Jesse M. Hunter

1.3k total citations
31 papers, 875 citations indexed

About

Jesse M. Hunter is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Jesse M. Hunter has authored 31 papers receiving a total of 875 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 12 papers in Genetics and 8 papers in Physiology. Recurrent topics in Jesse M. Hunter's work include Genomics and Rare Diseases (9 papers), Alzheimer's disease research and treatments (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Jesse M. Hunter is often cited by papers focused on Genomics and Rare Diseases (9 papers), Alzheimer's disease research and treatments (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Jesse M. Hunter collaborates with scholars based in United States, Argentina and Canada. Jesse M. Hunter's co-authors include Chera L. Maarouf, Tyler A. Kokjohn, Alex E. Roher, Thomas G. Beach, Peter J. Detloff, Marwan N. Sabbagh, Mathieu Lesort, Roger L. Albin, Sara J. Tallaksen‐Greene and Michael Malek‐Ahmadi and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Jesse M. Hunter

30 papers receiving 863 citations

Peers

Jesse M. Hunter

CMN

PHYSI

NEURO

Shu‐Hsien Sheu United States

Miriam Sciaccaluga Italy

Ian M. Williams United Kingdom

Raquel Pérez‐Sen Spain

Xiaotian T. Fang Sweden

Georg von Jonquières Australia

Esmerilda G. Delicado Spain

Stephan Verleysdonk Germany

Kathleen M. Schoch United States

George K. E. Umanah United States

Shu‐Hsien Sheu United States

Jesse M. Hunter

567 ×1.5

256 ×1.0

CMN

224 ×0.9

PHYSI

164 ×1.1

NEURO

80 ×0.6

NEURO

Citations per year, relative to Jesse M. Hunter Jesse M. Hunter (= 1×) peers Shu‐Hsien Sheu

Countries citing papers authored by Jesse M. Hunter

Since Specialization

Citations

This map shows the geographic impact of Jesse M. 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 Jesse M. Hunter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jesse M. Hunter more than expected).

Fields of papers citing papers by Jesse M. Hunter

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jesse M. 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 Jesse M. Hunter. The network helps show where Jesse M. Hunter may publish in the future.

Co-authorship network of co-authors of Jesse M. Hunter

This figure shows the co-authorship network connecting the top 25 collaborators of Jesse M. Hunter. A scholar is included among the top collaborators of Jesse M. 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 Jesse M. Hunter. Jesse M. Hunter is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Hunter, Jesse M., et al.. (2025). Harnessing the microbiome to improve clinical outcomes for cancer, transplant, and immunocompromised patients in the intensive care unit (ICU). Frontiers in Cellular and Infection Microbiology. 15. 1577108–1577108. 1 indexed citations

Koboldt, Daniel C., Hui Mei, Ying‐Chen Claire Hou, et al.. (2024). Clinically significant findings in a decade‐long retrospective study of prenatal chromosomal microarray testing. Molecular Genetics & Genomic Medicine. 12(3). e2349–e2349. 3 indexed citations

Macke, Erica L., Anthony R. Miller, M. Isabel González, et al.. (2024). Optical Genome Mapping (OGM) Identifies Multiple Structural Variants in a Case With Atypical Phelan‐McDermid Syndrome. American Journal of Medical Genetics Part A. 197(3). e63929–e63929. 1 indexed citations

Ramadesikan, Swetha, Allison C. Daley, Liz Varga, et al.. (2024). Expanding the phenotypic spectrum of CSNK2A1-associated Okur-Chung neurodevelopmental syndrome. Human Genetics and Genomics Advances. 6(1). 100379–100379. 1 indexed citations

Ramadesikan, Swetha, Allison C. Daley, Matthew Pastore, et al.. (2024). Long-read genome sequencing resolves complex genomic rearrangements in rare genetic syndromes. npj Genomic Medicine. 9(1). 66–66. 2 indexed citations

Umamaheswaran, Gurusamy, Swetha Ramadesikan, Jesse M. Hunter, et al.. (2024). Biallelic variants in HTRA2 cause 3-methylglutaconic aciduria mitochondrial disorder: case report and literature review. Frontiers in Genetics. 14. 1298574–1298574.

