Jon Thor Bergthorsson
Jon Thor Bergthorsson
PL Biomedical Center, University of Iceland
Verified email at
Cited by
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A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
TE Thorgeirsson, F Geller, P Sulem, T Rafnar, A Wiste, KP Magnusson, ...
Nature 452 (7187), 638-642, 2008
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
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
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
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
Sequence variant on 8q24 confers susceptibility to urinary bladder cancer
LA Kiemeney, S Thorlacius, P Sulem, F Geller, KKH Aben, SN Stacey, ...
Nature genetics 40 (11), 1307-1312, 2008
Common variants on 9q22. 33 and 14q13. 3 predispose to thyroid cancer in European populations
J Gudmundsson, P Sulem, DF Gudbjartsson, JG Jonasson, A Sigurdsson, ...
Nature genetics 41 (4), 460-464, 2009
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
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
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
Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12–q13
J Gudmundsson, G Johannesdottir, JT Bergthorsson, A Arason, ...
Cancer research 55 (21), 4830-4832, 1995
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
J Vallon-Christersson, C Cayanan, K Haraldsson, N Loman, ...
Human molecular genetics 10 (4), 353-360, 2001
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits
SN Stacey, DF Gudbjartsson, P Sulem, JT Bergthorsson, R Kumar, ...
Nature genetics 40 (11), 1313-1318, 2008
A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes
E Rozenblum, P Vahteristo, T Sandberg, J Bergthorsson, K Syrjakoski, ...
Human genetics 110, 111-121, 2002
High frequency of LOH, MSI and abnormal expression of FHIT in gastric cancer
C Huiping, S Kristjansdottir, JT Bergthorsson, JG Jonasson, J Magnusson, ...
European Journal of Cancer 38 (5), 728-735, 2002
The BARD1 Cys557Ser variant and breast cancer risk in Iceland
SN Stacey, P Sulem, OT Johannsson, A Helgason, J Gudmundsson, ...
PLoS medicine 3 (7), e217, 2006
Mutation analysis of the CHK2 gene in breast carcinoma and other cancers
S Ingvarsson, BI Sigbjornsdottir, C Huiping, SH Hafsteinsdottir, ...
Breast Cancer Research 4 (3), 1-6, 2002
Frequent occurrence of BRCA2 linkage in Icelandic breast cancer families and segregation of a common BRCA2 haplotype.
J Gudmundsson, G Johannesdottir, A Arason, JT Bergthorsson, ...
American journal of human genetics 58 (4), 749, 1996
BRCA1 andBRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age
JT Bergthorsson, B Ejlertsen, JH Olsen, A Borg, KV Nielsen, ...
Journal of medical genetics 38 (6), 361-368, 2001
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