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Familial endometrial cancer in female carriers of MSH6 germline mutations.
Wijnen J, de Leeuw W, Vasen H, van der Klift H, Møller P, Stormorken A, Meijers-Heijboer H, Lindhout D, Menko F, Vossen S, Möslein G, Tops C, Bröcker-Vriends A, Wu Y, Hofstra R, Sijmons R, Cornelisse C, Morreau H, Fodde R. Wijnen J, et al. Among authors: van der klift h. Nat Genet. 1999 Oct;23(2):142-4. doi: 10.1038/13773. Nat Genet. 1999. PMID: 10508506 No abstract available.
MSH2 genomic deletions are a frequent cause of HNPCC.
Wijnen J, van der Klift H, Vasen H, Khan PM, Menko F, Tops C, Meijers Heijboer H, Lindhout D, Møller P, Fodde R. Wijnen J, et al. Among authors: van der klift h. Nat Genet. 1998 Dec;20(4):326-8. doi: 10.1038/3795. Nat Genet. 1998. PMID: 9843200 No abstract available.
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations.
Johannesma PC, van der Klift HM, van Grieken NC, Troost D, Te Riele H, Jacobs MA, Postma TJ, Heideman DA, Tops CM, Wijnen JT, Menko FH. Johannesma PC, et al. Among authors: van der klift hm, van grieken nc. Clin Genet. 2011 Sep;80(3):243-55. doi: 10.1111/j.1399-0004.2011.01635.x. Epub 2011 Feb 20. Clin Genet. 2011. PMID: 21261604
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. Among authors: van leeuwen cornelisse i, van den broek m, van der klift h. Am J Hum Genet. 1996 Feb;58(2):300-7. Am J Hum Genet. 1996. PMID: 8571956 Free PMC article.
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. Among authors: van leeuwen cornelisse i, van der klift h. Am J Hum Genet. 1997 Aug;61(2):329-35. doi: 10.1086/514847. Am J Hum Genet. 1997. PMID: 9311737 Free PMC article.
Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP).
Nielsen M, Franken PF, Reinards TH, Weiss MM, Wagner A, van der Klift H, Kloosterman S, Houwing-Duistermaat JJ, Aalfs CM, Ausems MG, Bröcker-Vriends AH, Gomez Garcia EB, Hoogerbrugge N, Menko FH, Sijmons RH, Verhoef S, Kuipers EJ, Morreau H, Breuning MH, Tops CM, Wijnen JT, Vasen HF, Fodde R, Hes FJ. Nielsen M, et al. Among authors: van der klift h. J Med Genet. 2005 Sep;42(9):e54. doi: 10.1136/jmg.2005.033217. J Med Genet. 2005. PMID: 16140997 Free PMC article.
Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.
ten Broeke SW, Brohet RM, Tops CM, van der Klift HM, Velthuizen ME, Bernstein I, Capellá Munar G, Gomez Garcia E, Hoogerbrugge N, Letteboer TG, Menko FH, Lindblom A, Mensenkamp AR, Moller P, van Os TA, Rahner N, Redeker BJ, Sijmons RH, Spruijt L, Suerink M, Vos YJ, Wagner A, Hes FJ, Vasen HF, Nielsen M, Wijnen JT. ten Broeke SW, et al. Among authors: van der klift hm, van os ta. J Clin Oncol. 2015 Feb 1;33(4):319-25. doi: 10.1200/JCO.2014.57.8088. Epub 2014 Dec 15. J Clin Oncol. 2015. PMID: 25512458
The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers.
Suerink M, van der Klift HM, Ten Broeke SW, Dekkers OM, Bernstein I, Capellá Munar G, Gomez Garcia E, Hoogerbrugge N, Letteboer TG, Menko FH, Lindblom A, Mensenkamp A, Moller P, van Os TA, Rahner N, Redeker BJ, Olderode-Berends MJ, Spruijt L, Vos YJ, Wagner A, Morreau H, Hes FJ, Vasen HF, Tops CM, Wijnen JT, Nielsen M. Suerink M, et al. Among authors: van der klift hm, van os ta. Genet Med. 2016 Apr;18(4):405-9. doi: 10.1038/gim.2015.83. Epub 2015 Jun 25. Genet Med. 2016. PMID: 26110232 Free article.
52 results