Jessica Ezzell Hunter

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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

Lessons learned about harmonizing survey measures for the CSER consortium

Clustering of comorbid conditions among women who carry an FMR1 premutation

The association between maternal occupation and Down syndrome: A report from the national Down syndrome project

Recommended care and care adherence following a diagnosis of Lynch syndrome: A mixed-methods study

Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders

Clinical molecular marker testing data capture to promote precision medicine research within the Cancer Research Network

Implementation of a systematic tumor screening program for Lynch Syndrome in an integrated health care setting

Feasibility of an app-based mindfulness intervention among women with an FMR1 premutation experiencing maternal stress

The Healthcare Systems Research Network (HCSRN) as an environment for dissemination and implementation research: A case study of developing a multi-site research study in precision medicine

Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group

Implementing universal Lynch syndrome screening (IMPULSS): Protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts

Patient and provider perspectives on adherence to and care coordination of Lynch Syndrome surveillance recommendations: Findings from qualitative interviews

Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation