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Óskar Jóhannsson
Óskar Jóhannsson
Unknown affiliation
Verified email at landspitali.is
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Year
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies
A Antoniou, PDP Pharoah, S Narod, HA Risch, JE Eyfjord, JL Hopper, ...
The American Journal of Human Genetics 72 (5), 1117-1130, 2003
47592003
Gene-expression profiles in hereditary breast cancer
I Hedenfalk, D Duggan, Y Chen, M Radmacher, M Bittner, R Simon, ...
New England Journal of Medicine 344 (8), 539-548, 2001
21632001
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer
SN Stacey, A Manolescu, P Sulem, T Rafnar, J Gudmundsson, ...
Nature genetics 39 (7), 865-869, 2007
9002007
Parental origin of sequence variants associated with complex diseases
A Kong, V Steinthorsdottir, G Masson, G Thorleifsson, P Sulem, ...
Nature 462 (7275), 868-874, 2009
6592009
The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
AC Antoniou, AP Cunningham, J Peto, DG Evans, F Lalloo, SA Narod, ...
British journal of cancer 98 (8), 1457-1466, 2008
6262008
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer
SN Stacey, A Manolescu, P Sulem, S Thorlacius, SA Gudjonsson, ...
Nature genetics 40 (6), 703-706, 2008
5492008
Distinct Somatic Genetic Changes Associated with Tumor Progression in Carriers of BRCA1 and BRCA2 Germ-line Mutations
M Tirkkonen, O Johannsson, BA Agnarsson, H Olsson, S Ingvarsson, ...
Cancer research 57 (7), 1222-1227, 1997
4831997
High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families
A Borg, T Sandberg, K Nilsson, O Johannsson, M Klinker, A Måsbäck, ...
Journal of the National Cancer Institute 92 (15), 1260-1266, 2000
4352000
Frequent amplification of chromosomal region 20q12-q13 in ovarian cancer
MM Tanner, S Grenman, A Koul, O Johannsson, P Meltzer, T Pejovic, ...
Clinical Cancer Research 6 (5), 1833-1839, 2000
4342000
Tumour biological features of BRCA1-induced breast and ovarian cancer
OT Johannsson, I Idvall, C Anderson, Ĺ Borg, RB Barkardottir, V Egilsson, ...
European Journal of Cancer 33 (3), 362-371, 1997
4321997
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer
N Loman, O Johannsson, U Kristoffersson, H Olsson, A Borg
Journal of the National Cancer Institute 93 (16), 1215-1223, 2001
3582001
Survival of BRCA1 breast and ovarian cancer patients: a population-based study from southern Sweden
OT Johannsson, J Ranstam, Ĺ Borg, H Olsson
Journal of Clinical Oncology 16 (2), 397-404, 1998
3251998
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility
SN Stacey, P Sulem, A Jonasdottir, G Masson, J Gudmundsson, ...
Nature genetics 43 (11), 1098-1103, 2011
3172011
High prevalence of the 999del5 mutation in Icelandic breast and ovarian cancer patients
G Johannesdottir, J Gudmundsson, JT Bergthorsson, A Arason, ...
Cancer research 56 (16), 3663-3665, 1996
3151996
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
KB Kuchenbaecker, SJ Ramus, J Tyrer, A Lee, HC Shen, J Beesley, ...
Nature genetics 47 (2), 164-171, 2015
3112015
Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study
EK Bancroft, EC Page, E Castro, H Lilja, A Vickers, D Sjoberg, M Assel, ...
European urology 66 (3), 489-499, 2014
2912014
Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics
G Jönsson, J Staaf, J Vallon-Christersson, M Ringnér, K Holm, C Hegardt, ...
Breast Cancer Research 12, 1-14, 2010
2532010
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer.
S Hĺkansson, O Johannsson, U Johansson, G Sellberg, N Loman, ...
American journal of human genetics 60 (5), 1068, 1997
2251997
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
T Kainu, SHH Juo, R Desper, AA Schäffer, E Gillanders, E Rozenblum, ...
Proceedings of the National Academy of Sciences 97 (17), 9603-9608, 2000
2242000
Steroid receptors in hereditary breast carcinomas associated with BRCA1 or BRCA2 mutations or unknown susceptibility genes
N Loman, O Johannsson, PO Bendahl, Ĺ Borg, M Fernö, H Olsson
Cancer: Interdisciplinary International Journal of the American Cancer …, 1998
2231998
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