Jessica Ezzell Hunter

Author

Kaiser Permanente Center for Health Research ORCID

Also Known As

Boya Guo, Buchanan, Adam, Hunter, Jessica Ezzell, J E Hunter, J Hunter, J. E. Hunter, J. Hunter, James B. Hunter, James M Hoffman, Jessica E. Hunter

121

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Kaiser Permanente Center for Health Research Emory University Kaiser Permanente University of Washington Harvard University

About

Jessica Ezzell Hunter is an author at Kaiser Permanente Center for Health Research specializing in medicine, social sciences, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	336
2	Public Health	3	3	112
3	Health Sciences	2	2	120
4	Education	1	1	12
5	Nursing	1	1	44

Jessica Ezzell Hunter

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Evaluating Gene Expression in C57BL/6J and DBA/2J Mouse Striatum Using RNA-Seq and Microarrays Daniel Bottomly, Nicole A. R. Walter, Jessica Ezzell Hunter, PLoS ONE	2011	241
A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation Jessica Ezzell Hunter, Stephanie A. Irving, Leslie G. Biesecker, Genetics in Medicine	2016	146
A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation Bin Tang, Karoni Dutt, Ligia A. Papale, Neurobiology of Disease Generalized EpilepsySynaptic PlasticityMolecular NeuroscienceNeurophysiologyNeurological Function	2009	96
An Epilepsy Mutation in the Sodium Channel<i>SCN1A</i>That Decreases Channel Excitability Arthur J. Barela, Salina P. Waddy, Jay Lickfett, Journal of Neuroscience	2006	94
Fragile X‐associated primary ovarian insufficiency: evidence for additional genetic contributions to severity Jessica Ezzell Hunter, Michael P. Epstein, Stuart W. Tinker, Genetic Epidemiology	2008	79
The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project Jessica Ezzell Hunter, Emily G. Allen, Mikyong Shin, Genetics in Medicine Down SyndromeChild Well-beingChild HealthPediatricsLow Socioeconomic Status	2013	76
No Evidence for a Difference in Neuropsychological Profile among Carriers and Noncarriers of the FMR1 Premutation in Adults under the Age of 50 Jessica Ezzell Hunter, Emily G. Allen, Ann Abramowitz, The American Journal of Human Genetics Neuropsychological FunctioningNeuropsychologyNeuropsychological ProfileBrain FunctionNeuropsychiatry	2008	73
Investigation of Phenotypes Associated with Mood and Anxiety Among Male and Female Fragile X Premutation Carriers Jessica Ezzell Hunter, Emily G. Allen, Ann Abramowitz, Behavior Genetics Behavioral SciencesPsychiatryPhenotypes AssociatedMood SymptomFragile X Spectrum	2008	70
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 Alanna Kulchak Rahm, Deborah Cragun, Jessica Ezzell Hunter, BMC Health Services Research	2018	52
The FMR1 Premutation and Attention-Deficit Hyperactivity Disorder (ADHD): Evidence for a Complex Inheritance Jessica Ezzell Hunter, Michael P. Epstein, Stuart W. Tinker, Behavior Genetics NeuropsychologyNeuropsychiatryAttentionPsychologySocial Sciences	2011	44

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