Berkman BE - Search Results

1

Incidental medical information in whole-exome sequencing.

Solomon BD, Hadley DW, Pineda-Alvarez DE; NISC Comparative Sequencing Program; Kamat A, Teer JK, Cherukuri PF, Hansen NF, Cruz P, Young AC, Berkman BE, Chandrasekharappa SC, Mullikin JC. Solomon BD, et al. Among authors: berkman be. Pediatrics. 2012 Jun;129(6):e1605-11. doi: 10.1542/peds.2011-0080. Epub 2012 May 14. Pediatrics. 2012. PMID: 22585771 Free PMC article.

2

Response to open peer commentaries on "Genomic inheritances: disclosing individual research results from whole-exome sequencing to deceased participants' relatives".

Hull SC, Chan B, Biesecker LG, Berkman BE. Hull SC, et al. Among authors: berkman be. Am J Bioeth. 2012;12(12):W9-10. doi: 10.1080/15265161.2012.739836. Am J Bioeth. 2012. PMID: 23215942 Free PMC article. No abstract available.

3

Do researchers have an obligation to actively look for genetic incidental findings?

Gliwa C, Berkman BE. Gliwa C, et al. Among authors: berkman be. Am J Bioeth. 2013;13(2):32-42. doi: 10.1080/15265161.2012.754062. Am J Bioeth. 2013. PMID: 23391059 Free PMC article.

4

Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.

Abdul-Karim R, Berkman BE, Wendler D, Rid A, Khan J, Badgett T, Hull SC. Abdul-Karim R, et al. Among authors: berkman be. Pediatrics. 2013 Mar;131(3):564-71. doi: 10.1542/peds.2012-0084. Epub 2013 Feb 11. Pediatrics. 2013. PMID: 23400601 Free PMC article. Review.

5

Grappling with genomic incidental findings in the clinical realm.

Hull SC, Berkman BE. Hull SC, et al. Among authors: berkman be. Chest. 2014 Feb;145(2):226-230. doi: 10.1378/chest.13-1976. Chest. 2014. PMID: 24493507 Free PMC article.

6

Institutional review board perspectives on obligations to disclose genetic incidental findings to research participants.

Gliwa C, Yurkiewicz IR, Lehmann LS, Hull SC, Jones N, Berkman BE. Gliwa C, et al. Among authors: berkman be. Genet Med. 2016 Jul;18(7):705-11. doi: 10.1038/gim.2015.149. Epub 2015 Nov 19. Genet Med. 2016. PMID: 26583685 Free PMC article.

7

Development of a consensus approach for return of pathology incidental findings in the Genotype-Tissue Expression (GTEx) project.

Lockhart NC, Weil CJ, Carithers LJ, Koester SE, Little AR, Volpi S, Moore HM, Berkman BE. Lockhart NC, et al. Among authors: berkman be. J Med Ethics. 2018 Sep;44(9):643-645. doi: 10.1136/medethics-2017-104691. Epub 2018 Jun 14. J Med Ethics. 2018. PMID: 29903854 Free PMC article.

8

When to Disclose a Borderline Incidental Finding.

McGrew S, Berkman BE. McGrew S, et al. Among authors: berkman be. Am J Bioeth. 2022 Oct;22(10):91-93. doi: 10.1080/15265161.2022.2110975. Am J Bioeth. 2022. PMID: 36170085 No abstract available.

9

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research.

Tabor HK, Berkman BE, Hull SC, Bamshad MJ. Tabor HK, et al. Among authors: berkman be. Am J Med Genet A. 2011 Dec;155A(12):2916-24. doi: 10.1002/ajmg.a.34357. Epub 2011 Oct 28. Am J Med Genet A. 2011. PMID: 22038764 Free PMC article.

10

Genomic inheritances: disclosing individual research results from whole-exome sequencing to deceased participants' relatives.

Chan B, Facio FM, Eidem H, Hull SC, Biesecker LG, Berkman BE. Chan B, et al. Among authors: berkman be. Am J Bioeth. 2012;12(10):1-8. doi: 10.1080/15265161.2012.699138. Am J Bioeth. 2012. PMID: 22974017 Free PMC article.

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