Sickle cell carriers' unmet information needs: Beyond knowing trait status

Author:

Mayo‐Gamble Tilicia L.1ORCID,Schlundt David2,Cunningham‐Erves Jennifer3,Murry Velma McBride4,Bonnet Kemberlee2,Quasie‐Woode Delores1,Mouton Charles P.5

Affiliation:

1. Department of Health Policy and Community Health, Management and Behavior Jiann‐Ping Hsu College of Public Health, Georgia Southern University Statesboro Georgia

2. Department of Psychology College of Arts and Sciences, Vanderbilt University Nashville Tennessee

3. Department of Internal Medicine Meharry Medical College Nashville Tennessee

4. Department of Human and Organizational Development College of Education and Human Development, Vanderbilt University Nashville Tennessee

5. Department of Family Medicine, Office of Academic Affairs University of Texas Medical Branch Galveston Texas

Funder

National Center for Research Resources

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Genetics (clinical)

Reference39 articles.

1. A pilot study to explore knowledge, attitude, and meaning about sickle cell trait and disease;Acharya K.;Journal of the National Medical Association,2009

2. Human agency in social cognitive theory;Bandura A.;American Psychologist,1989

3. Social cognitive theory: An agentic perspective;Bandura A.;Annual Review of Psychology,2001

4. Sickle cell trait and development of microvascular complications in diabetes mellitus;Bleyer A. J.;Clinical Journal of the American Society of Nephrology,2010

5. Inadequate community knowledge about sickle cell disease among African‐American women;Boyd J. H.;Journal of the National Medical Association,2005

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