Assessing the Costs and Cost-Effectiveness of Genomic Sequencing

por Christensen, Kurt D., Dukhovny, Dmitry, Siebert, Uwe, Green, Robert C.
Publicado 2015

Adopting Genetics: Motivations and Outcomes of Personal Genomic Testing in Adult Adoptees

por Baptista, Natalie M., Christensen, Kurt D., Carere, Deanna Alexis, Broadley, Simon A., Roberts, J. Scott, Green, Robert C.
Publicado 2016

Primary care providers’ responses to unsolicited Lynch syndrome secondary findings of varying clinical significance

por Galbraith, Lauren N., Preys, Charlene L., Rehm, Heidi L., Scheuner, Maren T., Hajek, Catherine, Green, Robert C., Christensen, Kurt D.
Publicado 2021

Estimated Cost-effectiveness of Genetic Testing in Siblings of Newborns With Cancer Susceptibility Gene Variants

por O’Brien, Grace, Christensen, Kurt D., Sullivan, Haley K., Stout, Natasha K., Diller, Lisa, Yeh, Jennifer M., Wu, Ann Chen
Publicado 2021

A Cost–Consequence Analysis of Preemptive SLCO1B1 Testing for Statin Myopathy Risk Compared to Usual Care

por Brunette, Charles A., Dong, Olivia M., Vassy, Jason L., Danowski, Morgan E., Alexander, Nicholas, Antwi, Ashley A., Christensen, Kurt D.
Publicado 2021

Associations between self-referral and health behavior responses to genetic risk information

por Christensen, Kurt D, Roberts, J Scott, Zikmund-Fisher, Brian J, Kardia, Sharon LR, McBride, Colleen M, Linnenbringer, Erin, Green, Robert C
Publicado 2015

Patient understanding of, satisfaction with, and perceived utility of whole genome sequencing: Findings from the MedSeq Project

por Roberts, J. Scott, Robinson, Jill O., Diamond, Pamela M., Bharadwaj, Archana, Christensen, Kurt D., Lee, Kaitlyn B., Green, Robert C., McGuire, Amy L.
Publicado 2018

Behavioral and psychological impact of genome sequencing: a pilot randomized trial of primary care and cardiology patients

por Christensen, Kurt D., Schonman, Erica F., Robinson, Jill O., Roberts, J. Scott, Diamond, Pamela M., Lee, Kaitlyn B., Green, Robert C., McGuire, Amy L.
Publicado 2021

Workforce Considerations When Building a Precision Medicine Program

por Blout Zawatsky, Carrie L., Leonhard, Jennifer R., Bell, Megan, Moore, Michelle M., Petry, Natasha J., Platt, Dylan M., Green, Robert C., Hajek, Catherine, Christensen, Kurt D.
Publicado 2022

Family Health History Reporting is Sensitive to Small Changes in Wording

por Conway-Pearson, Liam S., Christensen, Kurt D., Savage, Sarah K., Huntington, Noelle L., Weitzman, Elissa R., Ziniel, Sonja I., Bacon, Phoebe, Cacioppo, Cara N., Green, Robert C., Holm, Ingrid A.
Publicado 2016

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

por Armstrong, Brittan, Christensen, Kurt D., Genetti, Casie A., Parad, Richard B., Robinson, Jill Oliver, Blout Zawatsky, Carrie L., Zettler, Bethany, Beggs, Alan H., Holm, Ingrid A., Green, Robert C., McGuire, Amy L., Smith, Hadley Stevens, Pereira, Stacey
Publicado 2022

A Randomized Controlled Trial of Disclosing Genetic Risk Information for Alzheimer’s Disease via Telephone

por Christensen, Kurt D., Uhlmann, Wendy R., Roberts, J. Scott, Linnenbringer, Erin, Whitehouse, Peter J., Royal, Charmaine D. M., Obisesan, Thomas O., Cupples, L. Adrienne, Butson, Melissa B., Fasaye, Grace-Ann, Hiraki, Susan, Chen, Clara A., Siebert, Uwe, Cook-Deegan, Robert, Green, Robert C.
Publicado 2017

