E. R. Brunt

6.9k citations

55 papers · 3.7k indexed · 1 hit paper · h-index 35

Molecular Biology top 2%
Cellular and Molecular Neuroscience top 0.5%
Neurology top 1%
Cardiology and Cardiovascular Medicine top 5%
Neurology top 5%

Co-authors: Udo Rüb Kay Seidel Wilfred F.A. den Dunnen M. Litt D.L. Browne John G. Nutt Stephen T. Gancher Eric A. Smith
Topics: Genetic Neurodegenerative Diseases (50 papers)Mitochondrial Function and Pathology (33 papers)Neurological disorders and treatments (20 papers)
Cited by: Cellular and Molecular Neuroscience Neurology Aging
Journals: Nature Genetics Journal of Neuroscience Brain
Partner nations: Netherlands Germany United States

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

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

#	Work	Indexed citations
1	Brain pathology of spinocerebellar ataxias 2012 ·Acta Neuropathologica ·Kay Seidel,(unknown),E. R. Brunt,Wilfred F.A. den Dunnen,Horst‐Werner Korf,Udo Rüb	301
2	Cellular protein quality control and the evolution of aggregates in spinocerebellar ataxia type 3 (SCA3) 2011 ·Neuropathology and Applied Neurobiology ·Kay Seidel,Melanie Meister,George J. Dugbartey,(unknown),Jonathan Vinet,E. R. Brunt,F.W. van Leeuwen,Udo Rüb,Harm H. Kampinga,Wilfred F.A. den Dunnen	39
3	Pathoanatomy of Cerebellar Degeneration in Spinocerebellar Ataxia Type 2 (SCA2) and Type 3 (SCA3) 2011 ·The Cerebellum ·(unknown),E. R. Brunt,Helmut Heinsen,(unknown),Kay Seidel,Katrin Bürk,Lüdger Schöls,Georg Auburger,Domenico Del Turco,Thomas Deller,Horst‐Werner Korf,Wilfred F.A. den Dunnen,Udo Rüb	77
4	HSPB7 is the most potent polyQ aggregation suppressor within the HSPB family of molecular chaperones 2010 ·Human Molecular Genetics ·Michel J. Vos,(unknown),Bart Kanon,(unknown),E. R. Brunt,(unknown),Serena Carra,Ody C.M. Sibon,Harm H. Kampinga	118
5	Levels of DNAJB family members (HSP40) correlate with disease onset in patients with spinocerebellar ataxia type 3 2010 ·European Journal of Neuroscience ·(unknown),Maria A. Rujano,(unknown),(unknown),E. R. Brunt,Harm H. Kampinga	31
6	The p62 antibody reveals various cytoplasmic protein aggregates in spinocerebellar ataxia Type 6 2009 ·Clinical Neuropathology ·Kay Seidel,E. R. Brunt,Rob A. I. de Vos,Freerk van Dijk,(unknown),(unknown),Udo Rüb,(unknown)	17
7	The human premotor oculomotor brainstem system – can it help to understand oculomotor symptoms in Huntington's disease? 2009 ·Neuropathology and Applied Neurobiology ·Udo Rüb,Helmut Heinsen,E. R. Brunt,G. Bernhard Landwehrmeyer,Wilfred F.A. den Dunnen,K. Gierga,Thomas Deller	18
8	Clinical spectrum of ataxia-telangiectasia in adulthood 2009 ·Neurology ·M.M.M. Verhagen,Wilson F. Abdo,Michèl A.A.P. Willemsen,F.B.L. Hogervorst,Dominique Smeets,J.A.P. Hiel,E. R. Brunt,Monique A. van Rijn,(unknown),Reinhard Oldenburg,Annegien Broeks,J. I. Last,Laura J. van’t Veer,Marina A.J. Tijssen,(unknown),Hannie Kremer,Corry M.R. Weemaes,A. Malcolm R. Taylor,Marcel van Deuren	108
9	Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites 2009 ·Neuropathology and Applied Neurobiology ·K. Gierga,Helenius J. Schelhaas,E. R. Brunt,Kay Seidel,(unknown),Rupert Egensperger,Rob A. I. de Vos,Wilfred F.A. den Dunnen,P.F. Ippel,Elisabeth Petrasch‐Parwez,Thomas Deller,Lüdger Schöls,Udo Rüb	36
