Powell CM - Search Results

1

The North Carolina Experience with Mucopolysaccharidosis Type I Newborn Screening.

Taylor JL, Clinard K, Powell CM, Rehder C, Young SP, Bali D, Beckloff SE, Gehtland LM, Kemper AR, Lee S, Millington D, Patel HS, Shone SM, Woodell C, Zimmerman SJ, Bailey DB Jr, Muenzer J. Taylor JL, et al. Among authors: powell cm. J Pediatr. 2019 Aug;211:193-200.e2. doi: 10.1016/j.jpeds.2019.04.027. Epub 2019 May 24. J Pediatr. 2019. PMID: 31133280

2

Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.

Bailey DB Jr, Skinner D, Davis AM, Whitmarsh I, Powell C. Bailey DB Jr, et al. Pediatrics. 2008 Mar;121(3):e693-704. doi: 10.1542/peds.2007-0820. Pediatrics. 2008. PMID: 18310190 Review.

3

Parents' decisions to screen newborns for FMR1 gene expansions in a pilot research project.

Skinner D, Choudhury S, Sideris J, Guarda S, Buansi A, Roche M, Powell C, Bailey DB Jr. Skinner D, et al. Pediatrics. 2011 Jun;127(6):e1455-63. doi: 10.1542/peds.2010-3078. Epub 2011 May 29. Pediatrics. 2011. PMID: 21624881 Free PMC article.

4

Design and evaluation of a decision aid for inviting parents to participate in a fragile X newborn screening pilot study.

Bailey DB Jr, Lewis MA, Harris SL, Grant T, Bann C, Bishop E, Roche M, Guarda S, Barnum L, Powell C, Therrell BL Jr. Bailey DB Jr, et al. J Genet Couns. 2013 Feb;22(1):108-17. doi: 10.1007/s10897-012-9511-0. Epub 2012 Jun 27. J Genet Couns. 2013. PMID: 22736213

5

Maternal Consequences of the Detection of Fragile X Carriers in Newborn Screening.

Bailey DB Jr, Wheeler A, Berry-Kravis E, Hagerman R, Tassone F, Powell CM, Roche M, Gane LW, Sideris J. Bailey DB Jr, et al. Among authors: powell cm. Pediatrics. 2015 Aug;136(2):e433-40. doi: 10.1542/peds.2015-0414. Epub 2015 Jul 13. Pediatrics. 2015. PMID: 26169437 Free PMC article.

6

Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.

Berg JS, Powell CM. Berg JS, et al. Among authors: powell cm. Cold Spring Harb Perspect Med. 2015 Oct 5;5(12):a023150. doi: 10.1101/cshperspect.a023150. Cold Spring Harb Perspect Med. 2015. PMID: 26438605 Free PMC article. Review.

7

Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid.

Lewis MA, Paquin RS, Roche MI, Furberg RD, Rini C, Berg JS, Powell CM, Bailey DB Jr. Lewis MA, et al. Among authors: powell cm. Pediatrics. 2016 Jan;137 Suppl 1(Suppl 1):S16-23. doi: 10.1542/peds.2015-3731E. Pediatrics. 2016. PMID: 26729698 Free PMC article.

8

Newborn Sequencing in Genomic Medicine and Public Health.

Berg JS, Agrawal PB, Bailey DB Jr, Beggs AH, Brenner SE, Brower AM, Cakici JA, Ceyhan-Birsoy O, Chan K, Chen F, Currier RJ, Dukhovny D, Green RC, Harris-Wai J, Holm IA, Iglesias B, Joseph G, Kingsmore SF, Koenig BA, Kwok PY, Lantos J, Leeder SJ, Lewis MA, McGuire AL, Milko LV, Mooney SD, Parad RB, Pereira S, Petrikin J, Powell BC, Powell CM, Puck JM, Rehm HL, Risch N, Roche M, Shieh JT, Veeraraghavan N, Watson MS, Willig L, Yu TW, Urv T, Wise AL. Berg JS, et al. Among authors: powell bc, powell cm. Pediatrics. 2017 Feb;139(2):e20162252. doi: 10.1542/peds.2016-2252. Epub 2017 Jan 17. Pediatrics. 2017. PMID: 28096516 Free PMC article. Clinical Trial.

9

Co-occurring Down syndrome and SUCLA2-related mitochondrial depletion syndrome.

Couser NL, Marchuk DS, Smith LD, Arreola A, Kaiser-Rogers KA, Muenzer J, Pandya A, Gucsavas-Calikoglu M, Powell CM. Couser NL, et al. Among authors: powell cm. Am J Med Genet A. 2017 Oct;173(10):2720-2724. doi: 10.1002/ajmg.a.38351. Epub 2017 Jul 27. Am J Med Genet A. 2017. PMID: 28749033

10

Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete-choice experiment.

Lewis MA, Stine A, Paquin RS, Mansfield C, Wood D, Rini C, Roche MI, Powell CM, Berg JS, Bailey DB Jr. Lewis MA, et al. Among authors: powell cm. Genet Med. 2018 Feb;20(2):181-189. doi: 10.1038/gim.2017.93. Epub 2017 Aug 3. Genet Med. 2018. PMID: 28771249 Free PMC article.

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