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Evaluating parents' decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol.
Milko LV, Rini C, Lewis MA, Butterfield RM, Lin FC, Paquin RS, Powell BC, Roche MI, Souris KJ, Bailey DB Jr, Berg JS, Powell CM. Milko LV, et al. Among authors: powell bc, powell cm. Trials. 2018 Jun 28;19(1):344. doi: 10.1186/s13063-018-2686-4. Trials. 2018. PMID: 29950170 Free PMC article.
Emerging dilemmas in newborn screening.
Bailey DB Jr, Skinner D, Roche MI, Powell C. Bailey DB Jr, et al. Virtual Mentor. 2009 Sep 1;11(9):709-13. doi: 10.1001/virtualmentor.2009.11.9.pfor2-0909. Virtual Mentor. 2009. PMID: 23199468 Free article. No abstract available.
A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.
Berg JS, Foreman AK, O'Daniel JM, Booker JK, Boshe L, Carey T, Crooks KR, Jensen BC, Juengst ET, Lee K, Nelson DK, Powell BC, Powell CM, Roche MI, Skrzynia C, Strande NT, Weck KE, Wilhelmsen KC, Evans JP. Berg JS, et al. Among authors: powell bc, powell cm. Genet Med. 2016 May;18(5):467-75. doi: 10.1038/gim.2015.104. Epub 2015 Aug 13. Genet Med. 2016. PMID: 26270767 Free PMC article.
178 results