日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

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

对冰岛大规模SARS-CoV-2感染疫情的重建为疫苗接种策略提供了信息

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

Molecular benchmarks of a SARS-CoV-2 epidemic

SARS-CoV-2 流行病的分子基准

Hakon Jonsson, Olafur T Magnusson, Pall Melsted, Jonas Berglund, Arna B Agustsdottir, Berglind Eiríksdottir, Run Fridriksdottir, Elisabet Eir Garðarsdottir, Gudmundur Georgsson, Olafia S Gretarsdottir, Kjartan R Guðmundsson, Thora Rosa Gunnarsdottir, Hannes Eggertsson, Arnaldur Gylfason, Hilma Holm,

Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis

88个变异体突显了T细胞调节和气道重塑在哮喘发病机制中的作用。

Thorunn A Olafsdottir ,Fannar Theodors ,Kristbjorg Bjarnadottir ,Unnur Steina Bjornsdottir ,Arna B Agustsdottir ,Olafur A Stefansson ,Erna V Ivarsdottir ,Jon K Sigurdsson ,Stefania Benonisdottir ,Gudmundur I Eyjolfsson ,David Gislason ,Thorarinn Gislason ,Steinunn Guðmundsdóttir ,Arnaldur Gylfason ,Bjarni V Halldorsson ,Gisli H Halldorsson ,Thorhildur Juliusdottir ,Anna M Kristinsdottir ,Dora Ludviksdottir ,Bjorn R Ludviksson ,Gisli Masson ,Kristjan Norland ,Pall T Onundarson ,Isleifur Olafsson ,Olof Sigurdardottir ,Lilja Stefansdottir ,Gardar Sveinbjornsson ,Vinicius Tragante ,Daniel F Gudbjartsson ,Gudmar Thorleifsson ,Patrick Sulem ,Unnur Thorsteinsdottir ,Gudmundur L Norddahl ,Ingileif Jonsdottir ,Kari Stefansson

Kidney Transplant Outcomes in Patients With Adenine Phosphoribosyltransferase Deficiency

腺嘌呤磷酸核糖转移酶缺乏症患者的肾移植结果

Runolfsdottir, Hrafnhildur Linnet; Palsson, Runolfur; Agustsdottir, Inger M Sch; Indridason, Olafur S; Li, Jennifer; Dao, Myriam; Knebelmann, Bertrand; Milliner, Dawn S; Edvardsson, Vidar O

GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

骨骼大小的 GWAS 得出了 12 个基因位点,这些基因位点也会影响身高、BMD、骨关节炎或骨折

Unnur Styrkarsdottir, Olafur A Stefansson, Kristbjorg Gunnarsdottir, Gudmar Thorleifsson, Sigrun H Lund, Lilja Stefansdottir, Kristinn Juliusson, Arna B Agustsdottir, Florian Zink, Gisli H Halldorsson, Erna V Ivarsdottir, Stefania Benonisdottir, Hakon Jonsson, Arnaldur Gylfason, Kristjan Norland, Ka

Melt movement through the Icelandic crust

冰岛地壳的熔融运动

White, Robert S; Edmonds, Marie; Maclennan, John; Greenfield, Tim; Agustsdottir, Thorbjorg

Urinary 2,8-dihydroxyadenine excretion in patients with adenine phosphoribosyltransferase deficiency, carriers and healthy control subjects

腺嘌呤磷酸核糖转移酶缺乏症患者、携带者和健康对照组的尿2,8-二羟基腺嘌呤排泄情况

Runolfsdottir, Hrafnhildur L; Palsson, Runolfur; Thorsteinsdottir, Unnur A; Indridason, Olafur S; Agustsdottir, Inger M Sch; Oddsdottir, G Steinunn; Thorsteinsdottir, Margret; Edvardsson, Vidar O

Long-term renal outcomes of APRT deficiency presenting in childhood

儿童期出现APRT缺乏症的长期肾脏预后

Runolfsdottir, Hrafnhildur Linnet; Palsson, Runolfur; Agustsdottir, Inger MSch; Indridason, Olafur S; Edvardsson, Vidar O

A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

导致 CYBC1 缺陷的纯合功能丧失突变会引起慢性肉芽肿病

Gudny A Arnadottir, Gudmundur L Norddahl, Steinunn Gudmundsdottir, Arna B Agustsdottir, Snaevar Sigurdsson, Brynjar O Jensson, Kristbjorg Bjarnadottir, Fannar Theodors, Stefania Benonisdottir, Erna V Ivarsdottir, Asmundur Oddsson, Ragnar P Kristjansson, Gerald Sulem, Kristjan F Alexandersson, Thorhi

MAP1B mutations cause intellectual disability and extensive white matter deficit

MAP1B 突变导致智力障碍和广泛性白质缺陷

G Bragi Walters, Omar Gustafsson, Gardar Sveinbjornsson, Valgerdur K Eiriksdottir, Arna B Agustsdottir, Gudrun A Jonsdottir, Stacy Steinberg, Arni F Gunnarsson, Magnus I Magnusson, Unnur Unnsteinsdottir, Amy L Lee, Adalbjorg Jonasdottir, Asgeir Sigurdsson, Aslaug Jonasdottir, Astros Skuladottir, Lin