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Browsing by Author Ouweland, A.M.W. van den

Full Text	Issue Date	Title	Author(s)
	2010	A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.	Antoniou, A.C.; Wang, X.; Fredericksen, Z.; McGuffog, L.; Tarrell, R., et al
	2009	A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example	Mohammadi, L.; Vreeswijk, M.P.; Oldenburg, R.; Ouweland, A.M.W. van den; Oosterwijk-Wakka, J.C., et al
	2009	A method to assess the clinical significance of unclassified variants in the BRCA1 and BRCA2 genes based on cancer family history.	Gomez Garcia, E.B.; Oosterwijk-Wakka, J.C.; Timmermans, M.; Asperen, C.J. van; Hogervorst, F.B.L., et al
	2009	Attitude towards pre-implantation genetic diagnosis for hereditary cancer.	Lammens, C.; Bleiker, E.M.A.; Aaronson, N.K.; Vriends, A.H.; Ausems, M.G.E.M., et al
	2009	Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA).	Osorio, A.; Milne, R.L.; Pita, G.; Peterlongo, P.; Heikkinen, T., et al
	2007	Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.	Hes, F.J.; Luijt, R.B. van der; Janssen, A.L.; Zewald, R.A.; Jong, G.J. de, et al
	2006	A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting.	Hout, A.H. van der; Ouweland, A.M.W. van den; Luijt, R.B. van der; Gille, H.J.; Bodmer, D., et al
	2004	Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapy.	Seynaeve, C.; Verhoog, L.C.; Bosch, L.M. van de; Geel, A.N. van; Menke-Pluymers, M., et al
	1997	A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families	Peelen, T.; Vliet, M. van; Petrij-Bosch, A.; Mieremet, R.; Szabo, C., et al
	1996	Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotype	Keulemans, J.L.M.; Reuser, A.J.J.; Kroos, M.A.; Willemsen, R.; Hermans, M.M.P., et al
	1996	Mental status of females with a FMR1 gene full mutation	Vries, B.B. de; Wiegers, A.M.; Smits, A.P.T.; Mohkamsing, S.; Duivenvoorden, H.J., et al