A review and definition of 'usual care' in genetic counseling trials to standardize use in research
Biesecker BB, Lillie SE, Amendola LM, Donohue KE, East KM, Foreman AKM, Gilmore MJ, Greve V, Liangolou B, O'Daniel JM, Odgis JA, Rego S, Rolf B, Scollon S, Suckiel SA, Zepp J, Joseph G.. J Genet Couns. 2021;30(1):42-50. PubMed PMID: 33278053. PubMed Central PMCID: PMC7882019.
Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings
Duenas DM, Shipman KJ, Porter KM, Shuster E, Guerra C, Reyes A, Kauffman TL, Hunter JE, Goddard KAB, Wilfond BS, Kraft SA.Genet Med. 2021. PubMed PMID: 34906471.
A decision aid for additional findings in genomic sequencing: Development and pilot testing
Freed AS, Gruss I, McMullen CK, Leo MC, Kauffman TL, Porter KM, Muessig KR, Eubanks D, Goddard KAB, Wilfond BS, Liles EG. Educ Couns. 2021;104(5):960-968. PubMed PMID: 33191058. PubMed Central PMCID: PMC8099937.
Impact of expanded carrier screening on health care utilization
Kauffman TL, Dickerson JF, Lynch FL, Leo MC, Shuster E, Wilfond BS, Himes P, Gilmore MJ, Rollins NJ, Goddard KAB. Am J Manag Care. 2021;27(8):316-321. PubMed PMID: 34460173.
Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol
Kauffman TL, Prado YK, Reyes AA, Zepp JM, Sawyer J, White LL, Martucci J, Salas SB, Vertrees S, Rope AF, Weinmann S, Henrikson NB, Lee SS, Feigelson HS, Hunter JE. J Pers Med. 2021;11(11). PubMed PMID: 34834546. PubMed Central PMCID: PMC8625870.
Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study
Kraft SA, Porter KM, Duenas DM, Guerra C, Joseph G, Lee SS, Shipman KJ, Allen J, Eubanks D, Kauffman TL, Lindberg NM, Anderson K, Zepp JM, Gilmore MJ, Mittendorf KF, Shuster E, Muessig KR, Arnold B, Goddard KAB, Wilfond BS. AJOB Empir Bioeth. 2021;12(1):1-11. PubMed PMID: 32981477. PubMed Central PMCID: PMC7785634.
Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations
Mittendorf KF, Kauffman TL, Amendola LM, Anderson KP, Biesecker BB, Dorschner MO, Duenas DM, Eubanks DJ, Feigelson HS, Gilmore MJ, Hunter JE, Joseph G, Kraft SA, Lee SSJ, Leo MC, Liles EG, Lindberg NM, Muessig KR, Okuyama S, Porter KM, Riddle LS, Rolf BA, Rope AF, Zepp JM, Jarvik GP, Wilfond BS, Goddard KAB, CHARM study team. Contemp Clin Trials. 2021;106:106432. PubMed PMID: 33984519. PubMed Central PMCID: PMC8336568.
Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities
Mittendorf KF, Knerr S, Kauffman TL, Lindberg NM, Anderson KP, Feigelson HS, Gilmore MJ, Hunter JE, Joseph G, Kraft SA, Zepp JM, Syngal S, Wilfond BS, Goddard KAB. JCO Precis Oncol. 2021;5(5):1709-1718. PubMed PMID: 34778694. PubMed Central PMCID: PMC8585306.
Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5) for lynch syndrome risk assessment in a diverse population
Mittendorf KF, Ukaegbu C, Gilmore MJ, Lindberg NM, Kauffman TL, Eubanks DJ, Shuster E, Allen J, McMullen C, Feigelson HS, Anderson KP, Leo MC, Hunter JE, Sasaki SO, Zepp JM, Syngal S, Wilfond BS, Goddard KAB. Fam Cancer. 2021. PubMed PMID: 33754278. PubMed Central PMCID: PMC8458476.
Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model.
Riddle L, Amendola LM, Gilmore MJ, Guerra C, Biesecker B, Kauffman TL, Anderson K, Rope AF, Leo MC, Caruncho M, Jarvik GP, Wilfond B, Goddard KAB, Joseph G. Patient Educ Couns. 2021;104(5):969-978. PubMed PMID: 33549385.
Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment.
Rolf BA, Schneider JL, Amendola LM, Davis JV, Mittendorf KF, Schmidt MA, Jarvik GP, Wilfond BS, Goddard KAB, Ezzell Hunter J. J Genet Couns. 2021. PubMed PMID: 34302314. PubMed Central PMCID: PMC8783924.
Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings
Suckiel SA, O'Daniel JM, Donohue KE, Gallagher KM, Gilmore MJ, Hendon LG, Joseph G, Lianoglou BR, Mathews JM, Norton ME, Odgis JA, Poss AF, Rego S, Scollon S, Yip T, Amendola LM. Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium. J Pers Med. 2021;11(3). PubMed PMID: 33805616. PubMed Central PMCID: PMC7998798.