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FHIR Genomics: enabling standardization for precision medicine use cases.
Alterovitz G, Heale B, Jones J, Kreda D, Lin F, Liu L, Liu X, Mandl KD, Poloway DW, Ramoni R, Wagner A, Warner JL. Alterovitz G, et al. Among authors: kreda d. NPJ Genom Med. 2020 Mar 18;5:13. doi: 10.1038/s41525-020-0115-6. eCollection 2020. NPJ Genom Med. 2020. PMID: 32194985 Free PMC article.
Computational prediction and validation of specific EmbR binding site on PknH.
Na I, Dai H, Li H, Gupta A, Kreda D, Zhang P, Chen X, Zhang L, Alterovitz G. Na I, et al. Among authors: kreda d. Synth Syst Biotechnol. 2021 Nov 26;6(4):429-436. doi: 10.1016/j.synbio.2021.11.006. eCollection 2021 Dec. Synth Syst Biotechnol. 2021. PMID: 34901481 Free PMC article.
SMART on FHIR Genomics: facilitating standardized clinico-genomic apps.
Alterovitz G, Warner J, Zhang P, Chen Y, Ullman-Cullere M, Kreda D, Kohane IS. Alterovitz G, et al. Among authors: kreda d. J Am Med Inform Assoc. 2015 Nov;22(6):1173-8. doi: 10.1093/jamia/ocv045. Epub 2015 Jul 21. J Am Med Inform Assoc. 2015. PMID: 26198304
The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification.
Wagner AH, Babb L, Alterovitz G, Baudis M, Brush M, Cameron DL, Cline M, Griffith M, Griffith OL, Hunt SE, Kreda D, Lee JM, Li S, Lopez J, Moyer E, Nelson T, Patel RY, Riehle K, Robinson PN, Rynearson S, Schuilenburg H, Tsukanov K, Walsh B, Konopko M, Rehm HL, Yates AD, Freimuth RR, Hart RK. Wagner AH, et al. Among authors: kreda d. Cell Genom. 2021 Nov 10;1(2):100027. doi: 10.1016/j.xgen.2021.100027. Cell Genom. 2021. PMID: 35311178 Free PMC article.
16 results