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Author Details

Katrina A B Goddard
Center for Health Research, Kaiser Permanente Northwest
1993
153
39
PMIDPaper TitleJournal TitlePublished Year
36516964The PrU: Development and validation of a measure to assess personal utility of genomic results.Genet Med2023
37644850Risk management actions following genetic testing in the Cancer Health Assessments Reaching Many (CHARM) Study: A prospective cohort study.Cancer Med2023
37126135Evaluating cancer genetic services in a safety net system: overcoming barriers for a lasting impact beyond the CHARM research project.J Community Genet2023
37421176Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population.Genet Med2023
37470892Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system.Breast Cancer Res Treat2023
34302314Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.J Genet Couns2022
35679147Risk-reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system.Cancer2022
35348718Developing an algorithm across integrated healthcare systems to identify a history of cancer using electronic medical records.J Am Med Inform Assoc2022
35436948Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system.Hered Cancer Clin Pract2022
35341655ClinGen's Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents.Genet Med2022
35363504Establishing the Medical Actionability of Genomic Variants.Annu Rev Genomics Hum Genet2022
35689290Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews.Hered Cancer Clin Pract2022
35522237ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.Genet Med2022
35933674Engaging Patient Advisory Committees to Inform a Genomic Cancer Risk Study: Lessons for Future Efforts.Perm J2022
36053287An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial.Genet Med2022
33754278Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>â¿¢) for lynch syndrome risk assessment in a diverse population.Fam Cancer2022
35123916Corrigendum to "Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations" [Contemporary Clinical Trials 106 (2021) 106432].Contemp Clin Trials2022
34906471Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings.Genet Med2022
35144679Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system.Hered Cancer Clin Pract2022
32981477Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study.AJOB Empir Bioeth2021
33549385Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.Patient Educ Couns2021
34460173Impact of expanded carrier screening on health care utilization.Am J Manag Care2021
34778694Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities.JCO Precis Oncol2021
33984519Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations.Contemp Clin Trials2021
33191058A decision aid for additional findings in genomic sequencing: Development and pilot testing.Patient Educ Couns2021
32125936Assessing the implications of positive genomic screening results.Per Med2020
33948230Lessons learned about harmonizing survey measures for the CSER consortium.J Clin Transl Sci2020
32089547Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol's evolution.Genet Med2020
33416699Discordant Patient and Clinician Perspectives on the Potential Value of Genetic Services in Safety-Net Clinics.J Health Care Poor Underserved2020
33023975Demonstrating 'respect for persons' in clinical research: findings from qualitative interviews with diverse genomics research participants.J Med Ethics2020
30670880Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
32025627Cost-Effectiveness of Risk-Stratified Colorectal Cancer Screening Based on Polygenic Risk: Current Status and Future Potential.JNCI Cancer Spectr2019
31890059Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study.Hered Cancer Clin Pract2019
29875426Returning negative results to individuals in a genomic screening program: lessons learned.Genet Med2019
30245516The evolving landscape of expanded carrier screening: challenges and opportunities.Genet Med2019
30729418Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting.Fam Cancer2019
31028355Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders.Genet Med2019
31104772The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.Am J Hum Genet2019
30287922Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.Genet Med2019
29293279Patient actions and reactions after receiving negative results from expanded carrier screening.Clin Genet2018
30193136The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.Am J Hum Genet2018
30133189Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience.Mol Genet Genomic Med2018
30020962Assessment of willingness to pay for expanded carrier screening among women and couples undergoing preconception carrier screening.PLoS One2018
30455898A case for expanding carrier testing to include actionable X-linked disorders.Clin Case Rep2018
30311382Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group.Hum Mutat2018
29423569Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing.J Genet Couns2018
29754767Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.Am J Hum Genet2018
29388940Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.Genet Med2018
29760830Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews.Hered Cancer Clin Pract2018
29733724Lessons Learned From A Study Of Genomics-Based Carrier Screening For Reproductive Decision Making.Health Aff (Millwood)2018
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Collaborators

Kaiser Permanente Center for Health Research
Co-authored papers 45
University of Washington School of Medicine.
Co-authored papers 45
University of Washington Medical Center
Co-authored papers 29
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Co-authored papers 20
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Illumina Inc.
Co-authored papers 18
University of North Carolina
Co-authored papers 15
Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center
Co-authored papers 15
University of Washington School of Medicine
Co-authored papers 13
Oregon Health & Science University (OHSU)
Co-authored papers 13
Seattle Children's Hospital
Co-authored papers 12
and Translational Research Center
Co-authored papers 11
Centers for Disease Control and Prevention Atlanta GA USA.
Co-authored papers 10
University of Washington
Co-authored papers 9
University of Washington Medical Center
Co-authored papers 9
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 9
Co-authored papers 8
University of Minnesota Medical School, 1035 University Drive duluth
Co-authored papers 8
University of Washington
Co-authored papers 8
University of Washington Medical Center
Co-authored papers 8
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 8
Biomedical Research Institute, Stellenbosch University.
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Biomedical Research Institute, Stellenbosch University.
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Vanderbilt Genetics Institute, Vanderbilt University Medical Center
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National Institutes of Health
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Washington University School of Medicine
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Baylor College of Medicine.
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University of North Carolina
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University of Washington
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University of California San Francisco
Co-authored papers 6