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

Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction.

主动脉狭窄的基因组学和转录组学分析有助于发现治疗靶点和预测疾病。

Small Aeron M, Yang Ta-Yu, Itoh Shinsuke, Thériault Sébastien, Dufresne Line, Kurosawa Ryo, Komuro Issei, Matsuda Koichi, Vy Ha My T, Farber-Eger Eric H, Shaffer Lauren Lee, Boulier Kristin M, Corey Kristin M, Ramaker Megan E, Laporte Fabien, Schott Jean-Jacques, Le Scouarnec Solena, Singh Sasha A, Sonawane Abhijeet R, Smith Harry A, Rafaels Nicholas, Ghouse Jonas, Raja Anna A, Ostrowski Sisse R, Sørensen Erik, Mikkelsen Christina, Pedersen Ole B, Erikstrup Christian, Ullum Henrik, Sveinbjornsson Gardar, Gudbjartsson Daniel F, Abner Erik, Lee Jiwoo, Ganna Andrea, Nowak-Göttl Ulrike, Finer Sarah, Schumacher Johannes, Maj Carlo, Al-Kassou Baravan, Nickenig Georg, Trenkwalder Teresa, Dreβen Martina, Krane Markus, Nöthen Markus M, Moksnes Marta R, Brumpton Ben M, Knight Stacey, Knowlton Kirk U, Nadauld Lincoln, Debiec Radek, Musameh Muntaser D, Braund Peter S, Nelson Christopher P, Czuba Tomasz, Melander Olle, Selvaraj Margaret Sunitha, Koyama Satoshi, Bhukar Rohan, Ruan Yunfeng, Ljungberg Johan, Damrauer Scott M, Levin Michael G, Franke Andre, Berger Klaus, Ruff Christian T, Melloni Giorgio E M, Kamanu Frederick K, Ito Kaoru, Do Ron, Loos Ruth J F, Schunkert Heribert, Wells Quinn S, Shah Svati H, Le Tourneau Thierry, Messika-Zeitoun David, Gignoux Christopher, Bundgaard Henning, Larsson Susanna C, Michaëlsson Karl, Holm Hilma, Helgadottir Anna, Esko Tonu, van Heel David A, Mathieu Patrick, Samani Nilesh J, Smith J Gustav, Söderberg Stefan, Rader Daniel J, Marston Nicholas A, Sabatine Marc S, Pasaniuc Bogdan, Cho Kelly, Wilson Peter W F, O'Donnell Christopher J, Stefansson Kari, Bossé Yohan, Aikawa Elena, Engert James C, Peloso Gina M, Natarajan Pradeep, Thanassoulis George

Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication

味觉受体基因位点的变异与失眠药物使用方式的改变有关

Einarsson, Gudmundur; Arnason, Hannes K; Gisladottir, Rosa S; Bjornsdottir, Gyda; Thorgeirsson, Thorgeir E; Skuladottir, Astros; Walters, G Bragi; Saevarsdottir, Saedis; Magnusson, Magnus K; Halldorsson, Gisli H; Snaebjarnarson, Audunn S; Einarsson, Hafsteinn; Sveinbjornsson, Gardar; Helgason, Hannes; Tragante, Vinicius; Jonsdottir, Gudrun A; Aegisdottir, Hildur M; Jonsdottir, Ingileif; Gislason, Thorarinn; Thorleifsson, Gudmar; Sulem, Patrick; Stefansson, Hreinn; Gudbjartsson, Daniel F; Stefansson, Kari

A frameshift variant in PKP2 can be associated with a complex phenotype in sudden cardiac death: a case report

PKP2基因移码变异可能与猝死的复杂表型相关:病例报告

Davidsson, Gustav A; Arnadottir, Gudny A; Sveinbjornsson, Gardar; Ottarsdottir, Helga; Arnar, David O

