Skinner D - Search Results

1

Bailey DB Jr, Skinner D, Roche MI, Powell C. Bailey DB Jr, et al. Among authors: skinner d. 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.

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. Among authors: skinner d. Pediatrics. 2008 Mar;121(3):e693-704. doi: 10.1542/peds.2007-0820. Pediatrics. 2008. PMID: 18310190 Review.

3

How parents search, interpret, and evaluate genetic information obtained from the internet.

Roche MI, Skinner D. Roche MI, et al. Among authors: skinner d. J Genet Couns. 2009 Apr;18(2):119-29. doi: 10.1007/s10897-008-9198-4. Epub 2008 Oct 21. J Genet Couns. 2009. PMID: 18937062 Free PMC article.

4

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.

5

"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.

Tomlinson AN, Skinner D, Perry DL, Scollon SR, Roche MI, Bernhardt BA. Tomlinson AN, et al. Among authors: skinner d. J Genet Couns. 2016 Feb;25(1):62-72. doi: 10.1007/s10897-015-9842-8. Epub 2015 Apr 26. J Genet Couns. 2016. PMID: 25911622 Free PMC article.

6

Experiences with obtaining informed consent for genomic sequencing.

Bernhardt BA, Roche MI, Perry DL, Scollon SR, Tomlinson AN, Skinner D. Bernhardt BA, et al. Among authors: skinner d. Am J Med Genet A. 2015 Nov;167A(11):2635-46. doi: 10.1002/ajmg.a.37256. Epub 2015 Jul 21. Am J Med Genet A. 2015. PMID: 26198374 Free PMC article.

7

"Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing.

Skinner D, Roche MI, Weck KE, Raspberry KA, Foreman AKM, Strande NT, Berg JS, Evans JP, Henderson GE. Skinner D, et al. Genet Med. 2018 Mar;20(3):313-319. doi: 10.1038/gim.2017.135. Epub 2017 Oct 2. Genet Med. 2018. PMID: 29593351 Free PMC article.

8

Role of religion in the lives of Latino families of young children with developmental delays.

Skinner DG, Correa V, Skinner M, Bailey DB Jr. Skinner DG, et al. Among authors: skinner m. Am J Ment Retard. 2001 Jul;106(4):297-313. doi: 10.1352/0895-8017(2001)106<0297:RORITL>2.0.CO;2. Am J Ment Retard. 2001. PMID: 11414871

9

Family experiences and factors associated with the diagnosis of fragile X syndrome.

Bailey DB, Skinner D, Hatton D, Roberts J. Bailey DB, et al. Among authors: skinner d. J Dev Behav Pediatr. 2000 Oct;21(5):315-21. doi: 10.1097/00004703-200010000-00001. J Dev Behav Pediatr. 2000. PMID: 11064958

10

Needs and supports reported by Latino families of young children with developmental disabilities.

Bailey DB Jr, Skinner D, Correa V, Arcia E, Reyes-Blanes ME, Rodriguez P, Vázquez-Montilla E, Skinner M. Bailey DB Jr, et al. Among authors: skinner m, skinner d. Am J Ment Retard. 1999 Sep;104(5):437-51. doi: 10.1352/0895-8017(1999)104<0437:NASRBL>2.0.CO;2. Am J Ment Retard. 1999. PMID: 10541414

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