Burke W - Search Results

1

Wilfond BS, Magnus D, Antommaria AH, Appelbaum P, Aschner J, Barrington KJ, Beauchamp T, Boss RD, Burke W, Caplan AL, Capron AM, Cho M, Clayton EW, Cole FS, Darlow BA, Diekema D, Faden RR, Feudtner C, Fins JJ, Fost NC, Frader J, Hester DM, Janvier A, Joffe S, Kahn J, Kass NE, Kodish E, Lantos JD, McCullough L, McKinney R Jr, Meadow W, O'Rourke PP, Powderly KE, Pursley DM, Ross LF, Sayeed S, Sharp RR, Sugarman J, Tarnow-Mordi WO, Taylor H, Tomlinson T, Truog RD, Unguru YT, Weise KL, Woodrum D, Youngner S. Wilfond BS, et al. Among authors: burke w. N Engl J Med. 2013 Jun 20;368(25):e36. doi: 10.1056/NEJMc1307008. Epub 2013 Jun 5. N Engl J Med. 2013. PMID: 23738513 No abstract available.

2

Newborn screening technology: proceed with caution.

Botkin JR, Clayton EW, Fost NC, Burke W, Murray TH, Baily MA, Wilfond B, Berg A, Ross LF. Botkin JR, et al. Among authors: burke w. Pediatrics. 2006 May;117(5):1793-9. doi: 10.1542/peds.2005-2547. Pediatrics. 2006. PMID: 16651338 No abstract available.

3

Ethical issues arising from the participation of children in genetic research.

Burke W, Diekema DS. Burke W, et al. J Pediatr. 2006 Jul;149(1 Suppl):S34-8. doi: 10.1016/j.jpeds.2006.04.049. J Pediatr. 2006. PMID: 16829241

4

Waiving informed consent in newborn screening research: balancing social value and respect.

Tarini BA, Burke W, Scott CR, Wilfond BS. Tarini BA, et al. Among authors: burke w. Am J Med Genet C Semin Med Genet. 2008 Feb 15;148C(1):23-30. doi: 10.1002/ajmg.c.30164. Am J Med Genet C Semin Med Genet. 2008. PMID: 18200521

5

Offering aggregate results to participants in genomic research: opportunities and challenges.

Beskow LM, Burke W, Fullerton SM, Sharp RR. Beskow LM, et al. Among authors: burke w. Genet Med. 2012 Apr;14(4):490-6. doi: 10.1038/gim.2011.62. Epub 2012 Jan 26. Genet Med. 2012. PMID: 22261761 Free PMC article.

6

Seeking Genomic Knowledge: The Case for Clinical Restraint.

Burke W, Trinidad SB, Clayton EW. Burke W, et al. Hastings Law J. 2013 Aug 1;64(6):1650-1664. Hastings Law J. 2013. PMID: 24688162 Free PMC article.

7

The translational potential of research on the ethical, legal, and social implications of genomics.

Burke W, Appelbaum P, Dame L, Marshall P, Press N, Pyeritz R, Sharp R, Juengst E. Burke W, et al. Genet Med. 2015 Jan;17(1):12-20. doi: 10.1038/gim.2014.74. Epub 2014 Jun 19. Genet Med. 2015. PMID: 24946153 Free PMC article. Review.

8

Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.

Wolf SM, Amendola LM, Berg JS, Chung WK, Clayton EW, Green RC, Harris-Wai J, Henderson GE, Jarvik GP, Koenig BA, Lehmann LS, McGuire AL, O'Rourke P, Somkin C, Wilfond BS, Burke W. Wolf SM, et al. Among authors: burke w. Genet Med. 2018 Apr;20(5):545-553. doi: 10.1038/gim.2017.137. Epub 2017 Aug 31. Genet Med. 2018. PMID: 28858330 Free PMC article.

9

Is there a duty to reinterpret genetic data? The ethical dimensions.

Appelbaum PS, Parens E, Berger SM, Chung WK, Burke W. Appelbaum PS, et al. Among authors: burke w. Genet Med. 2020 Mar;22(3):633-639. doi: 10.1038/s41436-019-0679-7. Epub 2019 Oct 15. Genet Med. 2020. PMID: 31616070 Free PMC article.

10

Deliberate deceit of family members: a challenge to providers of clinical genetics services.

Loud JT, Weissman NE, Peters JA, Giusti RM, Wilfond BS, Burke W, Greene MH. Loud JT, et al. Among authors: burke w. J Clin Oncol. 2006 Apr 1;24(10):1643-6. doi: 10.1200/JCO.2005.02.6203. J Clin Oncol. 2006. PMID: 16575016 No abstract available.

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