James M. Polke

4.9k citations

47 papers · 1.7k · h-index 21

Impact in

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 2%
- Neurological diseases and metabolism
- Amyotrophic Lateral Sclerosis Research
- Botulinum Toxin and Related Neurological Disorders
- Peripheral Neuropathies and Disorders

Papers in

Cellular and Molecular Neuroscience 32
- Hereditary Neurological Disorders 27
- Genetic Neurodegenerative Diseases 22
Molecular Biology 19
- Mitochondrial Function and Pathology 7

Co-authors: Henry Houlden (30 shared papers)Mary M. Reilly (29 shared papers)Alexander M. Rossor (11 shared papers)Matilde Laurá (20 shared papers)Julian Blake (16 shared papers)Sinéad M. Murphy (9 shared papers)Hadi Manji (5 shared papers)Mary B. Davis (3 shared papers)
Journals: Neurology (6 papers)Journal of the Peripheral Nervous System (6 papers)Journal of Neurology Neurosurgery & Psychiatry (6 papers)Neuromuscular Disorders (6 papers)Neurobiology of Aging (3 papers)
Partner nations: United Kingdom United States Italy

In The Last Decade

James M. Polke

47 papers receiving 1.7k citations

Peers

Countries citing papers authored by James M. Polke

Since Specialization

Citations

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

Fields of papers citing papers by James M. Polke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James M. Polke. 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 James M. Polke. The network helps show where James M. Polke may publish in the future.

