Publications by authors named "Renee C Niessen"

16Publications

Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines.

Authors:
Johanna C Herkert Renée C Niessen Maria J W Olderode-Berends Hermine E Veenstra-Knol Yvonne J Vos Heleen M van der Klift Rene Scheenstra Carli M J Tops Arend Karrenbeld Frans T M Peters Robert M W Hofstra Jan H Kleibeuker Rolf H Sijmons

Eur J Cancer 2011 May 4;47(7):965-82. Epub 2011 Mar 4.

Department of Genetics, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands.

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May 2011

Recurrence and variability of germline EPCAM deletions in Lynch syndrome.

Authors:
Roland P Kuiper Lisenka E L M Vissers Ramprasath Venkatachalam Danielle Bodmer Eveline Hoenselaar Monique Goossens Aline Haufe Eveline Kamping Renée C Niessen Frans B L Hogervorst Johan J P Gille Bert Redeker Carli M J Tops Marielle E van Gijn Ans M W van den Ouweland Nils Rahner Verena Steinke Philip Kahl Elke Holinski-Feder Monika Morak Matthias Kloor Susanne Stemmler Beate Betz Pierre Hutter David J Bunyan Sapna Syngal Julie O Culver Tracy Graham Tsun L Chan Iris D Nagtegaal J Han J M van Krieken Hans K Schackert Nicoline Hoogerbrugge Ad Geurts van Kessel Marjolijn J L Ligtenberg

Hum Mutat 2011 Apr 1;32(4):407-14. Epub 2011 Mar 1.

Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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April 2011

Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study.

Authors:
Marlies J E Kempers Roland P Kuiper Charlotte W Ockeloen Pierre O Chappuis Pierre Hutter Nils Rahner Hans K Schackert Verena Steinke Elke Holinski-Feder Monika Morak Matthias Kloor Reinhard Büttner Eugene T P Verwiel J Han van Krieken Iris D Nagtegaal Monique Goossens Rachel S van der Post Renée C Niessen Rolf H Sijmons Irma Kluijt Frans B L Hogervorst Edward M Leter Johan J P Gille Cora M Aalfs Egbert J W Redeker Frederik J Hes Carli M J Tops Bernadette P M van Nesselrooij Marielle E van Gijn Encarna B Gómez García Diana M Eccles David J Bunyan Sapna Syngal Elena M Stoffel Julie O Culver Melanie R Palomares Tracy Graham Lea Velsher Janos Papp Edith Oláh Tsun L Chan Suet Y Leung Ad Geurts van Kessel Lambertus A L M Kiemeney Nicoline Hoogerbrugge Marjolijn J L Ligtenberg

Lancet Oncol 2011 Jan 8;12(1):49-55. Epub 2010 Dec 8.

Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands.

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January 2011

Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patients.

Authors:
Ana M Ferreira Helga Westers Sónia Sousa Ying Wu Renée C Niessen Maran Olderode-Berends Tineke van der Sluis Peter T W Reuvekamp Raquel Seruca Jan H Kleibeuker Harry Hollema Rolf H Sijmons Robert M W Hofstra

J Pathol 2009 Sep;219(1):96-102

Department of Genetics, University Medical Centre Groningen, University of Groningen, Groningen, The Netherlands.

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September 2009

Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome.

Authors:
Renée C Niessen Robert M W Hofstra Helga Westers Marjolijn J L Ligtenberg Krista Kooi Paul O J Jager Marloes L de Groote Trijnie Dijkhuizen Maran J W Olderode-Berends Harry Hollema Jan H Kleibeuker Rolf H Sijmons

Genes Chromosomes Cancer 2009 Aug;48(8):737-44

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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August 2009

Do microsatellite instability profiles really differ between colorectal and endometrial tumors?

Authors:
Ana M Ferreira Helga Westers Ying Wu Renée C Niessen Maran Olderode-Berends Tineke van der Sluis Ate G van der Zee Harry Hollema Jan H Kleibeuker Rolf H Sijmons Robert M W Hofstra

Genes Chromosomes Cancer 2009 Jul;48(7):552-7

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

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July 2009

Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome.

