Olsson H - Search Results

1

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: olsson h. Cancer Res. 2005 Sep 1;65(17):7612-21. doi: 10.1158/0008-5472.CAN-05-0570. Cancer Res. 2005. PMID: 16140926

2

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: olsson h. 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

3

Mapping of a novel ocular and cutaneous malignant melanoma susceptibility locus to chromosome 9q21.32.

Jönsson G, Bendahl PO, Sandberg T, Kurbasic A, Staaf J, Sunde L, Crüger DG, Ingvar C, Olsson H, Borg A. Jönsson G, et al. Among authors: olsson h. J Natl Cancer Inst. 2005 Sep 21;97(18):1377-82. doi: 10.1093/jnci/dji280. J Natl Cancer Inst. 2005. PMID: 16174859

4

Chromosome 5 imbalance mapping in breast tumors from BRCA1 and BRCA2 mutation carriers and sporadic breast tumors.

Johannsdottir HK, Jonsson G, Johannesdottir G, Agnarsson BA, Eerola H, Arason A, Heikkila P, Egilsson V, Olsson H, Johannsson OT, Nevanlinna H, Borg A, Barkardottir RB. Johannsdottir HK, et al. Among authors: olsson h. Int J Cancer. 2006 Sep 1;119(5):1052-60. doi: 10.1002/ijc.21934. Int J Cancer. 2006. PMID: 16570289 Free article.

5

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: olsson h. 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

6

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: olsson h. Fam Cancer. 2007;6(4):445-52. doi: 10.1007/s10689-007-9141-0. Epub 2007 May 5. Fam Cancer. 2007. PMID: 17484040

7

Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair.

Saal LH, Gruvberger-Saal SK, Persson C, Lövgren K, Jumppanen M, Staaf J, Jönsson G, Pires MM, Maurer M, Holm K, Koujak S, Subramaniyam S, Vallon-Christersson J, Olsson H, Su T, Memeo L, Ludwig T, Ethier SP, Krogh M, Szabolcs M, Murty VV, Isola J, Hibshoosh H, Parsons R, Borg A. Saal LH, et al. Among authors: olsson h. Nat Genet. 2008 Jan;40(1):102-7. doi: 10.1038/ng.2007.39. Epub 2007 Dec 9. Nat Genet. 2008. PMID: 18066063 Free PMC article.

8

Genomic alterations in histopathologically normal breast tissue from BRCA1 mutation carriers may be caused by BRCA1 haploinsufficiency.

Rennstam K, Ringberg A, Cunliffe HE, Olsson H, Landberg G, Hedenfalk I. Rennstam K, et al. Among authors: olsson h. Genes Chromosomes Cancer. 2010 Jan;49(1):78-90. doi: 10.1002/gcc.20723. Genes Chromosomes Cancer. 2010. PMID: 19839046

9

Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.

Engel C, Versmold B, Wappenschmidt B, Simard J, Easton DF, Peock S, Cook M, Oliver C, Frost D, Mayes R, Evans DG, Eeles R, Paterson J, Brewer C; Epidemiological Study of Familial Breast Cancer (EMBRACE); McGuffog L, Antoniou AC, Stoppa-Lyonnet D, Sinilnikova OM, Barjhoux L, Frenay M, Michel C, Leroux D, Dreyfus H, Toulas C, Gladieff L, Uhrhammer N, Bignon YJ, Meindl A, Arnold N, Varon-Mateeva R, Niederacher D, Preisler-Adams S, Kast K, Deissler H, Sutter C, Gadzicki D, Chenevix-Trench G, Spurdle AB, Chen X, Beesley J; Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab); Olsson H, Kristoffersson U, Ehrencrona H, Liljegren A; Swedish Breast Cancer Study, Sweden (SWE-BRCA); van der Luijt RB, van Os TA, van Leeuwen FE; Hereditary Breast and Ovarian cancer group Netherlands (HEBON); Domchek SM, Rebbeck TR, Nathanson KL, Osorio A, Ramón y Cajal T, Konstantopoulou I, Benítez J, Friedman E, Kaufman B, Laitman Y, Mai PL, Greene MH, Nevanlinna H, Aittomäki K, Szabo CI, Caldes T, Couch FJ, Andrulis IL, Godwin AK, Hamann U, Schmutzler RK; Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA). Engel C, et al. Among authors: olsson h. Cancer Epidemiol Biomarkers Prev. 2010 Nov;19(11):2859-68. doi: 10.1158/1055-9965.EPI-10-0517. Epub 2010 Oct 26. Cancer Epidemiol Biomarkers Prev. 2010. PMID: 20978178 Free PMC article.

10

Deletions on chromosome 4 in sporadic and BRCA mutated tumors and association with pathological variables.

Johannsdottir HK, Johannesdottir G, Agnarsson BA, Eerola H, Arason A, Johannsson OT, Heikkilä P, Egilsson V, Olsson H, Borg A, Nevanlinna H, Barkardottir RB. Johannsdottir HK, et al. Among authors: olsson h. Anticancer Res. 2004 Sep-Oct;24(5A):2681-7. Anticancer Res. 2004. PMID: 15521105 Free article.

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