Claes K - Search Results

1

Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition.

Baeyens A, Thierens H, Claes K, Poppe B, Messiaen L, De Ridder L, Vral A. Baeyens A, et al. Among authors: claes k. Br J Cancer. 2002 Dec 2;87(12):1379-85. doi: 10.1038/sj.bjc.6600628. Br J Cancer. 2002. PMID: 12454765 Free PMC article.

2

Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online.

Claes K, Machackova E, De Vos M, Mortier G, De Paepe A, Messiaen L. Claes K, et al. Hum Mutat. 1999;13(3):256. doi: 10.1002/(SICI)1098-1004(1999)13:3<256::AID-HUMU12>3.0.CO;2-M. Hum Mutat. 1999. PMID: 10090482

3

Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G.

Claes K, Machackova E, De Vos M, Poppe B, De Paepe A, Messiaen L. Claes K, et al. Dis Markers. 1999 Oct;15(1-3):69-73. doi: 10.1155/1999/241046. Dis Markers. 1999. PMID: 10595255 Free PMC article.

4

Genetic counselling and testing for hereditary breast and ovarian cancer: the gent(le) approach.

De Vos M, Poppe B, Delvaux I, Mortier G, Claes K, Messiaen L, De Paepe A. De Vos M, et al. Among authors: claes k. Dis Markers. 1999 Oct;15(1-3):191-5. doi: 10.1155/1999/809125. Dis Markers. 1999. PMID: 10595277 Free PMC article.

5

A high occurrence of BRCA1 and BRCA2 mutations among Czech hereditary breast and breast-ovarian cancer families.

Machácková E, Foretová L, Navrátilová M, Valík D, Claes K, Messiaen L. Machácková E, et al. Among authors: claes k. Cas Lek Cesk. 2000 Oct 11;139(20):635-7. Cas Lek Cesk. 2000. PMID: 11192759

6

BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families.

Claes K, Poppe B, Coene I, Paepe AD, Messiaen L. Claes K, et al. Br J Cancer. 2004 Mar 22;90(6):1244-51. doi: 10.1038/sj.bjc.6601656. Br J Cancer. 2004. PMID: 15026808 Free PMC article.

7

Chromosomal radiosensitivity in BRCA1 and BRCA2 mutation carriers.

Baeyens A, Thierens H, Claes K, Poppe B, de Ridder L, Vral A. Baeyens A, et al. Among authors: claes k. Int J Radiat Biol. 2004 Oct;80(10):745-56. doi: 10.1080/09553000400017937. Int J Radiat Biol. 2004. PMID: 15799620

8

Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patients.

Wimmer K, Yao S, Claes K, Kehrer-Sawatzki H, Tinschert S, De Raedt T, Legius E, Callens T, Beiglböck H, Maertens O, Messiaen L. Wimmer K, et al. Among authors: claes k. Genes Chromosomes Cancer. 2006 Mar;45(3):265-76. doi: 10.1002/gcc.20289. Genes Chromosomes Cancer. 2006. PMID: 16283621

9

Two-tier approach for the detection of alpha-galactosidase A deficiency in a predominantly female haemodialysis population.

Terryn W, Poppe B, Wuyts B, Claes K, Maes B, Verbeelen D, Vanholder R, De Boeck K, Lameire N, De Paepe A, De Schoenmakere G. Terryn W, et al. Among authors: claes k. Nephrol Dial Transplant. 2008 Jan;23(1):294-300. doi: 10.1093/ndt/gfm532. Epub 2007 Sep 5. Nephrol Dial Transplant. 2008. PMID: 17804462

10

Polymorphisms in nonhomologous end-joining genes associated with breast cancer risk and chromosomal radiosensitivity.

Willems P, Claes K, Baeyens A, Vandersickel V, Werbrouck J, De Ruyck K, Poppe B, Van den Broecke R, Makar A, Marras E, Perletti G, Thierens H, Vral A. Willems P, et al. Among authors: claes k. Genes Chromosomes Cancer. 2008 Feb;47(2):137-48. doi: 10.1002/gcc.20515. Genes Chromosomes Cancer. 2008. PMID: 18000863

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