Wijnen J - Search Results

1

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.

2

A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis.

Tops CM, Breukel C, van der Klift HM, von Leeuwen IS, Wijnen JT, Griffioen G, Vasen HF, den Hartog Jager FC, Nagengast FM, Lamers CB, et al. Tops CM, et al. Among authors: wijnen jt. Hum Genet. 1991 Feb;86(4):365-8. doi: 10.1007/BF00201835. Hum Genet. 1991. PMID: 1671849

3

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

4

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.

5

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis.

van der Luijt RB, Khan PM, Vasen HF, Tops CM, van Leeuwen-Cornelisse IS, Wijnen JT, van der Klift HM, Plug RJ, Griffioen G, Fodde R. van der Luijt RB, et al. Among authors: wijnen jt. Hum Mutat. 1997;9(1):7-16. doi: 10.1002/(SICI)1098-1004(1997)9:1<7::AID-HUMU2>3.0.CO;2-8. Hum Mutat. 1997. PMID: 8990002

6

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.

7

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.

8

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

9

Eight novel inactivating germ line mutations at the APC gene identified by denaturing gradient gel electrophoresis.

Fodde R, van der Luijt R, Wijnen J, Tops C, van der Klift H, van Leeuwen-Cornelisse I, Griffioen G, Vasen H, Khan PM. Fodde R, et al. Among authors: wijnen j. Genomics. 1992 Aug;13(4):1162-8. doi: 10.1016/0888-7543(92)90032-n. Genomics. 1992. PMID: 1324223

10

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.

Wijnen J, Vasen H, Khan PM, Menko FH, van der Klift H, van Leeuwen C, van den Broek M, van Leeuwen-Cornelisse I, Nagengast F, Meijers-Heijboer A, et al. Wijnen J, et al. Am J Hum Genet. 1995 May;56(5):1060-6. Am J Hum Genet. 1995. PMID: 7726159 Free PMC article.

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