O'Daniel JM - Search Results

1

Reflections on 'common' genetic medical history questions: Time to examine the what, why, and how.

Waltz M, Foreman AKM, Canter C, Cadigan RJ, O'Daniel JM. Waltz M, et al. Among authors: o daniel jm. Patient Educ Couns. 2024 May;122:108190. doi: 10.1016/j.pec.2024.108190. Epub 2024 Feb 5. Patient Educ Couns. 2024. PMID: 38340501

2

TRIG on TRACK: educating pathology residents in genomic medicine.

Haspel RL, Atkinson JB, Barr FG, Kaul KL, Leonard DG, O'Daniel J, Rinder HM, Scott J, Sobel ME, Speights VO. Haspel RL, et al. Per Med. 2012 May;9(3):287-293. doi: 10.2217/pme.12.6. Per Med. 2012. PMID: 29758790

3

Determining user preferences between touch and pen data entry methods in the Tablet PC computing environment.

Silvey GM, Haga SB, O'Daniel JM, Deverka P, Ermentrout DM, Anstrom KJ, Lobach DF. Silvey GM, et al. AMIA Annu Symp Proc. 2007 Oct 11:1115. AMIA Annu Symp Proc. 2007. PMID: 18694212

4

Enhancing geneticists' perspectives of the public through community engagement.

O'Daniel JM, Rosanbalm KD, Boles L, Tindall GM, Livingston TM, Haga SB. O'Daniel JM, et al. Genet Med. 2012 Feb;14(2):243-9. doi: 10.1038/gim.2011.29. Epub 2012 Jan 19. Genet Med. 2012. PMID: 22241095 Free PMC article.

5

CORRIGENDUM: ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

Green RC, Berg JS, Grody WW, Kalia SS, Korf BR, Martin CL, McGuire AL, Nussbaum RL, O'Daniel JM, Ormond KE, Rehm HL, Watson MS, Williams MS, Biesecker LG. Green RC, et al. Genet Med. 2017 May;19(5):606. doi: 10.1038/gim.2017.18. Genet Med. 2017. PMID: 28492529 Free article. No abstract available.

6

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. 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.

7

The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study.

Rini C, Khan CM, Moore E, Roche MI, Evans JP, Berg JS, Powell BC, Corbie-Smith G, Foreman AKM, Griesemer I, Lee K, O'Daniel JM, Henderson GE. Rini C, et al. Genet Med. 2018 Jul;20(7):760-769. doi: 10.1038/gim.2017.176. Epub 2017 Oct 26. Genet Med. 2018. PMID: 29261173 Free PMC article.

8

Factors influencing NCGENES research participants' requests for non-medically actionable secondary findings.

Roche MI, Griesemer I, Khan CM, Moore E, Lin FC, O'Daniel JM, Foreman AKM, Lee K, Powell BC, Berg JS, Evans JP, Henderson GE, Rini C. Roche MI, et al. Genet Med. 2019 May;21(5):1092-1099. doi: 10.1038/s41436-018-0294-z. Epub 2018 Sep 21. Genet Med. 2019. PMID: 30237575 Free PMC article.

9

An Age-Based Framework for Evaluating Genome-Scale Sequencing Results in Newborn Screening.

Milko LV, O'Daniel JM, DeCristo DM, Crowley SB, Foreman AKM, Wallace KE, Mollison LF, Strande NT, Girnary ZS, Boshe LJ, Aylsworth AS, Gucsavas-Calikoglu M, Frazier DM, Vora NL, Roche MI, Powell BC, Powell CM, Berg JS. Milko LV, et al. J Pediatr. 2019 Jun;209:68-76. doi: 10.1016/j.jpeds.2018.12.027. Epub 2019 Mar 7. J Pediatr. 2019. PMID: 30851990 Free PMC article.

10

Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes.

Rini C, Henderson GE, Evans JP, Berg JS, Foreman AKM, Griesemer I, Waltz M, O'Daniel JM, Roche MI. Rini C, et al. Genet Med. 2020 Jan;22(1):60-68. doi: 10.1038/s41436-019-0600-4. Epub 2019 Jul 17. Genet Med. 2020. PMID: 31312045 Free PMC article.

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