Authors:
Jianghua Ou Merete Rasmussen Helga Westers Sofie D Andersen Paul O Jager Krista A Kooi Renée C Niessen Bart J L Eggen Finn C Nielsen Jan H Kleibeuker Rolf H Sijmons Lene J Rasmussen Robert M W Hofstra

Genes Chromosomes Cancer 2009 Apr;48(4):340-50

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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April 2009

PMS2 involvement in patients suspected of Lynch syndrome.

Authors:
Renée C Niessen Jan H Kleibeuker Helga Westers Paul O J Jager Dennie Rozeveld Krista K Bos Wytske Boersma-van Ek Harry Hollema Rolf H Sijmons Robert M W Hofstra

Genes Chromosomes Cancer 2009 Apr;48(4):322-9

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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April 2009

A database to support the interpretation of human mismatch repair gene variants.

Authors:
Jianghua Ou Renée C Niessen Jan Vonk Helga Westers Robert M W Hofstra Rolf H Sijmons

Hum Mutat 2008 Nov;29(11):1337-41

Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

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November 2008

A novel MSH2 germline mutation in a Druze HNPCC family.

Authors:
Jamal Zidan Renée C Niessen Yael Laitman Dennie Rozeveld Robert M W Hofstra Eitan Friedman

Fam Cancer 2008 29;7(2):135-9. Epub 2007 Jul 29.

Oncology Unit, Rivkah Ziv Medical Center, Zefat, Israel.

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October 2008

Functional analysis helps to clarify the clinical importance of unclassified variants in DNA mismatch repair genes.

Authors:
Jianghua Ou Renée C Niessen Anne Lützen Rolf H Sijmons Jan H Kleibeuker Niels de Wind Lene Juel Rasmussen Robert M W Hofstra

Hum Mutat 2007 Nov;28(11):1047-54

Department of Genetics, University Medical Center Groningen, Groningen, The Netherlands.

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November 2007

Getting rid of the PMS2 pseudogenes: mission impossible?

Authors:
Renée C Niessen Jan H Kleibeuker Paul O J Jager Rolf H Sijmons Robert M W Hofstra

Hum Mutat 2007 Apr;28(4):414; author reply 415

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April 2007

MUTYH and the mismatch repair system: partners in crime?

Authors:
Renée C Niessen Rolf H Sijmons J Ou Sandra G M Olthof Jan Osinga Marjolijn J Ligtenberg Frans B L Hogervorst Marjan M Weiss Carli M J Tops Frederik J Hes Geertruida H de Bock Charles H C M Buys Jan H Kleibeuker Robert M W Hofstra

Hum Genet 2006 Mar 12;119(1-2):206-11. Epub 2006 Jan 12.

Department of Medical Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

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March 2006

Pigmentary mosaicism following the lines of Blaschko in a girl with a double aneuploidy mosaicism: (47,XX,+7/45,X).

Authors:
Renée C Niessen Marcel F Jonkman Nies Muis Roel Hordijk Anthonie J van Essen

Am J Med Genet A 2005 Sep;137A(3):313-22

Department of Clinical Genetics, University Medical Center Groningen, Groningen, The Netherlands.

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September 2005

Colorectal cancer and the CHEK2 1100delC mutation.

Authors:
Mirjam M de Jong Ilja M Nolte Gerard J Te Meerman Winette T A van der Graaf Marcel J Mulder Gerrit van der Steege Marcel Bruinenberg Michael Schaapveld Renée C Niessen Maran J W Berends Rolf H Sijmons Robert M W Hofstra Elisabeth G E de Vries Jan H Kleibeuker

Genes Chromosomes Cancer 2005 Aug;43(4):377-82

Department of Gastroenterology, University of Groningen Medical Center, The Netherlands.

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August 2005

BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes.

Authors:
Enric Domingo Renée C Niessen Carla Oliveira Pia Alhopuro Catia Moutinho Eloi Espín Manel Armengol Rolf H Sijmons Jan H Kleibeuker Raquel Seruca Lauri A Aaltonen Kohzoh Imai Hiroyuki Yamamoto Simó Schwartz Robert M W Hofstra

Oncogene 2005 Jun;24(24):3995-8

Molecular Oncology and Aging Research, Centre d'Investigacions en Bioquímica i Biologia Molecular (CIBBIM), Hospital Universitari Vall d'Hebron, Passeig Vall d'Hebron 119-129, Barcelona 08035, Spain.

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June 2005