E.M.G. Joosten

2.4k total citations
81 papers, 1.7k citations indexed

About

E.M.G. Joosten is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, E.M.G. Joosten has authored 81 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Cellular and Molecular Neuroscience, 26 papers in Molecular Biology and 23 papers in Neurology. Recurrent topics in E.M.G. Joosten's work include Hereditary Neurological Disorders (16 papers), Genetic Neurodegenerative Diseases (13 papers) and Glycogen Storage Diseases and Myoclonus (12 papers). E.M.G. Joosten is often cited by papers focused on Hereditary Neurological Disorders (16 papers), Genetic Neurodegenerative Diseases (13 papers) and Glycogen Storage Diseases and Myoclonus (12 papers). E.M.G. Joosten collaborates with scholars based in Netherlands, Curacao and United States. E.M.G. Joosten's co-authors include F.J.M. Gabreëls, A.A.W.M. Gabreëls‐Festen, Dick F. Stegeman, R. A. Binkhorst, Ron A. Wevers, S. L. H. Notermans, H.M. Vingerhoets, H. J. ter Laak, Wim H.J.P. Linssen and Anneke Gabreëls-Festen and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

E.M.G. Joosten

81 papers receiving 1.6k citations

Peers

E.M.G. Joosten
D. G. F. Harriman United Kingdom
D J Dick United Kingdom
Nicholas J. Pantazis United States
Michael Sinnreich Switzerland
G. MILTON SHY United States
D. G. F. Harriman United Kingdom
E.M.G. Joosten
Citations per year, relative to E.M.G. Joosten E.M.G. Joosten (= 1×) peers D. G. F. Harriman

Countries citing papers authored by E.M.G. Joosten

Since Specialization
Citations

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

Fields of papers citing papers by E.M.G. Joosten

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E.M.G. Joosten. 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.M.G. Joosten. The network helps show where E.M.G. Joosten may publish in the future.

Co-authorship network of co-authors of E.M.G. Joosten

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

All Works

20 of 20 papers shown
1.
Verhagen, W. I. M., et al.. (1993). Hereditary neuropathy with liability to pressure palsies: A clinical, electroneurophysiological and morphological study. Journal of the Neurological Sciences. 116(2). 176–184. 80 indexed citations
2.
Gabreëls‐Festen, A.A.W.M., et al.. (1992). Autosomal recessive form of hereditary motor and sensory neuropathy type I. Neurology. 42(9). 1755–1755. 33 indexed citations
3.
Gabreëls‐Festen, A.A.W.M., et al.. (1992). Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I). Journal of the Neurological Sciences. 107(2). 145–154. 71 indexed citations
4.
Joosten, E.M.G., et al.. (1992). Cerebrotendinous xanthomatosis. Clinical Neurology and Neurosurgery. 94. 165–167. 7 indexed citations
5.
Gabreëls‐Festen, A.A.W.M., et al.. (1992). Hereditary Neuropathy with Liability to Pressure Palsies in Childhood*. Neuropediatrics. 23(3). 138–143. 35 indexed citations
6.
Engelen, Baziel G.M. van, F.J.M. Gabreëls, E.M.G. Joosten, et al.. (1992). Familial adult‐onset muscular dystrophy with leukoencephalopathy. Annals of Neurology. 32(4). 577–580. 5 indexed citations
7.
Poels, P.J.E., E.M.G. Joosten, R. C. A. Sengers, et al.. (1991). In vitro contraction test for malignant hyperthermia in patients with unexplained recurrent rhabdomyolysis. Journal of the Neurological Sciences. 105(1). 67–72. 22 indexed citations
8.
Linssen, W.H.J.P., Dick F. Stegeman, E.M.G. Joosten, et al.. (1991). FORCE AND FATIGUE IN HUMAN TYPE I MUSCLE FIBRES: A SURFACE EMG STUDY IN PATIENTS WITH CONGENITAL MYOPATHY AND TYPE I FIBRE PREDOMINANCE. Brain. 114(5). 2123–2132. 27 indexed citations
9.
Gabreëls‐Festen, A.A.W.M., E.M.G. Joosten, F.J.M. Gabreëls, et al.. (1991). HEREDITARY MOTOR AND SENSORY NEUROPATHY OF NEURONAL TYPE WITH ONSET IN EARLY CHILDHOOD. Brain. 114(4). 1855–1870. 47 indexed citations
10.
Gabreëls‐Festen, A.A.W.M., et al.. (1991). Adult polyglucosan body disease: The diagnostic value of axilla skin biopsy. Annals of Neurology. 29(4). 448–451. 14 indexed citations
11.
Wevers, Ron A., et al.. (1990). Excessive plasma K+ increase after ischemic exercise in myotonic muscular dystrophy. Muscle & Nerve. 13(1). 27–32. 16 indexed citations
12.
Poels, P.J.E., et al.. (1990). Dantrolene sodium does influence the second wind phenomenon in McArdle's disease. Journal of the Neurological Sciences. 100(1-2). 108–112. 16 indexed citations
13.
Gabreëls‐Festen, A.A.W.M., et al.. (1990). CONGENITAL DEMYELINATING MOTOR AND SENSORY NEUROPATHY WITH FOCALLY FOLDED MYELIN SHEATHS. Brain. 113(6). 1629–1643. 53 indexed citations
14.
Joosten, E.M.G., et al.. (1990). Muscle cramp: Main theories as to aetiology. European Archives of Psychiatry and Clinical Neuroscience. 239(5). 337–342. 36 indexed citations
15.
Laak, H. J. ter, et al.. (1989). Polyglucosan bodies in intramuscular motor nerves. Acta Neuropathologica. 77(6). 629–633. 13 indexed citations
16.
Verhagen, W. I. M., et al.. (1989). Hereditary vestibulo-cochlear dysfunction and vascular disorders. Journal of the Neurological Sciences. 92(1). 55–63. 22 indexed citations
17.
Stegeman, Dick F., et al.. (1989). Increase in median power frequency of the myoelectric signal in pathological fatigue. Electroencephalography and Clinical Neurophysiology. 73(2). 151–156. 16 indexed citations
18.
Thijssen, H.O.M., et al.. (1988). CT in neuromuscular disorders: a comparison of CT and histology. Neuroradiology. 30(5). 421–425. 13 indexed citations
19.
Pasman, Jaco W., E.M.G. Joosten, & Hans Wouters. (1988). Increased daytime sleepiness and snoring-obstructive sleep apnea syndrome caused by webbing of the soft palate. Clinical Neurology and Neurosurgery. 90(1). 75–78. 2 indexed citations
20.
Notermans, S. L. H., et al.. (1982). Kearns Syndrome or Kearns Disease. Ophthalmologica. 184(1). 40–50. 10 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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