Jason Hehir

784 total citations
5 papers, 252 citations indexed

About

Jason Hehir is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Jason Hehir has authored 5 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Neurology, 2 papers in Cellular and Molecular Neuroscience and 2 papers in Neurology. Recurrent topics in Jason Hehir's work include Parkinson's Disease Mechanisms and Treatments (4 papers), Lysosomal Storage Disorders Research (2 papers) and Neurological diseases and metabolism (2 papers). Jason Hehir is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (4 papers), Lysosomal Storage Disorders Research (2 papers) and Neurological diseases and metabolism (2 papers). Jason Hehir collaborates with scholars based in United Kingdom, United States and Spain. Jason Hehir's co-authors include Henry Houlden, Andrea Haworth, Sarah J. Tabrizi, James M. Polke, Jon Beck, Ese Mudanohwo, Peter McColgan, Davina J. Hensman Moss, Mark Poulter and Tracy Campbell and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Jason Hehir

5 papers receiving 244 citations

Peers

Jason Hehir
Daniela Corongiu Italy
R. Ou China
L. E. Hjermind Denmark
Diana A. Olszewska Ireland
Mario Cornejo‐Olivas Peru
Josja Graafland Netherlands
Hatice Karasoy Türkiye
Heike Pawlack Germany
Monica Federoff United States
Maximilian Naujock Germany
Daniela Corongiu Italy
Jason Hehir
Citations per year, relative to Jason Hehir Jason Hehir (= 1×) peers Daniela Corongiu

Countries citing papers authored by Jason Hehir

Since Specialization
Citations

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

Fields of papers citing papers by Jason Hehir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jason Hehir. 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 Jason Hehir. The network helps show where Jason Hehir may publish in the future.

Co-authorship network of co-authors of Jason Hehir

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

All Works

5 of 5 papers shown
1.
Lubbe, Steven, Bernabé I. Bustos, Jing Hu, et al.. (2021). Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk. Human Molecular Genetics. 30(1). 78–86. 37 indexed citations
2.
Bandrés‐Ciga, Sara, Niccolò E. Mencacci, Raquel Durán, et al.. (2015). Analysis of the genetic variability in Parkinson's disease from Southern Spain. Neurobiology of Aging. 37. 210.e1–210.e5. 22 indexed citations
3.
Poulter, Mark, Jon Beck, Tracy Campbell, et al.. (2014). K11 C9orf72 Expansions Are The Most Common Genetic Cause Of Huntington's Disease Phenocopy Presentations In A Uk Cohort. Journal of Neurology Neurosurgery & Psychiatry. 85(Suppl 1). A82–A82. 2 indexed citations
4.
Kara, Eleanna, Aoife P. Kiely, Christos Proukakis, et al.. (2014). A 6.4 Mb Duplication of the α-Synuclein Locus Causing Frontotemporal Dementia and Parkinsonism. JAMA Neurology. 71(9). 1162–1162. 54 indexed citations
5.
Moss, Davina J. Hensman, Mark Poulter, Jon Beck, et al.. (2013). C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology. 82(4). 292–299. 137 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.

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2026