Joanna C. Jen

9.3k total citations · 1 hit paper
88 papers, 5.1k citations indexed

About

Joanna C. Jen is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Joanna C. Jen has authored 88 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cellular and Molecular Neuroscience, 43 papers in Molecular Biology and 29 papers in Neurology. Recurrent topics in Joanna C. Jen's work include Genetic Neurodegenerative Diseases (39 papers), Mitochondrial Function and Pathology (25 papers) and Vestibular and auditory disorders (18 papers). Joanna C. Jen is often cited by papers focused on Genetic Neurodegenerative Diseases (39 papers), Mitochondrial Function and Pathology (25 papers) and Vestibular and auditory disorders (18 papers). Joanna C. Jen collaborates with scholars based in United States, Germany and Switzerland. Joanna C. Jen's co-authors include Robert W. Baloh, Jijun Wan, Paul Greengard, Angus C. Nairn, Charles F. Stevens, Stanley F. Nelson, Qing Yue, Ji‐Soo Kim, Dominik Straumann and Michael Strupp and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Joanna C. Jen

87 papers receiving 5.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Bilateral vestibulopathy: Diagnostic criteria Consensus document of the Classification Committee of the Bárány Society1

2017 405 citations Michael Strupp, Ji‐Soo Kim et al. Journal of Vestibular Research profile →

Peers

Countries citing papers authored by Joanna C. Jen

Since Specialization

Citations

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

Fields of papers citing papers by Joanna C. Jen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joanna C. Jen. 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 Joanna C. Jen. The network helps show where Joanna C. Jen may publish in the future.

Co-authorship network of co-authors of Joanna C. Jen

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	The episodic ataxias 2024 ·Handbook of clinical neurology ·Tracey D. Graves, (unknown), Kamran Khodakhah, Robert C. Griggs, Joanna C. Jen	1
2	Episodic ataxias 2018 ·Handbook of clinical neurology ·Joanna C. Jen, Jijun Wan	5
3	Mutations of EXOSC3/Rrp40p associated with neurological diseases impact ribosomal RNA processing functions of the exosome in S. cerevisiae 2017 ·RNA ·(unknown), (unknown), Joanna C. Jen, Guillaume Chanfreau	24
4	Bilateral vestibulopathy: Diagnostic criteria Consensus document of the Classification Committee of the Bárány Society1 breakdown → 2017 ·Journal of Vestibular Research ·Michael Strupp, Ji‐Soo Kim, Toshihisa Murofushi, Dominik Straumann, Joanna C. Jen, Sally M. Rosengren, Charles C. Della Santina, Herman Kingma	405
5	A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism 2009 ·Human Molecular Genetics ·Patricia Blanco, Anja P. Einholm, Hafsa Mamsa, (unknown), Hugo Gutiérrez‐de‐Terán, J. Romero, Mads S. Toustrup-Jensen, Ãngel Carracedo, Joanna C. Jen, Bente Vilsen, M.J. Sobrido	45
6	Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake 2009 ·Archives of Neurology ·Boukje de Vries, Hafsa Mamsa, Anine H Stam, Jijun Wan, S. L. M. Bakker, Kaate R. J. Vanmolkot, Joost Haan, Gisela M. Terwindt, Elles M. J. Boon, Bruce D. Howard, Rune R. Frants, Robert W. Baloh, Michel D. Ferrari, Joanna C. Jen, Arn M. J. M. van den Maagdenberg	99
7	Familial Episodic Ataxia 2009 ·Annals of the New York Academy of Sciences ·Joanna C. Jen, Robert W. Baloh	17
8	Recent advances in the genetics of recurrent vertigo and vestibulopathy 2008 ·Current Opinion in Neurology ·Joanna C. Jen	19
9	Progressive Cerebellar Ataxia with Variable Episodic Symptoms – Phenotypic Diversity of R1668W CACNA1A Mutation 2008 ·European Neurology ·Sarah Marti, Robert W. Baloh, Joanna C. Jen, Dominik Straumann, Hans H. Jung	17
10	Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea 2007 ·Muscle & Nerve ·Steven J. Shook, Hafsa Mamsa, Joanna C. Jen, Robert W. Baloh, Lan Zhou	27
11	Association of progesterone receptor with migraine-associated vertigo 2007 ·Neurogenetics ·Hane Lee, (unknown), Joanna C. Jen, Yoon‐Hee Cha, Robert W. Baloh, Stanley F. Nelson	30
12	Prolonged hemiplegic episodes in children due to mutations in ATP1A2 2006 ·Journal of Neurology Neurosurgery & Psychiatry ·Joanna C. Jen, Andrea Klein, Eugen Boltshauser, Michael S. Cartwright, E. Steve Roach, Hafsa Mamsa, Robert W. Baloh	39
13	HERNS 2005 ·Der Nervenarzt ·Carola Seifried, Matthias Sitzer, Joanna C. Jen, Georg Auburger	4
14	Three brothers with a very‐late‐onset writer's cramp 2005 ·Movement Disorders ·Roongroj Bhidayasiri, Joanna C. Jen, Robert W. Baloh	12
15	Late-onset pure cerebellar ataxia: Differentiating those with and without identifiable mutations 2005 ·Journal of the Neurological Sciences ·Kevin A. Kerber, Joanna C. Jen, Susan Perlman, Robert W. Baloh	28
16	A novel mutation in KCNA1 causes episodic ataxia without myokymia 2004 ·Human Mutation ·Hane Lee, Hui Wang, Joanna C. Jen, Chiara Sabatti, Robert W. Baloh, Stanley F. Nelson	40
17	No Mutations in CACNA1A and ATP1A2 in Probands With Common Types of Migraine 2004 ·Archives of Neurology ·Joanna C. Jen, (unknown), (unknown), Robert W. Baloh	58
18	Genetics of episodic ataxia. 2002 ·PubMed ·Joanna C. Jen, Robert W. Baloh	16
19	Genetics of Familial Episodic Vertigo and Ataxia 2002 ·Annals of the New York Academy of Sciences ·Robert W. Baloh, Joanna C. Jen	28
20	De novo mutation in CACNA1A caused acetazolamide-responsive episodic ataxia 1998 ·American Journal of Medical Genetics ·Qing Yue, Joanna C. Jen, (unknown), Stanley F. Nelson, Robert W. Baloh	60

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.

Explore authors with similar magnitude of impact