM
Genes, chromosomes & cancer 48(7):552-7, 2009 Jul - Who cited this? | PubMed ID: 19373783 | Fulltext
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PMS2 involvement in patients suspected of Lynch syndrome.
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Niessen RC, Kleibeuker JH, Westers H, Jager PO, Rozeveld D, Bos KK, Boersma-van Ek W, Hollema H, Sijmons RH, and Hofstra RM
Genes, chromosomes & cancer 48(4):322-9, 2009 Apr - Who cited this? | PubMed ID: 19132747 | Fulltext
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Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome.
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Ou J, Rasmussen M, Westers H, Andersen SD, Jager PO, Kooi KA, Niessen RC, Eggen BJ, Nielsen FC, Kleibeuker JH, Sijmons RH, Rasmussen LJ, and Hofstra RM
Genes, chromosomes & cancer 48(4):340-50, 2009 Apr - Who cited this? | PubMed ID: 19156873 | Fulltext
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A database to support the interpretation of human mismatch repair gene variants.
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Ou J, Niessen RC, Vonk J, Westers H, Hofstra RM, and Sijmons RH
Human mutation 29(11):1337-41, 2008 Nov - Who cited this? | PubMed ID: 18951442 | Fulltext
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A novel MSH2 germline mutation in a Druze HNPCC family.
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Zidan J, Niessen RC, Laitman Y, Rozeveld D, Hofstra RM, and Friedman E
Familial cancer 7(2):135-9, 2008 - Who cited this? | PubMed ID: 17661183 | Fulltext
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Functional analysis helps to clarify the clinical importance of unclassified variants in DNA mismatch repair genes.
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Ou J, Niessen RC, Lützen A, Sijmons RH, Kleibeuker JH, de Wind N, Rasmussen LJ, and Hofstra RM
Human mutation 28(11):1047-54, 2007 Nov - Who cited this? | PubMed ID: 17594722 | Fulltext
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Getting rid of the PMS2 pseudogenes: mission impossible?.
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Niessen RC, Kleibeuker JH, Jager PO, Sijmons RH, and Hofstra RM
Human mutation 28(4):414; author reply 415, 2007 Apr - Who cited this? | PubMed ID: 17139668 | Fulltext
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High EPHB2 mutation rate in gastric but not endometrial tumors with microsatellite instability.
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Davalos V, Dopeso H, Velho S, Ferreira AM, Cirnes L, Díaz-Chico N, Bilbao C, Ramírez R, Rodríguez G, Falcón O, León L, Niessen RC, Keller G, Dallenbach-Hellweg G, Espín E, Armengol M, 
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Oncogene 26(2):308-11, 2007 Jan 11 - Who cited this? | PubMed ID: 16819508 | Fulltext
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Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer.
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Niessen RC, Berends MJ, Wu Y, Sijmons RH, Hollema H, Ligtenberg MJ, de Walle HE, de Vries EG, Karrenbeld A, Buys CH, van der Zee AG, Hofstra RM, and Kleibeuker JH
Gut 55(12):1781-8, 2006 Dec - Who cited this? | PubMed ID: 16636019 | Fulltext
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MUTYH and the mismatch repair system: partners in crime?.
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Niessen RC, Sijmons RH, Ou J, Olthof SG, Osinga J, Ligtenberg MJ, Hogervorst FB, Weiss MM, Tops CM, Hes FJ, de Bock GH, Buys CH, Kleibeuker JH, and Hofstra RM
Human genetics 119(1-2):206-11, 2006 Mar - Who cited this? | PubMed ID: 16408224 | Fulltext
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Pigmentary mosaicism following the lines of Blaschko in a girl with a double aneuploidy mosaicism: (47,XX,+7/45,X).
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Niessen RC, Jonkman MF, Muis N, Hordijk R, and van Essen AJ
American journal of medical genetics. Part A 137(3):313-22, 2005 Sep 1 - Who cited this? | PubMed ID: 16092121 | Fulltext
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Colorectal cancer and the CHEK2 1100delC mutation.
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de Jong MM, Nolte IM, Te Meerman GJ, van der Graaf WT, Mulder MJ, van der Steege G, Bruinenberg M, Schaapveld M, Niessen RC, Berends MJ, Sijmons RH, Hofstra RM, de Vries EG, and Kleibeuker JH
Genes, chromosomes & cancer 43(4):377-82, 2005 Aug - Who cited this? | PubMed ID: 15852425 | Fulltext
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BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes.
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Domingo E, Niessen RC, Oliveira C, Alhopuro P, Moutinho C, Espín E, Armengol M, Sijmons RH, Kleibeuker JH, Seruca R, Aaltonen LA, Imai K, Yamamoto H, Schwartz S, and Hofstra RM
Oncogene 24(24):3995-8, 2005 Jun 2 - Who cited this? | PubMed ID: 15782118 | Fulltext
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Hereditary non-polyposis colorectal cancer: identification of mutation carriers and assessing pathogenicity of mutations.
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Niessen RC, Sijmons RH, Berends MJ, Ou J, Hofstra RM, and Kleibeuker JH
Scandinavian journal of gastroenterology. Supplement(241):70-7, 2004 - Who cited this? | PubMed ID: 15696853 | Fulltext
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