Zobrazeno 1 - 10
of 39
pro vyhledávání: '"T, Sverrisson"'
Autor:
Sverrir T. Sverrisson, Daniel F. Gudbjartsson, Droplaug N Magnusdottir, Ragnar P. Kristjansson, Gisli Masson, Bjarni Torfason, Snaedis Kristmundsdottir, Patrick Sulem, Olof Sigurdardottir, Doruk Beyter, Isleifur Olafsson, Guillaume Holley, Bjarni A Atlason, Aslaug Jonasdottir, Gudmundur I. Eyjolfsson, Helga Ingimundardottir, Hilma Holm, Marteinn T. Hardarson, Asmundur Oddsson, Kari Stefansson, Olafur A. Stefansson, Sigurjon A. Gudjonsson, Hannes P. Eggertsson, Agnar Helgason, Unnur Thorsteinsdottir, Eythor Bjornsson, Svenja Mehringer, Hakon Jonsson, Gunnar K. Pálsson, Adalbjorg Jonasdottir, Bjarni V. Halldorsson, Olafur T. Magnusson
Publikováno v:
Nature Genetics. 53:779-786
Long-read sequencing (LRS) promises to improve the characterization of structural variants (SVs). We generated LRS data from 3,622 Icelanders and identified a median of 22,636 SVs per individual (a median of 13,353 insertions and 9,474 deletions). We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5075d64883958b1e3306dfba5531fd2c
https://doi.org/10.1038/s41588-021-00865-4
https://doi.org/10.1038/s41588-021-00865-4
Autor:
Jona Saemundsdottir, Arnaldur Gylfason, Hreinn Stefansson, Steinunn Snorradottir, Gudmar Thorleifsson, Brynjar O. Jensson, Sverrir T. Sverrisson, Gisli Masson, Brynjar Sigurdsson, Olafur Th Magnusson, Agnar Helgason, Unnur Styrkarsdottir, Olafur A. Stefansson, Sigurjon A. Gudjonsson, Hannes Hauswedell, Pall I. Olason, Margret Asgeirsdottir, Páll Melsted, Droplaug N Magnusdottir, Marteinn T. Hardarson, Asmundur Oddsson, Gisli H. Halldorsson, Kristjan Norland, Hannes P. Eggertsson, Thorunn Rafnar, Kari Stefansson, Hilma Holm, Unnur Thorsteinsdottir, Emilia Sobech, Doruk Beyter, Ogmundur Eiriksson, Kristjan H. S. Moore, Brynja D. Sigurpalsdottir, Gunnar Th. Sigurdsson, Ingileif Jonsdottir, Guillaume Holley, Snaedis Kristmundsdottir, Kari Kristinsson, Bjarni V. Halldorsson, Gunnar K. Pálsson, Magnus O. Ulfarsson, Frosti Jonsson, Daniel F. Gudbjartsson, Vinicius Tragante, Patrick Sulem, Florian Zink, Gardar Sveinbjornsson, Hakon Jonsson
We describe the analysis of whole genome sequences (WGS) of 150,119 individuals from the UK biobank (UKB). This constitutes a set of high quality variants, including 585,040,410 SNPs, representing 7.0% of all possible human SNPs, and 58,707,036 indel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ec97dcc172cfe882dfcfb8c2d1ae42a
https://doi.org/10.1101/2021.11.16.468246
https://doi.org/10.1101/2021.11.16.468246
Autor:
Bjarni V, Halldorsson, Hannes P, Eggertsson, Kristjan H S, Moore, Hannes, Hauswedell, Ogmundur, Eiriksson, Magnus O, Ulfarsson, Gunnar, Palsson, Marteinn T, Hardarson, Asmundur, Oddsson, Brynjar O, Jensson, Snaedis, Kristmundsdottir, Brynja D, Sigurpalsdottir, Olafur A, Stefansson, Doruk, Beyter, Guillaume, Holley, Vinicius, Tragante, Arnaldur, Gylfason, Pall I, Olason, Florian, Zink, Margret, Asgeirsdottir, Sverrir T, Sverrisson, Brynjar, Sigurdsson, Sigurjon A, Gudjonsson, Gunnar T, Sigurdsson, Gisli H, Halldorsson, Gardar, Sveinbjornsson, Kristjan, Norland, Unnur, Styrkarsdottir, Droplaug N, Magnusdottir, Steinunn, Snorradottir, Kari, Kristinsson, Emilia, Sobech, Helgi, Jonsson, Arni J, Geirsson, Isleifur, Olafsson, Palmi, Jonsson, Ole Birger, Pedersen, Christian, Erikstrup, Søren, Brunak, Sisse Rye, Ostrowski, Gudmar, Thorleifsson, Frosti, Jonsson, Pall, Melsted, Ingileif, Jonsdottir, Thorunn, Rafnar, Hilma, Holm, Hreinn, Stefansson, Jona, Saemundsdottir, Daniel F, Gudbjartsson, Olafur T, Magnusson, Gisli, Masson, Unnur, Thorsteinsdottir, Agnar, Helgason, Hakon, Jonsson, Patrick, Sulem, Thomas, Werge
