Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersANTONIOU, Antonis C; SINILNIKOVA, Olga M; NEUHAUSEN, Susan L et al.Human molecular genetics (Print). 2009, Vol 18, Num 22, pp 4442-4456, issn 0964-6906, 15 p.Article

Common variants on chromosome 5pl2 confer susceptibility to estrogen receptor-positive breast cancerSTACEY, Simon N; MANOLESCU, Andrei; STROBBE, Luc J et al.Nature genetics. 2008, Vol 40, Num 6, pp 703-706, issn 1061-4036, 4 p.Article

From chromosomes to molecular karyotyping : Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to ∼650 kbSCHOUMANS, Jacqueline; STAAF, Johan; JÖNSSON, Göran et al.European journal of medical genetics. 2005, Vol 48, Num 3, pp 290-300, issn 1769-7212, 11 p.Article

The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriersLAITMAN, Yael; KUCHENBAECKER, Karoline B; SCHMUTZLER, Rita K et al.Breast cancer research and treatment. 2012, Vol 132, Num 3, pp 1119-1126, issn 0167-6806, 8 p.Article

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk PredictionANTONIOU, Antonis C; BEESLEY, Jonathan; ISAACS, Claudine et al.Cancer research (Chicago, Ill.). 2010, Vol 70, Num 23, pp 9742-9754, issn 0008-5472, 13 p.Article