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List of works by Jessica Ezzell Hunter

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

scientific article published on 28 April 2016

An epilepsy mutation in the sodium channel SCN1A that decreases channel excitability

scientific article

Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts

scientific article published on 16 January 2012

Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms ⬇️

scientific article published on 09 May 2012

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

scientific article published on 03 April 2014

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

scientific article

Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

scientific article

Genetic effects on sleep/wake variation of seizures

scientific article

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

scientific article published on February 2009

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

scientific article published on May 1, 2011

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

scientific article

The FMR1 Premutation and Attention-Deficit Hyperactivity Disorder (ADHD): Evidence for a Complex Inheritance ⬇️

scientific article published on November 19, 2011

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