Peter Hedera

8.2k total citations
176 papers, 5.3k citations indexed

About

Peter Hedera is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Peter Hedera has authored 176 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 87 papers in Neurology, 65 papers in Cellular and Molecular Neuroscience and 35 papers in Neurology. Recurrent topics in Peter Hedera's work include Neurological disorders and treatments (57 papers), Parkinson's Disease Mechanisms and Treatments (42 papers) and Genetic Neurodegenerative Diseases (29 papers). Peter Hedera is often cited by papers focused on Neurological disorders and treatments (57 papers), Parkinson's Disease Mechanisms and Treatments (42 papers) and Genetic Neurodegenerative Diseases (29 papers). Peter Hedera collaborates with scholars based in United States, Italy and Germany. Peter Hedera's co-authors include John K. Fink, Robert P. Friedland, George J. Brewer, Rajesh N. Kalaria, Thomas L. Davis, Fenna T. Phibbs, Raj N. Kalaria, Daniel R. Premkumar, David Cohen and Karen J. Kluin and has published in prestigious journals such as The Lancet, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Peter Hedera

167 papers receiving 5.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Peter Hedera United States 37 1.8k 1.5k 936 934 720 176 5.3k
Keyoumars Ashkan United Kingdom 40 3.9k 2.2× 2.4k 1.6× 870 0.9× 483 0.5× 700 1.0× 254 7.1k
Roberta Ghidoni Italy 43 1.4k 0.8× 646 0.4× 995 1.1× 1.9k 2.0× 496 0.7× 158 5.6k
Jean‐Jacques Hauw France 42 2.1k 1.2× 995 0.7× 1.7k 1.8× 2.6k 2.7× 693 1.0× 140 6.6k
Sun Ju Chung South Korea 34 2.9k 1.6× 872 0.6× 390 0.4× 465 0.5× 169 0.2× 211 4.3k
Luisa Benussi Italy 39 1.3k 0.7× 504 0.3× 953 1.0× 1.7k 1.9× 343 0.5× 138 5.0k
Takehiko Yanagihara Japan 48 1.8k 1.0× 2.1k 1.4× 1.8k 1.9× 2.6k 2.8× 286 0.4× 232 7.6k
Sharon Menzies United States 20 936 0.5× 327 0.2× 745 0.8× 813 0.9× 997 1.4× 22 3.6k
Stephen B. Wharton United Kingdom 51 2.6k 1.4× 1.3k 0.9× 2.3k 2.4× 2.8k 3.0× 264 0.4× 170 8.9k
Oliver Kempski Germany 45 1.9k 1.0× 1.3k 0.9× 940 1.0× 1.5k 1.6× 241 0.3× 226 6.4k
Hélène Girouard Canada 28 535 0.3× 598 0.4× 1.1k 1.2× 826 0.9× 218 0.3× 66 4.4k

Countries citing papers authored by Peter Hedera

Since Specialization
Citations

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

Fields of papers citing papers by Peter Hedera

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Hedera

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

All Works

20 of 20 papers shown
1.
Wylie, Scott A., Ahmad Alhourani, Ajmal Zemmar, et al.. (2025). Theta and beta power in the subthalamic nucleus respond to conflict across subregion and hemisphere. Brain Communications. 7(1). fcaf021–fcaf021.
2.
Dato, Fabiola Di & Peter Hedera. (2024). Zinc for Wilson’s Disease: What We Know and What We Don’t Know. SHILAP Revista de lepidopterología. 84–95.
3.
Cukier, Holly N., Anthony J. Griswold, Simona G. Codreanu, et al.. (2022). Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions. npj Parkinson s Disease. 8(1). 84–84. 6 indexed citations
4.
Pascual, Belén, Susanne T. de Bot, Marcondes C. França, et al.. (2019). “Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia. American Journal of Neuroradiology. 40(1). 199–203. 39 indexed citations
5.
Hedera, Peter. (2019). Clinical management of Wilson disease. Annals of Translational Medicine. 7(S2). S66–S66. 28 indexed citations
6.
Sukul, Vishad, William J. Rodriguez, Srivatsan Pallavaram, et al.. (2018). Confined Thalamic Deep Brain Stimulation in Refractory Essential Tremor. Stereotactic and Functional Neurosurgery. 96(5). 296–304. 11 indexed citations
7.
Pallavaram, Srivatsan, Fenna T. Phibbs, Christopher Tolleson, et al.. (2013). Neurologist Consistency in Interpreting Information Provided by an Interactive Visualization Software for Deep Brain Stimulation Postoperative Programming Assistance. Neuromodulation Technology at the Neural Interface. 17(1). 11–15. 6 indexed citations
8.
Charles, David, Chandler E. Gill, Thomas L. Davis, et al.. (2011). Deep brain stimulation in early Parkinson’s disease: Enrollment experience from a pilot trial. Parkinsonism & Related Disorders. 18(3). 268–273. 36 indexed citations
9.
10.
Blair, Marcia, et al.. (2007). Infantile Onset of Hereditary Spastic Paraplegia Poorly Predicts the Genotype. Pediatric Neurology. 36(6). 382–386. 17 indexed citations
11.
Hedera, Peter, Shaochun Ma, Marcia Blair, et al.. (2006). Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22. Epilepsia. 47(10). 1622–1628. 34 indexed citations
12.
Hedera, Peter, John K. Fink, Paula Bockenstedt, & George J. Brewer. (2003). Myelopolyneuropathy and Pancytopenia Due to Copper Deficiency and High Zinc Levels of Unknown Origin. Archives of Neurology. 60(9). 1303–6. 72 indexed citations
13.
Hedera, Peter, et al.. (2002). Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1. Journal of Medical Genetics. 39(7). 484–488. 10 indexed citations
14.
Hedera, Peter & Raymond Scott Turner. (2002). Inherited dementias. Neurologic Clinics. 20(3). 779–808. 8 indexed citations
15.
Zhao, Xinping, David M. Alvarado, Shirley Rainier, et al.. (2001). Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. Nature Genetics. 29(3). 326–331. 255 indexed citations
16.
Hedera, Peter. (2000). Clinical Diagnosis and Management of Alzheimer's Disease, 2nd ed. Archives of Neurology. 57(5). 756–756. 8 indexed citations
17.
Hedera, Peter, Shirley Rainier, David M. Alvarado, et al.. (1999). Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q. The American Journal of Human Genetics. 64(2). 563–569. 71 indexed citations
18.
Hedera, Peter & Robert P. Friedland. (1997). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy:. Journal of the Neurological Sciences. 146(1). 27–33. 27 indexed citations
19.
Lerner, Alan J., Peter Hedera, Elisabeth Koss, Jon C. Stuckey, & Robert P. Friedland. (1997). Delirium in Alzheimer Disease. Alzheimer Disease & Associated Disorders. 11(1). 16–20. 87 indexed citations
20.
Cohen, David, Peter Hedera, Daniel R. Premkumar, Robert P. Friedland, & Raj N. Kalaria. (1997). Amyloid‐β Protein Angiopathies Masquerading as Alzheimer's Disease?a. Annals of the New York Academy of Sciences. 826(1). 390–395. 21 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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