Jessica Ezzell Hunter

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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

RTI to serve as coordinating center for new Down syndrome research initiative

ASHG Annual Meeting 2022

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

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

The association of low socioeconomic status and the risk of having a child with Down syndrome: A report from the National Down Syndrome Project

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

A variance-component framework for pedigree analysis of continuous and categorical outcomes

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

Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation?: A review of current literature

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

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

No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50

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

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

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

Epidemiology of fragile X syndrome: A systematic review and meta-analysis

Evaluating gene expression in C57BL/6J and DBA/2J mouse striatum using RNA-Seq and microarrays