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

Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder

HECTD2 和 AKAP11 中罕见的失活变异会增加患双相情感障碍的风险。

Thorgeirsson, Thorgeir E; Tragante, Vinicius; Sveinbjornsson, Gardar; Jonsdottir, Gudrun A; Walters, G Bragi; Ivarsdottir, Erna V; Arnadottir, Gudny A; Sturluson, Arni; Jensson, Brynjar O; Fridriksdottir, Run; Skuladottir, Astros Th; Einarsson, Gudmundur; Bjornsdottir, Gyda; Gunnarsson, Arni F; Gisladottir, Rosa S; Sigurdsson, Asgeir; Oddsson, Asmundur; Jonsson, Hakon; Magnusson, Olafur Th; Helgason, Hannes; Norddahl, Gudmundur; Thorleifsson, Gudmar; Haraldsson, Magnus; Sigurdsson, Engilbert; Holm, Hilma; Masson, Gisli; Gudbjartsson, Daniel F; Stefansson, Hreinn; Sulem, Patrick; Stefansson, Kari

African-ancestry-specific variant IKKβ p.Glu502Lys confers high lupus risk

非洲裔特有的IKKβ p.Glu502Lys变异体与较高的狼疮风险相关

Thorlacius, Gudny Ella; Ivarsdottir, Erna V; Saevarsdottir, Saedis; Moore, Kristjan H S; Gudjonsson, Sigurjon A; Halldorsson, Bjarni V; Holm, Hilma; Jonasdottir, Aslaug; Jonsson, Frosti; Kristmundsdottir, Snaedis; Masson, Gisli; Magnusson, Olafur T; Norddahl, Gudmundur L; Oddsson, Asmundur; Olafsdottir, Thorunn A; Olason, Pall I; Skaftason, Aron; Stefansdottir, Lilja; Sturluson, Arni; Thorsteinsdottir, Unnur; Thorleifsson, Gudmar; Walker, Valentin Y; Zink, Florian; Steingrimsson, Eirikur; Gudbjartsson, Daniel F; Jonsdottir, Ingileif; Helgason, Agnar; Sulem, Patrick; Stefansson, Kari

Missense variants in FRS3 affect body mass index in populations of diverse ancestries

FRS3基因的错义变异会影响不同种族人群的体重指数。

Jonsdottir, Andrea B; Sveinbjornsson, Gardar; Thorolfsdottir, Rosa B; Tamlander, Max; Tragante, Vinicius; Olafsdottir, Thorhildur; Rognvaldsson, Solvi; Sigurdsson, Asgeir; Eggertsson, Hannes P; Aegisdottir, Hildur M; Arnar, David O; Banasik, Karina; Beyter, Doruk; Bjarnason, Ragnar G; Bjornsdottir, Gyda; Brunak, Søren; Topholm Bruun, Mie; Dowsett, Joseph; Einarsson, Eythor; Einarsson, Gudmundur; Erikstrup, Christian; Fridriksdottir, Run; Ghouse, Jonas; Gretarsdottir, Solveig; Halldorsson, Gisli H; Hansen, Torben; Helgadottir, Anna; Holm, Peter C; Ivarsdottir, Erna V; Iversen, Kasper Karmark; Jensen, Bitten Aagaard; Jonsdottir, Ingileif; Knight, Stacey; Knowlton, Kirk U; Kristmundsdottir, Snaedis; Larusdottir, Adalheidur E; Magnusson, Olafur Th; Masson, Gisli; Melsted, Pall; Mikkelsen, Christina; Moore, Kristjan H S; Oddsson, Asmundur; Olason, Pall I; Palsson, Frosti; Pedersen, Ole Birger; Schwinn, Michael; Sigurdsson, Emil L; Skaftason, Aron; Stefansdottir, Lilja; Stefansson, Hreinn; Steingrimsdottir, Thora; Sturluson, Arni; Styrkarsdottir, Unnur; Sørensen, Erik; Teitsdottir, Unnur D; Thorgeirsson, Thorgeir E; Thorisson, Gudmundur A; Thorsteinsdottir, Unnur; Ulfarsson, Magnus O; Ullum, Henrik; Vikingsson, Arnor; Walters, G Bragi; Nadauld, Lincoln D; Bundgaard, Henning; Ostrowski, Sisse Rye; Helgason, Agnar; Halldorsson, Bjarni V; Norddahl, Gudmundur L; Ripatti, Samuli; Gudbjartsson, Daniel F; Thorleifsson, Gudmar; Steinthorsdottir, Valgerdur; Holm, Hilma; Sulem, Patrick; Stefansson, Kari

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

整合常见和罕见变异分析有助于深入了解肝硬化的遗传结构。

Ghouse, Jonas; Sveinbjörnsson, Gardar; Vujkovic, Marijana; Seidelin, Anne-Sofie; Gellert-Kristensen, Helene; Ahlberg, Gustav; Tragante, Vinicius; Rand, Søren A; Brancale, Joseph; Vilarinho, Silvia; Lundegaard, Pia Rengtved; Sørensen, Erik; Erikstrup, Christian; Bruun, Mie Topholm; Jensen, Bitten Aagaard; Brunak, Søren; Banasik, Karina; Ullum, Henrik; Verweij, Niek; Lotta, Luca; Baras, Aris; Mirshahi, Tooraj; Carey, David J; Kaplan, David E; Lynch, Julie; Morgan, Timothy; Schwantes-An, Tae-Hwi; Dochtermann, Daniel R; Pyarajan, Saiju; Tsao, Philip S; Laisk, Triin; Mägi, Reedik; Kozlitina, Julia; Tybjærg-Hansen, Anne; Jones, David; Knowlton, Kirk U; Nadauld, Lincoln; Ferkingstad, Egil; Björnsson, Einar S; Ulfarsson, Magnus O; Sturluson, Árni; Sulem, Patrick; Pedersen, Ole B; Ostrowski, Sisse R; Gudbjartsson, Daniel F; Stefansson, Kari; Olesen, Morten Salling; Chang, Kyong-Mi; Holm, Hilma; Bundgaard, Henning; Stender, Stefan

