Jessica Ezzell Hunter

2.5k total citations
57 papers, 1.3k citations indexed

About

Jessica Ezzell Hunter is a scholar working on Genetics, Pathology and Forensic Medicine and Cognitive Neuroscience. According to data from OpenAlex, Jessica Ezzell Hunter has authored 57 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 14 papers in Pathology and Forensic Medicine and 12 papers in Cognitive Neuroscience. Recurrent topics in Jessica Ezzell Hunter's work include BRCA gene mutations in cancer (15 papers), Genetic factors in colorectal cancer (14 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Jessica Ezzell Hunter is often cited by papers focused on BRCA gene mutations in cancer (15 papers), Genetic factors in colorectal cancer (14 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Jessica Ezzell Hunter collaborates with scholars based in United States, United Kingdom and Canada. Jessica Ezzell Hunter's co-authors include Stephanie L. Sherman, José Leal, Iain Fotheringham, Angel Angelov, Oliver Rivero‐Arias, Edward Kim, Ann Abramowitz, Krista Charen, Emily G. Allen and Lisa Shubeck and has published in prestigious journals such as Journal of Neuroscience, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Jessica Ezzell Hunter

50 papers receiving 1.3k citations

Peers

Countries citing papers authored by Jessica Ezzell Hunter

Since Specialization

Citations

This map shows the geographic impact of Jessica Ezzell Hunter's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jessica Ezzell Hunter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jessica Ezzell Hunter more than expected).

Fields of papers citing papers by Jessica Ezzell Hunter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jessica Ezzell Hunter. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jessica Ezzell Hunter. The network helps show where Jessica Ezzell Hunter may publish in the future.

