Pramstaller, Peter P

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Number of items: 12.

Journal Article

Young, William J; Haessler, Jeffrey; Benjamins, Jan-Walter; Repetto, Linda; Yao, Jie; Isaacs, Aaron; Harper, Andrew R; Ramirez, Julia; Garnier, Sophie; van Duijvenboden, Stefan; Baldassari, Antoine R; Concas, Maria Pina; Duong, ThuyVy; Foco, Luisa; Isaksen, Jonas L; Mei, Hao; Noordam, Raymond; Nursyifa, Casia; Richmond, Anne; Santolalla, Meddly L; ... (2023). Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Nature communications, 14(1), p. 1411. Nature Publishing Group 10.1038/s41467-023-36997-w

Pramstaller, Peter P; Berlit, Peter; Bassetti, Claudio L A; Klein, Christine (2022). What if I could become the doctor I always wanted to be? European journal of neurology, 29(12), pp. 3481-3483. Wiley 10.1111/ene.15548

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

Liu, Jun; de Vries, Paul S; Del Greco M, Fabiola; Johansson, Åsa; Schraut, Katharina E; Hayward, Caroline; van Dijk, Ko Willems; Franco, Oscar H.; Hicks, Andrew A; Vitart, Veronique; Rudan, Igor; Campbell, Harry; Polašek, Ozren; Pramstaller, Peter P; Wilson, James F; Gyllensten, Ulf; van Duijn, Cornelia M; Dehghan, Abbas; Demirkan, Ayşe (2022). A multi-omics study of circulating phospholipid markers of blood pressure. Scientific Reports, 12(1), p. 574. Nature Publishing Group 10.1038/s41598-021-04446-7

Clark, David W; Okada, Yukinori; Moore, Kristjan H S; Mason, Dan; Pirastu, Nicola; Gandin, Ilaria; Mattsson, Hannele; Barnes, Catriona L K; Lin, Kuang; Zhao, Jing Hua; Deelen, Patrick; Rohde, Rebecca; Schurmann, Claudia; Guo, Xiuqing; Giulianini, Franco; Zhang, Weihua; Medina-Gomez, Carolina; Karlsson, Robert; Bao, Yanchun; Bartz, Traci M; ... (2019). Associations of autozygosity with a broad range of human phenotypes. Nature communications, 10(1), p. 4957. Nature Publishing Group 10.1038/s41467-019-12283-6

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

Wuttke, Matthias; Li, Yong; Li, Man; Sieber, Karsten B; Feitosa, Mary F; Gorski, Mathias; Tin, Adrienne; Wang, Lihua; Chu, Audrey Y; Hoppmann, Anselm; Kirsten, Holger; Giri, Ayush; Chai, Jin-Fang; Sveinbjornsson, Gardar; Tayo, Bamidele O; Nutile, Teresa; Fuchsberger, Christian; Marten, Jonathan; Cocca, Massimiliano; Ghasemi, Sahar; ... (2019). A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nature genetics, 51(6), pp. 957-972. Nature America 10.1038/s41588-019-0407-x

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

Pattaro, Cristian; Teumer, Alexander; Gorski, Mathias; Chu, Audrey Y; Li, Man; Mijatovic, Vladan; Garnaas, Maija; Tin, Adrienne; Sorice, Rossella; Li, Yong; Taliun, Daniel; Olden, Matthias; Foster, Meredith; Yang, Qiong; Chen, Ming-Huei; Pers, Tune H; Johnson, Andrew D; Ko, Yi-An; Fuchsberger, Christian; Tayo, Bamidele; ... (2016). Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nature communications, 7, p. 10023. Nature Publishing Group 10.1038/ncomms10023

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

Oexle, Konrad; Ried, Janina S; Hicks, Andrew A; Tanaka, Toshiko; Hayward, Caroline; Bruegel, Mathias; Gögele, Martin; Lichtner, Peter; Müller-Myhsok, Bertram; Döring, Angela; Illig, Thomas; Schwienbacher, Christine; Minelli, Cosetta; Pichler, Irene; Fiedler, G Martin; Thiery, Joachim; Rudan, Igor; Wright, Alan F; Campbell, Harry; Ferrucci, Luigi; ... (2011). Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Human molecular genetics, 20(5), pp. 1042-7. Oxford: Oxford University Press 10.1093/hmg/ddq538

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