Claes KBM - Search Results

1

Prevalence of Germline Pathogenic Variants in Cancer Predisposing Genes in Czech and Belgian Pancreatic Cancer Patients.

Wieme G, Kral J, Rosseel T, Zemankova P, Parton B, Vocka M, Van Heetvelde M, Kleiblova P, Blaumeiser B, Soukupova J, van den Ende J, Nehasil P, Tejpar S, Borecka M, Gómez García EB, Blok MJ, Safarikova M, Kalousova M, Geboes K, De Putter R, Poppe B, De Leeneer K, Kleibl Z, Janatova M, Claes KBM. Wieme G, et al. Among authors: claes kbm. Cancers (Basel). 2021 Sep 2;13(17):4430. doi: 10.3390/cancers13174430. Cancers (Basel). 2021. PMID: 34503238 Free PMC article.

2

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.

3

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. Dis Markers. 1999 Oct;15(1-3):191-5. doi: 10.1155/1999/809125. Dis Markers. 1999. PMID: 10595277 Free PMC article.

4

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.

5

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. Nephrol Dial Transplant. 2008 Jan;23(1):294-300. doi: 10.1093/ndt/gfm532. Epub 2007 Sep 5. Nephrol Dial Transplant. 2008. PMID: 17804462

6

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. Genes Chromosomes Cancer. 2008 Feb;47(2):137-48. doi: 10.1002/gcc.20515. Genes Chromosomes Cancer. 2008. PMID: 18000863

7

Rapid and sensitive detection of BRCA1/2 mutations in a diagnostic setting: comparison of two high-resolution melting platforms.

De Leeneer K, Coene I, Poppe B, De Paepe A, Claes K. De Leeneer K, et al. Clin Chem. 2008 Jun;54(6):982-9. doi: 10.1373/clinchem.2007.098764. Epub 2008 Apr 10. Clin Chem. 2008. PMID: 18403564 Free article.

8

Genotyping of frequent BRCA1/2 SNPs with unlabeled probes: a supplement to HRMCA mutation scanning, allowing the strong reduction of sequencing burden.

De Leeneer K, Coene I, Poppe B, De Paepe A, Claes K. De Leeneer K, et al. J Mol Diagn. 2009 Sep;11(5):415-9. doi: 10.2353/jmoldx.2009.090032. Epub 2009 Jul 30. J Mol Diagn. 2009. PMID: 19644020 Free PMC article.

9

Massive parallel amplicon sequencing of the breast cancer genes BRCA1 and BRCA2: opportunities, challenges, and limitations.

De Leeneer K, Hellemans J, De Schrijver J, Baetens M, Poppe B, Van Criekinge W, De Paepe A, Coucke P, Claes K. De Leeneer K, et al. Hum Mutat. 2011 Mar;32(3):335-44. doi: 10.1002/humu.21428. Epub 2011 Feb 8. Hum Mutat. 2011. PMID: 21305653

10

Prevalence of BRCA1/2 mutations in sporadic breast/ovarian cancer patients and identification of a novel de novo BRCA1 mutation in a patient diagnosed with late onset breast and ovarian cancer: implications for genetic testing.

De Leeneer K, Coene I, Crombez B, Simkens J, Van den Broecke R, Bols A, Stragier B, Vanhoutte I, De Paepe A, Poppe B, Claes K. De Leeneer K, et al. Breast Cancer Res Treat. 2012 Feb;132(1):87-95. doi: 10.1007/s10549-011-1544-9. Epub 2011 May 7. Breast Cancer Res Treat. 2012. PMID: 21553119

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