Health care providers and direct-to-consumer access and advertising of genetic testing in the United States

per Myers, Melanie F
Publicat 2011

Adolescents’ and Parents’ Genomic Testing Decisions: Associations with Age, Race, and Sex

per Myers, Melanie F., Martin, Lisa J., Prows, Cynthia A.
Publicat a J Adolesc Health (2019)

Put the Family Back in Family Health History: A Multiple-Informant Approach

per Lin, Jielu, Marcum, Christopher S., Myers, Melanie F., Koehly, Laura M.
Publicat a Am J Prev Med (2017)

Racial differences in family health history knowledge of type 2 diabetes: exploring the role of interpersonal mechanisms

per Lin, Jielu, Marcum, Christopher S, Myers, Melanie F, Koehly, Laura M
Publicat a Transl Behav Med (2018)

A Bayesian hierarchical logistic regression model of multiple informant family health histories

per Lin, Jielu, Myers, Melanie F., Koehly, Laura M., Marcum, Christopher Steven
Publicat a BMC Med Res Methodol (2019)

Activating Communal Coping Related to Diabetes Risk in Mexican-Heritage Families

per Lin, Jielu, Myers, Melanie F., Wilkinson, Anna V., Koehly, Laura M.
Publicat a Fam Community Health (2019)

Decisional conflict among adolescents and parents making decisions about genomic sequencing results

per Raghuram Pillai, Preethi, Prows, Cynthia A., Martin, Lisa J., Myers, Melanie F.
Publicat a Clin Genet (2019)

The Underdeveloped “Gift”: Ethics in Implementing Precision Medicine Research

per Blumling, Amy A., Childers-Buschle, Kristin E., Lynch, John A., Myers, Melanie F., McGowan, Michelle L.
Publicat a Am J Bioeth (2021)

Familial Risk for Chronic Disease and Intent to Share Family History With a Health Care Provider Among Urban Appalachian Women, Southwestern Ohio, 2007

per Myers, Melanie F., Au, Margaret G., Warren, Nancy S., Cornett, Sandra J., Nick, Todd G., Wang, Yu, Wallace, Jody
Publicat 2009

Pediatric epilepsy surgery: The prognostic value of central nervous system comorbidities in patients and their families

per Qualmann, Krista J, Spaeth, Christine G, Myers, Melanie F, Horn, Paul S, Holland, Katherine, Mangano, Francesco T, Greiner, Hansel M
Publicat a J Child Neurol (2017)

Adolescent and Parental Attitudes about Return of Genomic Research Results: Focus Group Findings Regarding Decisional Preferences

per McGowan, Michelle L., Prows, Cynthia A., DeJonckheere, Melissa, Brinkman, William B., Vaughn, Lisa, Myers, Melanie F.
Publicat a J Empir Res Hum Res Ethics (2018)

Parental Perception of Self-Empowerment in Pediatric Pharmacogenetic Testing: The Reactions of Parents to the Communication of Actual and Hypothetical CYP2D6 Test Results

per Adelsperger, Sarah, Prows, Cynthia A., Myers, Melanie F., Perry, Cassandra L., Chandler, Ariel, Holm, Ingrid A., Lynch, John A.
Publicat a Health Commun (2016)

Development and Evaluation of a Genetics Literacy Assessment Instrument for Undergraduates

per Bowling, Bethany Vice, Acra, Erin E., Wang, Lihshing, Myers, Melanie F., Dean, Gary E., Markle, Glenn C., Moskalik, Christine L., Huether, Carl A.
Publicat 2008

Prior opioid exposure influences parents’ sharing of their children's CYP2D6 research results

per Myers, Melanie F, Zhang, Xue, McLaughlin, Brooke, Kissell, Diane, Perry, Cassandra L, Veerkamp, Matthew, Zhang, Kejian, Holm, Ingrid A, Prows, Cynthia A
Publicat a Pharmacogenomics (2017)

Physicians' Perspectives on Receiving Unsolicited Genomic Results

per Pet, Douglas B., Holm, Ingrid A., Williams, Janet L., Myers, Melanie F., Novak, Laurie L., Brothers, Kyle B., Wiesner MD, Georgia L., Clayton, Ellen W.
Publicat a Genet Med (2018)

