Barkardottir R B
Barkardottir R B
Laboratory of Cell Biology, Department of Pathology, Landspitali University Hospital, Reykjavik
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Identification of the breast cancer susceptibility gene BRCA2
Wooster, R, Bignell, G, Lancaster, J, Swift, S, Seal, S, Mangion, J, Collins ...
Nature 378, 789-792, 1995
Breast and ovarian cancer incidence in BRCA1 mutation carriers
Easton, DF, Ford, D, Bishop, DT, Haites, N, Milner, B, Allan, L, Ponder, BAJ ...
Am. J. Hum. Genet. 56 (1), 1995
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
D Ford, DF Easton, M Stratton, S Narod, D Goldgar, P Devilee, DT Bishop, ...
The American Journal of Human Genetics 62 (3), 676-689, 1998
Risks of cancer in BRCA1 mutation carriers
Ford, D, Easton, DF, Bishop, DT, Narod, SA, Goldgar, DE and the Breast ...
Lancet 343, 692-695, 1994
Genetic Linkage Analysis in Familial Breast and Ovarian Cancer: Results from 214 families
Easton, DF, Bishop, DT, Ford, D, Crockford GP and the Breast Cancer Linkage ...
Am. J. Hum. Genet. 52, 678-701, 1993
Cancer Risks in BRCA2 Mutation Carriers
The Breast Cancer Linkage Consortium
The Journal of the National Cancer Institute 91 (15), 1999
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
J Gudmundsson, P Sulem, A Manolescu, LT Amundadottir, ...
Nature genetics 39 (5), 631-637, 2007
A common variant associated with prostate cancer in European and African populations
LT Amundadottir, P Sulem, J Gudmundsson, A Helgason, A Baker, ...
Nature genetics 38 (6), 652-658, 2006
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
J Gudmundsson, P Sulem, V Steinthorsdottir, JT Bergthorsson, ...
Nature genetics 39 (8), 977-983, 2007
Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations
SR Lakhani, J Jacquemier, JP Sloane, BA Gusterson, TJ Anderson, ...
Journal of the National Cancer Institute 90 (15), 1138-1145, 1998
Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
N Mavaddat, D Barrowdale, IL Andrulis, SM Domchek, D Eccles, ...
Cancer Epidemiology, Biomarkers & Prevention 21 (1), 134-147, 2012
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types
T Rafnar, P Sulem, SN Stacey, F Geller, J Gudmundsson, A Sigurdsson, ...
Nature genetics 41 (2), 221-227, 2009
Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases
MR Stratton
The Lancet 349 (9064), 1505-1510, 1997
Variation in Cancer Risks by Mutation Position in BRCA2 mutation carriers
Thompson DJ, Easton DF, Breast Cancer Linkage Consortium
Am J Hum Genet 68 (2), 410-419, 2001
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
TR Rebbeck, N Mitra, F Wan, OM Sinilnikova, S Healey, L McGuffog, ...
Jama 313 (13), 1347-1361, 2015
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
Common sequence variants on 2p15 and Xp11. 22 confer susceptibility to prostate cancer
J Gudmundsson, P Sulem, T Rafnar, JT Bergthorsson, A Manolescu, ...
Nature genetics 40 (3), 281-283, 2008
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility
J Gudmundsson, P Sulem, DF Gudbjartsson, T Blondal, A Gylfason, ...
Nature genetics 41 (10), 1122-1126, 2009
Tumour biological features of BRCA1-induced breast and ovarian cancer
OT Johannsson, I Idvall, C Anderson, Borg, RB Barkardottir, V Egilsson, ...
European journal of cancer 33 (3), 362-371, 1997
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families
SA Narod, D Ford, P Devilee, RB Barkardottir, HT Lynch, SA Smith, ...
American journal of human genetics 56 (1), 254, 1995
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