West KM - Search Results

1

At the Research-Clinical Interface: Returning Individual Genetic Results to Research Participants.

West KM, Blacksher E, Cavanaugh KL, Fullerton SM, Umeukeje EM, Young BA, Burke W. West KM, et al. Clin J Am Soc Nephrol. 2020 Aug 7;15(8):1181-1189. doi: 10.2215/CJN.09670819. Epub 2020 Feb 10. Clin J Am Soc Nephrol. 2020. PMID: 32041801 Free PMC article. Review.

2

dbGaP data access requests: a call for greater transparency.

Walker L, Starks H, West KM, Fullerton SM. Walker L, et al. Among authors: west km. Sci Transl Med. 2011 Dec 14;3(113):113cm34. doi: 10.1126/scitranslmed.3002788. Sci Transl Med. 2011. PMID: 22174311 Free PMC article.

3

Exploring pathways to trust: a tribal perspective on data sharing.

James R, Tsosie R, Sahota P, Parker M, Dillard D, Sylvester I, Lewis J, Klejka J, Muzquiz L, Olsen P, Whitener R, Burke W; Kiana Group. James R, et al. Genet Med. 2014 Nov;16(11):820-6. doi: 10.1038/gim.2014.47. Epub 2014 May 15. Genet Med. 2014. PMID: 24830328 Free PMC article. Review.

4

Genomics, Health Disparities, and Missed Opportunities for the Nation's Research Agenda.

West KM, Blacksher E, Burke W. West KM, et al. JAMA. 2017 May 9;317(18):1831-1832. doi: 10.1001/jama.2017.3096. JAMA. 2017. PMID: 28346599 Free PMC article. No abstract available.

5

Identifying "ownership" through role descriptions to support implementing universal colorectal cancer tumor screening for Lynch syndrome.

West KM, Burke W, Korngiebel DM. West KM, et al. Genet Med. 2017 Nov;19(11):1236-1244. doi: 10.1038/gim.2017.39. Epub 2017 May 4. Genet Med. 2017. PMID: 28471433 Free PMC article.

6

Clinician-Stakeholders' Perspectives on Using Patient Portals to Return Lynch Syndrome Screening Results.

Korngiebel DM, West KM, Burke W. Korngiebel DM, et al. Among authors: west km. J Genet Couns. 2018 Apr;27(2):349-357. doi: 10.1007/s10897-017-0179-3. Epub 2017 Nov 21. J Genet Couns. 2018. PMID: 29159545 Free PMC article.

7

Responsible Research With Urban American Indians and Alaska Natives.

James RD, West KM, Claw KG, EchoHawk A, Dodge L, Dominguez A, Taualii M, Forquera R, Thummel K, Burke W. James RD, et al. Among authors: west km. Am J Public Health. 2018 Dec;108(12):1613-1616. doi: 10.2105/AJPH.2018.304708. Epub 2018 Oct 25. Am J Public Health. 2018. PMID: 30359103 Free PMC article. Review.

8

Apolipoprotein L1 Testing in African Americans: Involving the Community in Policy Discussions.

Young BA, Blacksher E, Cavanaugh KL, Freedman BI, Fullerton SM, Kopp JB, Umeukeje EM, West KM, Wilson JG, Burke W; APOL1 Stakeholders Project. Young BA, et al. Among authors: west km. Am J Nephrol. 2019;50(4):303-311. doi: 10.1159/000502675. Epub 2019 Sep 3. Am J Nephrol. 2019. PMID: 31480040 Free PMC article.

9

Preimplantation Genetic Testing for Genetic Kidney Disease: Addressing Moral Uncertainties and Access Inequity.

Burke W, West KM. Burke W, et al. Among authors: west km. Clin J Am Soc Nephrol. 2020 Sep 7;15(9):1231-1233. doi: 10.2215/CJN.11790720. Epub 2020 Aug 27. Clin J Am Soc Nephrol. 2020. PMID: 32895299 Free PMC article. No abstract available.

10

Stakeholder Perspectives on Returning Nonactionable Apolipoprotein L1 (APOL1) Genetic Results to African American Research Participants.

West KM, Cavanaugh KL, Blacksher E, Fullerton SM, Umeukeje EM, Young B, Burke W. West KM, et al. J Empir Res Hum Res Ethics. 2022 Feb-Apr;17(1-2):4-14. doi: 10.1177/15562646211063267. Epub 2021 Dec 6. J Empir Res Hum Res Ethics. 2022. PMID: 34870514 Free PMC article.

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