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

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

Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development

全基因组荟萃分析确定了9个与肝细胞癌发生风险增加相关的基因位点。

Ghouse, Jonas; Gellert-Kristensen, Helene; O'Rourke, Colm J; Seidelin, Anne-Sofie; Thorleifsson, Gudmar; Sveinbjörnsson, Gardar; Tragante, Vinicius; Konkwo, Chigoziri; Brancale, Joseph; Vilarinho, Silvia; Eyrich, Tim M; Ahlberg, Gustav; Bundgaard, Johan S; Rand, Søren A; Lundegaard, Pia R; Sørensen, Erik; Mikkelsen, Christina; Træholt, Jacob; Erikstrup, Christian; Dinh, Khoa M; Bruun, Mie T; Jensen, Bitten Aa; Bay, Jakob T; Brunak, Søren; Banasik, Karina; Ullum, Henrik; Laisk, Triin; Mägi, Reedik; Nadauld, Lincoln D; Knowlton, Kirk U; Knight, Stacey; Gluud, Lise L; Vistisen, Kirsten; Björnsson, Einar S; Ulfarsson, Magnus O; Sulem, Patrick; Holm, Hilma; Pedersen, Ole B; Ostrowski, Sisse R; Gudbjartsson, Daniel F; Rafnar, Thorunn; Stefansson, Kari; Lassen, Ulrik; Pommergaard, Hans-Christian; Hillingsø, Jens G; Andersen, Jesper B; Bundgaard, Henning; Stender, Stefan

Histologically verified penile lichen sclerosus-Incidence in Denmark over 26 years and long-term risk of penile and non-penile cancer

经组织学证实的阴茎硬化性苔藓——丹麦26年间的发病率及阴茎癌和非阴茎癌的长期风险

Stærk, Marianne Gardar; Kaderly Rasmussen, Emma L; Hannibal, Charlotte Gerd; Hertzum-Larsen, Rasmus; Baandrup, Louise; Kjær, Susanne K

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

POPDC2基因的双等位基因变异会导致一种常染色体隐性遗传综合征,其特征为心脏传导缺陷和肥厚型心肌病。

Nicastro, Michele; Vermeer, Alexa M C; Postema, Pieter G; Tadros, Rafik; Bowling, Forrest Z; Aegisdottir, Hildur M; Tragante, Vinicius; Mach, Lukas; Postma, Alex V; Lodder, Elisabeth M; van Duijvenboden, Karel; Zwart, Rob; Beekman, Leander; Wu, Lingshuang; Jurgens, Sean J; van der Zwaag, Paul A; Alders, Mariëlle; Allouba, Mona; Aguib, Yasmine; Santome, J Luis; de Una, David; Monserrat, Lorenzo; Miranda, Antonio M A; Kanemaru, Kazumasa; Cranley, James; van Zeggeren, Ingeborg E; Aronica, Eleonora M A; Ripolone, Michela; Zanotti, Simona; Sveinbjornsson, Gardar; Ivarsdottir, Erna V; Hólm, Hilma; Guðbjartsson, Daníel F; Skúladóttir, Ástrós Th; Stefánsson, Kári; Nadauld, Lincoln; Knowlton, Kirk U; Ostrowski, Sisse Rye; Sørensen, Erik; Vesterager Pedersen, Ole Birger; Ghouse, Jonas; Rand, Søren A; Bundgaard, Henning; Ullum, Henrik; Erikstrup, Christian; Aagaard, Bitten; Bruun, Mie Topholm; Christiansen, Mette; Jensen, Henrik K; Carere, Deanna Alexis; Cummings, Christopher T; Fishler, Kristen; Tørring, Pernille Mathiesen; Brusgaard, Klaus; Juul, Trine Maxel; Saaby, Lotte; Winkel, Bo Gregers; Mogensen, Jens; Fortunato, Francesco; Comi, Giacomo Pietro; Ronchi, Dario; van Tintelen, J Peter; Noseda, Michela; Airola, Michael V; Christiaans, Imke; Wilde, Arthur A M; Wilders, Ronald; Clur, Sally-Ann; Verkerk, Arie O; Bezzina, Connie R; Lahrouchi, Najim