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

CCDC201基因中终止密码子突变的纯合子会导致原发性卵巢功能不全。

Oddsson, Asmundur; Steinthorsdottir, Valgerdur; Oskarsson, Gudjon R; Styrkarsdottir, Unnur; Moore, Kristjan H S; Isberg, Salvor; Halldorsson, Gisli H; Sveinbjornsson, Gardar; Westergaard, David; Nielsen, Henriette Svarre; Fridriksdottir, Run; Jensson, Brynjar O; Arnadottir, Gudny A; Jonsson, Hakon; Sturluson, Arni; Snaebjarnarson, Audunn S; Andreassen, Ole A; Walters, G Bragi; Nyegaard, Mette; Erikstrup, Christian; Steingrimsdottir, Thora; Lie, Rolv T; Melsted, Pall; Jonsdottir, Ingileif; Halldorsson, Bjarni V; Thorleifsson, Gudmar; Saemundsdottir, Jona; Magnusson, Olafur Th; Banasik, Karina; Sorensen, Erik; Masson, Gisli; Pedersen, Ole Birger; Tryggvadottir, Laufey; Haavik, Jan; Ostrowski, Sisse Rye; Stefansson, Hreinn; Holm, Hilma; Rafnar, Thorunn; Gudbjartsson, Daniel F; Sulem, Patrick; Stefansson, Kari

Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease

LAG3基因起始密码子变异与LAG-3表达降低和自身免疫性甲状腺疾病风险增加相关。

Saedis Saevarsdottir ,Kristbjörg Bjarnadottir ,Thorsteinn Markusson ,Jonas Berglund ,Thorunn A Olafsdottir ,Gisli H Halldorsson ,Gudrun Rutsdottir ,Kristbjorg Gunnarsdottir ,Asgeir Orn Arnthorsson ,Sigrun H Lund ,Lilja Stefansdottir ,Julius Gudmundsson ,Ari J Johannesson ,Arni Sturluson ,Asmundur Oddsson ,Bjarni Halldorsson ,Björn R Ludviksson ,Egil Ferkingstad ,Erna V Ivarsdottir ,Gardar Sveinbjornsson ,Gerdur Grondal ,Gisli Masson ,Grimur Hjorleifsson Eldjarn ,Gudmundur A Thorisson ,Katla Kristjansdottir ,Kirk U Knowlton ,Kristjan H S Moore ,Sigurjon A Gudjonsson ,Solvi Rognvaldsson ,Stacey Knight ,Lincoln D Nadauld ,Hilma Holm ,Olafur T Magnusson ,Patrick Sulem ,Daniel F Gudbjartsson ,Thorunn Rafnar ,Gudmar Thorleifsson ,Pall Melsted ,Gudmundur L Norddahl ,Ingileif Jonsdottir ,Kari Stefansson

Variants at the Interleukin 1 Gene Locus and Pericarditis

白细胞介素 1 基因位点变异与心包炎

Thorolfsdottir, Rosa B; Jonsdottir, Andrea B; Sveinbjornsson, Gardar; Aegisdottir, Hildur M; Oddsson, Asmundur; Stefansson, Olafur A; Halldorsson, Gisli H; Saevarsdottir, Saedis; Thorleifsson, Gudmar; Stefansdottir, Lilja; Pedersen, Ole B; Sørensen, Erik; Ghouse, Jonas; Raja, Anna Axelsson; Zheng, Chaoqun; Silajdzija, Elvira; Rand, Søren Albertsen; Erikstrup, Christian; Ullum, Henrik; Mikkelsen, Christina; Banasik, Karina; Brunak, Søren; Ivarsdottir, Erna V; Sigurdsson, Asgeir; Beyter, Doruk; Sturluson, Arni; Einarsson, Hafsteinn; Tragante, Vinicius; Helgason, Hannes; Lund, Sigrun H; Halldorsson, Bjarni V; Sigurpalsdottir, Brynja D; Olafsson, Isleifur; Arnar, David O; Thorgeirsson, Gudmundur; Knowlton, Kirk U; Nadauld, Lincoln D; Gretarsdottir, Solveig; Helgadottir, Anna; Ostrowski, Sisse R; Gudbjartssson, Daniel F; Jonsdottir, Ingileif; Bundgaard, Henning; Holm, Hilma; Sulem, Patrick; Stefansson, Kari

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

ITSN1基因功能缺失变异会增加患帕金森病的风险。

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; Sulem, Patrick; Stefansson, Hreinn; Stefansson, Kari

Understanding Gas Storage in Cuboctahedral Porous Coordination Cages

了解立方八面体多孔配位笼中的气体存储

Lorzing, Gregory R; Gosselin, Aeri J; Trump, Benjamin A; York, Arthur H P; Sturluson, Arni; Rowland, Casey A; Yap, Glenn P A; Brown, Craig M; Simon, Cory M; Bloch, Eric D

The role of molecular modelling and simulation in the discovery and deployment of metal-organic frameworks for gas storage and separation

分子建模和模拟在发现和部署用于气体储存和分离的金属有机框架中的作用

Sturluson, Arni; Huynh, Melanie T; Kaija, Alec R; Laird, Caleb; Yoon, Sunghyun; Hou, Feier; Feng, Zhenxing; Wilmer, Christopher E; Colón, Yamil J; Chung, Yongchul G; Siderius, Daniel W; Simon, Cory M