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Chapdelaine-Trepanier, Vincent; Shenoy, Shamika; Masud, Wardah; Minju-OP, Amisha; Berube, Marie-Anne; Schoenherr, Sebastian; Forer, Lukas; Fradet-Turcotte, Amelie; Taliun, Daniel; Cuella-Martin, Raquel .png)
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收藏分享 收藏 Genome-Wide Characterization of a Highly Penetrant Form of Hyperlipoprotein(a)emia Associated With Genetically Elevated Cardiovascular RiskCoassin, Stefan; Chemello, Kevin; Khantalin, Ilya; Forer, Lukas; Dottelmayer, Patricia; Schonherr, Sebastian; Gruneis, Rebecca; Chong-Hong-Fong, Clement; Nativel, Brice; Ramin-Mangata, Stephane; Gallo, Antonio; Roche, Mathias; Muhlegger, Beatrix; Gieger, Christian; Peters, Annette; Zschocke, Johannes; Marimoutou, Catherine; Meilhac, Olivier; Lamina, Claudia; Kronenberg, Florian; Blanchard, Valentin; Lambert, Gilles 分享 收藏 Discontinuation versus continuation of renin-angiotensin-system inhibitors in COVID-19 (ACEI-COVID): a prospective, parallel group, randomised, controlled, open-label trialBauer, Axel; Schreinlechner, Michael; Sappler, Nikolay; Dolejsi, Theresa; Tilg, Herbert; Aulinger, Benedikt A.; Weiss, Guenter; Bellmann-Weiler, Rosa; Adolf, Christian; Wolf, Dominik; Pirklbauer, Markus; Graziadei, Ivo; Gaenzer, Hannes; von Bary, Christian; May, Andreas E.; Woell, Ewald; von Scheidt, Wolfgang; Rassaf, Tienush; Duerschmied, Daniel; Brenner, Christoph; Kaeaeb, Stefan; Metzler, Bernhard; Joannidis, Michael; Kain, Hans-Ulrich; Kaiser, Norbert; Schwinger, Robert; Witzenbichler, Bernhard; Alber, Hannes; Straube, Florian; Hartmann, Niels; Achenbach, Stephan; von Bergwelt-Baildon, Michael; von Stuelpnagel, Lukas; Schoenherr, Sebastian; Forer, Lukas; Embacher-Aichhorn, Sabine; Mansmann, Ulrich; Rizzast, Konstantinos D.; Massberg, Steffen 分享 收藏 分享 收藏 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease功能丧失的基因组变异突出了心血管疾病的潜在治疗靶点Nielsen, Jonas B.; Rom, Oren; Surakka, Ida; Graham, Sarah E.; Zhou, Wei; Roychowdhury, Tanmoy; Fritsche, Lars G.; Taliun, Sarah A. Gagliano; Sidore, Carlo; Liu, Yuhao; Gabrielsen, Maiken E.; Skogholt, Anne Heidi; Wolford, Brooke; Overton, William; Zhao, Ying; Chen, Jin; Zhang, He; Hornsby, Whitney E.; Acheampong, Akua; Grooms, Austen; Schaefer, Amanda; Zajac, Gregory J. M.; Villacorta, Luis; Zhang, Jifeng; Brumpton, Ben; Loset, Mari; Rai, Vivek; Lundegaard, Pia R.; Olesen, Morten S.; Taylor, Kent D.; Palmer, Nicholette D.; Chen, Yii-Der; Choi, Seung H.; Lubitz, Steven A.; Ellinor, Patrick T.; Barnes, Kathleen C.; Daya, Michelle; Rafaels, Nicholas; Weiss, Scott T.; Lasky-Su, Jessica; Tracy, Russell P.; Vasan, Ramachandran S.; Cupples, L. Adrienne; Mathias, Rasika A.; Yanek, Lisa R.; Becker, Lewis C.; Peyser, Patricia A.; Bielak, Lawrence F.; Smith, Jennifer A.; Aslibekyan, Stella; Hidalgo, Bertha A.; Arnett, Donna K.; Irvin, Marguerite R.; Wilson, James G.; Musani, Solomon K.; Correa, Adolfo; Rich, Stephen S.; Guo, Xiuqing; Rotter, Jerome I.; Konkle, Barbara A.; Johnsen, Jill M.; Ashley-Koch, Allison E.; Telen, Marilyn J.; Sheehan, Vivien A.; Blangero, John; Curran, Joanne E.; Peralta, Juan M.; Montgomery, Courtney; Sheu, Wayne H-H; Chung, Ren-Hua; Schwander, Karen; Nouraie, Seyed M.; Gordeuk, Victor R.; Zhang, Yingze; Kooperberg, Charles; Reiner, Alexander P.; Jackson, Rebecca D.; Bleecker, Eugene R.; Meyers, Deborah A.; Li, Xingnan; Das, Sayantan; Yu, Ketian; LeFaive, Jonathon; Smith, Albert; Blackwell, Tom; Taliun, Daniel; Zollner, Sebastian; Forer, Lukas; Schoenherr, Sebastian; Fuchsberger, Christian; Pandit, Anita; Zawistowski, Matthew; Kheterpal, Sachin; Brummett, Chad M.; Natarajan, Pradeep; Schlessinger, David; Lee, Seunggeun; Kang, Hyun Min; Cucca, Francesco; Holmen, Oddgeir L.; Asvold, Bjorn O.; Boehnke, Michael; Kathiresan, Sekar; Abecasis, Goncalo R.; Chen, Y. Eugene; Willer, Cristen J.; Hveem, Kristian 分享 收藏 Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individualsDi Maio, Silvia; Grueneis, Rebecca; Streiter, Gertraud; Lamina, Claudia; Maglione, Manuel; Schoenherr, Sebastian; Ofner, Dietmar; Thorand, Barbara; Peters, Annette; Eckardt, Kai-Uwe; Koettgen, Anna; Kronenberg, Florian; Coassin, Stefan 分享 收藏 The Natural History of Ferroportin Disease-First Results of the International, Multicenter EASL non-HFE RegistrySchaefer, Benedikt; Viveiros, Andre; Corradini, Elena; Fiorini, Massimo; Scarlini, Stefania; Rametta, Raffaela; Pelucchi, Sara; Busti, Fabiana; Weissensteiner, Hansi; Schoenherr, Sebastian; Forer, Lukas; Subramaniam, Nathan; Bardou-Jacquet, Edouard; Ryan, John; Loreal, Olivier; Swinkels, Dorine; Sanchez, Mayka; Muckenthaler, Martina; Drakesmith, Alexander; Tilg, Herbert; Weiss, Gunter; Theurl, Igor; Kronenberg, Florian; Girelli, Domenico; Piperno, Alberto; Pietrangelo, Antonello; Valenti, Luca; Porto, Graca; Zoller, Heinz 分享 收藏 Reference-based phasing using the Haplotype Reference Consortium panel使用单倍型参考联盟小组进行基于参考的分阶段Loh, Po-Ru; Danecek, Petr; Palamara, Pier Francesco; Fuchsberger, Christian; Reshef, Yakir A.; Finucane, Hilary K.; Schoenherr, Sebastian; Forer, Lukas; McCarthy, Shane; Abecasis, Goncalo R.; Durbin, Richard; Price, Alkes L. 分享 收藏 
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