Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice

por Roche, Myra I., Berg, Jonathan S.
Publicado 2015

Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision-Making Research in Genomic Sequencing

por Langer, Michelle M., Roche, Myra I., Brewer, Noel T., Berg, Jonathan S., Khan, Cynthia M., Leos, Cristina, Moore, Elizabeth, Brown, Michelle, Rini, Christine
Publicado 2017

Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete choice experiment

por Lewis, Megan A., Stine, Alex, Paquin, Ryan S., Mansfield, Carol, Wood, Dallas, Rini, Christine, Roche, Myra I., Powell, Cynthia M., Berg, Jonathan S., Bailey, Donald B.
Publicado 2017

“Possibly positive or certainly uncertain?”: Participants’ responses to uncertain diagnostic results from exome sequencing

por Skinner, Debra, Roche, Myra I., Weck, Karen E., Raspberry, Kelly A., Foreman, A. Katherine M., Strande, Natasha T., Berg, Jonathan S., Evans, James P., Henderson, Gail E.
Publicado 2017

Genomic Knowledge in the Context of Diagnostic Exome Sequencing: Changes over Time, Persistent Subgroup Differences, and Associations with Psychological Sequencing Outcomes

por Rini, Christine, Henderson, Gail E., Evans, James P., Berg, Jonathan S., Foreman, Ann Katherine M., Griesemer, Ida, Waltz, Margaret, O’Daniel, Julianne M., Roche, Myra I.
Publicado 2019

Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized...

por Milko, Laura V., Rini, Christine, Lewis, Megan A., Butterfield, Rita M., Lin, Feng-Chang, Paquin, Ryan S., Powell, Bradford C., Roche, Myra I., Souris, Katherine J., Bailey, Donald B., Berg, Jonathan S., Powell, Cynthia M.
Publicado 2018

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

por Rini, Christine, Khan, Cynthia M., Moore, Elizabeth, Roche, Myra I., Evans, James P., Berg, Jonathan S., Powell, Bradford C., Corbie-Smith, Giselle, Foreman, Ann Katherine M., Griesemer, Ida, Lee, Kristy, O’Daniel, Julianne M., Henderson, Gail E.
Publicado 2017

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

por Roche, Myra I., Griesemer, Ida, Khan, Cynthia M., Moore, Elizabeth, Lin, Feng-Chang, O’Daniel, Julianne M., Foreman, Ann Katherine M., Lee, Kristy, Powell, Bradford C., Berg, Jonathan S., Evans, James P., Henderson, Gail E., Rini, Christine
Publicado 2018

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

por Berg, Jonathan S., Foreman, Ann Katherine M., O'Daniel, Julianne M., Booker, Jessica K., Boshe, Lacey, Carey, Timothy, Crooks, Kristy R., Jensen, Brian C., Juengst, Eric T., Lee, Kristy, Nelson, Daniel K., Powell, Bradford C., Powell, Cynthia M., Roche, Myra I., Skrzynia, Cecile, Strande, Natasha T., Weck, Karen E., Wilhelmsen, Kirk C., Evans, James P.
Publicado 2016