Publikováno v:
Nature. 607(7920)
Detailed knowledge of how diversity in the sequence of the human genome affects phenotypic diversity depends on a comprehensive and reliable characterization of both sequences and phenotypic variation. Over the past decade, insights into this relatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7fc382f82eda30e2487a10b47c2249b6
https://pubmed.ncbi.nlm.nih.gov/35859178
https://pubmed.ncbi.nlm.nih.gov/35859178
Autor:
Isleifur Olafsson, Ragnar P. Kristjansson, Olof Sigurdardottir, Gudmundur I. Eyjolfsson, Hakon Jonsson, Daniel F. Gudbjartsson, Gisli Masson, Eythor Bjornsson, Adalbjorg Jonasdottir, Sverrir T. Sverrisson, Patrick Sulem, Snaedis Kristmundsdottir, Droplaug N Magnusdottir, Hannes P. Eggertsson, Marteinn T. Hardarson, Asmundur Oddsson, Kari Stefansson, Aslaug Jonasdottir, Helga Ingimundardottir, Bjarni A Atlason, Unnur Thorsteinsdottir, Doruk Beyter, Bjarni Torfason, Svenja Mehringer, Olafur A. Stefansson, Guillaume Holley, Sigurjon A. Gudjonsson, Agnar Helgason, Bjarni V. Halldorsson, Gunnar K. Pálsson, Olafur T. Magnusson, Hilma Holm
Long-read sequencing (LRS) promises to improve characterization of structural variants (SVs), a major source of genetic diversity. We generated LRS data on 3,622 Icelanders using Oxford Nanopore Technologies, and identified a median of 22,636 SVs per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c710c770a4a46b10f0795eac798d8a0
https://doi.org/10.1101/848366
https://doi.org/10.1101/848366
Autor:
Doruk, Beyter, Helga, Ingimundardottir, Asmundur, Oddsson, Hannes P, Eggertsson, Eythor, Bjornsson, Hakon, Jonsson, Bjarni A, Atlason, Snaedis, Kristmundsdottir, Svenja, Mehringer, Marteinn T, Hardarson, Sigurjon A, Gudjonsson, Droplaug N, Magnusdottir, Aslaug, Jonasdottir, Adalbjorg, Jonasdottir, Ragnar P, Kristjansson, Sverrir T, Sverrisson, Guillaume, Holley, Gunnar, Palsson, Olafur A, Stefansson, Gudmundur, Eyjolfsson, Isleifur, Olafsson, Olof, Sigurdardottir, Bjarni, Torfason, Gisli, Masson, Agnar, Helgason, Unnur, Thorsteinsdottir, Hilma, Holm, Daniel F, Gudbjartsson, Patrick, Sulem, Olafur T, Magnusson, Bjarni V, Halldorsson, Kari, Stefansson
Publikováno v:
Nature genetics. 53(6)
Long-read sequencing (LRS) promises to improve the characterization of structural variants (SVs). We generated LRS data from 3,622 Icelanders and identified a median of 22,636 SVs per individual (a median of 13,353 insertions and 9,474 deletions). We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a0cdd5750adf4da02aa997e3b764f93
https://pubmed.ncbi.nlm.nih.gov/33972781
https://pubmed.ncbi.nlm.nih.gov/33972781
Autor:
Rosa B, Thorolfsdottir, Gardar, Sveinbjornsson, Patrick, Sulem, Jonas B, Nielsen, Stefan, Jonsson, Gisli H, Halldorsson, Pall, Melsted, Erna V, Ivarsdottir, Olafur B, Davidsson, Ragnar P, Kristjansson, Gudmar, Thorleifsson, Anna, Helgadottir, Solveig, Gretarsdottir, Gudmundur, Norddahl, Sridharan, Rajamani, Bjarni, Torfason, Atli S, Valgardsson, Jon T, Sverrisson, Vinicius, Tragante, Oddgeir L, Holmen, Folkert W, Asselbergs, Dan M, Roden, Dawood, Darbar, Terje R, Pedersen, Marc S, Sabatine, Cristen J, Willer, Maja-Lisa, Løchen, Bjarni V, Halldorsson, Ingileif, Jonsdottir, Kristian, Hveem, David O, Arnar, Unnur, Thorsteinsdottir, Daniel F, Gudbjartsson, Hilma, Holm, Kari, Stefansson
Publikováno v:
Communications biology. 1
Most sequence variants identified hitherto in genome-wide association studies (GWAS) of atrial fibrillation are common, non-coding variants associated with risk through unknown mechanisms. We performed a meta-analysis of GWAS of atrial fibrillation a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::43f478e9af9a9e02f82048d9f1dc863a
https://pubmed.ncbi.nlm.nih.gov/30271950
https://pubmed.ncbi.nlm.nih.gov/30271950
Autor:
Daniel F. Gudbjartsson, Michael L. Frigge, Agnar Helgason, Unnur Thorsteinsdottir, Gudrun M. Jonsdottir, Theodora Thorlacius, Aslaug Jonasdottir, Gisli Masson, Stefan T Palsson, Augustine Kong, Sverrir T. Sverrisson, Hreinn Stefansson, Gudmundur A. Hardarson, Sigurjon A. Gudjonsson, Jeffrey R. Gulcher, Kari Stefansson, Gudmar Thorleifsson
Publikováno v:
Science. 319:1398-1401
The genome-wide recombination rate varies between individuals, but the mechanism controlling this variation in humans has remained elusive. A genome-wide search identified sequence variants in the 4p16.3 region correlated with recombination rate in b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a6e49445962f3ce2f8e5c6466c0e916
https://doi.org/10.1126/science.1152422
https://doi.org/10.1126/science.1152422
Publikováno v:
Acta Ophthalmologica. 68:71-73
Chronic open angle glaucoma (COAG) is to a great extent a disease of the elderly,- a population often affected by other diseases reducing vision. The visual reduction in older patients affected by COAG is thus often the cause of other diseases than g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cd6aa2342784adbce9156b4e275fd63
https://doi.org/10.1111/j.1755-3768.1990.tb01964.x
https://doi.org/10.1111/j.1755-3768.1990.tb01964.x
Autor:
G T, Gunnarsson, J T, Sverrisson
Publikováno v:
Laeknabladid. 81(6)
In the last years there has been an increase in serious invasive group A streptococcal infections. Necrotizing fasciitis is one of them. These infections have mostly affected young and middle aged people without known risk factors. The first symptoms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::582ca78b9139d40273876f24324c816b
https://pubmed.ncbi.nlm.nih.gov/20065481
https://pubmed.ncbi.nlm.nih.gov/20065481
Publikováno v:
Journal of glaucoma. 8(5)
To compare the 2.0% dorzolamide/0.5% timolol fixed combination (COSOPT; MerckCo., Whitehouse Station, NJ) to 0.5% timolol plus 2.0% pilocarpine given concomitantly, and to determine patient preference, tolerability, and impact on daily life in patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4d5a8b14ff6d5dc2ab323e56231d1889
https://pubmed.ncbi.nlm.nih.gov/10529932
https://pubmed.ncbi.nlm.nih.gov/10529932