Jesse M. Hunter

1.3k citations
31 papers · 875 · h-index 16

Impact in

  • Neurology top 5%
    • Neuroinflammation and Neurodegeneration Mechanisms
    • Neurological Disease Mechanisms and Treatments
    • Genetic Neurodegenerative Diseases
    • Neuroscience and Neuropharmacology Research

Papers in

    • Mitochondrial Function and Pathology 5
    • Genomics and Rare Diseases 9
    • Genomic variations and chromosomal abnormalities 7
    • Genetics and Neurodevelopmental Disorders 3

Jesse M. Hunter

30 papers receiving 863 citations

Peers

Jesse M. Hunter
Comparison fields: 5 of 84
  • Neurology 148
  • Cellular and Molecular Neuroscience 266
  • Biological Psychiatry 30
  • Physiology 263
  • Neurology 132
Replace Shu‐Hsien Sheu with:
Shu‐Hsien Sheu United States
Matthew J. Crisp United States
Nicholas T. Seyfried United States
Kyota Fujita Japan
Pierre De Rossi United States
Hirohide Sawada Japan
Georg von Jonquières Australia
Michael Kurnellas United States
Nicholas Mitsios Sweden
Yu‐Wen Alvin Huang United States
Jesse M. Hunter relative to Shu‐Hsien Sheu United States Shu‐Hsien Sheu's profile →
Citations per field
00.5×4.7×
Shu‐Hsien Sheu · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Jesse M. Hunter, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jesse M. Hunter Line = papers co-authored together Jesse M. Hunter links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2012145
2 201099
3 201961
4 200960
5 200058
6 201154
7 200549
8 201146
9 200738
10 201535
11 201232
12 201229
13 200925
14 201824
15 200321
16 201121
17 201514
18 201113
19 202210
20 200410

About Jesse M. Hunter

Jesse M. Hunter is a scholar working on Molecular Biology, Genetics, Physiology, Cellular and Molecular Neuroscience and Neurology, having authored 31 papers that have together received 875 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Alzheimer's disease research and treatments (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic Neurodegenerative Diseases (5 papers), Mitochondrial Function and Pathology (5 papers), Dementia and Cognitive Impairment Research (4 papers), Genetic factors in colorectal cancer (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Neurology (148 citations), Cellular and Molecular Neuroscience (266 citations), Biological Psychiatry (30 citations), Physiology (263 citations) and Neurology (132 citations). Jesse M. Hunter has collaborated with scholars based in United States, Argentina and Canada. Frequent co-authors include Tyler A. Kokjohn, Alex E. Roher, Chera L. Maarouf, Thomas G. Beach, Peter J. Detloff, Marwan N. Sabbagh, Mathieu Lesort, Sara J. Tallaksen‐Greene, Roger L. Albin and Michael Malek‐Ahmadi. Their work appears in journals such as Genetics in Medicine, Journal of Alzheimer s Disease, PLoS ONE, Human Genetics and Genomics Advances and Journal of Neuroscience.

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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