Co-authorship network of co-authors of Jessica Ezzell Hunter

This figure shows the co-authorship network connecting the top 25 collaborators of Jessica Ezzell Hunter. A scholar is included among the top collaborators of Jessica Ezzell Hunter based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jessica Ezzell Hunter. Jessica Ezzell Hunter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	5952 The determinants of intraventricular hemorrhage among neonates at a public hospital in South Africa (2013–2020) 2024 ·Jessica Ezzell Hunter, B. Krüger, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	1
2	“Go ahead and screen” - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients 2023 ·Hereditary Cancer in Clinical Practice ·Jennifer L. Schneider, Alison Firemark, (unknown), James V. Davis, Pamala A. Pawloski, Su‐Ying Liang, Mara M. Epstein, Jan T. Lowery, Christine Y. Lu, Ravi Sharaf, Andrea N. Burnett‐Hartman, (unknown), Zachary Salvati, Deborah Cragun, Alanna Kulchak Rahm, Jessica Ezzell Hunter	0
3	Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system 2022 ·Hereditary Cancer in Clinical Practice ·(unknown), Jamilyn M. Zepp, (unknown), (unknown), Tia L. Kauffman, Elizabeth Shuster, Katrina A.B. Goddard, Benjamin S. Wilfond, Jessica Ezzell Hunter	7
4	Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol 2021 ·Journal of Personalized Medicine ·Tia L. Kauffman, (unknown), (unknown), Jamilyn M. Zepp, (unknown), (unknown), (unknown), (unknown), (unknown), Alan F. Rope, Sheila Weinmann, Nora B. Henrikson, Sandra Soo‐Jin Lee, Heather Spencer Feigelson, Jessica Ezzell Hunter	4
5	Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities 2021 ·JCO Precision Oncology ·Kathleen F. Mittendorf, Sarah Knerr, Tia L. Kauffman, Nangel M. Lindberg, Katherine Anderson, Heather Spencer Feigelson, Marian J. Gilmore, Jessica Ezzell Hunter, Galen Joseph, Stephanie A. Kraft, Jamilyn M. Zepp, Sapna Syngal, Benjamin S. Wilfond, Katrina A.B. Goddard	19
6	Congenital Cytomegalovirus and Human Immunodeficiency Virus: Effects on Hearing, Speech and Language Development, and Clinical Outcomes in Children 2021 ·Frontiers in Pediatrics ·(unknown), (unknown), Jessica Ezzell Hunter, Yonghee Oh	4
7	Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings 2021 ·Genetics in Medicine ·Devan M. Duenas, Kelly J. Shipman, Kathryn M. Porter, Elizabeth Shuster, Cláudia Guerra, (unknown), Tia L. Kauffman, Jessica Ezzell Hunter, Katrina A.B. Goddard, Benjamin S. Wilfond, Stephanie A. Kraft	5
8	Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population 2021 ·Familial Cancer ·Kathleen F. Mittendorf, Chinedu Ukaegbu, Marian J. Gilmore, Nangel M. Lindberg, Tia L. Kauffman, Donna J. Eubanks, Elizabeth Shuster, (unknown), Carmit K. McMullen, Heather Spencer Feigelson, Katherine Anderson, Michael C. Leo, Jessica Ezzell Hunter, Sonia Okuyama, Jamilyn M. Zepp, Sapna Syngal, Benjamin S. Wilfond, Katrina A.B. Goddard	9
9	Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders 2019 ·Genetics in Medicine ·Ryan S. Paquin, Kathleen F. Mittendorf, Megan A. Lewis, Jessica Ezzell Hunter, Kristy Lee, Jonathan S. Berg, Marc S. Williams, Katrina A.B. Goddard	3
10	Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews 2018 ·Hereditary Cancer in Clinical Practice ·Jennifer L. Schneider, Katrina A.B. Goddard, Kristin R. Muessig, James V. Davis, Alan F. Rope, Jessica Ezzell Hunter, Susan K. Peterson, Louise S. Acheson, Sapna Syngal, Georgia L. Wiesner, Jacob A. Reiss	24
11	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 2018 ·BMC Health Services Research ·Alanna Kulchak Rahm, Deborah Cragun, Jessica Ezzell Hunter, Mara M. Epstein, Jan T. Lowery, Christine Y. Lu, Pamala A. Pawloski, Ravi Sharaf, Su‐Ying Liang, Andrea N. Burnett‐Hartman, (unknown), Jing Hao, Susan Snyder, Radhika Gogoi, Ilene Ladd, Marc S. Williams	29
12	Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives 2017 ·Familial Cancer ·Jessica Ezzell Hunter, Kathleen Arnold, (unknown), Jamilyn M. Zepp, Marian J. Gilmore, Alan F. Rope, James V. Davis, (unknown), Elizabeth Esterberg, Kristin R. Muessig, Susan K. Peterson, Sapna Syngal, Louise S. Acheson, Georgia L. Wiesner, Jacob A. Reiss, Katrina A.B. Goddard	12
13	The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project 2013 ·Genetics in Medicine ·Jessica Ezzell Hunter, Emily G. Allen, Mikyong Shin, Lora Jh Bean, Adolfo Correa, Charlotte M. Druschel, Charlotte A. Hobbs, Leslie A. O’Leary, Paul A. Romitti, Marjorie H. Royle, Claudine P. Torfs, Sallie B. Freeman, Stephanie L. Sherman	40
14	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 2012 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Jessica Ezzell Hunter, Mary Leslie, (unknown), Debra Hamilton, Lisa Shubeck, Krista Charen, Ann Abramowitz, Michael P. Epstein, Adriana Lori, Elisabeth B. Binder, Joseph F. Cubells, Stephanie L. Sherman	32
15	Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome. 2011 ·Neuropsychology ·Emily G. Allen, Jessica Ezzell Hunter, (unknown), Jorge L. Juncos, (unknown), Debra Hamilton, Lisa Shubeck, Krista Charen, Stephanie L. Sherman	15
16	The FMR1 Premutation and Attention-Deficit Hyperactivity Disorder (ADHD): Evidence for a Complex Inheritance 2011 ·Behavior Genetics ·Jessica Ezzell Hunter, Michael P. Epstein, Stuart W. Tinker, Ann Abramowitz, Stephanie L. Sherman	35
17	A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes 2009 ·Statistics in Biosciences ·Michael P. Epstein, Jessica Ezzell Hunter, Emily G. Allen, Stephanie L. Sherman, Xihong Lin, Michael Boehnke	2
18	A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation 2009 ·Neurobiology of Disease ·Bin Tang, (unknown), Ligia A. Papale, Raffaella Rusconi, Anupama Shankar, Jessica Ezzell Hunter, (unknown), Frank H. Yu, William A. Catterall, Massimo Mantegazza, Alan L. Goldin, Andrew Escayg	77
19	Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature 2009 ·Genetics in Medicine ·Jessica Ezzell Hunter, Ann Abramowitz, (unknown), Stephanie L. Sherman	35
20	Subthreshold changes of voltage-dependent activation of the KV7.2 channel in neonatal epilepsy 2006 ·Neurobiology of Disease ·Jessica Ezzell Hunter, Snezana Maljevic, Anupama Shankar, Anne Siegel, Barbara Weissman, (unknown), (unknown), Holger Lerche, Andrew Escayg	27

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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