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

Development and validation of a neural network survival prediction model for ischemic heart disease

缺血性心脏病神经网络生存预测模型的开发与验证

Holm, Peter C; Haue, Amalie D; Westergaard, David; Röder, Timo; Banasik, Karina; Tragante, Vinicius; Johansen, Christian H; Christensen, Alex H; Thomas, Laurent; Nøst, Therese H; Skogholt, Anne-Heidi; Iversen, Kasper K; Pedersen, Frants; Høfsten, Dan E; Pedersen, Ole B; Ostrowski, Sisse Rye; Ullum, Henrik; Svendsen, Mette N; Gjødsbøl, Iben M; Gudnason, Thorarinn; Guðbjartsson, Daníel F; Helgadottir, Anna; Hveem, Kristian; Køber, Lars V; Holm, Hilma; Stefansson, Kari; Brunak, Søren; Bundgaard, Henning

Meaning in Life Mediates Associations Between Gratitude, Forgiveness, Spirituality, and Mental Health in Postgraduate Students

人生意义在研究生感恩、宽恕、灵性和心理健康之间起着中介作用

Adeeb, Muhammad; Ghani, Mariny Abdul; Hillaluddin, Azlin Hilma; Flesia, Luca

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

Genome-wide association study and polygenic risk prediction of hypothyroidism

全基因组关联研究和甲状腺功能减退症的多基因风险预测

Rand, Søren A; Ahlberg, Gustav; Tragante, Vinicius; Monfort, Laia M; Zheng, Chaoqun; Feldt-Rasmussen, Ulla; Klose, Marianne C; Teder-Laving, Maris; Metspalu, Andres; Poulsen, Henrik E; Ellervik, Christina; Nygaard, Birte; Erikstrup, Christian; Bruun, Mie T; A Jensen, Bitten; Ullum, Henrik; Brunak, Søren; Schwinn, Michael; Ostrowski, Sisse R; Pedersen, Ole B; Sørensen, Erik; Jonsdottir, Ingileif; Gudbjartsson, Daniel F; Thorleifsson, Gudmar; Holm, Hilma; Saevarsdottir, Saedis; Stefansson, Kari; Salling Olesen, Morten; Bundgaard, Henning; Ghouse, Jonas

Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

全基因组分析鉴定出25个不孕症基因位点,并揭示了这些位点与等位基因频率范围内生殖性状的关联。

Venkatesh, Samvida S; Wittemans, Laura B L; Palmer, Duncan S; Baya, Nikolas A; Ferreira, Teresa; Hill, Barney; Lassen, Frederik Heymann; Parker, Melody J; Reibe, Saskia; Elhakeem, Ahmed; Banasik, Karina; Bruun, Mie T; Erikstrup, Christian; Aagard Jensen, Bitten; Juul, Anders; Mikkelsen, Christina; Nielsen, Henriette S; Ostrowski, Sisse R; Pedersen, Ole B; Rohde, Palle Duun; Sørensen, Erik; Ullum, Henrik; Westergaard, David; Haraldsson, Asgeir; Holm, Hilma; Jonsdottir, Ingileif; Olafsson, Isleifur; Steingrimsdottir, Thora; Steinthorsdottir, Valgerdur; Thorleifsson, Gudmar; Figueredo, Jessica; Karjalainen, Minna K; Pasanen, Anu; Jacobs, Benjamin M; Kalantzis, Georgios; Hubers, Nikki; Lippincott, Margaret; Fraser, Abigail; Lawlor, Deborah A; Timpson, Nicholas J; Nyegaard, Mette; Stefansson, Kari; Magi, Reedik; Laivuori, Hannele; van Heel, David A; Boomsma, Dorret I; Balasubramanian, Ravikumar; Seminara, Stephanie B; Chan, Yee-Ming; Laisk, Triin; Lindgren, Cecilia M

