Výsledky vyhledávání - "Thorolfsdottir, Rosa B"

Genetic variants associated with syncope implicate neural and autonomic processes

Autor: Aegisdottir, Hildur M., Thorolfsdottir, Rosa B., Sveinbjornsson, Gardar, Stefansson, Olafur A., Gunnarsson, Bjarni, Tragante, Vinicius, Thorleifsson, Gudmar, Stefansdottir, Lilja, Thorgeirsson, Thorgeir E., Ferkingstad, Egil, Sulem, Patrick, Norddahl, Gudmundur, Rutsdottir, Gudrun, Banasik, Karina, Christensen, Alex Hoerby, Mikkelsen, Christina, Pedersen, Ole Birger, Brunak, Søren, Bruun, Mie Topholm, Erikstrup, Christian, Jacobsen, Rikke Louise, Nielsen, Kaspar Rene, Sørensen, Erik, Frigge, Michael L., Hjorleifsson, Kristjan E., Ivarsdottir, Erna V., Helgadottir, Anna, Gretarsdottir, Solveig, Steinthorsdottir, Valgerdur, Oddsson, Asmundur, Eggertsson, Hannes P., Halldorsson, Gisli H., Jones, David A., Anderson, Jeffrey L., Knowlton, Kirk U., Nadauld, Lincoln D., Nyegaard, Mette, Haraldsson, Magnus, Thorgeirsson, Gudmundur, Bundgaard, Henning, Arnar, David O., Thorsteinsdottir, Unnur, Gudbjartsson, Daniel F., Ostrowski, Sisse R., Holm, Hilma, Stefansson, Kari

Publikováno v: Aegisdottir, H M, Thorolfsdottir, R B, Sveinbjornsson, G, Stefansson, O A, Gunnarsson, B, Tragante, V, Thorleifsson, G, Stefansdottir, L, Thorgeirsson, T E, Ferkingstad, E, Sulem, P, Norddahl, G, Rutsdottir, G, Banasik, K, Christensen, A H, Mikkelsen, C, Pedersen, O B, Brunak, S, Bruun, M T, Erikstrup, C, Jacobsen, R L, Nielsen, K R, Sørensen, E, Frigge, M L, Hjorleifsson, K E, Ivarsdottir, E V, Helgadottir, A, Gretarsdottir, S, Steinthorsdottir, V, Oddsson, A, Eggertsson, H P, Halldorsson, G H, Jones, D A, Anderson, J L, Knowlton, K U, Nadauld, L D, DBDS Genomic Consortium, Nyegaard, M, Haraldsson, M, Thorgeirsson, G, Bundgaard, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Ostrowski, S R, Holm, H & Stefansson, K 2023, ' Genetic variants associated with syncope implicate neural and autonomic processes ', European Heart Journal, vol. 44, no. 12, ehad016, pp. 1070-1080 . https://doi.org/10.1093/eurheartj/ehad016
Aegisdottir, H M, Thorolfsdottir, R B, Sveinbjornsson, G, Stefansson, O A, Gunnarsson, B, Tragante, V, Thorleifsson, G, Stefansdottir, L, Thorgeirsson, T E, Ferkingstad, E, Sulem, P, Norddahl, G, Rutsdottir, G, Banasik, K, Christensen, A H, Mikkelsen, C, Pedersen, O B, Brunak, S, Bruun, M T, Erikstrup, C, Jacobsen, R L, Nielsen, K R, Sørensen, E, Frigge, M L, Hjorleifsson, K E, Ivarsdottir, E V, Helgadottir, A, Gretarsdottir, S, Steinthorsdottir, V, Oddsson, A, Eggertsson, H P, Halldorsson, G H, Jones, D A, Anderson, J L, Knowlton, K U, Nadauld, L D, Haraldsson, M, Thorgeirsson, G, Bundgaard, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Ostrowski, S R, Holm, H, Stefansson, K & DBDS Genomic Consortium 2023, ' Genetic variants associated with syncope implicate neural and autonomic processes ', European Heart Journal, vol. 44, no. 12, pp. 1070-1080 . https://doi.org/10.1093/eurheartj/ehad016

