Borg A - Search Results

1

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.

Borg A, Haile RW, Malone KE, Capanu M, Diep A, Törngren T, Teraoka S, Begg CB, Thomas DC, Concannon P, Mellemkjaer L, Bernstein L, Tellhed L, Xue S, Olson ER, Liang X, Dolle J, Børresen-Dale AL, Bernstein JL. Borg A, et al. Hum Mutat. 2010 Mar;31(3):E1200-40. doi: 10.1002/humu.21202. Hum Mutat. 2010. PMID: 20104584 Free PMC article.

2

Cancer incidence in relatives of a population-based set of cases of early-onset breast cancer with a known BRCA1 and BRCA2 mutation status.

Loman N, Bladström A, Johannsson O, Borg A, Olsson H. Loman N, et al. Among authors: borg a. Breast Cancer Res. 2003;5(6):R175-86. doi: 10.1186/bcr632. Epub 2003 Aug 7. Breast Cancer Res. 2003. PMID: 14580253 Free PMC article.

3

Impact of teenage oral contraceptive use in a population-based series of early-onset breast cancer cases who have undergone BRCA mutation testing.

Jernström H, Loman N, Johannsson OT, Borg A, Olsson H. Jernström H, et al. Among authors: borg a. Eur J Cancer. 2005 Oct;41(15):2312-20. doi: 10.1016/j.ejca.2005.03.035. Epub 2005 Aug 22. Eur J Cancer. 2005. PMID: 16118051

4

Distinct genomic profiles in hereditary breast tumors identified by array-based comparative genomic hybridization.

Jönsson G, Naylor TL, Vallon-Christersson J, Staaf J, Huang J, Ward MR, Greshock JD, Luts L, Olsson H, Rahman N, Stratton M, Ringnér M, Borg A, Weber BL. Jönsson G, et al. Among authors: borg a. Cancer Res. 2005 Sep 1;65(17):7612-21. doi: 10.1158/0008-5472.CAN-05-0570. Cancer Res. 2005. PMID: 16140926

5

RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability.

Heikkinen K, Rapakko K, Karppinen SM, Erkko H, Knuutila S, Lundán T, Mannermaa A, Børresen-Dale AL, Borg A, Barkardottir RB, Petrini J, Winqvist R. Heikkinen K, et al. Among authors: borg a. Carcinogenesis. 2006 Aug;27(8):1593-9. doi: 10.1093/carcin/bgi360. Epub 2006 Feb 12. Carcinogenesis. 2006. PMID: 16474176 Free PMC article.

6

Differences in IGFBP-3 regulation between young healthy women from BRCAX families and those belonging to BRCA1/2 families.

Jernström H, Sellberg G, Borg A, Olsson H. Jernström H, et al. Among authors: borg a. Eur J Cancer Prev. 2006 Jun;15(3):233-41. doi: 10.1097/01.cej.0000203615.77183.97. Eur J Cancer Prev. 2006. PMID: 16679866

7

Absence of the common IGF1 19 CA-repeat allele is more common among BRCA1 mutation carriers than among non-carriers from BRCA1 families.

Henningson M, Bågeman E, Sandberg T, Borg A, Olsson H, Jernström H. Henningson M, et al. Among authors: borg a. Fam Cancer. 2007;6(4):445-52. doi: 10.1007/s10689-007-9141-0. Epub 2007 May 5. Fam Cancer. 2007. PMID: 17484040

8

Risk for contralateral breast cancer among carriers of the CHEK2*1100delC mutation in the WECARE Study.

Mellemkjaer L, Dahl C, Olsen JH, Bertelsen L, Guldberg P, Christensen J, Børresen-Dale AL, Stovall M, Langholz B, Bernstein L, Lynch CF, Malone KE, Haile RW, Andersson M, Thomas DC, Concannon P, Capanu M, Boice JD Jr; WECARE Study Collaborative Group; Bernstein JL. Mellemkjaer L, et al. Br J Cancer. 2008 Feb 26;98(4):728-33. doi: 10.1038/sj.bjc.6604228. Epub 2008 Feb 5. Br J Cancer. 2008. PMID: 18253122 Free PMC article.

9

Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).

Staaf J, Törngren T, Rambech E, Johansson U, Persson C, Sellberg G, Tellhed L, Nilbert M, Borg A. Staaf J, et al. Among authors: borg a. Hum Mutat. 2008 Apr;29(4):555-64. doi: 10.1002/humu.20678. Hum Mutat. 2008. PMID: 18330910

10

Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.

Magnusson S, Borg A, Kristoffersson U, Nilbert M, Wiebe T, Olsson H. Magnusson S, et al. Among authors: borg a. Fam Cancer. 2008;7(4):331-7. doi: 10.1007/s10689-008-9195-7. Epub 2008 May 15. Fam Cancer. 2008. PMID: 18481196

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