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

The influence of social content on episodic memory retrieval

社会内容对情景记忆提取的影响

Ghouse, Ameer; Kaplan, Raphael

Drivers of Diagnostic Delay in Mitochondrial Disease: Missed Recognition of Canonical Features

线粒体疾病诊断延迟的驱动因素:未能识别典型特征

Tinker, Rory J; Jacob, Neil; Syed, Mohammad Ghouse; Kelkar, Janhawi; Donnelly, Colleen; Elsharkawi, Ibrahim; Ganesh, Jaya; Gelb, Bruce D; Pejaver, Vikas; Kozicz, Tamas; Morava, Eva

Optic Nerve Sheath Diameter as a Prognostic Tool for Mortality in Intensive Care Unit Patients

视神经鞘直径作为重症监护病房患者死亡率的预后指标

Syed, Fahimuddin; Hendi, Mohamed F; Ghouse Mohammed, Nayeem; Faoor Medhat Alrais, Zeyad; Sheikh, Waseem

Global High-Cited Pediatric Fracture Research: Bibliometric Assessment of Scopus Publications (1929-2024)

全球高被引儿科骨折研究:Scopus 出版物的文献计量学评估(1929-2024)

Vaishya, Raju; Johari, Ashok N; Gupta, Brij Mohan; Kappi, Mallikarjun M; Mamdapur, Ghouse Modin Naseesab; Vaish, Abhishek

Developing a phenotype risk score for TTR V142I to capture undiagnosed variant transthyretin amyloidosis in health systems

为TTR V142I开发表型风险评分,以在医疗系统中发现未确诊的变异型转甲状腺素蛋白淀粉样变性。

Sarkar, Deepa; Ferar, Kathleen D; Syed, Mohammad Ghouse; Bastarache, Lisa A; Kenny, Eimear E; Abul-Husn, Noura S; Pejaver, Vikas; Kontorovich, Amy R

Within-person stability of lipoprotein(a) concentration

脂蛋白(a)浓度的个体内部稳定性

Ghouse, Jonas; Ahlberg, Gustav; Albertsen Rand, Søren; Salling Olesen, Morten; Vilhjalmsson, Bjarni; Stender, Stefan; Bundgaard, Henning

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 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

Genomics of chronic dry cough unravels neurological pathways

慢性干咳的基因组学研究揭示了神经通路

Coley, Kayesha; John, Catherine; Ghouse, Jonas; Shepherd, David J; Shrine, Nick; Izquierdo, Abril G; Kanoni, Stavroula; Magavern, Emma F; Packer, Richard; McGarvey, Lorcan; Smith, Jaclyn A; Bundgaard, Henning; Ostrowski, Sisse R; Erikstrup, Christian; Pedersen, Ole B V; van Heel, David A; Hennah, William; Marttila, Mikko; Free, Robert C; Hollox, Edward J; Wain, Louise V; Tobin, Martin D; Batini, Chiara