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Asmundur Oddsson
Asmundur Oddsson
Research associate, deCODE genetics/AMGEN
decode.is üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
The nature of nurture: Effects of parental genotypes
A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ...
Science 359 (6374), 424-428, 2018
9112018
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
8942015
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
8052021
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
3352022
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
3132019
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits
U Styrkarsdottir, G Thorleifsson, P Sulem, DF Gudbjartsson, A Sigurdsson, ...
Nature 497 (7450), 517-520, 2013
2932013
Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits
D Beyter, H Ingimundardottir, A Oddsson, HP Eggertsson, E Bjornsson, ...
Nature genetics 53 (6), 779-786, 2021
2652021
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
2642015
Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease
A Helgadottir, S Gretarsdottir, G Thorleifsson, E Hjartarson, A Sigurdsson, ...
Nature genetics 48 (6), 634-639, 2016
2622016
Weighting sequence variants based on their annotation increases power of whole-genome association studies
G Sveinbjornsson, A Albrechtsen, F Zink, SA Gudjonsson, A Oddson, ...
Nature genetics 48 (3), 314-317, 2016
2192016
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
U Styrkarsdottir, SH Lund, G Thorleifsson, F Zink, OA Stefansson, ...
Nature genetics 50 (12), 1681-1687, 2018
1862018
Loss-of-function variants in ATM confer risk of gastric cancer
H Helgason, T Rafnar, HS Olafsdottir, JG Jonasson, A Sigurdsson, ...
Nature genetics 47 (8), 906-910, 2015
1862015
Large-scale plasma proteomics comparisons through genetics and disease associations
GH Eldjarn, E Ferkingstad, SH Lund, H Helgason, OT Magnusson, ...
Nature 622 (7982), 348-358, 2023
1702023
Common and rare variants associated with kidney stones and biochemical traits
A Oddsson, P Sulem, H Helgason, VO Edvardsson, G Thorleifsson, ...
Nature communications 6 (1), 7975, 2015
1592015
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis
S Bell, AS Rigas, MK Magnusson, E Ferkingstad, E Allara, G Bjornsdottir, ...
Communications biology 4 (1), 156, 2021
1302021
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
RP Kristjansson, S Benonisdottir, OB Davidsson, A Oddsson, V Tragante, ...
Nature genetics 51 (2), 267-276, 2019
1202019
A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease
GA Arnadottir, GL Norddahl, S Gudmundsdottir, AB Agustsdottir, ...
Nature Communications 9 (1), 4447, 2018
1132018
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation
DF Gudbjartsson, H Holm, P Sulem, G Masson, A Oddsson, ...
European heart journal, ehw379, 2016
1092016
The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms
A Oddsson, SY Kristinsson, H Helgason, DF Gudbjartsson, G Masson, ...
Leukemia 28 (6), 1371-1374, 2014
1092014
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
T Rafnar, B Gunnarsson, OA Stefansson, P Sulem, A Ingason, ML Frigge, ...
Nature communications 9 (1), 3636, 2018
1072018
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