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Items: 15

1.

Trust in provider care teams and health information technology-mediated communication.

Raj M, Platt JE, Wilk AS.

Am J Manag Care. 2020 Jan;26(1):23-25.

2.

Dynamics of Physicians' Trust in Fellow Health Care Providers and the Role of Health Information Technology.

Raj M, Wilk AS, Platt JE.

Med Care Res Rev. 2019 Dec 11:1077558719892349. doi: 10.1177/1077558719892349. [Epub ahead of print]

PMID:
31822195
3.

Willingness to Participate in Health Information Networks with Diverse Data Use: Evaluating Public Perspectives.

Platt J, Raj M, Büyüktür AG, Trinidad MG, Olopade O, Ackerman MS, Kardia S.

EGEMS (Wash DC). 2019 Jul 25;7(1):33. doi: 10.5334/egems.288.

4.

Encouraging Participation And Transparency In Biobank Research.

Spector-Bagdady K, De Vries RG, Gornick MG, Shuman AG, Kardia S, Platt J.

Health Aff (Millwood). 2018 Aug;37(8):1313-1320. doi: 10.1377/hlthaff.2018.0159.

5.

Ethical, legal, and social implications of learning health systems.

Platt J, Spector-Bagdady K, Platt T, De Vries R, Markel D, Hutchinson R, Manion F, Ziegler G, Rubin J, Kardia S.

Learn Health Syst. 2018 Jan 3;2(1):e10051. doi: 10.1002/lrh2.10051. eCollection 2018 Jan. No abstract available.

6.

Improving the Informed Consent Process in Hematopoietic Cell Transplantation: Patient, Caregiver, and Provider Perspectives.

Raj M, Choi SW, Gurtekin TS, Platt J.

Biol Blood Marrow Transplant. 2018 Jan;24(1):156-162. doi: 10.1016/j.bbmt.2017.08.037. Epub 2017 Sep 4.

7.

Engaging a state: Facebook comments on a large population biobank.

Platt T, Platt J, Thiel D, Kardia SLR.

J Community Genet. 2017 Jul;8(3):183-197. doi: 10.1007/s12687-017-0302-z. Epub 2017 Apr 5.

8.

Public Trust in Health Information Sharing: A Measure of System Trust.

Platt JE, Jacobson PD, Kardia SLR.

Health Serv Res. 2018 Apr;53(2):824-845. doi: 10.1111/1475-6773.12654. Epub 2017 Jan 18.

9.

Measuring physicians' trust: A scoping review with implications for public policy.

Wilk AS, Platt JE.

Soc Sci Med. 2016 Sep;165:75-81. doi: 10.1016/j.socscimed.2016.07.039. Epub 2016 Jul 29. Review.

PMID:
27497858
10.

Facebook Advertising Across an Engagement Spectrum: A Case Example for Public Health Communication.

Platt T, Platt J, Thiel DB, Kardia SL.

JMIR Public Health Surveill. 2016 May 30;2(1):e27. doi: 10.2196/publichealth.5623.

11.
12.

Testing an online, dynamic consent portal for large population biobank research.

Thiel DB, Platt J, Platt T, King SB, Fisher N, Shelton R, Kardia SL.

Public Health Genomics. 2015;18(1):26-39. doi: 10.1159/000366128. Epub 2014 Oct 30.

13.

'Cool! and creepy': engaging with college student stakeholders in Michigan's biobank.

Platt T, Platt J, Thiel DB, Fisher N, Kardia SL.

J Community Genet. 2014 Oct;5(4):349-62. doi: 10.1007/s12687-014-0190-4. Epub 2014 Jun 12.

14.

Community perspectives on public health biobanking: an analysis of community meetings on the Michigan BioTrust for Health.

Thiel DB, Platt T, Platt J, King SB, Kardia SL.

J Community Genet. 2014 Apr;5(2):125-38. doi: 10.1007/s12687-013-0162-0. Epub 2013 Jul 27.

15.

Public preferences regarding informed consent models for participation in population-based genomic research.

Platt J, Bollinger J, Dvoskin R, Kardia SL, Kaufman D.

Genet Med. 2014 Jan;16(1):11-8. doi: 10.1038/gim.2013.59. Epub 2013 May 9.

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