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Year Number of Results
2012 1
2013 1
2014 1
2015 2
2016 2
2017 2
2018 1
2019 1
2020 2
2021 1
2022 1
2023 4
2024 0

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Page 1
Connecting the Dots in Atrial Fibrillation.
Nurnberg ST. Nurnberg ST. Circ Cardiovasc Genet. 2017 Oct;10(5):e001908. doi: 10.1161/CIRCGENETICS.117.001908. Circ Cardiovasc Genet. 2017. PMID: 28974515 No abstract available.
Pragmatic screening for heart failure in the general population using an electrocardiogram-based neural network.
Surendra K, Nürnberg S, Bremer JP, Knorr MS, Ückert F, Wenzel JP, Bei der Kellen R, Westermann D, Schnabel RB, Twerenbold R, Magnussen C, Kirchhof P, Blankenberg S, Neumann J, Schrage B. Surendra K, et al. Among authors: nurnberg s. ESC Heart Fail. 2023 Apr;10(2):975-984. doi: 10.1002/ehf2.14263. Epub 2022 Dec 8. ESC Heart Fail. 2023. PMID: 36482800 Free PMC article.
Transcriptional diversity during lineage commitment of human blood progenitors.
Chen L, Kostadima M, Martens JHA, Canu G, Garcia SP, Turro E, Downes K, Macaulay IC, Bielczyk-Maczynska E, Coe S, Farrow S, Poudel P, Burden F, Jansen SBG, Astle WJ, Attwood A, Bariana T, de Bono B, Breschi A, Chambers JC, Consortium B, Choudry FA, Clarke L, Coupland P, van der Ent M, Erber WN, Jansen JH, Favier R, Fenech ME, Foad N, Freson K, van Geet C, Gomez K, Guigo R, Hampshire D, Kelly AM, Kerstens HHD, Kooner JS, Laffan M, Lentaigne C, Labalette C, Martin T, Meacham S, Mumford A, Nürnberg S, Palumbo E, van der Reijden BA, Richardson D, Sammut SJ, Slodkowicz G, Tamuri AU, Vasquez L, Voss K, Watt S, Westbury S, Flicek P, Loos R, Goldman N, Bertone P, Read RJ, Richardson S, Cvejic A, Soranzo N, Ouwehand WH, Stunnenberg HG, Frontini M, Rendon A. Chen L, et al. Among authors: nurnberg s. Science. 2014 Sep 26;345(6204):1251033. doi: 10.1126/science.1251033. Science. 2014. PMID: 25258084 Free PMC article.
Genetic Regulatory Mechanisms of Smooth Muscle Cells Map to Coronary Artery Disease Risk Loci.
Liu B, Pjanic M, Wang T, Nguyen T, Gloudemans M, Rao A, Castano VG, Nurnberg S, Rader DJ, Elwyn S, Ingelsson E, Montgomery SB, Miller CL, Quertermous T. Liu B, et al. Among authors: nurnberg s. Am J Hum Genet. 2018 Sep 6;103(3):377-388. doi: 10.1016/j.ajhg.2018.08.001. Epub 2018 Aug 23. Am J Hum Genet. 2018. PMID: 30146127 Free PMC article.
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseases.
Nurnberg ST, Guerraty MA, Wirka RC, Rao HS, Pjanic M, Norton S, Serrano F, Perisic L, Elwyn S, Pluta J, Zhao W, Testa S, Park Y, Nguyen T, Ko YA, Wang T, Hedin U, Sinha S, Barash Y, Brown CD, Quertermous T, Rader DJ. Nurnberg ST, et al. PLoS Genet. 2020 Jan 9;16(1):e1008538. doi: 10.1371/journal.pgen.1008538. eCollection 2020 Jan. PLoS Genet. 2020. PMID: 31917787 Free PMC article.
17 results