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Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer.
Lindblom A, Tannergård P, Werelius B, Nordenskjöld M. Lindblom A, et al. Among authors: werelius b. Nat Genet. 1993 Nov;5(3):279-82. doi: 10.1038/ng1193-279. Nat Genet. 1993. PMID: 7903889
Definition of candidate low risk APC alleles in a Swedish population.
Zhou XL, Eriksson U, Werelius B, Kressner U, Sun XF, Lindblom A. Zhou XL, et al. Among authors: werelius b. Int J Cancer. 2004 Jul 1;110(4):550-7. doi: 10.1002/ijc.20173. Int J Cancer. 2004. PMID: 15122587 Free article.
A screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancer.
Zhou XL, Werelius B, Lindblom A. Zhou XL, et al. Among authors: werelius b. Breast Cancer Res. 2004;6(3):R187-90. doi: 10.1186/bcr774. Epub 2004 Mar 9. Breast Cancer Res. 2004. PMID: 15084242 Free PMC article.
CDH1 mutations are present in both ductal and lobular breast cancer, but promoter allelic variants show no detectable breast cancer risk.
Lei H, Sjöberg-Margolin S, Salahshor S, Werelius B, Jandáková E, Hemminki K, Lindblom A, Vorechovský I. Lei H, et al. Among authors: werelius b. Int J Cancer. 2002 Mar 10;98(2):199-204. doi: 10.1002/ijc.10176. Int J Cancer. 2002. PMID: 11857408 Free article.
BRCA1 mutations in a population-based study of breast cancer in Stockholm County.
Margolin S, Werelius B, Fornander T, Lindblom A. Margolin S, et al. Among authors: werelius b. Genet Test. 2004 Summer;8(2):127-32. doi: 10.1089/gte.2004.8.127. Genet Test. 2004. PMID: 15345109
The estrogen receptor alpha C975G variant in familial and sporadic breast cancer: a case-control study.
Skoglund J, Margolin S, Zhou XL, Maguire P, Werelius B, Lindblom A. Skoglund J, et al. Among authors: werelius b. Anticancer Res. 2006 Jul-Aug;26(4B):3077-81. Anticancer Res. 2006. PMID: 16886637 Free article.
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.
Stacey SN, Manolescu A, Sulem P, Rafnar T, Gudmundsson J, Gudjonsson SA, Masson G, Jakobsdottir M, Thorlacius S, Helgason A, Aben KK, Strobbe LJ, Albers-Akkers MT, Swinkels DW, Henderson BE, Kolonel LN, Le Marchand L, Millastre E, Andres R, Godino J, Garcia-Prats MD, Polo E, Tres A, Mouy M, Saemundsdottir J, Backman VM, Gudmundsson L, Kristjansson K, Bergthorsson JT, Kostic J, Frigge ML, Geller F, Gudbjartsson D, Sigurdsson H, Jonsdottir T, Hrafnkelsson J, Johannsson J, Sveinsson T, Myrdal G, Grimsson HN, Jonsson T, von Holst S, Werelius B, Margolin S, Lindblom A, Mayordomo JI, Haiman CA, Kiemeney LA, Johannsson OT, Gulcher JR, Thorsteinsdottir U, Kong A, Stefansson K. Stacey SN, et al. Among authors: werelius b. Nat Genet. 2007 Jul;39(7):865-9. doi: 10.1038/ng2064. Epub 2007 May 27. Nat Genet. 2007. PMID: 17529974
A screening for BRCA1 mutations in breast and breast-ovarian cancer families from the Stockholm region.
Zelada-Hedman M, Wasteson Arver B, Claro A, Chen J, Werelius B, Kok H, Sandelin K, Håkansson S, Andersen TI, Borg A, Børresen Dale AL, Lindblom A. Zelada-Hedman M, et al. Among authors: werelius b. Cancer Res. 1997 Jun 15;57(12):2474-7. Cancer Res. 1997. PMID: 9192828
Loss of heterozygosity in familial breast carcinomas.
Lindblom A, Skoog L, Rotstein S, Werelius B, Larsson C, Nordenskjöld M. Lindblom A, et al. Among authors: werelius b. Cancer Res. 1993 Sep 15;53(18):4356-61. Cancer Res. 1993. PMID: 8364930
Physical mapping of the NF2/meningioma region on human chromosome 22q12.
Ruttledge MH, Xie YG, Han FY, Giovannini M, Janson M, Fransson I, Werelius B, Delattre O, Thomas G, Evans G, et al. Ruttledge MH, et al. Among authors: werelius b. Genomics. 1994 Jan 1;19(1):52-9. doi: 10.1006/geno.1994.1012. Genomics. 1994. PMID: 8188242
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