Kishore R. Kumar

4.8k total citations · 1 hit paper
95 papers, 1.9k citations indexed

About

Kishore R. Kumar is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Kishore R. Kumar has authored 95 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Cellular and Molecular Neuroscience, 36 papers in Neurology and 32 papers in Molecular Biology. Recurrent topics in Kishore R. Kumar's work include Genetic Neurodegenerative Diseases (28 papers), Neurological diseases and metabolism (21 papers) and Hereditary Neurological Disorders (19 papers). Kishore R. Kumar is often cited by papers focused on Genetic Neurodegenerative Diseases (28 papers), Neurological diseases and metabolism (21 papers) and Hereditary Neurological Disorders (19 papers). Kishore R. Kumar collaborates with scholars based in Australia, Germany and United States. Kishore R. Kumar's co-authors include Carolyn M. Sue, Anne Grünewald, Ryan L. Davis, Mark J. Cowley, Christine Klein, Katja Lohmann, Fangzhi Jia, Avi Fellner, Jannik Prasuhn and Karl Ng and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Scientific Reports.

In The Last Decade

Kishore R. Kumar

80 papers receiving 1.9k 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.

New insights into the complex role of mitochondria in Parkinson’s disease

2018 283 citations Kishore R. Kumar, Carolyn M. Sue et al. profile →

Peers

Countries citing papers authored by Kishore R. Kumar

Since Specialization

Citations

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

Fields of papers citing papers by Kishore R. Kumar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kishore R. Kumar. 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 Kishore R. Kumar. The network helps show where Kishore R. Kumar may publish in the future.

Co-authorship network of co-authors of Kishore R. Kumar

This figure shows the co-authorship network connecting the top 25 collaborators of Kishore R. Kumar. A scholar is included among the top collaborators of Kishore R. Kumar 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 Kishore R. Kumar. Kishore R. Kumar 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