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

对超过18万例房颤病例进行全基因组关联和多基因风险预测的荟萃分析

Roselli, Carolina; Surakka, Ida; Olesen, Morten S; Sveinbjornsson, Gardar; Marston, Nicholas A; Choi, Seung Hoan; Holm, Hilma; Chaffin, Mark; Gudbjartsson, Daniel; Hill, Matthew C; Aegisdottir, Hildur; Albert, Christine M; Alonso, Alvaro; Anderson, Christopher D; Arking, Dan E; Arnar, David O; Barnard, John; Benjamin, Emelia J; Braunwald, Eugene; Brumpton, Ben; Campbell, Archie; Chami, Nathalie; Chasman, Daniel I; Cho, Kelly; Choi, Eue-Keun; Christophersen, Ingrid E; Chung, Mina K; Conen, David; Crijns, Harry J; Cutler, Michael J; Czuba, Tomasz; Damrauer, Scott M; Dichgans, Martin; Dörr, Marcus; Dudink, Elton; Duong, ThuyVy; Erikstrup, Christian; Esko, Tõnu; Fatkin, Diane; Faul, Jessica D; Ferreira, Manuel; Freitag, Daniel F; Ganesh, Santhi K; Gaziano, J Michael; Geelhoed, Bastiaan; Ghouse, Jonas; Gieger, Christian; Giulianini, Franco; Graham, Sarah E; Gudnason, Vilmundur; Guo, Xiuqing; Haggerty, Christopher; Hayward, Caroline; Heckbert, Susan R; Hveem, Kristian; Ito, Kaoru; Johnson, Renee; Jukema, J Wouter; Jurgens, Sean J; Kääb, Stefan; Kane, John P; Kany, Shinwan; Kardia, Sharon L R; Kavousi, Maryam; Khurshid, Shaan; Kamanu, Frederick K; Kirchhof, Paulus; Kleber, Marcus E; Knight, Stacey; Komuro, Issei; Krieger, Jose E; Launer, Lenore J; Li, Dadong; Lin, Honghuang; Lin, Henry J; Loos, Ruth J F; Lotta, Luca; Lubitz, Steven A; Lunetta, Kathryn L; Macfarlane, Peter W; Magnusson, Patrik K E; Malik, Rainer; Mantineo, Helene; Marcus, Gregory M; März, Winfried; McManus, David D; Melander, Olle; Melloni, Giorgio E M; Meyre, Pascal B; Miyazawa, Kazuo; Mohanty, Sanghamitra; Monfort, Laia M; Müller-Nurasyid, Martina; Nafissi, Navid A; Natale, Andrea; Nazarian, Saman; Ostrowski, Sisse R; Pak, Hui-Nam; Pang, Shichao; Pedersen, Ole B; Pedersen, Nancy L; Pereira, Alexandre C; Pirruccello, James P; Preuss, Michael; Psaty, Bruce M; Pullinger, Clive R; Rader, Daniel J; Rämö, Joel T; Ridker, Paul M; Rienstra, Michiel; Risch, Lorenz; Roden, Dan M; Rotter, Jerome I; Sabatine, Marc S; Schunkert, Heribert; Shah, Svati H; Shim, Jaemin; Shoemaker, M Benjamin; Simonson, Bridget; Sinner, Moritz F; Smit, Roelof A J; Smith, Jennifer A; Smith, Nicholas L; Smith, J Gustav; Soliman, Elsayed Z; Sørensen, Erik; Sotoodehnia, Nona; Strbian, Daniel; Stricker, Bruno H; Teder-Laving, Maris; Sun, Yan V; Thériault, Sébastien; Thorolfsdottir, Rosa B; Thorsteinsdottir, Unnur; Tveit, Arnljot; van der Harst, Pim; van Meurs, Joyce; Wang, Biqi; Weiss, Stefan; Wells, Quinn S; Weng, Lu-Chen; Wilson, Peter W; Xiao, Ling; Yang, Pil-Sung; Yao, Jie; Yoneda, Zachary T; Zeller, Tanja; Zeng, Lingyao; Zhao, Wei; Zhou, Xiang; Zöllner, Sebastian; Ruff, Christian T; Bundgaard, Henning; Willer, Cristen; Stefansson, Kari; Ellinor, Patrick T

Author Correction: Large-scale plasma proteomics comparisons through genetics and disease associations

作者更正:通过遗传学和疾病关联进行大规模血浆蛋白质组学比较

Eldjarn, Grimur Hjorleifsson; Ferkingstad, Egil; Lund, Sigrun H; Helgason, Hannes; Magnusson, Olafur Th; Gunnarsdottir, Kristbjorg; Olafsdottir, Thorunn A; Halldorsson, Bjarni V; Olason, Pall I; Zink, Florian; Gudjonsson, Sigurjon A; Sveinbjornsson, Gardar; Magnusson, Magnus I; Helgason, Agnar; Oddsson, Asmundur; Halldorsson, Gisli H; Magnusson, Magnus K; Saevarsdottir, Saedis; Eiriksdottir, Thjodbjorg; Masson, Gisli; Stefansson, Hreinn; Jonsdottir, Ingileif; Holm, Hilma; Rafnar, Thorunn; Melsted, Pall; Saemundsdottir, Jona; Norddahl, Gudmundur L; Thorleifsson, Gudmar; Ulfarsson, Magnus O; Gudbjartsson, Daniel F; Thorsteinsdottir, Unnur; Sulem, Patrick; Stefansson, Kari