Enrichment sampling for a multi-site patient survey using electronic health records and census data

per Mercaldo, Nathaniel D, Brothers, Kyle B, Carrell, David S, Clayton, Ellen W, Connolly, John J, Holm, Ingrid A, Horowitz, Carol R, Jarvik, Gail P, Kitchner, Terrie E, Li, Rongling, McCarty, Catherine A, McCormick, Jennifer B, McManus, Valerie D, Myers, Melanie F, Pankratz, Joshua J, Shrubsole, Martha J, Smith, Maureen E, Stallings, Sarah C, Williams, Janet L, Schildcrout, Jonathan S
Publicat a J Am Med Inform Assoc (2018)

Conducting a large, multi-site survey about patients’ views on broad consent: challenges and solutions

per Smith, Maureen E., Sanderson, Saskia C., Brothers, Kyle B., Myers, Melanie F., McCormick, Jennifer, Aufox, Sharon, Shrubsole, Martha J., Garrison, Nanibaá A., Mercaldo, Nathaniel D., Schildcrout, Jonathan S., Clayton, Ellen Wright, Antommaria, Armand H. Matheny, Basford, Melissa, Brilliant, Murray, Connolly, John J., Fullerton, Stephanie M., Horowitz, Carol R., Jarvik, Gail P., Kaufman, Dave, Kitchner, Terri, Li, Rongling, Ludman, Evette J., McCarty, Catherine, McManus, Valerie, Stallings, Sarah, Williams, Janet L., Holm, Ingrid A.
Publicat a BMC Med Res Methodol (2016)

Parents’ Attitudes toward Consent and Data Sharing in Biobanks: A Multi-Site Experimental Survey

per Antommaria, Armand H. Matheny, Brothers, Kyle B., Myers, John A., Feygin, Yana B., Aufox, Sharon A., Brilliant, Murray H., Conway, Pat, Fullerton, Stephanie M., Garrison, Nanibaa’ A., Horowitz, Carol R., Jarvik, Gail P., Li, Rongling, Ludman, Evette J., McCarty, Catherine A., McCormick, Jennifer B., Mercaldo, Nathaniel D., Myers, Melanie F., Sanderson, Saskia C., Shrubsole, Martha J., Schildcrout, Jonathan S., Williams, Janet L., Smith, Maureen E., Clayton, Ellen Wright, Holm, Ingrid A.
Publicat a AJOB Empir Bioeth (2018)

Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US

per Sanderson, Saskia C., Brothers, Kyle B., Mercaldo, Nathaniel D., Clayton, Ellen Wright, Antommaria, Armand H. Matheny, Aufox, Sharon A., Brilliant, Murray H., Campos, Diego, Carrell, David S., Connolly, John, Conway, Pat, Fullerton, Stephanie M., Garrison, Nanibaa’ A., Horowitz, Carol R., Jarvik, Gail P., Kaufman, David, Kitchner, Terrie E., Li, Rongling, Ludman, Evette J., McCarty, Catherine A., McCormick, Jennifer B., McManus, Valerie D., Myers, Melanie F., Scrol, Aaron, Williams, Janet L., Shrubsole, Martha J., Schildcrout, Jonathan S., Smith, Maureen E., Holm, Ingrid A.
Publicat a Am J Hum Genet (2017)

Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience

per Fossey, Robyn, Kochan, David, Winkler, Erin, Pacyna, Joel E., Olson, Janet, Thibodeau, Stephen, Connolly, John J., Harr, Margaret, Behr, Meckenzie A., Prows, Cynthia A., Cobb, Beth, Myers, Melanie F., Leslie, Nancy D., Namjou-Khales, Bahram, Milo Rasouly, Hila, Wynn, Julia, Fedotov, Alexander, Chung, Wendy K., Gharavi, Ali, Williams, Janet L., Pais, Lynn, Holm, Ingrid, Aufox, Sharon, Smith, Maureen E., Scrol, Aaron, Leppig, Kathleen, Jarvik, Gail P., Wiesner, Georgia L., Li, Rongling, Stroud, Mary, Smoller, Jordan W., Sharp, Richard R., Kullo, Iftikhar J.
Publicat a J Pers Med (2018)