Asmundur Oddsson
Asmundur Oddsson
Research associate, deCODE genetics/AMGEN
Verified email at - Homepage
Cited by
Cited by
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
The nature of nurture: Effects of parental genotypes
A Kong, G Thorleifsson, ML Frigge, BJ Vilhjalmsson, AI Young, ...
Science 359 (6374), 424-428, 2018
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
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, 2015
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
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, 2016
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
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), 1-9, 2015
Characterizing mutagenic effects of recombination through a sequence-level genetic map
BV Halldorsson, G Palsson, OA Stefansson, H Jonsson, MT Hardarson, ...
Science 363 (6425), 2019
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
Expression and subcellular distribution of novel glomerulus-associated proteins dendrin, ehd3, sh2d4a, plekhh2, and 2310066E14Rik
J Patrakka, Z Xiao, M Nukui, M Takemoto, L He, A Oddsson, L Perisic, ...
Journal of the American Society of Nephrology 18 (3), 689-697, 2007
Zebrafish: a model system for the study of vertebrate renal development, function, and pathophysiology
L Ebarasi, A Oddsson, K Hultenby, C Betsholtz, K Tryggvason
Current opinion in nephrology and hypertension 20 (4), 416-424, 2011
Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
U Styrkarsdottir, H Helgason, A Sigurdsson, GL Norddahl, AB Agustsdottir, ...
Nature genetics 49 (5), 801-805, 2017
Sequence variants from whole genome sequencing a large group of Icelanders
DF Gudbjartsson, P Sulem, H Helgason, A Gylfason, SA Gudjonsson, ...
Scientific data 2 (1), 1-11, 2015
Identification of sequence variants influencing immunoglobulin levels
S Jonsson, G Sveinbjornsson, AL de Lapuente Portilla, B Swaminathan, ...
Nature genetics 49 (8), 1182, 2017
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
RP Kristjansson, A Oddsson, H Helgason, G Sveinbjornsson, ...
Nature communications 7 (1), 1-8, 2016
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
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
Epigenetic and genetic components of height regulation
S Benonisdottir, A Oddsson, A Helgason, RP Kristjansson, ...
Nature communications 7 (1), 1-10, 2016
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), 1-9, 2018
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