Publications by authors named "Kurt D Christensen"

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A Lack of Information About Family Health History Motivates Adopted Individuals to Pursue Elective Genomic Testing.
Madison R Hickingbotham, Megan Bell, Emilie S Zoltick, Dylan Platt, Jennifer R Leonhard, Kurt D Christensen

Am J Med Genet A· November 2025

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Primary care providers' perspectives on receiving opportunistic genomic results from a national study: The Million Veteran Program Return Of Actionable Results (MVP-ROAR) Study.
Anna L Johannsen, Morgan E Danowski, Kailyn E Sitter, Charlene L Preys, Haley L Gerety, Kurt D Christensen

Genet Med· June 2025

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Opportunities amid complexities in returning genetic results to black precision medicine research participants: Interview themes in context with open data.
Rachele M Hendricks-Sturrup, Nora Emmott, Maryam Nafie, Stephanie Argetsinger, Lauren Edgar, Kurt D Christensen

J Clin Transl Sci· April 2025

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Familial communication and cascade testing following elective genomic testing.
Sophia M Adelson, Carrie L Blout Zawatsky, Madison R Hickingbotham, Megan E Bell, Dylan M Platt, Kurt D Christensen

J Genet Couns· February 2025

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Primary Care Providers' Experiences With an Active Elective Genetic Testing Program.
Dylan M Platt, Carrie L Blout Zawatsky, Kurt D Christensen, Robert C Green, Catherine Hajek

Health Educ Behav· February 2025

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Modernizing Newborn Screening in the Genomic Era: Importance of Health-Related Quality of Life.
Ellen Kim DeLuca, Ann Chen Wu, Kurt D Christensen, Davene R Wright, Jennifer Yeh

Pharmacoecon Open· November 2024

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Design and pilot results from the Million Veteran Program Return Of Actionable Results (MVP-ROAR) Study.
Jason L Vassy, Charles A Brunette, Thomas Yi, Alicia Harrison, Mark P Cardellino, Kurt D Christensen

Am Heart J· October 2024

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Attitudes, knowledge, and risk perceptions of patients who received elective genomic testing as a clinical service.
Emilie S Zoltick, Megan Bell, Madison R Hickingbotham, Ann Chen Wu, Lauren N Galbraith, Kurt D Christensen

Genet Med· October 2024

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The BabySeq Project: A clinical trial of genome sequencing in a diverse cohort of infants.
Hadley Stevens Smith, Bethany Zettler, Casie A Genetti, Madison R Hickingbotham, Tanner F Coleman, Kurt D Christensen

Am J Hum Genet· October 2024

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Diverse Participant Recruitment for Infant Sequencing in the BabySeq Project.
Maya C Del Rosario, Sheyenne A Walmsley, Barbara W Harrison, Crystal T Stephens, Bethany Zettler, Kurt D Christensen

medRxiv· October 2024

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Evaluation of pharmacogenetic automated clinical decision support for clopidogrel.
Amanda Massmann, Joel Van Heukelom, Max Weaver, April Schultz, Debbie M Figueroa, Kurt D Christensen

Pharmacogenomics· September 2024

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Clinical impact of preemptive pharmacogenomic testing on antiplatelet therapy in a real-world setting.
Amanda Massmann, Kurt D Christensen, Joel Van Heukelom, April Schultz, Muhammad Hamza Saad Shaukat

Eur J Hum Genet· August 2024

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Evaluating the utility of multi-gene, multi-disease population-based panel testing accounting for uncertainty in penetrance estimates.
Jane W Liang, Kurt D Christensen, Robert C Green, Peter Kraft

NPJ Genom Med· May 2024

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Paving the path for implementation of clinical genomic sequencing globally: Are we ready?
Deborah A Marshall, Nicolle Hua, James Buchanan, Kurt D Christensen, Geert W J Frederix

Health Aff Sch· May 2024

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Development and utility of a clinical research informatics application for participant recruitment and workflow management for a return of results pilot trial in familial hypercholesterolemia in the Million Veteran Program.
Charles A Brunette, Thomas Yi, Morgan E Danowski, Mark Cardellino, Alicia Harrison, Kurt D Christensen

JAMIA Open· April 2024

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Returning personalized, genetic health test results to individuals of African descent or ancestry in precision medicine research.
Rachele M Hendricks-Sturrup, Nora Emmott, Maryam Nafie, Lauren Edgar, Tracey Johnson-Glover, Kurt D Christensen

Health Aff Sch· December 2023

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The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care.
Jason L Vassy, Charles A Brunette, Matthew S Lebo, Katharine MacIsaac, Thomas Yi, Kurt D Christensen

Am J Hum Genet· November 2023

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Public perspective on medications to delay Alzheimer's disease symptoms.
Matthew B Rich, Carrie L Blout Zawatsky, Joseph J Botta, Kurt D Christensen

J Genet Couns· October 2023

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Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project.
Robert C Green, Nidhi Shah, Casie A Genetti, Timothy Yu, Bethany Zettler, Kurt D Christensen

Am J Hum Genet· July 2023

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Attitudes about pharmacogenomic testing vary by healthcare specialty.
Charlene L Preys, Carrie L Blout Zawatsky, Amanda Massmann, Joel Van Heukelom, Robert C Green, Kurt D Christensen

Pharmacogenomics· July 2023

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gene-based clinical decision support reduces statin-associated muscle symptoms risk with simvastatin.
Amanda Massmann, Joel Van Heukelom, Robert C Green, Catherine Hajek, Madison R Hickingbotham, Kurt D Christensen

Pharmacogenomics· May 2023

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Benefits, harms, and costs of newborn genetic screening for hypertrophic cardiomyopathy: Estimates from the PreEMPT model.
Kurt D Christensen, Pamela M McMahon, Lauren N Galbraith, Jennifer M Yeh, Natasha K Stout

Genet Med· April 2023

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Parents' decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project.
Stacey Pereira, Amanda M Gutierrez, Jill Oliver Robinson, Kurt D Christensen, Casie A Genetti

Genet Med· March 2023

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Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos.
Kurt D Christensen, Mengran Zhang, Lauren N Galbraith, Einat Granot-Hershkovitz, Sarah C Nelson

HGG Adv· January 2023

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Workforce Considerations When Building a Precision Medicine Program.
Carrie L Blout Zawatsky, Jennifer R Leonhard, Megan Bell, Michelle M Moore, Natasha J Petry, Kurt D Christensen

J Pers Med· November 2022

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