Audrey Strongosky

2.4k total citations
43 papers, 1.3k citations indexed

About

Audrey Strongosky is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Audrey Strongosky has authored 43 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Neurology, 12 papers in Cellular and Molecular Neuroscience and 12 papers in Neurology. Recurrent topics in Audrey Strongosky's work include Parkinson's Disease Mechanisms and Treatments (24 papers), Neurological disorders and treatments (12 papers) and Neurological diseases and metabolism (10 papers). Audrey Strongosky is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (24 papers), Neurological disorders and treatments (12 papers) and Neurological diseases and metabolism (10 papers). Audrey Strongosky collaborates with scholars based in United States, Canada and Poland. Audrey Strongosky's co-authors include Ryan J. Uitti, Zbigniew K. Wszołek, Dennis W. Dickson, A. Jon Stoessl, Matthew J. Farrer, Donald B. Calne, Owen A. Ross, Thomas Gasser, Z.K. Wszolek and M.F. Turk and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Audrey Strongosky

41 papers receiving 1.3k citations

Peers

Audrey Strongosky

NEURO

CMN

NEURO

PHYSI

Benjámin Bereznai Hungary

Tomokazu Obi Japan

Alexandra I. Soto‐Ortolaza United States

Oswaldo Lorenzo‐Betancor Spain

Mari Tada Japan

Charles Duyckaerts France

Yasmine T. Asi United Kingdom

Vanessa Brochard France

Chi Wang Ip Germany

Yi‐Min Sun China

Benjámin Bereznai Hungary

Audrey Strongosky

940 ×0.9

NEURO

584 ×1.3

CMN

243 ×0.8

NEURO

146 ×0.5

PHYSI

247 ×1.0

Citations per year, relative to Audrey Strongosky Audrey Strongosky (= 1×) peers Benjámin Bereznai

Countries citing papers authored by Audrey Strongosky

Since Specialization

Citations

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

Fields of papers citing papers by Audrey Strongosky

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Audrey Strongosky

This figure shows the co-authorship network connecting the top 25 collaborators of Audrey Strongosky. A scholar is included among the top collaborators of Audrey Strongosky 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 Audrey Strongosky. Audrey Strongosky 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

Mannheim, Julia G., Jessie Fanglu Fu, Ivan S. Klyuzhin, et al.. (2024). Multi-tracer PET correlation analysis reveals disease-specific patterns in Parkinson’s disease and asymptomatic LRRK2 pathogenic variant carriers compared to healthy controls. NeuroImage Clinical. 42. 103600–103600.

Rush, Beth, Philip W. Tipton, Audrey Strongosky, & Zbigniew K. Wszołek. (2023). Neuropsychological profile of CSF1R-related leukoencephalopathy. Frontiers in Neurology. 14. 1155387–1155387. 1 indexed citations

Ikezu, Tsuneya, et al.. (2020). Crohn’s and Parkinson’s Disease-Associated LRRK2 Mutations Alter Type II Interferon Responses in Human CD14+ Blood Monocytes Ex Vivo. Journal of Neuroimmune Pharmacology. 15(4). 794–800. 17 indexed citations

Wernick, Anna I., Audrey Strongosky, Alexandra I. Soto‐Beasley, et al.. (2020). Spinocerebellar ataxia type 6 family with phenotypic overlap with Multiple System Atrophy. Neurologia i Neurochirurgia Polska. 54(4). 350–355. 5 indexed citations

Caulfield, Thomas R., Audrey Strongosky, Karen Jansen‐West, et al.. (2018). TRIO gene segregation in a family with cerebellar ataxia. Neurologia i Neurochirurgia Polska. 52(6). 743–749. 3 indexed citations

Markopoulou, Katerina, Bruce A. Chase, Piotr Robowski, et al.. (2016). Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction. PLoS ONE. 11(11). e0165112–e0165112. 11 indexed citations

Tipton, Philip W., et al.. (2016). Spinocerebellar ataxia 15: A phenotypic review and expansion. Neurologia i Neurochirurgia Polska. 51(1). 86–91. 13 indexed citations

Tacik, Paweł, Audrey Strongosky, Daniel F. Broderick, et al.. (2015). Whole-Exome Sequencing as a Diagnostic Tool in a Family With Episodic Ataxia Type 1. Mayo Clinic Proceedings. 90(3). 366–371. 12 indexed citations

Tacik, Paweł, Michael DeTure, Wen-Lang Lin, et al.. (2015). A novel tau mutation, p.K317N, causes globular glial tauopathy. Acta Neuropathologica. 130(2). 199–214. 39 indexed citations

10.

Wren, Melissa C., Jing Zhao, Chia‐Chen Liu, et al.. (2015). Frontotemporal dementia-associated N279K tau mutant disrupts subcellular vesicle trafficking and induces cellular stress in iPSC-derived neural stem cells. Molecular Neurodegeneration. 10(1). 46–46. 54 indexed citations

11.

Fujioka, Shinsuke, Mónica Sánchez-Contreras, Audrey Strongosky, et al.. (2014). Three sib-pairs of autopsy-confirmed progressive supranuclear palsy. Parkinsonism & Related Disorders. 21(2). 101–105. 32 indexed citations

12.

Tacik, Paweł, Fabienne C. Fiesel, Shinsuke Fujioka, et al.. (2014). Three families with Perry syndrome from distinct parts of the world. Parkinsonism & Related Disorders. 20(8). 884–888. 22 indexed citations

13.

Baker, Matt, Audrey Strongosky, Mónica Sánchez-Contreras, et al.. (2013). SLC20A2 and THAP1 deletion in familial basal ganglia calcification with dystonia. Neurogenetics. 15(1). 23–30. 46 indexed citations

14.

Labbé, Catherine, Alexandra I. Soto‐Ortolaza, Sruti Rayaprolu, et al.. (2013). Investigating the role of FUS exonic variants in Essential Tremor. Parkinsonism & Related Disorders. 19(8). 755–757. 25 indexed citations

15.

DeJesus‐Hernandez, Mariely, Sruti Rayaprolu, Alexandra I. Soto‐Ortolaza, et al.. (2012). Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome. Parkinsonism & Related Disorders. 19(2). 198–201. 31 indexed citations

16.

Shinotoh, Hitoshi, Zbigniew K. Wszołek, Audrey Strongosky, et al.. (2010). In vivo detection of neuropathologic changes in presymptomatic MAPT mutation carriers: A PET and MRI study. Parkinsonism & Related Disorders. 16(6). 404–408. 52 indexed citations

17.

Spector, Andrew R., Brittany N. Dugger, Zbigniew K. Wszołek, et al.. (2010). Anatomy of disturbed sleep in pallido‐ponto‐nigral degeneration. Annals of Neurology. 69(6). 1014–1025. 7 indexed citations

18.

Słowiński, Jerzy, Akiko Imamura, Ryan J. Uitti, et al.. (2007). MR imaging of brainstem atrophy in progressive supranuclear palsy. Journal of Neurology. 255(1). 37–44. 46 indexed citations

19.

Wszołek, Zbigniew K., Yasuhiko Baba, Ian R. Mackenzie, et al.. (2006). Autosomal dominant dystonia-plus with cerebral calcifications. Neurology. 67(4). 620–625. 28 indexed citations

20.

Adams, John R., Michael Schulzer, Edwin Mak, et al.. (2005). PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation. Brain. 128(12). 2777–2785. 196 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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