Co-authors

The 25 scholars most cited alongside James M. Polke, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with James M. Polke Line = papers co-authored together James M. Polke links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 47 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing Journal of Neurology Neurosurgery & Psychiatry ·Sinéad M. Murphy, Matilde Laurá, Katherine A. Fawcett, Amelie Pandraud, Yo‐Tsen Liu, Gabrielle L. Davidson, Alexander M. Rossor, James M. Polke, Victoria Castleman, Hadi Manji, Michael P. Lunn, Karen Bull, Gita Ramdharry, Mary B. Davis, Julian Blake, Henry Houlden, Mary M. Reilly	2012	257
2	Clinical implications of genetic advances in Charcot–Marie–Tooth disease Nature Reviews Neurology ·Alexander M. Rossor, James M. Polke, Henry Houlden, Mary M. Reilly	2013	242
3	C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies Neurology ·Davina J. Hensman Moss, Mark Poulter, Jon Beck, Jason Hehir, James M. Polke, Tracy Campbell, Garry Adamson, Ese Mudanohwo, Peter McColgan, Andrea Haworth, Edward J. Wild, Mary G. Sweeney, Henry Houlden, Simon Mead, Sarah J. Tabrizi	2013	137
4	Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia Acta Neuropathologica ·Pietro Fratta, Mark Poulter, Tammaryn Lashley, Jonathan D. Rohrer, James M. Polke, Jon Beck, Natalie S. Ryan, Davina J. Hensman Moss, Sarah Mizielinska, Adrian J. Waite, Mang Ching Lai, Tania F. Gendron, Leonard Petrucelli, Elizabeth Fisher, Tamás Révész, Jason D. Warren, John Collinge, Adrian M. Isaacs, Simon Mead	2013	104
5	NDUFA4 Mutations Underlie Dysfunction of a Cytochrome c Oxidase Subunit Linked to Human Neurological Disease Cell Reports ·Robert D. S. Pitceathly, Shamima Rahman, Yehani Wedatilake, James M. Polke, Sebahattin Çirak, A. Reghan Foley, Anna Sailer, Matthew E. Hurles, Jim Stalker, Iain P. Hargreaves, Cathy E. Woodward, M G Sweeney, Francesco Muntoni, Henry Houlden, Jan‐Willem Taanman, Michael G. Hanna	2013	101
6	Extended phenotypic spectrum of KIF5A mutations 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	2014	80
7	Targeted next-generation sequencing panels in the diagnosis of Charcot-Marie-Tooth disease Neurology ·Andrea Cortese, Janel E. Wilcox, James M. Polke, Roy Poh, Mariola Skorupinska, Alexander M. Rossor, Matilde Laurá, Pedro José Tomaselli, Henry Houlden, Michael E. Shy, Mary M. Reilly	2019	68
8	Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations Neurology ·James M. Polke, Matilde Laurá, Davide Pareyson, Franco Taroni, M Milani, Giorgia Bergamin, V.S. Gibbons, Henry Houlden, S.C. Chamley, J. Blake, Catherine DeVile, Richard Sandford, Mary G. Sweeney, Mary B. Davis, Mary M. Reilly	2011	63
9	Reduction of Gstm1 Expression in the Stroke-Prone Spontaneously Hypertension Rat Contributes to Increased Oxidative Stress Hypertension ·Martin McBride, M. Julia Brosnan, Joanne Mathers, Lesley I. McLellan, William H. Miller, Delyth Graham, Neil Hanlon, Carlene A. Hamilton, James M. Polke, Wai Lee, Anna F. Dominiczak	2005	55
10	Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT Neurology ·Pedro José Tomaselli, Alexander M. Rossor, Alejandro Horga, Zane Jaunmuktane, Aisling Carr, Paola Saveri, Giuseppe Piscosquito, Davide Pareyson, Matilde Laurá, Julian Blake, Roy Poh, James M. Polke, Henry Houlden, Mary M. Reilly	2017	43
11	Variable phenotypes are associated with PMP22 missense mutations Neuromuscular Disorders ·Massimo Russo, Matilde Laurá, James M. Polke, Mary B. Davis, J. Blake, Sebastian Brandner, Richard AC Hughes, Henry Houlden, David Bennett, Michael P. Lunn, Mary M. Reilly	2010	42
12	Phenotype expression in women with CMT1X Journal of the Peripheral Nervous System ·Carly E. Siskind, Sinéad M. Murphy, Richard Ovens, James M. Polke, Mary M. Reilly, Michael E. Shy	2011	37
13	Candidate Genes That Determine Response to Salt in the Stroke-Prone Spontaneously Hypertensive Rat Hypertension ·Delyth Graham, Martin McBride, Michelle Gaasenbeek, Kirsten Gilday, Elisabeth Beattie, William H. Miller, John McClure, James M. Polke, Augusto C. Montezano, Rhian M. Touyz, Anna F. Dominiczak	2007	37
14	Hereditary sensory and autonomic neuropathy type 1 (HSANI) caused by a novel mutation in SPTLC2 Neurology ·Sinéad M. Murphy, Daniela Ernst, Wei Yu, Matilde Laurá, Yo-Tsen Liu, James M. Polke, Julian Blake, J. Winer, Henry Houlden, Thorsten Hornemann, Mary M. Reilly	2013	35
15	High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients Neurobiology of Aging ·Kin Y. Mok, Georgios Koutsis, Lucía Schottlaender, James M. Polke, Μάριος Πάνας, Henry Houlden	2012	33
16	Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines European Journal of Human Genetics ·Eleni Mavraki, Robyn Labrum, Kate Sergeant, Charlotte L. Alston, Cathy E. Woodward, Conrad Smith, Charlotte V. Y. Knowles, Yogen Patel, Philip Hodsdon, Jack P. Baines, Emma L. Blakely, James M. Polke, Robert W. Taylor, Carl Fratter	2022	33
17	Genetic and clinical characteristics ofNEFL-related Charcot-Marie-Tooth disease Journal of Neurology Neurosurgery & Psychiatry ·Alejandro Horga, Matilde Laurá, Zane Jaunmuktane, Nivedita U. Jerath, Michael Gonzalez, James M. Polke, Roy Poh, Julian Blake, Yo-Tsen Liu, Sarah Wiethoff, Conceição Bettencourt, Michael P. Lunn, Hadi Manji, Michael G. Hanna, Henry Houlden, Sebastian Brandner, Stephan Züchner, Michael E. Shy, Mary M. Reilly	2017	32
18	A 30-unit hexanucleotide repeat expansion in C9orf72 induces pathological lesions with dipeptide-repeat proteins and RNA foci, but not TDP-43 inclusions and clinical disease Acta Neuropathologica ·Priya Gami‐Patel, Christina E. Murray, Schottlaender Lucia, Conceição Bettencourt, Eduardo De Pablo‐Fernández, Ese Mudanohwo, Sarah Mizielinska, James M. Polke, Janice L. Holton, Adrian M. Isaacs, Henry Houlden, Tamás Révész, Tammaryn Lashley	2015	28
19	A novel mutation in the nerve‐specific 5′UTR of the GJB1 gene causes X‐linked Charcot‐Marie‐Tooth disease Journal of the Peripheral Nervous System ·Sinéad M. Murphy, James M. Polke, Hadi Manji, Julian Blake, Lilla Reiniger, Mary G. Sweeney, Henry Houlden, Sebastian Brandner, Mary M. Reilly	2011	26
20	Charcot-Marie-Tooth Type 2B: A New Phenotype Associated with a Novel RAB7A Mutation and Inhibited EGFR Degradation Cells ·Paola Saveri, Maria De Luca, Veronica Nisi, Chiara Pisciotta, Roberta Romanò, Giuseppe Piscosquito, Mary M. Reilly, James M. Polke, Tiziana Cavallaro, Gian Maria Fabrizi, Paola Fossa, Elena Cichero, Raffaella Lombardi, Giuseppe Lauria, Stefania Magri, Franco Taroni, Davide Pareyson, Cecilia Bucci	2020	24

About James M. Polke

James M. Polke is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Neurology and Genetics, having authored 47 papers that have together received 1.7k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (27 papers), Genetic Neurodegenerative Diseases (22 papers), Botulinum Toxin and Related Neurological Disorders (10 papers), Neurological diseases and metabolism (9 papers), Mitochondrial Function and Pathology (7 papers), Amyotrophic Lateral Sclerosis Research (5 papers), Parkinson's Disease Mechanisms and Treatments (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (1.1k citations), Neurology (416 citations), Neurology (651 citations), Genetics (239 citations) and Clinical Biochemistry (99 citations). James M. Polke has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include Henry Houlden, Mary M. Reilly, Alexander M. Rossor, Matilde Laurá, Julian Blake, Sinéad M. Murphy, Hadi Manji, Mary B. Davis, Mary G. Sweeney and Michael P. Lunn. Their work appears in journals such as Neurology, Journal of the Peripheral Nervous System, Journal of Neurology Neurosurgery & Psychiatry, Neuromuscular Disorders and Neurobiology of Aging.

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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