#	Work	Indexed citations
1	Long‐Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia 2025 ·Movement Disorders ·Thomas Wirth, Kishore R. Kumar, Michael Zech	2
2	Targeted Long‐Read Sequencing as a Single Assay Improves the Diagnosis of Spastic‐Ataxia Disorders 2025 ·Annals of Clinical and Translational Neurology ·(unknown), Igor Stevanovski, (unknown), (unknown), Sanjog R. Chintalaphani, Pak Leng Cheong, Hasindu Gamaarachchi, Lisa Worgan, Kate Ahmad, Mike Hayes, Andrew Hannaford, Samuel Kim, Victor S.C. Fung, G. Michael Hálmagyi, Andrew J. Martin, (unknown), Michel Tchan, (unknown), Marina Kennerson, Ira W. Deveson, Kishore R. Kumar	3
3	Diagnostic work up when suspecting early onset Parkinson disease (EOPD). Recommendations from the MDS EOPD study group 2025 ·Parkinsonism & Related Disorders ·Raja Mehanna, (unknown), Jori Fleisher, Bart Post, Kishore R. Kumar, Alastair J. Noyce, Roy N. Alcalay, Huw R. Morris, (unknown), Mehri Salari, Katarzyna Śmiłowska, Yih‐Ru Wu, Baorong Zhang, Eng‐King Tan, Rodolfo Savica	1
4	Long-read sequencing for diagnosis of genetic myopathies 2025 ·BMJ Neurology Open ·(unknown), (unknown), Ryan L. Davis, Karl Ng, Roula Ghaoui, Pak Leng Cheong, Gianina Ravenscroft, Marina Kennerson, Ira W. Deveson, Kishore R. Kumar	1
5	Chronic Pain in Parkinson’s Disease: Prevalence, Sex Differences, Regional Anatomy and Comorbidities 2025 ·Annals of Clinical and Translational Neurology ·(unknown), (unknown), Fangyuan Cao, (unknown), (unknown), (unknown), (unknown), Luis M. García‐Marín, Scott F. Farrell, Kishore R. Kumar, Jane Alty, George D. Mellick, Trung T. Ngo, Miguel E. Rentería	1
6	Case Series of Cerebellar Ataxia with Tremor Due to Heterozygous STUB1 Variants (SCA48) without TBP Expansions: Further Evidence for SCA48 as a Monogenic Disease 2024 ·The Cerebellum ·(unknown), Kishore R. Kumar, (unknown), Paul Darveniza, Michel Tchan, (unknown), (unknown), Kathy H. C. Wu, Stephen Tisch	0
7	Genetic Testing of Movements Disorders: A Review of Clinical Utility 2024 ·Tremor and Other Hyperkinetic Movements ·(unknown), (unknown), (unknown), Ryan L. Davis, Kishore R. Kumar	4
8	An Inversion Affecting the GCH1 Gene as a Novel Finding in Dopa‐Responsive Dystonia 2024 ·Movement Disorders Clinical Practice ·(unknown), Avi Fellner, Matthew Hobbs, (unknown), Ira W. Deveson, Igor Stevanovski, (unknown), Danqing Zhu, Ramesh K. Narayanan, (unknown), Lisa Worgan, Pak Leng Cheong, (unknown), (unknown), Md Mehedi Hasan, Vanessa M. Hayes, Marina Kennerson, Kishore R. Kumar, Mike Hayes	2
9	Two Novel Variants in PI4KA in a Family Presenting With Hereditary Spastic Paraparesis 2024 ·Neurology Genetics ·J. Parmar, Elyshia McNamara, Phillipa J. Lamont, Kishore R. Kumar, (unknown), (unknown), Pak Leng Cheong, Gianina Ravenscroft	3
10	An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches 2024 ·The Cerebellum ·(unknown), (unknown), Karl Ng, Ira W. Deveson, Marina Kennerson, Kishore R. Kumar	16
11	Global Perspectives on Returning Genetic Research Results in Parkinson Disease 2024 ·Neurology Genetics ·Ai Huey Tan, Paula Saffie Awad, Artur Francisco Schumacher Schuh, Shen‐Yang Lim, Harutyun Madoev, Azlina Ahmad, J Solle, Claire Wegel, (unknown), Sumit Dey, María Teresa Periñán, Mary B. Makarious, Brian P. Fiske, Huw R. Morris, Alastair J. Noyce, Roy N. Alcalay, Kishore R. Kumar, Christine Klein, (unknown)	1
12	A deep intronic variant in MME causes autosomal recessive Charcot–Marie–Tooth neuropathy through aberrant splicing 2024 ·Journal of the Peripheral Nervous System ·(unknown), J. Parmar, Melina Ellis, Samantha J. Bryen, Cas Simons, (unknown), Igor Stevanovski, Ira W. Deveson, Garth A. Nicholson, Nigel G. Laing, Mathew Wallis, Gianina Ravenscroft, Kishore R. Kumar, Steve Vucic, Marina Kennerson	1
13	Unmet Need in Early-Onset Parkinson’s Disease: Deep Brain Stimulation and Pregnancy 2024 ·Journal of Parkinson s Disease ·Katarzyna Śmiłowska, Raja Mehanna, Jori Fleisher, Roy N. Alcalay, Kishore R. Kumar, Connie Marras, (unknown), Bart Post, Owen A. Ross, Maria Elisa Pimentel Piemonte, Valérie Fraix, Elena Moro, Eng‐King Tan, Rodolfo Savica, (unknown)	3
14	Reduced acetylated α-tubulin in SPAST hereditary spastic paraplegia patient PBMCs 2023 ·Frontiers in Neuroscience ·Gautam Wali, (unknown), (unknown), Kishore R. Kumar, Alan Mackay‐Sim, Carolyn M. Sue	2
15	Outcome Measures and Biomarkers for Clinical Trials in Hereditary Spastic Paraplegia: A Scoping Review 2023 ·Genes ·(unknown), (unknown), (unknown), Fangzhi Jia, Gautam Wali, Carolyn M. Sue, Kishore R. Kumar	7
16	Decompensation of cardiorespiratory function and emergence of anemia during pregnancy in a case of mitochondrial myopathy, lactic acidosis, and sideroblastic anemia 2 with compound heterozygous YARS2 pathogenic variants 2022 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Kishore R. Kumar, Patricia A. Sullivan, Mark J. Cowley, Ryan L. Davis, Carolyn M. Sue	5
17	Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy 2022 ·Journal of the Peripheral Nervous System ·(unknown), Igor Stevanovski, Sara Negri, Melina Ellis, Stephanie L. Barnes, Stephen Reddel, Steve Vucic, Garth A. Nicholson, Andrea Cortese, Kishore R. Kumar, Ira W. Deveson, Marina Kennerson	9
18	Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force – An Update 2022 ·Movement Disorders ·Lara M. Lange, Paulina González-Latapí, Rajasumi Rajalingam, Marina A.J. Tijssen, Darius Ebrahimi‐Fakhari, (unknown), Christos Ganos, Rhia Ghosh, Kishore R. Kumar, Anthony E. Lang, Malco Rossi, Sterre van der Veen, Bart P.C. van de Warrenburg, Thomas T. Warner, Katja Lohmann, Christine Klein, Connie Marras, (unknown)	58
19	Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis 2022 ·Neurology ·Ryan L. Davis, Kishore R. Kumar, Clare Puttick, Christina Liang, Kate Ahmad, (unknown), Jin‐Sung Park, André E. Minoche, Velimir Gayevskiy, Amali Mallawaarachchi, John Christodoulou, Deborah Schofield, Marcel E. Dinger, Mark J. Cowley, Carolyn M. Sue	32
20	Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS) 2021 ·Journal of Medical Genetics ·(unknown), Ying Zhu, Claudine M. Kraan, Kishore R. Kumar, David E. Godler, Michael Field	5

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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