Wijnen JT - Search Results

1

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

Vasen HF, Stormorken A, Menko FH, Nagengast FM, Kleibeuker JH, Griffioen G, Taal BG, Moller P, Wijnen JT. Vasen HF, et al. Among authors: wijnen jt. J Clin Oncol. 2001 Oct 15;19(20):4074-80. doi: 10.1200/JCO.2001.19.20.4074. J Clin Oncol. 2001. PMID: 11600610

2

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

Vasen HF, Wijnen JT, Menko FH, Kleibeuker JH, Taal BG, Griffioen G, Nagengast FM, Meijers-Heijboer EH, Bertario L, Varesco L, Bisgaard ML, Mohr J, Fodde R, Khan PM. Vasen HF, et al. Among authors: wijnen jt. Gastroenterology. 1996 Apr;110(4):1020-7. doi: 10.1053/gast.1996.v110.pm8612988. Gastroenterology. 1996. PMID: 8612988

3

Genetic counseling in hereditary nonpolyposis colorectal cancer.

Menko FH, Wijnen JT, Khan PM, Vasen HF, Oosterwijk MH. Menko FH, et al. Among authors: wijnen jt. Oncology (Williston Park). 1996 Jan;10(1):71-6; discussion 81-2. Oncology (Williston Park). 1996. PMID: 8924367 Free article.

4

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

Wijnen JT, Vasen HF, Khan PM, Zwinderman AH, van der Klift H, Mulder A, Tops C, Møller P, Fodde R. Wijnen JT, et al. N Engl J Med. 1998 Aug 20;339(8):511-8. doi: 10.1056/NEJM199808203390804. N Engl J Med. 1998. PMID: 9709044 Free article.

5

Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.

Wijnen J, Khan PM, Vasen H, Menko F, van der Klift H, van den Broek M, van Leeuwen-Cornelisse I, Nagengast F, Meijers-Heijboer EJ, Lindhout D, Griffioen G, Cats A, Kleibeuker J, Varesco L, Bertario L, Bisgaard ML, Mohr J, Kolodner R, Fodde R. Wijnen J, et al. Am J Hum Genet. 1996 Feb;58(2):300-7. Am J Hum Genet. 1996. PMID: 8571956 Free PMC article.

6

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.

Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, Losekoot M, Møller P, Fodde R. Wijnen J, et al. Am J Hum Genet. 1997 Aug;61(2):329-35. doi: 10.1086/514847. Am J Hum Genet. 1997. PMID: 9311737 Free PMC article.

7

Clinical implications of genetic testing of hereditary nonpolyposis colorectal cancer.

Vasen HF, Wijnen J. Vasen HF, et al. Cytogenet Cell Genet. 1999;86(2):136-9. doi: 10.1159/000015366. Cytogenet Cell Genet. 1999. PMID: 10545704 Review. No abstract available.

8

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach.

Gille JJ, Hogervorst FB, Pals G, Wijnen JT, van Schooten RJ, Dommering CJ, Meijer GA, Craanen ME, Nederlof PM, de Jong D, McElgunn CJ, Schouten JP, Menko FH. Gille JJ, et al. Among authors: wijnen jt. Br J Cancer. 2002 Oct 7;87(8):892-7. doi: 10.1038/sj.bjc.6600565. Br J Cancer. 2002. PMID: 12373605 Free PMC article.

9

Endometrial cancer in four sisters: report of a kindred with presumed cancer family syndrome.

Menko FH, Verheijen RH, Everhardt E, Louwé LA, Wijnen JT, Band SC, Felt-Bersma RJ, Vasen HF, Khan PM. Menko FH, et al. Among authors: wijnen jt. Gynecol Oncol. 1994 Aug;54(2):171-4. doi: 10.1006/gyno.1994.1188. Gynecol Oncol. 1994. PMID: 8063241

10

Familial and hereditary non-polyposis colorectal cancer: issues relevant for surgical practice.

Menko FH, Wijnen JT, Vasen HF, Sijmons RH, Khan PM. Menko FH, et al. Among authors: wijnen jt. Recent Results Cancer Res. 1998;146:20-31. doi: 10.1007/978-3-642-71967-7_2. Recent Results Cancer Res. 1998. PMID: 9670246 Review.

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