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Young, William J; Lahrouchi, Najim; Isaacs, Aaron; Duong, ThuyVy; Foco, Luisa; Ahmed, Farah; Brody, Jennifer A; Salman, Reem; Noordam, Raymond; Benjamins, Jan-Walter; Haessler, Jeffrey; Lyytikäinen, Leo-Pekka; Repetto, Linda; Concas, Maria Pina; van den Berg, Marten E; Weiss, Stefan; Baldassari, Antoine R; Bartz, Traci M; Cook, James P; Evans, Daniel S; ... (2022). Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. Nature communications, 13(1), p. 5144. Nature Publishing Group 10.1038/s41467-022-32821-z
Wang, Zhe; Emmerich, Andrew; Pillon, Nicolas J; Moore, Tim; Hemerich, Daiane; Cornelis, Marilyn C; Mazzaferro, Eugenia; Broos, Siacia; Ahluwalia, Tarunveer S; Bartz, Traci M; Bentley, Amy R; Bielak, Lawrence F; Chong, Mike; Chu, Audrey Y; Berry, Diane; Dorajoo, Rajkumar; Dueker, Nicole D; Kasbohm, Elisa; Feenstra, Bjarke; Feitosa, Mary F; ... (2022). Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nature genetics, 54(9), pp. 1332-1344. Nature America 10.1038/s41588-022-01165-1
Castaneda, Andy B; Petty, Lauren E; Scholz, Markus; Jansen, Rick; Weiss, Stefan; Zhang, Xiaoling; Schramm, Katharina; Beutner, Frank; Kirsten, Holger; Schminke, Ulf; Hwang, Shih-Jen; Marzi, Carola; Dhana, Klodian; Seldenrijk, Adrie; Krohn, Knut; Homuth, Georg; Wolf, Petra; Peters, Marjolein J; Dörr, Marcus; Peters, Annette; ... (2022). Associations of carotid intima media thickness with gene expression in whole blood and genetically predicted gene expression across 48 tissues. Human molecular genetics, 31(7), pp. 1171-1182. Oxford University Press 10.1093/hmg/ddab236
Barc, Julien; Tadros, Rafik; Glinge, Charlotte; Chiang, David Y.; Jouni, Mariam; Simonet, Floriane; Jurgens, Sean J.; Baudic, Manon; Nicastro, Michele; Potet, Franck; Offerhaus, Joost A.; Walsh, Roddy; Choi, Seung Hoan; Verkerk, Arie O.; Mizusawa, Yuka; Anys, Soraya; Minois, Damien; Arnaud, Marine; Duchateau, Josselin; Wijeyeratne, Yanushi D.; ... (2022). Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature genetics, 54(3), pp. 232-239. Springer Nature 10.1038/s41588-021-01007-6
Ochoa-Rosales, Carolina; Portilla-Fernandez, Eliana; Nano, Jana; Wilson, Rory; Lehne, Benjamin; Mishra, Pashupati P; Gao, Xu; Ghanbari, Mohsen; Rueda-Ochoa, Oscar L; Juvinao-Quintero, Diana; Loh, Marie; Zhang, Weihua; Kooner, Jaspal S; Grabe, Hans J; Felix, Stephan B; Schöttker, Ben; Zhang, Yan; Gieger, Christian; Müller-Nurasyid, Martina; Heier, Margit; ... (2020). Epigenetic Link Between Statin Therapy and Type 2 Diabetes. Diabetes care, 43(4), pp. 875-884. American Diabetes Association 10.2337/dc19-1828
Teumer, Alexander; Li, Yong; Ghasemi, Sahar; Prins, Bram P; Wuttke, Matthias; Hermle, Tobias; Giri, Ayush; Sieber, Karsten B; Qiu, Chengxiang; Kirsten, Holger; Tin, Adrienne; Chu, Audrey Y; Bansal, Nisha; Feitosa, Mary F; Wang, Lihua; Chai, Jin-Fang; Cocca, Massimiliano; Fuchsberger, Christian; Gorski, Mathias; Hoppmann, Anselm; ... (2019). Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nature communications, 10(1), p. 4130. Nature Publishing Group 10.1038/s41467-019-11576-0
Fiorito, Giovanni; McCrory, Cathal; Robinson, Oliver; Carmeli, Cristian; Rosales, Carolina Ochoa; Zhang, Yan; Colicino, Elena; Dugué, Pierre-Antoine; Artaud, Fanny; McKay, Gareth J; Jeong, Ayoung; Mishra, Pashupati P; Nøst, Therese H; Krogh, Vittorio; Panico, Salvatore; Sacerdote, Carlotta; Tumino, Rosario; Palli, Domenico; Matullo, Giuseppe; Guarrera, Simonetta; ... (2019). Socioeconomic position, lifestyle habits and biomarkers of epigenetic aging: a multi-cohort analysis. Aging, 11(7), pp. 2045-2070. Impact Journals 10.18632/aging.101900
