Tops CM - Search Results

1

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.

Talseth-Palmer BA, Wijnen JT, Andreassen EK, Barker D, Jagmohan-Changur S, Tops CM, Meldrum C; Dutch Cancer Genetics Group; Spigelman A, Hes FJ, Van Wezel T, Vasen HF, Scott RJ. Talseth-Palmer BA, et al. Among authors: tops cm. Hered Cancer Clin Pract. 2013 Dec 29;11(1):20. doi: 10.1186/1897-4287-11-20. Hered Cancer Clin Pract. 2013. PMID: 24373140 Free PMC article.

2

Delineating genotype and parent-of-origin effect on the phenotype in MSH6-associated Lynch syndrome.

van der Werf-'t Lam AS, Rodriguez-Girondo M, Villasmil M, Tops CM, van Hest L, Gille HJP, Duijkers FAM, Wagner A, Eikenboom E, Letteboer TGW, de Jong MM, Bajwa-Ten Broeke SW, Bleeker F, Gomez Garcia EB, Dominguez-Valentin M, Møller P, Suerink M, Nielsen M. van der Werf-'t Lam AS, et al. Among authors: tops cm. Genes Chromosomes Cancer. 2024 May;63(5):e23237. doi: 10.1002/gcc.23237. Genes Chromosomes Cancer. 2024. PMID: 38722212

3

Close linkage of a highly polymorphic marker (D5S37) to familial adenomatous polyposis (FAP) and confirmation of FAP localization on chromosome 5q21-q22.

Meera Khan P, Tops CM, vd Broek M, Breukel C, Wijnen JT, Oldenburg M, vd Bos J, van Leeuwen-Cornelisse IS, Vasen HF, Griffioen G, et al. Meera Khan P, et al. Among authors: tops cm. Hum Genet. 1988 Jun;79(2):183-5. doi: 10.1007/BF00280563. Hum Genet. 1988. PMID: 2839409

4

Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.

van der Luijt RB, Meera Khan P, Vasen HF, Breukel C, Tops CM, Scott RJ, Fodde R. van der Luijt RB, et al. Among authors: tops cm. Hum Genet. 1996 Dec;98(6):727-34. doi: 10.1007/s004390050293. Hum Genet. 1996. PMID: 8931709

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: tops cm. 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

[Genetics of colorectal cancer. I. Non-polyposis and polyposis forms of hereditary colorectal cancer].

Menko FH, Griffioen G, Wijnen JT, Tops CM, Fodde R, Vasen HF. Menko FH, et al. Among authors: tops cm. Ned Tijdschr Geneeskd. 1999 Jun 5;143(23):1201-6. Ned Tijdschr Geneeskd. 1999. PMID: 10389534 Review. Dutch.

7

[Genetics of colorectal cancer. II. Hereditary background of sporadic and familial colorectal cancer].

Menko FH, Griffioen G, Wijnen JT, Tops CM, Fodde R, Vasen HF. Menko FH, et al. Among authors: tops cm. Ned Tijdschr Geneeskd. 1999 Jun 5;143(23):1207-11. Ned Tijdschr Geneeskd. 1999. PMID: 10389535 Review. Dutch.

8

[From gene to disease; the APC gene and familial adenomatous polyposis coli].

van der Luijt RB, Tops CM, Vasen HF. van der Luijt RB, et al. Among authors: tops cm. Ned Tijdschr Geneeskd. 2000 Oct 14;144(42):2007-9. Ned Tijdschr Geneeskd. 2000. PMID: 11072519 Review. Dutch.

9

Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures.

Wagner A, van Kessel I, Kriege MG, Tops CM, Wijnen JT, Vasen HF, van der Meer CA, van Oostrom II, Meijers-Heijboer H. Wagner A, et al. Among authors: tops cm. Fam Cancer. 2005;4(4):295-300. doi: 10.1007/s10689-005-0658-9. Fam Cancer. 2005. PMID: 16341806

10

Diagnostic approach and management of Lynch syndrome (hereditary nonpolyposis colorectal carcinoma): a guide for clinicians.

Hendriks YM, de Jong AE, Morreau H, Tops CM, Vasen HF, Wijnen JT, Breuning MH, Bröcker-Vriends AH. Hendriks YM, et al. Among authors: tops cm. CA Cancer J Clin. 2006 Jul-Aug;56(4):213-25. doi: 10.3322/canjclin.56.4.213. CA Cancer J Clin. 2006. PMID: 16870997 Free article. Review.

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