Jessica Ezzell Hunter

RTI uses cookies to offer you the best experience online. By clicking “accept” on this website, you opt in and you agree to the use of cookies. If you would like to know more about how RTI uses cookies and how to manage them please view our Privacy Policy here. You can “opt out” or change your mind by visiting: http://optout.aboutads.info/. Click “accept” to agree.

Search Results

Filter by Type

Filter by Year

Filter by Focus Area

Filter by Solution

Filter by Center

Search Results

Genetic load is associated with hypothalamic-pituitary-adrenal (HPA) axis dysregulation in macaques

Establishing the medical actionability of genomic variants

Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers

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

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

American Society of Human Genetics (ASHG) Annual Meeting 2023

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

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

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

A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation

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

Co-occuring diagnoses among FMR1 premutation allele carriers

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

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

Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome

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

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

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

Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers

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