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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 4
2005 5
2006 8
2007 10
2008 22
2009 23
2010 22
2011 28
2012 16
2013 16
2014 11
2015 7
2016 7
2017 4
2018 1
2020 0
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170 results
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Page 1
Azithromycin Causes a Novel Proarrhythmic Syndrome.
Yang Z, Prinsen JK, Bersell KR, Shen W, Yermalitskaya L, Sidorova T, Luis PB, Hall L, Zhang W, Du L, Milne G, Tucker P, George AL Jr, Campbell CM, Pickett RA, Shaffer CM, Chopra N, Yang T, Knollmann BC, Roden DM, Murray KT. Yang Z, et al. Circ Arrhythm Electrophysiol. 2017 Apr;10(4):e003560. doi: 10.1161/CIRCEP.115.003560. Circ Arrhythm Electrophysiol. 2017. PMID: 28408648 Free PMC article.
Pharmacogenetics of Potassium Channel Blockers.
Roden DM. Roden DM. Card Electrophysiol Clin. 2016 Jun;8(2):385-93. doi: 10.1016/j.ccep.2016.02.003. Card Electrophysiol Clin. 2016. PMID: 27261829 Free PMC article. Review.
Genomic architecture of pharmacological efficacy and adverse events.
Chhibber A, Kroetz DL, Tantisira KG, McGeachie M, Cheng C, Plenge R, Stahl E, Sadee W, Ritchie MD, Pendergrass SA. Chhibber A, et al. Pharmacogenomics. 2014 Dec;15(16):2025-48. doi: 10.2217/pgs.14.144. Pharmacogenomics. 2014. PMID: 25521360 Free PMC article. Review.
Somatic mutations and atrial fibrillation: the end or just the beginning?
Lubitz SA, Ellinor PT. Lubitz SA, et al. Circ Cardiovasc Genet. 2015 Feb;8(1):2-3. doi: 10.1161/CIRCGENETICS.115.000963. Circ Cardiovasc Genet. 2015. PMID: 25691683 Free PMC article. No abstract available.
Gene-gene Interaction Analyses for Atrial Fibrillation.
Lin H, Mueller-Nurasyid M, Smith AV, Arking DE, Barnard J, Bartz TM, Lunetta KL, Lohman K, Kleber ME, Lubitz SA, Geelhoed B, Trompet S, Niemeijer MN, Kacprowski T, Chasman DI, Klarin D, Sinner MF, Waldenberger M, Meitinger T, Harris TB, Launer LJ, Soliman EZ, Chen LY, Smith JD, Van Wagoner DR, Rotter JI, Psaty BM, Xie Z, Hendricks AE, Ding J, Delgado GE, Verweij N, van der Harst P, Macfarlane PW, Ford I, Hofman A, Uitterlinden A, Heeringa J, Franco OH, Kors JA, Weiss S, Völzke H, Rose LM, Natarajan P, Kathiresan S, Kääb S, Gudnason V, Alonso A, Chung MK, Heckbert SR, Benjamin EJ, Liu Y, März W, Rienstra M, Jukema JW, Stricker BH, Dörr M, Albert CM, Ellinor PT. Lin H, et al. Sci Rep. 2016 Nov 8;6:35371. doi: 10.1038/srep35371. Sci Rep. 2016. PMID: 27824142 Free PMC article.
PharmCAT: A Pharmacogenomics Clinical Annotation Tool.
Klein TE, Ritchie MD. Klein TE, et al. Version 2. Clin Pharmacol Ther. 2018 Jul;104(1):19-22. doi: 10.1002/cpt.928. Epub 2017 Dec 1. Clin Pharmacol Ther. 2018. PMID: 29194583 Free PMC article.
Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines.
Chhibber A, French CE, Yee SW, Gamazon ER, Theusch E, Qin X, Webb A, Papp AC, Wang A, Simmons CQ, Konkashbaev A, Chaudhry AS, Mitchel K, Stryke D, Ferrin TE, Weiss ST, Kroetz DL, Sadee W, Nickerson DA, Krauss RM, George AL, Schuetz EG, Medina MW, Cox NJ, Scherer SE, Giacomini KM, Brenner SE. Chhibber A, et al. Version 2. Pharmacogenomics J. 2017 Mar;17(2):137-145. doi: 10.1038/tpj.2015.93. Epub 2016 Feb 9. Pharmacogenomics J. 2017. PMID: 26856248 Free PMC article.
A biologically informed method for detecting rare variant associations.
Moore CCB, Basile AO, Wallace JR, Frase AT, Ritchie MD. Moore CCB, et al. BioData Min. 2016 Aug 30;9(1):27. doi: 10.1186/s13040-016-0107-3. eCollection 2016. BioData Min. 2016. PMID: 27582876 Free PMC article.
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