A systematic approach to the reporting of medically relevant findings from whole genome sequencing

por McLaughlin, Heather M, Ceyhan-Birsoy, Ozge, Christensen, Kurt D, Kohane, Isaac S, Krier, Joel, Lane, William J, Lautenbach, Denise, Lebo, Matthew S, Machini, Kalotina, MacRae, Calum A, Azzariti, Danielle R, Murray, Michael F, Seidman, Christine E, Vassy, Jason L, Green, Robert C, Rehm, Heidi L
Publicado 2014

Airmen and Healthcare Providers’ attitudes toward the use of genomic sequencing in the US Air Force: Findings from the MilSeq Project

por Pereira, Stacey, Hsu, Rebecca L., Islam, Rubaiya, Robinson, Jill Oliver, Ramapriyan, Rishab, Sirotich, Emily, Maxwell, Megan D., Majumder, Mary, Blout, Carrie L., Christensen, Kurt D., Mehlman, Maxwell, Parasidis, Efthimios, Gardner, Cubby L., Killian, Jacqueline M., De Castro, Mauricio, Green, Robert C., McGuire, Amy L.
Publicado 2020

Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos

por Christensen, Kurt D., Zhang, Mengran, Galbraith, Lauren N., Granot-Hershkovitz, Einat, Nelson, Sarah C., Gonzalez, Sara, Argos, Maria, Perreira, Krista M., Daviglus, Martha L., Isasi, Carmen R., Cai, Jianwen, Talavera, Gregory A., Blout Zawatsky, Carrie L., Green, Robert C., Isasi, Rosario, Kaplan, Robert, Sofer, Tamar
Publicado 2022

Short Term Costs of Integrating Whole Genome Sequencing into Primary Care and Cardiology Settings: A Pilot Randomized Trial

por Christensen, Kurt D., Vassy, Jason L., Phillips, Kathryn A., Blout, Carrie L., Azzariti, Danielle R., Lu, Christine Y., Robinson, Jill O., Lee, Kaitlyn, Douglas, Michael P., Yeh, Jennifer M., Machini, Kalotina, Stout, Natasha K., Rehm, Heidi L., McGuire, Amy L., Green, Robert C., Dukhovny, Dmitry
Publicado 2018

Disclosing genetic risk for Alzheimer's dementia to individuals with mild cognitive impairment

por Christensen, Kurt D., Karlawish, Jason, Roberts, J. Scott, Uhlmann, Wendy R., Harkins, Kristin, Wood, Elisabeth M., Obisesan, Thomas O., Le, Lan Q., Cupples, L. Adrienne, Zoltick, Emilie S., Johnson, Megan S., Bradbury, Margaret K., Waterston, Leo B., Chen, Clara A., Feldman, Sara, Perry, Denise L., Green, Robert C.
Publicado 2020

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

por Blout Zawatsky, Carrie L., Shah, Nidhi, Machini, Kalotina, Perez, Emma, Christensen, Kurt D., Zouk, Hana, Steeves, Marcie, Koch, Christopher, Uveges, Melissa, Shea, Janelle, Gold, Nina, Krier, Joel, Boutin, Natalie, Mahanta, Lisa, Rehm, Heidi L., Weiss, Scott T., Karlson, Elizabeth W., Smoller, Jordan W., Lebo, Matthew S., Green, Robert C.
Publicado 2021

Precision Population Medicine in Primary Care: The Sanford Chip Experience

por Christensen, Kurt D., Bell, Megan, Zawatsky, Carrie L. B., Galbraith, Lauren N., Green, Robert C., Hutchinson, Allison M., Jamal, Leila, LeBlanc, Jessica L., Leonhard, Jennifer R., Moore, Michelle, Mullineaux, Lisa, Petry, Natasha, Platt, Dylan M., Shaaban, Sherin, Schultz, April, Tucker, Bethany D., Van Heukelom, Joel, Wheeler, Elizabeth, Zoltick, Emilie S., Hajek, Catherine
Publicado 2021

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine

por Vassy, Jason L, Lautenbach, Denise M, McLaughlin, Heather M, Kong, Sek Won, Christensen, Kurt D, Krier, Joel, Kohane, Isaac S, Feuerman, Lindsay Z, Blumenthal-Barby, Jennifer, Roberts, J Scott, Lehmann, Lisa Soleymani, Ho, Carolyn Y, Ubel, Peter A, MacRae, Calum A, Seidman, Christine E, Murray, Michael F, McGuire, Amy L, Rehm, Heidi L, Green, Robert C
Publicado 2014