10	Neurophysiological evaluation in children with Friedreich's ataxia 2009 ·Early Human Development ·Deborah A. Sival,Gideon J. du Marchie Sarvaas,O.F. Brouwer,(unknown),Corien C. Verschuuren‐Bemelmans,Natasha M. Maurits,E. R. Brunt,Johannes H. van der Hoeven	9
11	New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado–Joseph disease) 2008 ·Current Opinion in Neurology ·Udo Rüb,E. R. Brunt,Thomas Deller	126
12	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 2007 ·Neuropathology and Applied Neurobiology ·Udo Rüb,E. R. Brunt,Kay Seidel,K. Gierga,Cornelia M. Mooy,Mattias Kettner,Christine Van Broeckhoven,Ingo Bechmann,Albert R. La Spada,Lüdger Schöls,Wilfred F.A. den Dunnen,Rob A. I. de Vos,Thomas Deller	28
13	Degeneration of ingestion‐related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7 2006 ·Neuropathology and Applied Neurobiology ·Udo Rüb,E. R. Brunt,Elisabeth Petrasch‐Parwez,Lüdger Schöls,Dirk Theegarten,Georg Auburger,Kay Seidel,Christian Schultz,K. Gierga,Henry L. Paulson,Christine Van Broeckhoven,Thomas Deller,Rob A. I. de Vos	65
14	Caspase‐mediated proteolysis of the polyglutamine disease protein ataxin‐3 2004 ·Journal of Neurochemistry ·(unknown),(unknown),E. R. Brunt,Lisa Ellerby,Henry L. Paulson	86
15	The nucleus raphe interpositus in spinocerebellar ataxia type 3 (Machado–Joseph disease) 2003 ·Journal of Chemical Neuroanatomy ·Udo Rüb,E. R. Brunt,K. Gierga,Christian Schultz,Henry L. Paulson,Rob A. I. de Vos,Heiko Braak	31
16	Degeneration of the external cuneate nucleus in spinocerebellar ataxia type 3 (Machado–Joseph disease) 2002 ·Brain Research ·Udo Rüb,Rob A. I. de Vos,E. R. Brunt,Christian Schultz,Henry L. Paulson,Kelly Del Tredici,Heiko Braak	25
17	Unique myoclonic pattern in corticobasal degeneration 1995 ·Movement Disorders ·E. R. Brunt,Tiemen W. van Weerden,Jan Pruim,(unknown)	39
18	Refinement by linkage analysis in two large families of the candidate region of the third locus (SCA3) for autosomal dominant cerebellar ataxia type I 1995 ·Human Genetics ·Corien C. Verschuuren‐Bemelmans,E. R. Brunt,(unknown),Rob G.J. Mensink,(unknown),(unknown),Irene Stolte‐Dijkstra,Charles H.C.M. Buys,Hans Scheffer	12
19	EPISODIC ATAXIA MYOKYMIA SYNDROME IS ASSOCIATED WITH POINT MUTATIONS IN THE HUMAN POTASSIUM CHANNEL GENE KCNA1 (KV1.1) 1994 ·The Journal of General Physiology ·M. Litt,D.L. Browne,S. Gancher,(unknown),E. R. Brunt,Eric A. Smith	3
20	FAMILIAL PAROXYSMAL KINESIGENIC ATAXIA AND CONTINUOUS MYOKYMIA 1990 ·Brain ·E. R. Brunt,Tiemen W. van Weerden	99

About E. R. Brunt

E. R. Brunt is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology, having authored 55 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (50 papers), Mitochondrial Function and Pathology (33 papers) and Neurological disorders and treatments (20 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.6k citations), Neurology (1.2k citations) and Aging (83 citations). E. R. Brunt has collaborated with scholars based in Netherlands, Germany and United States. Frequent 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. Their work appears in journals such as Nature Genetics, Journal of Neuroscience and Brain.

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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