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes

全基因组关联研究荟萃分析为心力衰竭及其亚型的病因学提供了新的见解

Henry, Albert; Mo, Xiaodong; Finan, Chris; Chaffin, Mark D; Speed, Doug; Issa, Hanane; Denaxas, Spiros; Ware, James S; Zheng, Sean L; Malarstig, Anders; Gratton, Jasmine; Bond, Isabelle; Roselli, Carolina; Miller, David; Chopade, Sandesh; Schmidt, A Floriaan; Abner, Erik; Adams, Lance; Andersson, Charlotte; Aragam, Krishna G; Ärnlöv, Johan; Asselin, Geraldine; Raja, Anna Axelsson; Backman, Joshua D; Bartz, Traci M; Biddinger, Kiran J; Biggs, Mary L; Bloom, Heather L; Boersma, Eric; Brandimarto, Jeffrey; Brown, Michael R; Brunak, Søren; Bruun, Mie Topholm; Buckbinder, Leonard; Bundgaard, Henning; Carey, David J; Chasman, Daniel I; Chen, Xing; Cook, James P; Czuba, Tomasz; de Denus, Simon; Dehghan, Abbas; Delgado, Graciela E; Doney, Alexander S; Dörr, Marcus; Dowsett, Joseph; Dudley, Samuel C; Engström, Gunnar; Erikstrup, Christian; Esko, Tõnu; Farber-Eger, Eric H; Felix, Stephan B; Finer, Sarah; Ford, Ian; Ghanbari, Mohsen; Ghasemi, Sahar; Ghouse, Jonas; Giedraitis, Vilmantas; Giulianini, Franco; Gottdiener, John S; Gross, Stefan; Guðbjartsson, Daníel F; Gui, Hongsheng; Gutmann, Rebecca; Hägg, Sara; Haggerty, Christopher M; Hedman, Åsa K; Helgadottir, Anna; Hemingway, Harry; Hillege, Hans; Hyde, Craig L; Aagaard Jensen, Bitten; Jukema, J Wouter; Kardys, Isabella; Karra, Ravi; Kavousi, Maryam; Kizer, Jorge R; Kleber, Marcus E; Køber, Lars; Koekemoer, Andrea; Kuchenbaecker, Karoline; Lai, Yi-Pin; Lanfear, David; Langenberg, Claudia; Lin, Honghuang; Lind, Lars; Lindgren, Cecilia M; Liu, Peter P; London, Barry; Lowery, Brandon D; Luan, Jian'an; Lubitz, Steven A; Magnusson, Patrik; Margulies, Kenneth B; Marston, Nicholas A; Martin, Hilary; März, Winfried; Melander, Olle; Mordi, Ify R; Morley, Michael P; Morris, Andrew P; Morrison, Alanna C; Morton, Lori; Nagle, Michael W; Nelson, Christopher P; Niessner, Alexander; Niiranen, Teemu; Noordam, Raymond; Nowak, Christoph; O'Donoghue, Michelle L; Ostrowski, Sisse Rye; Owens, Anjali T; Palmer, Colin N A; Paré, Guillaume; Pedersen, Ole Birger; Perola, Markus; Pigeyre, Marie; Psaty, Bruce M; Rice, Kenneth M; Ridker, Paul M; Romaine, Simon P R; Rotter, Jerome I; Ruff, Christian T; Sabatine, Marc S; Sallah, Neneh; Salomaa, Veikko; Sattar, Naveed; Shalaby, Alaa A; Shekhar, Akshay; Smelser, Diane T; Smith, Nicholas L; Sørensen, Erik; Srinivasan, Sundararajan; Stefansson, Kari; Sveinbjörnsson, Garðar; Svensson, Per; Tammesoo, Mari-Liis; Tardif, Jean-Claude; Teder-Laving, Maris; Teumer, Alexander; Thorgeirsson, Guðmundur; Thorsteinsdottir, Unnur; Torp-Pedersen, Christian; Tragante, Vinicius; Trompet, Stella; Uitterlinden, Andre G; Ullum, Henrik; van der Harst, Pim; van Heel, David; van Setten, Jessica; van Vugt, Marion; Veluchamy, Abirami; Verschuuren, Monique; Verweij, Niek; Vissing, Christoffer Rasmus; Völker, Uwe; Voors, Adriaan A; Wallentin, Lars; Wang, Yunzhang; Weeke, Peter E; Wiggins, Kerri L; Williams, L Keoki; Yang, Yifan; Yu, Bing; Zannad, Faiez; Zheng, Chaoqun; Asselbergs, Folkert W; Cappola, Thomas P; Dubé, Marie-Pierre; Dunn, Michael E; Lang, Chim C; Samani, Nilesh J; Shah, Svati; Vasan, Ramachandran S; Smith, J Gustav; Holm, Hilma; Shah, Sonia; Ellinor, Patrick T; Hingorani, Aroon D; Wells, Quinn; Lumbers, R Thomas

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

Intratumor heterogeneity of EGFR expression mediates targeted therapy resistance and formation of drug tolerant microenvironment

EGFR 表达的肿瘤内异质性介导靶向治疗耐药性和药物耐受微环境的形成

Bassel Alsaed, Linh Lin, Jieun Son, Jiaqi Li, Johannes Smolander, Timothy Lopez, Pinar Ö Eser, Atsuko Ogino, Chiara Ambrogio, Yoonji Eum, Tran Thai, Haiyun Wang, Eva Sutinen, Hilma Mutanen, Hanna Duàn, Nina Bobik, Kristian Borenius, William W Feng, Behnam Nabet, Satu Mustjoki, Sanna Laaksonen, Benja