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Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies

Autor: Hjorleifsson, Kristjan E., Rognvaldsson, Solvi, Jonsson, Hakon, Agustsdottir, Arna B., Andresdottir, Margret, Birgisdottir, Kolbrun, Eiriksson, Ogmundur, Eythorsson, Elias S., Fridriksdottir, Run, Georgsson, Gudmundur, Gudmundsson, Kjartan R., Gylfason, Arnaldur, Haraldsdottir, Gudbjorg, Jensson, Brynjar O., Jonasdotti, Adalbjorg, Jonasdottir, Aslaug, Josefsdottir, Kamilla S., Kristinsdottir, Nina, Kristjansdottir, Borghildur, Kristjansson, Thordur, Magnusdottir, Droplaug N., Palsson, Runolfur, le Roux, Louise, Sigurbergsdottir, Gudrun M., Sigurdsson, Asgeir, Sigurdsson, Martin I., Sveinbjornsson, Gardar, Thorarensen, Emil Aron, Thorbjornsson, Bjarni, Thordardottir, Marianna, Helgason, Agnar, Holm, Hilma, Jonsdottir, Ingileif, Jonsson, Frosti, Magnusson, Olafur T., Masson, Gisli, Norddahl, Gudmundur L., Saemundsdottir, Jona, Sulem, Patrick, Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Melsted, Pall, Stefansson, Kari

Publikováno v: In Clinical Microbiology and Infection June 2022 28(6):852-858

Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.

Autor: Skuladottir, Astros Th., Tragante, Vinicius, Sveinbjornsson, Gardar, Helgason, Hannes, Sturluson, Arni, Bjornsdottir, Anna, Jonsson, Palmi, Palmadottir, Vala, Sveinsson, Olafur A., Jensson, Brynjar O., Gudjonsson, Sigurjon A., Ivarsdottir, Erna V., Gisladottir, Rosa S., Gunnarsson, Arni F., Walters, G. Bragi, Jonsdottir, Gudrun A., Thorgeirsson, Thorgeir E., Bjornsdottir, Gyda, Holm, Hilma, Gudbjartsson, Daniel F.

Publikováno v: NPJ Parkinson's Disease; 8/15/2024, Vol. 10 Issue 1, p1-4, 4p

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Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

Autor: Oddsson, Asmundur, Sulem, Patrick, Sveinbjornsson, Gardar, Arnadottir, Gudny A, Steinthorsdottir, Valgerdur, Halldorsson, Gisli H, Atlason, Bjarni A, Oskarsson, Gudjon R, Helgason, Hannes, Nielsen, Henriette Svarre, Westergaard, David, Karjalainen, Juha M, Katrinardottir, Hildigunnur, Fridriksdottir, Run, Jensson, Brynjar O, Tragante, Vinicius, Ferkingstad, Egil, Jonsson, Hakon, Gudjonsson, Sigurjon A, Beyter, Doruk, Moore, Kristjan H S, Thordardottir, Helga B, Kristmundsdottir, Snaedis, Stefansson, Olafur A, Rantapää-Dahlqvist, Solbritt, Sonderby, Ida Elken, Didriksen, Maria, Stridh, Pernilla, Haavik, Jan, Tryggvadottir, Laufey, Frei, Oleksandr, Walters, G Bragi, Kockum, Ingrid, Hjalgrim, Henrik, Olafsdottir, Thorunn A, Selbaek, Geir, Nyegaard, Mette, Erikstrup, Christian, Brodersen, Thorsten, Saevarsdottir, Saedis, Olsson, Tomas, Nielsen, Kaspar Rene, Haraldsson, Asgeir, Bruun, Mie Topholm, Hansen, Thomas Folkmann, Steingrimsdottir, Thora, Jacobsen, Rikke Louise, Lie, Rolv T, Djurovic, Srdjan, Alfredsson, Lars, Lopez de Lapuente Portilla, Aitzkoa, Brunak, Soren, Melsted, Pall, Halldorsson, Bjarni V, Saemundsdottir, Jona, Magnusson, Olafur Th, Padyukov, Leonid, Banasik, Karina, Rafnar, Thorunn, Askling, Johan, Klareskog, Lars, Pedersen, Ole Birger, Masson, Gisli, Havdahl, Alexandra, Nilsson, Bjorn, Andreassen, Ole A, Daly, Mark, Ostrowski, Sisse Rye, Jonsdottir, Ingileif, Stefansson, Hreinn, Holm, Hilma, Helgason, Agnar, Thorsteinsdottir, Unnur, Stefansson, Kari, Gudbjartsson, Daniel F

Publikováno v: Oddsson, A, Sulem, P, Sveinbjornsson, G, Arnadottir, G A, Steinthorsdottir, V, Halldorsson, G H, Atlason, B A, Oskarsson, G R, Helgason, H, Nielsen, H S, Westergaard, D, Karjalainen, J M, Katrinardottir, H, Fridriksdottir, R, Jensson, B O, Tragante, V, Ferkingstad, E, Jonsson, H, Gudjonsson, S A, Beyter, D, Moore, K H S, Thordardottir, H B, Kristmundsdottir, S, Stefansson, O A, Rantapää-Dahlqvist, S, Sonderby, I E, Didriksen, M, Stridh, P, Haavik, J, Tryggvadottir, L, Frei, O, Walters, G B, Kockum, I, Hjalgrim, H, Olafsdottir, T A, Selbaek, G, Nyegaard, M, Erikstrup, C, Brodersen, T, Saevarsdottir, S, Olsson, T, Nielsen, K R, Haraldsson, A, Bruun, M T, Hansen, T F, DBDS Genomic Consortium, Steingrimsdottir, T, Jacobsen, R L, Lie, R T, Djurovic, S, Alfredsson, L, Lopez de Lapuente Portilla, A, Brunak, S, Melsted, P, Halldorsson, B V, Saemundsdottir, J, Magnusson, O T, Padyukov, L, Banasik, K, Rafnar, T, Askling, J, Klareskog, L, Pedersen, O B, Masson, G, Havdahl, A, Nilsson, B, Andreassen, O A, Daly, M, Ostrowski, S R, Jonsdottir, I, Stefansson, H, Holm, H, Helgason, A, Thorsteinsdottir, U, Stefansson, K & Gudbjartsson, D F 2023, ' Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality ', Nature Communications, vol. 14, no. 1, 3453 . https://doi.org/10.1038/s41467-023-38951-2

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 homozygosity among

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1266::374935cbc9fc6b65f251eb1881130c9f
https://vbn.aau.dk/ws/files/534278535/s41467_023_38951_2.pdf