Sledovat
Sigurjon A. Gudjonsson
Sigurjon A. Gudjonsson
Další jménaSigurjón Axel Guðjónsson, Sigurjón Guðjónsson, Sigurjon Gudjonsson
E-mailová adresa ověřena na: decode.is
Název
Citace
Citace
Rok
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
24322012
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
20042002
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
8982007
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
8352015
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
8322017
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
6882017
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
6612010
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
6562009
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
5482008
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
4962008
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
4582010
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
4482010
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
4302008
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
3762021
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
3672015
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
3672009
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
3492014
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
3132011
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
2502019
Identification of a large set of rare complete human knockouts
P Sulem, H Helgason, A Oddson, H Stefansson, SA Gudjonsson, F Zink, ...
Nature genetics 47 (5), 448-452, 2015
2482015
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Články 1–20