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Page 1
Enhanced specificity of clinical high-sensitivity tumor mutation profiling in cell-free DNA via paired normal sequencing using MSK-ACCESS.
Rose Brannon A, Jayakumaran G, Diosdado M, Patel J, Razumova A, Hu Y, Meng F, Haque M, Sadowska J, Murphy BJ, Baldi T, Johnson I, Ptashkin R, Hasan M, Srinivasan P, Rema AB, Rijo I, Agarunov A, Won H, Perera D, Brown DN, Samoila A, Jing X, Gedvilaite E, Yang JL, Stephens DP, Dix JM, DeGroat N, Nafa K, Syed A, Li A, Lebow ES, Bowman AS, Ferguson DC, Liu Y, Mata DA, Sharma R, Yang SR, Bale T, Benhamida JK, Chang JC, Dogan S, Hameed MR, Hechtman JF, Moung C, Ross DS, Vakiani E, Vanderbilt CM, Yao J, Razavi P, Smyth LM, Chandarlapaty S, Iyer G, Abida W, Harding JJ, Krantz B, O'Reilly E, Yu HA, Li BT, Rudin CM, Diaz L, Solit DB, Arcila ME, Ladanyi M, Loomis B, Tsui D, Berger MF, Zehir A, Benayed R. Rose Brannon A, et al. Among authors: degroat n. Nat Commun. 2021 Jun 18;12(1):3770. doi: 10.1038/s41467-021-24109-5. Nat Commun. 2021. PMID: 34145282 Free PMC article.
Implementation of an electronic genomic and family health history tool in primary prenatal care.
Edelman EA, Lin BK, Doksum T, Drohan B, Edelson V, Dolan SM, Hughes KS, O'Leary J, Galvin SL, Degroat N, Pardanani S, Feero WG, Adams C, Jones R, Scott J. Edelman EA, et al. Among authors: degroat n. Am J Med Genet C Semin Med Genet. 2014 Mar;166C(1):34-44. doi: 10.1002/ajmg.c.31389. Epub 2014 Mar 10. Am J Med Genet C Semin Med Genet. 2014. PMID: 24616345
Evaluation of a novel electronic genetic screening and clinical decision support tool in prenatal clinical settings.
Edelman EA, Lin BK, Doksum T, Drohan B, Edelson V, Dolan SM, Hughes K, O'Leary J, Vasquez L, Copeland S, Galvin SL, DeGroat N, Pardanani S, Gregory Feero W, Adams C, Jones R, Scott J. Edelman EA, et al. Among authors: degroat n. Matern Child Health J. 2014 Jul;18(5):1233-45. doi: 10.1007/s10995-013-1358-y. Matern Child Health J. 2014. PMID: 24101435