Ramesh, Naveen, Min Hu, Sayaka Hashimoto, et al.. (2022). A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. Journal of Molecular Diagnostics. 24(9). 1031–1040. 3 indexed citations

Hunter, Jesse M., Lauren Massingham, Kandamurugu Manickam, et al.. (2022). Inherited and de novo variants extend the etiology of TAOK1-associated neurodevelopmental disorder. Molecular Case Studies. 8(2). mcs.a006180–mcs.a006180. 10 indexed citations

Powis, Zöe, Kelly D. Farwell Hagman, Kirsten Blanco, et al.. (2019). When moments matter: Finding answers with rapid exome sequencing. Molecular Genetics & Genomic Medicine. 8(2). e1027–e1027. 9 indexed citations

10.

Powis, Zöe, Kelly D. Farwell Hagman, Virginia Speare, et al.. (2018). Exome sequencing in neonates: diagnostic rates, characteristics, and time to diagnosis. Genetics in Medicine. 20(11). 1468–1471. 24 indexed citations

11.

Kokjohn, Tyler A., Chera L. Maarouf, Ian D. Daugs, et al.. (2012). Neurochemical Profile of Dementia Pugilistica. Journal of Neurotrauma. 30(11). 981–997. 29 indexed citations

12.

Hunter, Jesse M., John R. Cirrito, Jessica L. Restivo, et al.. (2012). Emergence of a seizure phenotype in aged apolipoprotein epsilon 4 targeted replacement mice. Brain Research. 1467. 120–132. 32 indexed citations

13.

Kokjohn, Tyler A., Gregory D. Van Vickle, Chera L. Maarouf, et al.. (2011). Chemical characterization of pro-inflammatory amyloid-beta peptides in human atherosclerotic lesions and platelets. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1812(11). 1508–1514. 46 indexed citations

14.

Maarouf, Chera L., Ian D. Daugs, Tyler A. Kokjohn, et al.. (2011). Alzheimer's Disease and Non-Demented High Pathology Control Nonagenarians: Comparing and Contrasting the Biochemistry of Cognitively Successful Aging. PLoS ONE. 6(11). e27291–e27291. 54 indexed citations

15.

Heng, Mary Y., Roger L. Albin, Sara J. Tallaksen‐Greene, et al.. (2010). Early autophagic response in a novel knock-in model of Huntington disease. Human Molecular Genetics. 19(19). 3702–3720. 99 indexed citations

16.

Zhao, Lingzhi, Suizhen Lin, Kelly R. Bales, et al.. (2009). Macrophage-Mediated Degradation of β-Amyloid via an Apolipoprotein E Isoform-Dependent Mechanism. Journal of Neuroscience. 29(11). 3603–3612. 60 indexed citations

17.

Hunter, Jesse M., et al.. (2009). Role of Molecular Chaperones in G Protein β5/Regulator of G Protein Signaling Dimer Assembly and G Protein βγ Dimer Specificity. Journal of Biological Chemistry. 284(24). 16386–16399. 25 indexed citations

18.

Hunter, Jesse M., Mathieu Lesort, & Gail V.W. Johnson. (2007). Ubiquitin‐proteasome system alterations in a striatal cell model of huntington's disease. Journal of Neuroscience Research. 85(8). 1774–1788. 38 indexed citations

19.

Tallaksen‐Greene, Sara J., Andrew B. Crouse, Jesse M. Hunter, Peter J. Detloff, & Roger L. Albin. (2005). Neuronal intranuclear inclusions and neuropil aggregates in HdhCAG(150) knockin mice. Neuroscience. 131(4). 843–852. 49 indexed citations

20.

Hunter, Jesse M., Andrew B. Crouse, Mathieu Lesort, Gail V.W. Johnson, & Peter J. Detloff. (2004). Verification of somatic CAG repeat expansion by pre-PCR fractionation. Journal of Neuroscience Methods. 144(1). 11–17. 10 indexed citations

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.

Explore authors with similar magnitude of impact