Dinjens WNM - Search Results

1

Yield of Lynch Syndrome Surveillance for Patients With Pathogenic Variants in DNA Mismatch Repair Genes.

Goverde A, Eikenboom EL, Viskil EL, Bruno MJ, Doukas M, Dinjens WNM, Dubbink EJ, van den Ouweland AMW, Hofstra RMW, Wagner A, Spaander MCW. Goverde A, et al. Among authors: dinjens wnm. Clin Gastroenterol Hepatol. 2020 May;18(5):1112-1120.e1. doi: 10.1016/j.cgh.2019.08.043. Epub 2019 Aug 27. Clin Gastroenterol Hepatol. 2020. PMID: 31470178

2

Frequent loss of the AXIN1 locus but absence of AXIN1 gene mutations in adenocarcinomas of the gastro-oesophageal junction with nuclear beta-catenin expression.

Koppert LB, van der Velden AW, van de Wetering M, Abbou M, van den Ouweland AM, Tilanus HW, Wijnhoven BP, Dinjens WN. Koppert LB, et al. Br J Cancer. 2004 Feb 23;90(4):892-9. doi: 10.1038/sj.bjc.6601589. Br J Cancer. 2004. PMID: 14970870 Free PMC article.

3

Breast cancer in an MSH2 gene mutation carrier.

Westenend PJ, Schütte R, Hoogmans MM, Wagner A, Dinjens WN. Westenend PJ, et al. Hum Pathol. 2005 Dec;36(12):1322-6. doi: 10.1016/j.humpath.2005.08.025. Hum Pathol. 2005. PMID: 16311127

4

Mismatch repair and treatment resistance in ovarian cancer.

Helleman J, van Staveren IL, Dinjens WN, van Kuijk PF, Ritstier K, Ewing PC, van der Burg ME, Stoter G, Berns EM. Helleman J, et al. BMC Cancer. 2006 Jul 31;6:201. doi: 10.1186/1471-2407-6-201. BMC Cancer. 2006. PMID: 16879751 Free PMC article.

5

Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies.

Poley JW, Wagner A, Hoogmans MM, Menko FH, Tops C, Kros JM, Reddingius RE, Meijers-Heijboer H, Kuipers EJ, Dinjens WN; Rotterdam Initiative on Gastrointestinal Hereditary Tumors. Poley JW, et al. Cancer. 2007 Jun 1;109(11):2349-56. doi: 10.1002/cncr.22697. Cancer. 2007. PMID: 17440981 Free article.

6

A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.

Ramsoekh D, Wagner A, van Leerdam ME, Dinjens WN, Steyerberg EW, Halley DJ, Kuipers EJ, Dooijes D. Ramsoekh D, et al. Gut. 2008 Nov;57(11):1539-44. doi: 10.1136/gut.2008.156695. Epub 2008 Jul 14. Gut. 2008. PMID: 18625694

7

Underutilization of microsatellite instability analysis in colorectal cancer patients at high risk for Lynch syndrome.

Van Lier MG, De Wilt JH, Wagemakers JJ, Dinjens WN, Damhuis RA, Wagner A, Kuipers EJ, Van Leerdam ME. Van Lier MG, et al. Scand J Gastroenterol. 2009;44(5):600-4. doi: 10.1080/00365520802706008. Scand J Gastroenterol. 2009. PMID: 19153873

8

Deletion of exons 1a-2 of BRCA1: a rather frequent pathogenic abnormality.

van den Ouweland AM, Dinjens WN, Dorssers LC, van Veghel-Plandsoen MM, Brüggenwirth HT, Withagen-Hermans CJ, Collée JM, Joosse SA, Terlouw-Kromosoeto JN, Nederlof PM. van den Ouweland AM, et al. Genet Test Mol Biomarkers. 2009 Jun;13(3):399-406. doi: 10.1089/gtmb.2008.0155. Genet Test Mol Biomarkers. 2009. PMID: 19405878

9

A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory.

van Lier MG, Wagner A, van Leerdam ME, Biermann K, Kuipers EJ, Steyerberg EW, Dubbink HJ, Dinjens WN. van Lier MG, et al. J Cell Mol Med. 2010 Jan;14(1-2):181-97. doi: 10.1111/j.1582-4934.2009.00977.x. Epub 2009 Nov 19. J Cell Mol Med. 2010. PMID: 19929944 Free PMC article. Review.

10

On the advent of MSI testing of all colorectal cancers and a substantial part of other Lynch syndrome-related neoplasms.

Dinjens WN, van Leerdam ME, Wagner A. Dinjens WN, et al. Expert Rev Mol Diagn. 2010 May;10(4):381-4. doi: 10.1586/erm.10.37. Expert Rev Mol Diagn. 2010. PMID: 20465492 No abstract available.

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