Katrina Goddard is Distinguished Investigator and Associate Director of the Science Programs at Kaiser Permanente Center for Health Research in Portland, OR. Katrina is genetic epidemiologist who focuses on public health genomics and the translation of genetic testing into practice. Prior to joining the Kaiser Permanente Center for Health Research in 2007, she was faculty in the Department of Epidemiology and Biostatistics (now Population and Quantitative Health Sciences) at Case Western Reserve University in Cleveland, OH. She was also a mid-career fellow at the Centers for Disease Control and Prevention in Genetics & Public Health Research and Practice. At Kaiser, she was the founding director for the NW Biobank, and she is currently a PI of Kaiser's Cancer Health Assessments Reaching Many (CHARM) study as part of the National Human Genome Research Institute (NHGRI)-funded Clinical Sequencing Evidence-Generating Research (CSER2) consortium.
- Mittendorf, KF, Knerr, S, Kauffman, TL, Lindberg, NM, Anderson, KP, Feigelson, HS, Gilmore, MJ, Hunter, JE, Joseph, G, Kraft, SA et al.. Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities. JCO Precis Oncol 2021; 5 : . PubMed PMID:34778694 PubMed Central PMC8585306.
- Kauffman, TL, Dickerson, JF, Lynch, FL, Leo, MC, Shuster, E, Wilfond, BS, Himes, P, Gilmore, MJ, Rollins, NJ, Goddard, KAB et al.. Impact of expanded carrier screening on health care utilization. Am J Manag Care 2021; 27 (8): 316-321. PubMed PMID:34460173 .
- Rolf, BA, Schneider, JL, Amendola, LM, Davis, JV, Mittendorf, KF, Schmidt, MA, Jarvik, GP, Wilfond, BS, Goddard, KAB, Ezzell Hunter, J et al.. Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment. J Genet Couns 2021; : . PubMed PMID:34302314 .
- Mittendorf, KF, Kauffman, TL, Amendola, LM, Anderson, KP, Biesecker, BB, Dorschner, MO, Duenas, DM, Eubanks, DJ, Feigelson, HS, Gilmore, MJ et al.. Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations. Contemp Clin Trials 2021; 106 : 106432. PubMed PMID:33984519 PubMed Central PMC8336568.
- Goddard, KAB, Angelo, FAN, Ackerman, SL, Berg, JS, Biesecker, BB, Danila, MI, East, KM, Hindorff, LA, Horowitz, CR, Hunter, JE et al.. Lessons learned about harmonizing survey measures for the CSER consortium. J Clin Transl Sci 2020; 4 (6): 537-546. PubMed PMID:33948230 PubMed Central PMC8057449.
- Mittendorf, KF, Ukaegbu, C, Gilmore, MJ, Lindberg, NM, Kauffman, TL, Eubanks, DJ, Shuster, E, Allen, J, McMullen, C, Feigelson, HS et al.. Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population. Fam Cancer 2021; : . PubMed PMID:33754278 PubMed Central PMC8458476.
- Wand, H, Lambert, SA, Tamburro, C, Iacocca, MA, O'Sullivan, JW, Sillari, C, Kullo, IJ, Rowley, R, Dron, JS, Brockman, D et al.. Improving reporting standards for polygenic scores in risk prediction studies. Nature 2021; 591 (7849): 211-219. PubMed PMID:33692554 PubMed Central PMC8609771.
- Riddle, L, Amendola, LM, Gilmore, MJ, Guerra, C, Biesecker, B, Kauffman, TL, Anderson, K, Rope, AF, Leo, MC, Caruncho, M et al.. Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model. Patient Educ Couns 2021; 104 (5): 969-978. PubMed PMID:33549385 .
- Freed, AS, Gruß, I, McMullen, CK, Leo, MC, Kauffman, TL, Porter, KM, Muessig, KR, Eubanks, D, Goddard, KAB, Wilfond, BS et al.. A decision aid for additional findings in genomic sequencing: Development and pilot testing. Patient Educ Couns 2021; 104 (5): 960-968. PubMed PMID:33191058 PubMed Central PMC8099937.
- Kraft, SA, Rothwell, E, Shah, SK, Duenas, DM, Lewis, H, Muessig, K, Opel, DJ, Goddard, KAB, Wilfond, BS. Demonstrating 'respect for persons' in clinical research: findings from qualitative interviews with diverse genomics research participants. J Med Ethics 2020; : . PubMed PMID:33023975 PubMed Central PMC8021602.