Ligthart, Symen; Vaez, Ahmad; Võsa, Urmo; Stathopoulou, Maria G; de Vries, Paul S; Prins, Bram P; Van der Most, Peter J; Tanaka, Toshiko; Naderi, Elnaz; Rose, Lynda M; Wu, Ying; Karlsson, Robert; Barbalic, Maja; Lin, Honghuang; Pool, René; Zhu, Gu; Macé, Aurélien; Sidore, Carlo; Trompet, Stella; Mangino, Massimo; ... (2018). Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American journal of human genetics, 103(5), pp. 691-706. Cell Press 10.1016/j.ajhg.2018.09.009
Evangelou, Evangelos; Warren, Helen R; Mosen-Ansorena, David; Mifsud, Borbala; Pazoki, Raha; Gao, He; Ntritsos, Georgios; Dimou, Niki; Cabrera, Claudia P; Karaman, Ibrahim; Ng, Fu Liang; Evangelou, Marina; Witkowska, Katarzyna; Tzanis, Evan; Hellwege, Jacklyn N; Giri, Ayush; Velez Edwards, Digna R; Sun, Yan V; Cho, Kelly; Gaziano, J Michael; ... (2018). Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Nature genetics, 50(10), pp. 1412-1425. Nature America 10.1038/s41588-018-0205-x
Christophersen, Ingrid E; Rienstra, Michiel; Roselli, Carolina; Yin, Xiaoyan; Geelhoed, Bastiaan; Barnard, John; Lin, Honghuang; Arking, Dan E; Smith, Albert V; Albert, Christine M; Chaffin, Mark; Tucker, Nathan R; Li, Molong; Klarin, Derek; Bihlmeyer, Nathan A; Low, Siew-Kee; Weeke, Peter E; Müller-Nurasyid, Martina; Smith, J Gustav; Brody, Jennifer A; ... (2017). Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nature genetics, 49(6), pp. 946-952. Nature America 10.1038/ng.3843
Zewinger, Stephen; Drechsler, Christiane; Kleber, Marcus E; Dressel, Alexander; Riffel, Julia; Triem, Sarah; Lehmann, Marlene; Kopecky, Chantal; Säemann, Marcus D; Lepper, Philipp M; Silbernagel, Günther; Scharnagl, Hubert; Ritsch, Andreas; Thorand, Barbara; de las Heras Gala, Tonia; Wagenpfeil, Stefan; Koenig, Wolfgang; Peters, Annette; Laufs, Ulrich; Wanner, Christoph; ... (2015). Serum amyloid A: high-density lipoproteins interaction and cardiovascular risk. European Heart Journal, 36(43), pp. 3007-3016. Oxford University Press 10.1093/eurheartj/ehv352
Arking, Dan E; Pulit, Sara L; Crotti, Lia; van der Harst, Pim; Munroe, Patricia B; Koopmann, Tamara T; Sotoodehnia, Nona; Rossin, Elizabeth J; Morley, Michael; Wang, Xinchen; Johnson, Andrew D; Lundby, Alicia; Gudbjartsson, Daníel F; Noseworthy, Peter A; Eijgelsheim, Mark; Bradford, Yuki; Tarasov, Kirill V; Dörr, Marcus; Müller-Nurasyid, Martina; Lahtinen, Annukka M; ... (2014). Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature genetics, 46(8), pp. 826-836. Nature America 10.1038/ng.3014
Lubitz, Steven A; Lunetta, Kathryn L; Lin, Honghuang; Arking, Dan E; Trompet, Stella; Li, Guo; Krijthe, Bouwe P; Chasman, Daniel I; Barnard, John; Kleber, Marcus E; Dörr, Marcus; Ozaki, Kouichi; Smith, Albert V; Müller-Nurasyid, Martina; Walter, Stefan; Agarwal, Sunil K; Bis, Joshua C; Brody, Jennifer A; Chen, Lin Y; Everett, Brendan M; ... (2014). Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. Journal of the American College of Cardiology, 63(12), pp. 1200-1210. Elsevier 10.1016/j.jacc.2013.12.015
Oexle, Konrad; Schormair, Barbara; Ried, Janina S.; Czamara, Darina; Heim, Katharina; Frauscher, Birgit; Högl, Birgit; Trenkwalder, Claudia; Fiedler, G. Martin; Thiery, Joachim; Lichtner, Peter; Prokisch, Holger; Specht, Michael; Müller-Myhsok, Bertram; Döring, Angela; Gieger, Christian; Peters, Annette; Wichmann, H.-Erich; Meitinger, Thomas and Winkelmann, Juliane (2013). Dilution of candidates: the case of iron-related genes in restless legs syndrome. European journal of human genetics, 21(4), pp. 410-414. Nature Publishing Group 10.1038/ejhg.2012.193
Peters, Annette; Veronesi, Bellina; Calderón-Garcidueñas, Lilian; Gehr, Peter; Chen, Lung Chi; Geiser, Marianne; Reed, William; Rothen-Rutishauser, Barbara; Schürch, Samuel; Schulz, Holger (2006). Translocation and potential neurological effects of fine and ultrafine particles a critical update. Particle and fibre toxicology, 3, p. 13. London: BioMed Central 10.1186/1743-8977-3-13
