Twin pregnancies with diploid hydatidiform mole and co-existing normal fetus may originate from one oocyteNIEMANN, Isa; BOLUND, Lars; SUNDE, Lone et al.Human reproduction (Oxford. Print). 2008, Vol 23, Num 9, pp 2031-2035, issn 0268-1161, 5 p.Article

Neurofibromatosis von recklinghausen type I phenotype and early onset of cancers in siblings compound heterozygous for mutations in MSH6ØSTERGAARD, John R; SUNDE, Lone; OKKELS, Henrik et al.American journal of medical genetics. 2005, Vol 139A, Num 2, pp 96-105, issn 0148-7299, 10 p.Article

Predictors of low risk of persistent trophoblastic disease in molar pregnanciesNIEMANN, Isa; PETERSEN, Lone Kjeld; HANSEN, Estrid S et al.Obstetrics and gynecology (New York. 1953). 2006, Vol 107, Num 5, pp 1006-1011, issn 0029-7844, 6 p.Article

Mosaics and molesSUNDE, Lone; NIEMANN, Isa; STAEHR HANSEN, Estrid et al.European journal of human genetics. 2011, Vol 19, Num 10, pp 1026-1031, issn 1018-4813, 6 p.Article

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutationPEIXOTO, Ana; SANTOS, Catarina; THOMASSEN, Mads et al.Breast cancer research and treatment. 2011, Vol 127, Num 3, pp 671-679, issn 0167-6806, 9 p.Article

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

Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndromeJENSEN, Uffe Birk; SUNDE, Lone; TIMSHEL, Susanne et al.Breast cancer research and treatment. 2010, Vol 120, Num 3, pp 777-782, issn 0167-6806, 6 p.Article

The risk of extra-colonic, extra-endometrial cancer in the Lynch syndromeWATSON, Patrice; VASEN, Hans F. A; MECKLIN, Jukka-Pekka et al.International journal of cancer. 2008, Vol 123, Num 2, pp 444-449, issn 0020-7136, 6 p.Article

Polyposis and early cancer in a patient with low penetrant mutations in MSH6 and APC : hereditary colorectal cancer as a polygenic traitOKKELS, Henrik; SUNDE, Lone; LINDORFF-LARSEN, Karen et al.International journal of colorectal disease (Print). 2006, Vol 21, Num 8, pp 847-850, issn 0179-1958, 4 p.Article

A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicingTHOMASSEN, Mads; SØKILDE PEDERSEN, Inge; LUISE BISGAARD, Marie et al.Breast cancer research and treatment. 2011, Vol 128, Num 1, pp 179-185, issn 0167-6806, 7 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

Mapping of a novel ocular and cutaneous malignant melanoma susceptibility locus to chromosome 9q21.32JÖNSSON, Goran; BENDAHL, Pär-Ola; SANDBERG, Therese et al.Journal of the National Cancer Institute. 2005, Vol 97, Num 18, pp 1377-1382, issn 0027-8874, 6 p.Article

Genotype—phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysisVOS, Yvonne J; DE WALLE, Hermien E. K; FORTUNA, Ana Maria et al.Journal of medical genetics. 2010, Vol 47, Num 3, pp 169-175, issn 0022-2593, 7 p.Article