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Sigurjon A. Gudjonsson
Sigurjon A. Gudjonsson
Other namesSigurjón Axel Guðjónsson, Sigurjon Guðjonsson, Sigurjon Axel Gudjonsson
Verified email at decode.is
Title
Cited by
Cited by
Year
Rate of de novo mutations and the importance of father’s age to disease risk
A Kong, ML Frigge, G Masson, S Besenbacher, P Sulem, G Magnusson, ...
Nature 488 (7412), 471-475, 2012
24782012
A high-resolution recombination map of the human genome
A Kong, DF Gudbjartsson, J Sainz, GM Jonsdottir, SA Gudjonsson, ...
Nature genetics 31 (3), 241-247, 2002
20112002
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
8932007
Parental influence on human germline de novo mutations in 1,548 trios from Iceland
H Jónsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ...
Nature 549 (7673), 519-522, 2017
8622017
Large-scale whole-genome sequencing of the Icelandic population
DF Gudbjartsson, H Helgason, SA Gudjonsson, F Zink, A Oddson, ...
Nature genetics 47 (5), 435-444, 2015
8572015
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly
F Zink, SN Stacey, GL Norddahl, ML Frigge, OT Magnusson, I Jonsdottir, ...
Blood, The Journal of the American Society of Hematology 130 (6), 742-752, 2017
7152017
Fine-scale recombination rate differences between sexes, populations and individuals
A Kong, G Thorleifsson, DF Gudbjartsson, G Masson, A Sigurdsson, ...
Nature 467 (7319), 1099-1103, 2010
6672010
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
6632009
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
5472008
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
5032008
Large-scale integration of the plasma proteome with genetics and disease
E Ferkingstad, P Sulem, BA Atlason, G Sveinbjornsson, MI Magnusson, ...
Nature genetics 53 (12), 1712-1721, 2021
4882021
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
G Thorleifsson, GB Walters, AW Hewitt, G Masson, A Helgason, A DeWan, ...
Nature genetics 42 (10), 906-909, 2010
4582010
Several common variants modulate heart rate, PR interval and QRS duration
H Holm, DF Gudbjartsson, DO Arnar, G Thorleifsson, G Thorgeirsson, ...
Nature genetics 42 (2), 117-122, 2010
4562010
Two newly identified genetic determinants of pigmentation in Europeans
P Sulem, DF Gudbjartsson, SN Stacey, A Helgason, T Rafnar, ...
Nature genetics 40 (7), 835-837, 2008
4382008
Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
S Steinberg, H Stefansson, T Jonsson, H Johannsdottir, A Ingason, ...
Nature genetics 47 (5), 445-447, 2015
3752015
New common variants affecting susceptibility to basal cell carcinoma
SN Stacey, P Sulem, G Masson, SA Gudjonsson, G Thorleifsson, ...
Nature genetics 41 (8), 909-914, 2009
3662009
Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes
V Steinthorsdottir, G Thorleifsson, P Sulem, H Helgason, N Grarup, ...
Nature genetics 46 (3), 294-298, 2014
3552014
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
3202011
Characterizing mutagenic effects of recombination through a sequence-level genetic map
BV Halldorsson, G Palsson, OA Stefansson, H Jonsson, MT Hardarson, ...
Science 363 (6425), eaau1043, 2019
2702019
The sequences of 150,119 genomes in the UK Biobank
BV Halldorsson, HP Eggertsson, KHS Moore, H Hauswedell, O Eiriksson, ...
Nature 607 (7920), 732-740, 2022
2532022
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