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Author Correction: Analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Moynihan D, Monaco S, Ting TW, Narasimhalu K, Hsieh J, Kam S, Lim JY, Lim WK, Davila S, Bylstra Y, Balakrishnan ID, Heng M, Chia E, Yeo KK, Goh BK, Gupta R, Tan T, Baynam G, Jamuar SS. Moynihan D, et al. Among authors: monaco s. Sci Rep. 2024 May 2;14(1):10084. doi: 10.1038/s41598-024-60776-2. Sci Rep. 2024. PMID: 38698204 Free PMC article. No abstract available.
Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Moynihan D, Monaco S, Ting TW, Narasimhalu K, Hsieh J, Kam S, Lim JY, Lim WK, Davila S, Bylstra Y, Balakrishnan ID, Heng M, Chia E, Yeo KK, Goh BK, Gupta R, Tan T, Baynam G, Jamuar SS. Moynihan D, et al. Among authors: monaco s. Sci Rep. 2024 Mar 1;14(1):5056. doi: 10.1038/s41598-024-55424-8. Sci Rep. 2024. PMID: 38424111 Free PMC article.
Recommendations for accelerating open preprint peer review to improve the culture of science.
Avissar-Whiting M, Belliard F, Bertozzi SM, Brand A, Brown K, Clément-Stoneham G, Dawson S, Dey G, Ecer D, Edmunds SC, Farley A, Fischer TD, Franko M, Fraser JS, Funk K, Ganier C, Harrison M, Hatch A, Hazlett H, Hindle S, Hook DW, Hurst P, Kamoun S, Kiley R, Lacy MM, LaFlamme M, Lawrence R, Lemberger T, Leptin M, Lumb E, MacCallum CJ, Marcum CS, Marinello G, Mendonça A, Monaco S, Neves K, Pattinson D, Polka JK, Puebla I, Rittman M, Royle SJ, Saderi D, Sever R, Shearer K, Spiro JE, Stern B, Taraborelli D, Vale R, Vasquez CG, Waltman L, Watt FM, Weinberg ZY, Williams M. Avissar-Whiting M, et al. Among authors: monaco s. PLoS Biol. 2024 Feb 29;22(2):e3002502. doi: 10.1371/journal.pbio.3002502. eCollection 2024 Feb. PLoS Biol. 2024. PMID: 38421949 Free PMC article.
664 results