Aims Syncope is a common and clinically challenging condition. In this study, the genetics of syncope were investigated to seek knowledge about its pathophysiology and prognostic implications. Methods and results This genome-wide association meta-ana

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f58902f7bcd7236c79c568f1c47f041
https://vbn.aau.dk/da/publications/45c15d73-cc3c-41db-9edf-922b39228dc7

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Multiomics study of nonalcoholic fatty liver disease

Autor: Sveinbjornsson, Gardar, Ulfarsson, Magnus O, Thorolfsdottir, Rosa B, Jonsson, Benedikt A, Einarsson, Eythor, Gunnlaugsson, Gylfi, Rognvaldsson, Solvi, Arnar, David O, Baldvinsson, Magnus, Bjarnason, Ragnar G, Eiriksdottir, Thjodbjorg, Erikstrup, Christian, Ferkingstad, Egil, Halldorsson, Gisli H, Helgason, Hannes, Helgadottir, Anna, Hindhede, Lotte, Hjorleifsson, Grimur, Jones, David, Knowlton, Kirk U, Lund, Sigrun H, Melsted, Pall, Norland, Kristjan, Olafsson, Isleifur, Olafsson, Sigurdur, Oskarsson, Gudjon R, Ostrowski, Sisse Rye, Pedersen, Ole Birger, Snaebjarnarson, Auðunn S, Sigurdsson, Emil, Steinthorsdottir, Valgerdur, Schwinn, Michael, Thorgeirsson, Gudmundur, Thorleifsson, Gudmar, Jonsdottir, Ingileif, Bundgaard, Henning, Nadauld, Lincoln, Bjornsson, Einar S, Rulifson, Ingrid C, Rafnar, Thorunn, Norddahl, Gudmundur L, Thorsteinsdottir, Unnur, Sulem, Patrick, Gudbjartsson, Daniel F, Holm, Hilma, Stefansson, Kari

Publikováno v: Sveinbjornsson, G, Ulfarsson, M O, Thorolfsdottir, R B, Jonsson, B A, Einarsson, E, Gunnlaugsson, G, Rognvaldsson, S, Arnar, D O, Baldvinsson, M, Bjarnason, R G, Eiriksdottir, T, Erikstrup, C, Ferkingstad, E, Halldorsson, G H, Helgason, H, Helgadottir, A, Hindhede, L, Hjorleifsson, G, Jones, D, Knowlton, K U, Lund, S H, Melsted, P, Norland, K, Olafsson, I, Olafsson, S, Oskarsson, G R, Ostrowski, S R, Pedersen, O B, Snaebjarnarson, A S, Sigurdsson, E, Steinthorsdottir, V, Schwinn, M, Thorgeirsson, G, Thorleifsson, G, Jonsdottir, I, Bundgaard, H, Nadauld, L, Bjornsson, E S, Rulifson, I C, Rafnar, T, Norddahl, G L, Thorsteinsdottir, U, Sulem, P, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium 2022, ' Multiomics study of nonalcoholic fatty liver disease ', Nature Genetics, vol. 54, no. 11, pp. 1652-1663 . https://doi.org/10.1038/s41588-022-01199-5
DBDS Genomic Consortium 2022, ' Multiomics study of nonalcoholic fatty liver disease ', Nature Genetics, vol. 54, pp. 1652–1663 . https://doi.org/10.1038/s41588-022-01199-5

Nonalcoholic fatty liver (NAFL) and its sequelae are growing health problems. We performed a genome-wide association study of NAFL, cirrhosis and hepatocellular carcinoma, and integrated the findings with expression and proteomic data. For NAFL, we u

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3fc8772fb9337ecbc8c280a01928fea
https://pure.au.dk/portal/da/publications/multiomics-study-of-nonalcoholic-fatty-liver-disease(0ef7997b-73b5-420e-accf-5d2eea901078).html

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