Joshua Hersheson

3.0k total citations · 1 hit paper
15 papers, 1.8k citations indexed

About

Joshua Hersheson is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Joshua Hersheson has authored 15 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Joshua Hersheson's work include Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (7 papers) and Neurological diseases and metabolism (3 papers). Joshua Hersheson is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (7 papers) and Neurological diseases and metabolism (3 papers). Joshua Hersheson collaborates with scholars based in United Kingdom, Germany and Italy. Joshua Hersheson's co-authors include Douglass M. Turnbull, Joanne Betts, Christopher M. Morris, Thomas Klopstock, Kim J. Krishnan, Evelyn Jaros, Geoffrey A. Taylor, Robert H. Perry, Andreas Bender and Robert W. Taylor and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Joshua Hersheson

15 papers receiving 1.7k 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.

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

2006 1.2k citations Andreas Bender, Kim J. Krishnan et al. Nature Genetics profile →

Peers

Countries citing papers authored by Joshua Hersheson

Since Specialization

Citations

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

Fields of papers citing papers by Joshua Hersheson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joshua Hersheson

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Charcot-Marie-Tooth type 4B2 demyelinating neuropathy in miniature Schnauzer dogs caused by a novel splicing SBF2 (MTMR13) genetic variant: a new spontaneous clinical model 2019 ·PeerJ ·Nicolas Granger, Alejandro Luján Feliu‐Pascual, (unknown), Sally L. Ricketts, (unknown), Oliver P. Forman, Joshua Hersheson, Henry Houlden	4
2	Genotype‐phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14 2018 ·Movement Disorders ·Viorica Chelban, Sarah Wiethoff, (unknown), Nourelhoda A. Haridy, (unknown), Stéphanie Efthymiou, Esther B. E. Becker, Emer O’Connor, Joshua Hersheson, (unknown), (unknown), Pernille Axél Gregersen, Suzanne Granhøj Lindquist, Michael B. Petersen, Jørgen E. Nielsen, (unknown), Nicholas Wood, Paola Giunti, Henry Houlden	25
3	Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 Gene 2016 ·The Cerebellum ·Sarah Wiethoff, Conceição Bettencourt, Reema Paudel, Prochi F. Madon, Yo‐Tsen Liu, Joshua Hersheson, Noshir Wadia, Joy Desai, Henry Houlden	20
4	Heterogeneity in clinical features and disease severity in ataxia-associated SYNE1 mutations 2016 ·Journal of Neurology ·Sarah Wiethoff, Joshua Hersheson, Conceição Bettencourt, Nicholas Wood, Henry Houlden	20
5	ADCY5 mutations are another cause of benign hereditary chorea 2015 ·Neurology ·Niccolò E. Mencacci, Roberto Erro, Sarah Wiethoff, Joshua Hersheson, Mina Ryten, Bettina Balint, Christos Ganos, María Stamelou, Niall Quinn, Henry Houlden, Nicholas Wood, Kailash P. Bhatia	62
6	Expanding the Phenotype and Genetic Defects Associated with the GOSR 2 Gene 2015 ·Movement Disorders Clinical Practice ·(unknown), Bettina Balint, Niccolò E. Mencacci, Joshua Hersheson, Ignacio Rubio‐Agusti, Dimitri M. Kullmann, Conceição Bettencourt, Kailash P. Bhatia, Henry Houlden	20
7	Extended phenotypic spectrum of KIF5A mutations 2014 ·UCL Discovery (University College London) ·(unknown), Laura M. Sly, Joshua Hersheson, Alejandro Horga, Zane Jaunmuktane, Sebastian Brandner, Alan Pittman, David C. Hughes, (unknown), (unknown), Christos Proukakis, (unknown), Michaela Auer‐Grumbach, Stephan Züchner, (unknown), Mary M. Reilly, Henry Houlden	3
8	Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia 2014 ·JAMA Neurology ·Conceição Bettencourt, Mina Ryten, Paola Forabosco, Stéphanie Schorge, Joshua Hersheson, John Hardy, Henry Houlden	38
9	Cathepsin D deficiency causes juvenile-onset ataxia and distinctive muscle pathology 2014 ·Neurology ·Joshua Hersheson, Derek Burke, Robert Clayton, Glenn Anderson, Thomas S. Jacques, Philippa B. Mills, Nicholas Wood, Paul Gissen, Peter T. Clayton, Julian Fearnley, Sara Mole, Henry Houlden	32
10	H‐ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations? 2014 ·Movement Disorders ·Roberto Erro, Joshua Hersheson, Christos Ganos, Niccolò E. Mencacci, María Stamelou, Amit Batla, Stefanie Thust, José Brás, Rita Guerreiro, John Hardy, Niall Quinn, Henry Houlden, Kailash P. Bhatia	41
11	Extended phenotypic spectrum of KIF5A mutations 2014 ·Neurology ·Yo-Tsen Liu, Matilde Laurá, Joshua Hersheson, Alejandro Horga, Zane Jaunmuktane, Sebastian Brandner, Alan Pittman, Deborah Hughes, James M. Polke, Mary G. Sweeney, Christos Proukakis, John C. Janssen, Michaela Auer‐Grumbach, Stephan Züchner, Kevin Shields, Mary M. Reilly, Henry Houlden	80
12	Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation 2013 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown), Joshua Hersheson, Vincent Plagnol, Katherine A. Fawcett, Kate Duberley, Elisavet Preza, Iain P. Hargreaves, Annapurna Chalasani, Matilde Laurá, Nicholas Wood, Mary M. Reilly, Henry Houlden	43
13	The inherited ataxias: Genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics 2012 ·Human Mutation ·Joshua Hersheson, Andrea Haworth, Henry Houlden	69
14	Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia 2012 ·Annals of Neurology ·Joshua Hersheson, Niccolò E. Mencacci, Mary B. Davis, Nicola MacDonald, Daniah Trabzuni, Mina Ryten, Alan Pittman, Reema Paudel, Eleanna Kara, Katherine A. Fawcett, Vincent Plagnol, Kailash P. Bhatia, Alan Medlar, Horia Stanescu, John Hardy, Robert Kleta, Nicholas Wood, Henry Houlden	120
15	High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease breakdown → 2006 ·Nature Genetics ·Andreas Bender, Kim J. Krishnan, Christopher M. Morris, Geoffrey A. Taylor, Amy K. Reeve, Robert H. Perry, Evelyn Jaros, Joshua Hersheson, Joanne Betts, Thomas Klopstock, Robert W. Taylor, Douglass M. Turnbull	1195

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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