Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bjarni A. Atlason"'
Autor:
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, Gudny A. Arnadottir, Valgerdur Steinthorsdottir, Gisli H. Halldorsson, Bjarni A. Atlason, Gudjon R. Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M. Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Brynjar O. Jensson, Vinicius Tragante, Egil Ferkingstad, Hakon Jonsson, Sigurjon A. Gudjonsson, Doruk Beyter, Kristjan H. S. Moore, Helga B. Thordardottir, Snaedis Kristmundsdottir, Olafur A. Stefansson, Solbritt Rantapää-Dahlqvist, Ida Elken Sonderby, Maria Didriksen, Pernilla Stridh, Jan Haavik, Laufey Tryggvadottir, Oleksandr Frei, G. Bragi Walters, Ingrid Kockum, Henrik Hjalgrim, Thorunn A. Olafsdottir, Geir Selbaek, Mette Nyegaard, Christian Erikstrup, Thorsten Brodersen, Saedis Saevarsdottir, Tomas Olsson, Kaspar Rene Nielsen, Asgeir Haraldsson, Mie Topholm Bruun, Thomas Folkmann Hansen, DBDS Genomic Consortium, Thora Steingrimsdottir, Rikke Louise Jacobsen, Rolv T. Lie, Srdjan Djurovic, Lars Alfredsson, Aitzkoa Lopez de Lapuente Portilla, Soren Brunak, Pall Melsted, Bjarni V. Halldorsson, Jona Saemundsdottir, Olafur Th. Magnusson, Leonid Padyukov, Karina Banasik, Thorunn Rafnar, Johan Askling, Lars Klareskog, Ole Birger Pedersen, Gisli Masson, Alexandra Havdahl, Bjorn Nilsson, Ole A. Andreassen, Mark Daly, Sisse Rye Ostrowski, Ingileif Jonsdottir, Hreinn Stefansson, Hilma Holm, Agnar Helgason, Unnur Thorsteinsdottir, Kari Stefansson, Daniel F. Gudbjartsson
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract Genotypes causing pregnancy loss and perinatal mortality are depleted among living individuals and are therefore difficult to find. To explore genetic causes of recessive lethality, we searched for sequence variants with deficit of homozygos
Externí odkaz:
https://doaj.org/article/a4fa595277a74ef2949c5d74d9c4032d
Autor:
Asmundur Oddsson, Patrick Sulem, Gardar Sveinbjornsson, Gudny A. Arnadottir, Valgerdur Steinthorsdottir, Gisli H. Halldorsson, Bjarni A. Atlason, Gudjon R. Oskarsson, Hannes Helgason, Henriette Svarre Nielsen, David Westergaard, Juha M. Karjalainen, Hildigunnur Katrinardottir, Run Fridriksdottir, Brynjar O. Jensson, Vinicius Tragante, Egil Ferkingstad, Hakon Jonsson, Sigurjon A. Gudjonsson, Doruk Beyter, Kristjan H. S. Moore, Helga B. Thordardottir, Snaedis Kristmundsdottir, Olafur A. Stefansson, Solbritt Rantapää-Dahlqvist, Ida Elken Sonderby, Maria Didriksen, Pernilla Stridh, Jan Haavik, Laufey Tryggvadottir, Oleksandr Frei, G. Bragi Walters, Ingrid Kockum, Henrik Hjalgrim, Thorunn A. Olafsdottir, Geir Selbaek, Mette Nyegaard, Christian Erikstrup, Thorsten Brodersen, Saedis Saevarsdottir, Tomas Olsson, Kaspar Rene Nielsen, Asgeir Haraldsson, Mie Topholm Bruun, Thomas Folkmann Hansen, DBDS Genomic Consortium, Thora Steingrimsdottir, Rikke Louise Jacobsen, Rolv T. Lie, Srdjan Djurovic, Lars Alfredsson, Aitzkoa Lopez de Lapuente Portilla, Soren Brunak, Pall Melsted, Bjarni V. Halldorsson, Jona Saemundsdottir, Olafur Th. Magnusson, Leonid Padyukov, Karina Banasik, Thorunn Rafnar, Johan Askling, Lars Klareskog, Ole Birger Pedersen, Gisli Masson, Alexandra Havdahl, Bjorn Nilsson, Ole A. Andreassen, Mark Daly, Sisse Rye Ostrowski, Ingileif Jonsdottir, Hreinn Stefansson, Hilma Holm, Agnar Helgason, Unnur Thorsteinsdottir, Kari Stefansson, Daniel F. Gudbjartsson
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/5f67c08c01ba468598a7f011b98dd4d8
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:
Kristbjorg Gunnarsdottir, Daniel F. Gudbjartsson, Vinicius Tragante, Gisli Masson, Solvi Rognvaldsson, Simon N. Stacey, Gudny A. Arnadottir, Bjarni V. Halldorsson, Hilma Holm, Edda L Styrmisdottir, Páll Melsted, Magnus K. Magnusson, Saedis Saevarsdottir, Kristinn Juliusson, Thorunn Rafnar, Ingileif Jonsdottir, Run Fridriksdottir, Sigurjon A. Gudjonsson, Hildigunnur Katrinardottir, Jona Saemundsdottir, Patrick Sulem, Magnus O. Ulfarsson, Gisli H. Halldorsson, Thorunn A. Olafsdottir, Sigrun H. Lund, Valgerdur Steinthorsdottir, Bjarni A Atlason, Gudmundur L. Norddahl, Hreinn Stefansson, Brynjar O. Jensson, Asmundur Oddsson, Kari Stefansson, Florian Zink, Gardar Sveinbjornsson, Magnus I Magnusson, Olafur Th Magnusson, Agnar Helgason, Thjodbjorg Eiriksdottir, Unnur Thorsteinsdottir, Egil Ferkingstad
Publikováno v:
Nature genetics. 53(12)
The plasma proteome can help bridge the gap between the genome and diseases. Here we describe genome-wide association studies (GWASs) of plasma protein levels measured with 4,907 aptamers in 35,559 Icelanders. We found 18,084 associations between seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ee83c5a08ad76e6c7b09bb98df5ae78
https://pubmed.ncbi.nlm.nih.gov/34857953
https://pubmed.ncbi.nlm.nih.gov/34857953
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