E. R. Brunt

6.9k total citations · 1 hit paper
55 papers, 3.7k citations indexed

About

E. R. Brunt is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, E. R. Brunt has authored 55 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Cellular and Molecular Neuroscience, 43 papers in Molecular Biology and 29 papers in Neurology. Recurrent topics in E. R. Brunt's work include Genetic Neurodegenerative Diseases (50 papers), Mitochondrial Function and Pathology (33 papers) and Neurological disorders and treatments (20 papers). E. R. Brunt is often cited by papers focused on Genetic Neurodegenerative Diseases (50 papers), Mitochondrial Function and Pathology (33 papers) and Neurological disorders and treatments (20 papers). E. R. Brunt collaborates with scholars based in Netherlands, Germany and United States. E. R. Brunt's co-authors include Udo Rüb, Kay Seidel, Wilfred F.A. den Dunnen, M. Litt, D.L. Browne, John G. Nutt, Stephen T. Gancher, Eric A. Smith, Thomas Deller and Rob A. I. de Vos and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and Brain.

In The Last Decade

E. R. Brunt

55 papers receiving 3.6k 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.

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

1994 561 citations D.L. Browne, E. R. Brunt et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. R. Brunt Netherlands	35	2.7k	2.6k	1.2k	330	291	55	3.7k
Vikram G. Shakkottai United States	29	2.2k 0.8×	2.0k 0.7×	665 0.5×	239 0.7×	232 0.8×	68	3.1k
Katrin Bürk Germany	37	2.4k 0.9×	2.8k 1.1×	1.6k 1.3×	73 0.2×	477 1.6×	73	3.7k
Marina Frontali Italy	29	1.8k 0.7×	2.0k 0.8×	1.3k 1.1×	72 0.2×	314 1.1×	81	3.0k
Stefan M. Pulst United States	44	4.1k 1.5×	3.3k 1.3×	2.3k 1.9×	123 0.4×	457 1.6×	157	6.2k
Maria Pennuto Italy	31	1.9k 0.7×	1.6k 0.6×	532 0.4×	42 0.1×	204 0.7×	81	3.0k
Alexander Zimprich Austria	32	1.1k 0.4×	1.4k 0.5×	1.6k 1.4×	39 0.1×	504 1.7×	76	3.3k
J.-P. G. Vonsattel United States	16	2.6k 1.0×	3.2k 1.2×	2.0k 1.6×	25 0.1×	321 1.1×	22	4.4k
Maurizio De Fusco Italy	19	1.3k 0.5×	770 0.3×	351 0.3×	157 0.5×	455 1.6×	32	2.8k
Éric Leguern France	39	1.9k 0.7×	2.7k 1.0×	1.4k 1.1×	53 0.2×	936 3.2×	101	4.8k
Tie-Shan Tang United States	21	2.3k 0.8×	1.5k 0.6×	456 0.4×	60 0.2×	111 0.4×	22	2.9k

Countries citing papers authored by E. R. Brunt

Since Specialization

Citations

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

Fields of papers citing papers by E. R. Brunt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. R. Brunt

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

Seidel, Kay, et al.. (2012). Brain pathology of spinocerebellar ataxias. Acta Neuropathologica. 124(1). 1–21. 301 indexed citations

Seidel, Kay, Melanie Meister, George J. Dugbartey, et al.. (2011). Cellular protein quality control and the evolution of aggregates in spinocerebellar ataxia type 3 (SCA3). Neuropathology and Applied Neurobiology. 38(6). 548–558. 39 indexed citations

Brunt, E. R., Helmut Heinsen, Kay Seidel, et al.. (2011). Pathoanatomy of Cerebellar Degeneration in Spinocerebellar Ataxia Type 2 (SCA2) and Type 3 (SCA3). The Cerebellum. 11(3). 749–760. 77 indexed citations

Vos, Michel J., Bart Kanon, E. R. Brunt, et al.. (2010). HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones. Human Molecular Genetics. 19(23). 4677–4693. 118 indexed citations

Rujano, Maria A., et al.. (2010). Levels of DNAJB family members (HSP40) correlate with disease onset in patients with spinocerebellar ataxia type 3. European Journal of Neuroscience. 32(5). 760–770. 31 indexed citations

Seidel, Kay, et al.. (2009). The p62 antibody reveals various cytoplasmic protein aggregates in spinocerebellar ataxia Type 6. Clinical Neuropathology. 28(9). 344–349. 17 indexed citations

Rüb, Udo, Helmut Heinsen, E. R. Brunt, et al.. (2009). The human premotor oculomotor brainstem system – can it help to understand oculomotor symptoms in Huntington's disease?. Neuropathology and Applied Neurobiology. 35(1). 4–15. 18 indexed citations

Verhagen, M.M.M., Wilson F. Abdo, Michèl A.A.P. Willemsen, et al.. (2009). Clinical spectrum of ataxia-telangiectasia in adulthood. Neurology. 73(6). 430–437. 108 indexed citations

Gierga, K., Helenius J. Schelhaas, E. R. Brunt, et al.. (2009). Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites. Neuropathology and Applied Neurobiology. 35(5). 515–527. 36 indexed citations

10.

Sival, Deborah A., Gideon J. du Marchie Sarvaas, O.F. Brouwer, et al.. (2009). Neurophysiological evaluation in children with Friedreich's ataxia. Early Human Development. 85(10). 647–651. 9 indexed citations

11.

Rüb, Udo, E. R. Brunt, & Thomas Deller. (2008). New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado–Joseph disease). Current Opinion in Neurology. 21(2). 111–116. 126 indexed citations

12.

Rüb, Udo, E. R. Brunt, Kay Seidel, et al.. (2007). Spinocerebellar ataxia type 7 (SCA7): widespread brain damage in an adult‐onset patient with progressive visual impairments in comparison with an adult‐onset patient without visual impairments. Neuropathology and Applied Neurobiology. 34(2). 155–168. 28 indexed citations

13.

Rüb, Udo, E. R. Brunt, Elisabeth Petrasch‐Parwez, et al.. (2006). Degeneration of ingestion‐related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7. Neuropathology and Applied Neurobiology. 32(6). 635–649. 65 indexed citations

14.

Brunt, E. R., et al.. (2004). Caspase‐mediated proteolysis of the polyglutamine disease protein ataxin‐3. Journal of Neurochemistry. 89(4). 908–918. 86 indexed citations

15.

Rüb, Udo, E. R. Brunt, K. Gierga, et al.. (2003). The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado–Joseph disease). Journal of Chemical Neuroanatomy. 25(2). 115–127. 31 indexed citations

16.

Rüb, Udo, Rob A. I. de Vos, E. R. Brunt, et al.. (2002). Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado–Joseph disease). Brain Research. 953(1-2). 126–134. 25 indexed citations

17.

Brunt, E. R., et al.. (1995). Unique myoclonic pattern in corticobasal degeneration. Movement Disorders. 10(2). 132–142. 39 indexed citations

18.

Verschuuren‐Bemelmans, Corien C., E. R. Brunt, Rob G.J. Mensink, et al.. (1995). Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I. Human Genetics. 96(6). 691–694. 12 indexed citations

19.

Litt, M., et al.. (1994). EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE KCNA1 (KV1.1). The Journal of General Physiology. 104(6). 3 indexed citations

20.

Brunt, E. R. & Tiemen W. van Weerden. (1990). FAMILIAL PAROXYSMAL KINESIGENIC ATAXIA AND CONTINUOUS MYOKYMIA. Brain. 113(5). 1361–1382. 99 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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