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

Year Number of Results
1979 1
1995 1
2000 1
2001 1
2002 2
2006 1
2007 1
2008 1
2009 1
2010 1
2011 1
2012 4
2013 7
2014 13
2015 4
2016 6
2017 9
2018 13
2019 4
2020 6
2021 21
2022 4
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94 results
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Page 1
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.
Bastarache L, Hughey JJ, Hebbring S, Marlo J, Zhao W, Ho WT, Van Driest SL, McGregor TL, Mosley JD, Wells QS, Temple M, Ramirez AH, Carroll R, Osterman T, Edwards T, Ruderfer D, Velez Edwards DR, Hamid R, Cogan J, Glazer A, Wei WQ, Feng Q, Brilliant M, Zhao ZJ, Cox NJ, Roden DM, Denny JC. Bastarache L, et al. Among authors: mosley jd. Science. 2018 Mar 16;359(6381):1233-1239. doi: 10.1126/science.aal4043. Science. 2018. PMID: 29590070 Free PMC article.
Benefit of Preemptive Pharmacogenetic Information on Clinical Outcome.
Roden DM, Van Driest SL, Mosley JD, Wells QS, Robinson JR, Denny JC, Peterson JF. Roden DM, et al. Among authors: mosley jd. Clin Pharmacol Ther. 2018 May;103(5):787-794. doi: 10.1002/cpt.1035. Epub 2018 Mar 13. Clin Pharmacol Ther. 2018. PMID: 29377064 Free PMC article. Review.
Proteomic profiling reveals biomarkers and pathways in type 2 diabetes risk.
Ngo D, Benson MD, Long JZ, Chen ZZ, Wang R, Nath AK, Keyes MJ, Shen D, Sinha S, Kuhn E, Morningstar JE, Shi X, Peterson BD, Chan C, Katz DH, Tahir UA, Farrell LA, Melander O, Mosley JD, Carr SA, Vasan RS, Larson MG, Smith JG, Wang TJ, Yang Q, Gerszten RE. Ngo D, et al. Among authors: mosley jd. JCI Insight. 2021 Mar 8;6(5):e144392. doi: 10.1172/jci.insight.144392. JCI Insight. 2021. PMID: 33591955 Free PMC article.
Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics.
Li R, Duan R, Zhang X, Lumley T, Pendergrass S, Bauer C, Hakonarson H, Carrell DS, Smoller JW, Wei WQ, Carroll R, Velez Edwards DR, Wiesner G, Sleiman P, Denny JC, Mosley JD, Ritchie MD, Chen Y, Moore JH. Li R, et al. Among authors: mosley jd. Nat Commun. 2021 Jan 8;12(1):168. doi: 10.1038/s41467-020-20211-2. Nat Commun. 2021. PMID: 33420026 Free PMC article.
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants.
Kozek K, Wada Y, Sala L, Denjoy I, Egly C, O'Neill MJ, Aiba T, Shimizu W, Makita N, Ishikawa T, Crotti L, Spazzolini C, Kotta MC, Dagradi F, Castelletti S, Pedrazzini M, Gnecchi M, Leenhardt A, Salem JE, Ohno S, Zuo Y, Glazer AM, Mosley JD, Roden DM, Knollmann BC, Blume JD, Extramiana F, Schwartz PJ, Horie M, Kroncke BM. Kozek K, et al. Among authors: mosley jd. Circ Genom Precis Med. 2021 Aug;14(4):e003289. doi: 10.1161/CIRCGEN.120.003289. Epub 2021 Jul 26. Circ Genom Precis Med. 2021. PMID: 34309407
Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults.
Wells QS, Bagheri M, Aday AW, Gupta DK, Shaffer CM, Wei WQ, Vaitinadin NS, Khan SS, Greenland P, Wang TJ, Stein CM, Roden DM, Mosley JD. Wells QS, et al. Among authors: mosley jd. Circ Genom Precis Med. 2021 Oct;14(5):e003341. doi: 10.1161/CIRCGEN.121.003341. Epub 2021 Aug 31. Circ Genom Precis Med. 2021. PMID: 34463132
94 results