Snaevar Sigurdsson
Snaevar Sigurdsson
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Genome sequence, comparative analysis, and population genetics of the domestic horse
CM Wade, E Giulotto, S Sigurdsson, M Zoli, S Gnerre, F Imsland, TL Lear, ...
Science 326 (5954), 865-867, 2009
Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus
S Sigurdsson, G Nordmark, HHH Göring, K Lindroos, AC Wiman, ...
The American Journal of Human Genetics 76 (3), 528-537, 2005
Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus
RR Graham, C Kyogoku, S Sigurdsson, IA Vlasova, LRL Davies, ...
Proceedings of the National Academy of Sciences 104 (16), 6758-6763, 2007
Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping
A Vaysse, A Ratnakumar, T Derrien, E Axelsson, G Rosengren Pielberg, ...
PLoS genetics 7 (10), e1002316, 2011
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing
A Kirby, A Gnirke, DB Jaffe, V Barešová, N Pochet, B Blumenstiel, C Ye, ...
Nature genetics 45 (3), 299-303, 2013
Association of a haplotype in the promoter region of the interferon regulatory factor 5 gene with rheumatoid arthritis
S Sigurdsson, L Padyukov, FAS Kurreeman, U Liljedahl, AC Wiman, ...
Arthritis & Rheumatism: Official Journal of the American College of …, 2007
A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of …
S Sigurdsson, G Nordmark, S Garnier, E Grundberg, T Kwan, O Nilsson, ...
Human molecular genetics 17 (18), 2868-2876, 2008
Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus …
S Sigurdsson, HHH Göring, G Kristjansdottir, L Milani, G Nordmark, ...
Human molecular genetics 17 (6), 872-881, 2008
An insertion–deletion polymorphism in the interferon regulatory factor 5 (IRF5) gene confers risk of inflammatory bowel diseases
V Dideberg, G Kristjansdottir, L Milani, C Libioulle, S Sigurdsson, E Louis, ...
Human molecular genetics 16 (24), 3008-3016, 2007
Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA
L Lovmar, M Fredriksson, U Liljedahl, S Sigurdsson, AC Syvänen
Nucleic acids research 31 (21), e129-e129, 2003
Structural basis for the inhibitory efficacy of efavirenz (DMP‐266), MSC194 and PNU142721 towards the HIV‐1 RT K103N mutant
J Lindberg, S Sigurðsson, S Löwgren, H O. Andersson, C Sahlberg, ...
European Journal of Biochemistry 269 (6), 1670-1677, 2002
Genome-wide analyses implicate 33 loci in heritable dog osteosarcoma, including regulatory variants near CDKN2A/B
EK Karlsson, S Sigurdsson, E Ivansson, R Thomas, I Elvers, J Wright, ...
Genome biology 14, 1-16, 2013
Multiplex SNP genotyping in pooled DNA samples by a four‐colour microarray system
K Lindroos, S Sigurdsson, K Johansson, L Rönnblom, AC Syvänen
Nucleic acids research 30 (14), e70-e70, 2002
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations
G Kristjansdottir, JK Sandling, A Bonetti, IM Roos, L Milani, C Wang, ...
Journal of medical genetics 45 (6), 362-369, 2008
Genetic variants and disease‐associated factors contribute to enhanced interferon regulatory factor 5 expression in blood cells of patients with systemic lupus erythematosus
D Feng, RC Stone, ML Eloranta, N Sangster‐Guity, G Nordmark, ...
Arthritis & Rheumatism: Official Journal of the American College of …, 2010
Mutation discovery in mice by whole exome sequencing
H Fairfield, GJ Gilbert, M Barter, RR Corrigan, M Curtain, Y Ding, ...
Genome biology 12, 1-12, 2011
Candidate genes and functional noncoding variants identified in a canine model of obsessive-compulsive disorder
R Tang, HJ Noh, D Wang, S Sigurdsson, R Swofford, M Perloski, ...
Genome biology 15, 1-15, 2014
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
A STAT4 risk allele is associated with ischaemic cerebrovascular events and anti-phospholipid antibodies in systemic lupus erythematosus
E Svenungsson, J Gustafsson, D Leonard, J Sandling, I Gunnarsson, ...
Annals of the rheumatic diseases 69 (5), 834-840, 2010
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis
S Sigurdsson, KF Alexandersson, P Sulem, B Feenstra, S Gudmundsdottir, ...
Nature communications 8 (1), 15789, 2017
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
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