F.G.I. Jennekens

1.2k total citations
22 papers, 907 citations indexed

About

F.G.I. Jennekens is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, F.G.I. Jennekens has authored 22 papers receiving a total of 907 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in F.G.I. Jennekens's work include Muscle Physiology and Disorders (5 papers), Nerve injury and regeneration (5 papers) and Genetic Neurodegenerative Diseases (5 papers). F.G.I. Jennekens is often cited by papers focused on Muscle Physiology and Disorders (5 papers), Nerve injury and regeneration (5 papers) and Genetic Neurodegenerative Diseases (5 papers). F.G.I. Jennekens collaborates with scholars based in Netherlands and United Kingdom. F.G.I. Jennekens's co-authors include Pieter A. van Doorn, F.G.A. van der Meché, Jan Meulstee, H. Veldman, H.R. Scholte, C.J.M. van den Oord, Joost Verhaagen, Angela Vincent, H. F. M. Busch and F.J.M. Gabreëls and has published in prestigious journals such as Journal of Neuroscience, Brain and Neurology.

In The Last Decade

F.G.I. Jennekens

21 papers receiving 880 citations

Peers

F.G.I. Jennekens
L. M. E. Smit Netherlands
F. Jerusalem Germany
J. Bethlem Netherlands
Olavo M. Vasconcelos United States
F.G.I. Jennekens
Citations per year, relative to F.G.I. Jennekens F.G.I. Jennekens (= 1×) peers Z Kamieniecka

Countries citing papers authored by F.G.I. Jennekens

Since Specialization
Citations

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

Fields of papers citing papers by F.G.I. Jennekens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F.G.I. Jennekens. 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 F.G.I. Jennekens. The network helps show where F.G.I. Jennekens may publish in the future.

Co-authorship network of co-authors of F.G.I. Jennekens

This figure shows the co-authorship network connecting the top 25 collaborators of F.G.I. Jennekens. A scholar is included among the top collaborators of F.G.I. Jennekens 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 F.G.I. Jennekens. F.G.I. Jennekens 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.
Meché, F.G.A. van der, Pieter A. van Doorn, Jan Meulstee, & F.G.I. Jennekens. (2001). Diagnostic and Classification Criteria for the Guillain-Barré Syndrome. European Neurology. 45(3). 133–139. 196 indexed citations
2.
Kooi, Anneke J. van der, Willem G. de Voogt, P. G. Barth, et al.. (1998). The heart in limb girdle muscular dystrophy. Heart. 79(1). 73–77. 48 indexed citations
3.
Kooi, Anneke J. van der, Marianne de Visser, H.B. Ginjaar, et al.. (1998). A novel γ-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy. Neuromuscular Disorders. 8(5). 305–308. 16 indexed citations
4.
Gabreëls-Festen, Anneke, Jessica E. Hoogendijk, F.J.M. Gabreëls, et al.. (1996). Two divergent types of nerve pathology in patients with different P sub 0 mutations in Charcot-Marie-Tooth disease. Neurology. 47(3). 761–765. 116 indexed citations
5.
Kooi, Anneke J. van der, P. G. Barth, H. F. M. Busch, et al.. (1996). The clinical spectrum of limb girdle muscular dystrophy A survey in the Netherlands. Brain. 119(5). 1471–1480. 67 indexed citations
6.
Jennekens, F.G.I., et al.. (1993). Development of innervation of skeletal muscle fibers in man: Relation to acetylcholine receptors. The Anatomical Record. 236(3). 553–562. 100 indexed citations
7.
Kerkhoff, Henk & F.G.I. Jennekens. (1993). Peripheral nerve lesions: The neuropharmacological outlook. Clinical Neurology and Neurosurgery. 95. 103–108. 15 indexed citations
8.
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
9.
Scholte, H.R., Etienne Agsteribbe, H. F. M. Busch, et al.. (1990). Oxidative phosporylation in human muscle in patients with ocular myopathy and after general anaesthesia. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1018(2-3). 211–216. 9 indexed citations
10.
Jennekens, F.G.I., et al.. (1989). A light and electron microscopical study of B-50 (GAP-43) in human intramuscular nerve and neuromuscular junctions during development. Journal of the Neurological Sciences. 89(2-3). 301–311. 12 indexed citations
11.
Wokke, John H. J., et al.. (1989). Congenital paucity of secondary synaptic clefts (CPSC) syndrome in 2 adult sibs. Neurology. 39(5). 648–648. 21 indexed citations
12.
Jennekens, F.G.I., et al.. (1989). Immunoreactivity to foetal acetylcholine receptor disappears during the 33D week of human foetal development and reappears with denervation. Journal of Autoimmunity. 2(6). 921–921. 1 indexed citations
13.
Scholte, H.R., et al.. (1989). Carnitine deficiency, mitochondrial dysfunction and the heart. Identical defect of oxidative phosphorylation in muscle mitochondria in cardiomyopathy due to carnitine loss and in Duchenne muscular dystrophy.. PubMed. 101(1). 12–7. 11 indexed citations
14.
Gispen, W.H., et al.. (1988). Factors promoting peripheral nerve repair: I. Recovery from peripheral nerve transection in the rat is accelerated by subcutaneous application of á-MSH. Utrecht University Repository (Utrecht University). 6(2). 87–90. 4 indexed citations
15.
Verhaagen, Joost, P.M. Edwards, P.N.E. de Graan, et al.. (1986). The kinase c substrate protein b-50 and axonal regeneration. Brain Research Bulletin. 17(6). 737–741. 81 indexed citations
16.
Gispen, W.H., Wim A. Bijlsma, F.G.I. Jennekens, & P. Schotman. (1981). Corticotrophin (ACTH) like peptides stimulate peripheral nerve regeneration. Developmental Neuroscience. 13. 411–416. 13 indexed citations
17.
Scholte, H.R., et al.. (1979). Carnitine palmitoyltransferase II deficiency with normal carnitine palmitoyltransferase I in skeletal muscle and leucocytes. Journal of the Neurological Sciences. 40(1). 39–51. 74 indexed citations
18.
Jennekens, F.G.I., K. E. W. P. Tan, & T.U. Hoogenraad. (1976). Enzyme-Histochemistry of Normal External Ocular Muscles. Ophthalmologica. 173(3-4). 326–327. 3 indexed citations
19.
Bradley, Walter G. & F.G.I. Jennekens. (1971). Axonal degeneration in diphtheritic neuropathy. Journal of the Neurological Sciences. 13(4). 415–430. 14 indexed citations
20.
Dijkstra, Sipke, et al.. (1969). Maximum conduction velocity and range of conduction velocity in motor fibers of the deep peroneal nerve in patients with chronic renal insufficiency. Electroencephalography and Clinical Neurophysiology. 27(7). 715–715. 2 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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