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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: ullman cullere m. 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
OncDRS: An integrative clinical and genomic data platform for enabling translational research and precision medicine.
Orechia J, Pathak A, Shi Y, Nawani A, Belozerov A, Fontes C, Lakhiani C, Jawale C, Patel C, Quinn D, Botvinnik D, Mei E, Cotter E, Byleckie J, Ullman-Cullere M, Chhetri P, Chalasani P, Karnam P, Beaudoin R, Sahu S, Belozerova Y, Mathew JP. Orechia J, et al. Among authors: ullman cullere m. Appl Transl Genom. 2015 Sep 14;6:18-25. doi: 10.1016/j.atg.2015.08.005. eCollection 2015 Sep. Appl Transl Genom. 2015. PMID: 27054074 Free PMC article.
Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.
Lubin IM, Aziz N, Babb LJ, Ballinger D, Bisht H, Church DM, Cordes S, Eilbeck K, Hyland F, Kalman L, Landrum M, Lockhart ER, Maglott D, Marth G, Pfeifer JD, Rehm HL, Roy S, Tezak Z, Truty R, Ullman-Cullere M, Voelkerding KV, Worthey EA, Zaranek AW, Zook JM. Lubin IM, et al. Among authors: ullman cullere m. J Mol Diagn. 2017 May;19(3):417-426. doi: 10.1016/j.jmoldx.2016.12.001. Epub 2017 Mar 18. J Mol Diagn. 2017. PMID: 28315672 Free PMC article.
12 results