Jessica Ezzell Hunter

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Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population

"Go ahead and screen" - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients

Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population

Insight and recommendations for fragile x-premutation-associated conditions from the fifth international conference on FMR1 premutation

A picture is worth a thousand words: Advancing the use of visualization tools in implementation science through process mapping and matrix heat mapping

An examination of the ethical and legal limits in implementing "traceback testing" for deceased patients

An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial

Should health systems share genetic findings with at-risk relatives when the proband is deceased?: Interviews with individuals diagnosed with Lynch syndrome

Establishing the medical actionability of genomic variants

EE139 Using a user-friendly modeling tool to inform and guide local decision-making for lynch syndrome screening at healthcare systems

ClinGen's Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents

Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system

Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population

Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings

Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system

Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment

Systemic barriers to risk-reducing interventions for hereditary cancer syndromes: Implications for health care inequities

Feasibility of a traceback approach for using pathology specimens to facilitate genetic testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) study protocol

Predictors of comorbid conditions in women who carry an FMR1 premutation

Cancer health assessments reaching many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations