Ami Rosen

2.3k total citations
23 papers, 832 citations indexed

About

Ami Rosen is a scholar working on Neurology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Ami Rosen has authored 23 papers receiving a total of 832 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 7 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Ami Rosen's work include Neurological disorders and treatments (9 papers), Botulinum Toxin and Related Neurological Disorders (8 papers) and Genetic Neurodegenerative Diseases (6 papers). Ami Rosen is often cited by papers focused on Neurological disorders and treatments (9 papers), Botulinum Toxin and Related Neurological Disorders (8 papers) and Genetic Neurodegenerative Diseases (6 papers). Ami Rosen collaborates with scholars based in United States, Canada and India. Ami Rosen's co-authors include Mahlon R. DeLong, Marian L. Evatt, Natasha Khazai, Shirley Triche, Vin Tangpricha, Hyder A. Jinnah, Stewart A. Factor, Joel S. Perlmutter, Cynthia Comella and Wendy R. Galpern and has published in prestigious journals such as Neurology, PEDIATRICS and Neurobiology of Aging.

In The Last Decade

Ami Rosen

22 papers receiving 812 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ami Rosen United States 14 503 192 174 129 67 23 832
Masayuki Yoshioka Japan 10 190 0.4× 162 0.8× 103 0.6× 27 0.2× 89 1.3× 21 510
András Király Hungary 16 131 0.3× 170 0.9× 102 0.6× 123 1.0× 47 0.7× 59 755
Patricia M. Washington United States 12 425 0.8× 47 0.2× 137 0.8× 139 1.1× 261 3.9× 15 894
A Muratorio Italy 18 423 0.8× 116 0.6× 236 1.4× 113 0.9× 143 2.1× 68 1.0k
Yoshiki Imamura Japan 20 317 0.6× 187 1.0× 336 1.9× 869 6.7× 117 1.7× 69 1.3k
E. Kapaki Greece 15 308 0.6× 37 0.2× 198 1.1× 359 2.8× 178 2.7× 24 893
Maja Relja Croatia 19 752 1.5× 135 0.7× 325 1.9× 356 2.8× 211 3.1× 41 1.3k
J. Leston France 10 479 1.0× 527 2.7× 43 0.2× 155 1.2× 87 1.3× 11 1.0k
Nadežda Šternić Serbia 16 515 1.0× 200 1.0× 156 0.9× 138 1.1× 69 1.0× 53 924
Michael Teepker Germany 15 197 0.4× 142 0.7× 53 0.3× 202 1.6× 61 0.9× 27 667

Countries citing papers authored by Ami Rosen

Since Specialization
Citations

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

Fields of papers citing papers by Ami Rosen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ami Rosen

This figure shows the co-authorship network connecting the top 25 collaborators of Ami Rosen. A scholar is included among the top collaborators of Ami Rosen 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 Ami Rosen. Ami Rosen 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.
Kenneson, Aileen, et al.. (2025). Qualitative assessment of primary care providers’ attitudes toward genetic services and genetics education. Journal of Community Genetics. 16(2). 131–137. 1 indexed citations
2.
Wang, Yunting, et al.. (2024). Patient experiences of receiving a diagnosis of hypermobile Ehlers–Danlos syndrome. American Journal of Medical Genetics Part A. 194(8). e63613–e63613. 3 indexed citations
3.
Laney, Dawn A., et al.. (2022). Validation of a suspicion index to identify patients at risk for hereditary angioedema. Journal of Allergy and Clinical Immunology Global. 2(1). 76–78. 2 indexed citations
4.
Laney, Dawn A., et al.. (2022). Development and implementation of an automated severity scoring system to identify patients at possible increased risk for ten lysosomal disorders. Molecular Genetics and Metabolism. 135(2). S70–S71. 1 indexed citations
5.
Rosen, Ami, et al.. (2019). Spinocerebellar Ataxia Patient Perceptions Regarding Reproductive Options. Movement Disorders Clinical Practice. 7(1). 37–44. 7 indexed citations
6.
Quillin, John M., et al.. (2018). The Changing Age of Individuals Seeking Presymptomatic Genetic Testing for Huntington Disease. Journal of Genetic Counseling. 27(5). 1157–1166. 8 indexed citations
7.
Jinnah, Hyder A., et al.. (2016). Botulinum toxin treatment failures in cervical dystonia: causes, management, and outcomes. Journal of Neurology. 263(6). 1188–1194. 51 indexed citations
8.
Young, Sarah P., et al.. (2016). Potential mechanisms for low uric acid in Parkinson disease. Journal of Neural Transmission. 123(4). 365–370. 15 indexed citations
9.
Comella, Cynthia, Joel S. Perlmutter, Hyder A. Jinnah, et al.. (2015). Reliability of the Severity subscale of the revised Toronto Spasmodic Torticollis Rating Scale (TWSTRS-2) (S15.001). Neurology. 84(14_supplement). 8 indexed citations
10.
Creighton, Francis X., Edie R. Hapner, Adam M. Klein, et al.. (2015). Diagnostic Delays in Spasmodic Dysphonia: A Call for Clinician Education. Journal of Voice. 29(5). 592–594. 40 indexed citations
11.
Comella, Cynthia, Christy L. Ludlow, Hyder A. Jinnah, et al.. (2015). Secured web-based video repository for multicenter studies. Parkinsonism & Related Disorders. 21(4). 366–371. 15 indexed citations
12.
Comella, Cynthia, Susan H. Fox, Kailash P. Bhatia, et al.. (2015). Development of the Comprehensive Cervical Dystonia Rating Scale: Methodology. Movement Disorders Clinical Practice. 2(2). 135–141. 43 indexed citations
13.
Rosen, Ami, Edie R. Hapner, Michael M. Johns, et al.. (2013). How long does it take to diagnose cervical dystonia?. Journal of the Neurological Sciences. 335(1-2). 72–74. 27 indexed citations
14.
Jinnah, Hyder A., Alfredo Berardelli, Cynthia Comella, et al.. (2013). The focal dystonias: Current views and challenges for future research. Movement Disorders. 28(7). 926–943. 149 indexed citations
15.
Factor, Stewart A., N. Kyle Steenland, Donald S. Higgins, et al.. (2011). Disease‐related and genetic correlates of psychotic symptoms in Parkinson's disease. Movement Disorders. 26(12). 2190–2195. 53 indexed citations
16.
Wingo, Thomas S., Ami Rosen, David J. Cutler, James J. Lah, & Allan I. Levey. (2010). Paraoxonase-1 polymorphisms in Alzheimer's disease, Parkinson's disease, and AD-PD spectrum diseases. Neurobiology of Aging. 33(1). 204.e13–204.e15. 27 indexed citations
17.
Evatt, Marian L., Mahlon R. DeLong, Natasha Khazai, et al.. (2008). Prevalence of Vitamin D Insufficiency in Patients With Parkinson Disease and Alzheimer Disease. Archives of Neurology. 65(10). 1348–52. 291 indexed citations
18.
Rosen, Ami, N. Kyle Steenland, John Hanfelt, et al.. (2007). Evidence of shared risk for Alzheimer’s disease and Parkinson’s disease using family history. Neurogenetics. 8(4). 263–270. 16 indexed citations
19.
Rosen, Ami. (2004). 10 Most Commonly Asked Questions About Genetic Testing. The Neurologist. 10(2). 107–109. 2 indexed citations
20.
Rosen, Ami, Sylvan Wallenstein, & Margaret M. McGovern. (2002). Attitudes of Pediatric Residents Toward Ethical Issues Associated With Genetic Testing in Children. PEDIATRICS. 110(2). 360–363. 15 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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