Gert C. Scheper

9.7k total citations
80 papers, 3.9k citations indexed

About

Gert C. Scheper is a scholar working on Molecular Biology, Cell Biology and Immunology. According to data from OpenAlex, Gert C. Scheper has authored 80 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 14 papers in Cell Biology and 9 papers in Immunology. Recurrent topics in Gert C. Scheper's work include RNA regulation and disease (49 papers), RNA and protein synthesis mechanisms (20 papers) and RNA Research and Splicing (18 papers). Gert C. Scheper is often cited by papers focused on RNA regulation and disease (49 papers), RNA and protein synthesis mechanisms (20 papers) and RNA Research and Splicing (18 papers). Gert C. Scheper collaborates with scholars based in Netherlands, United States and United Kingdom. Gert C. Scheper's co-authors include Christopher G. Proud, Marjo S. van der Knaap, Harry O. Voorma, Miranda Kleijn, Barbara van Kollenburg, Adri A.M. Thomas, Jan C. Pronk, Marianna Bugiani, James M. Powers and Carola G.M. van Berkel and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Gert C. Scheper

78 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gert C. Scheper Netherlands 37 3.3k 481 366 351 349 80 3.9k
Katsuya Kominami Japan 20 2.0k 0.6× 357 0.7× 175 0.5× 387 1.1× 453 1.3× 31 3.7k
Vera L. Bonilha United States 27 1.8k 0.5× 438 0.9× 226 0.6× 229 0.7× 282 0.8× 71 2.8k
Jan C. Pronk Netherlands 31 3.4k 1.0× 499 1.0× 250 0.7× 237 0.7× 222 0.6× 77 4.1k
Sylvie Bannwarth France 27 1.6k 0.5× 244 0.5× 161 0.4× 148 0.4× 241 0.7× 62 2.0k
Yosaburo Shibata Japan 31 1.8k 0.5× 419 0.9× 440 1.2× 109 0.3× 424 1.2× 87 2.9k
Mark Berryman United States 24 1.8k 0.6× 767 1.6× 81 0.2× 287 0.8× 221 0.6× 34 3.0k
Christian Delphin France 22 2.4k 0.7× 441 0.9× 114 0.3× 232 0.7× 263 0.8× 29 2.9k
Christof Haffner Germany 23 1.2k 0.4× 753 1.6× 379 1.0× 181 0.5× 171 0.5× 36 2.5k
Julien Fauré France 28 2.5k 0.8× 1.1k 2.2× 133 0.4× 260 0.7× 411 1.2× 82 3.6k
Patricia J. Gallagher United States 35 2.8k 0.8× 1.2k 2.6× 115 0.3× 250 0.7× 419 1.2× 56 4.0k

Countries citing papers authored by Gert C. Scheper

Since Specialization
Citations

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

Fields of papers citing papers by Gert C. Scheper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gert C. Scheper. 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 Gert C. Scheper. The network helps show where Gert C. Scheper may publish in the future.

Co-authorship network of co-authors of Gert C. Scheper

This figure shows the co-authorship network connecting the top 25 collaborators of Gert C. Scheper. A scholar is included among the top collaborators of Gert C. Scheper 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 Gert C. Scheper. Gert C. Scheper 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.
2.
Vujadinovic, Marija, Selina Khan, Koen Oosterhuis, et al.. (2018). Adenovirus based HPV L2 vaccine induces broad cross-reactive humoral immune responses. Vaccine. 36(30). 4462–4470. 18 indexed citations
3.
Dooves, Stephanie, Marianna Bugiani, Nienke L. Postma, et al.. (2016). Astrocytes are central in the pathomechanisms of vanishing white matter. Journal of Clinical Investigation. 126(4). 1512–1524. 106 indexed citations
4.
Schwenzer, Hagen, Gert C. Scheper, Nathalie Zorn, et al.. (2013). Released selective pressure on a structural domain gives new insights on the functional relaxation of mitochondrial aspartyl-tRNA synthetase. Biochimie. 100. 18–26. 4 indexed citations
5.
López-Hernández, Tania, Sònia Sirisi, Xavier Capdevila‐Nortes, et al.. (2011). Molecular mechanisms of MLC1 and GLIALCAM mutations in megalencephalic leukoencephalopathy with subcortical cysts. Human Molecular Genetics. 20(16). 3266–3277. 78 indexed citations
6.
Scheper, Gert C., Carola G.M. van Berkel, Lilia Leisle, et al.. (2010). Analysis of CLCN2 as Candidate Gene for Megalencephalic Leukoencephalopathy with Subcortical Cysts. Genetic Testing and Molecular Biomarkers. 14(2). 255–257. 21 indexed citations
7.
Bugiani, Marianna, Ilja Boor, Barbara van Kollenburg, et al.. (2010). Defective Glial Maturation in Vanishing White Matter Disease. Journal of Neuropathology & Experimental Neurology. 70(1). 69–82. 104 indexed citations
8.
Mejaški‐Bošnjak, Vlatka, et al.. (2009). Vanishing white matter disease. Paediatria Croatica. 53(3). 149–152.
9.
Duarri, Anna, Óscar Teijido, Tania López-Hernández, et al.. (2008). Molecular pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts: mutations in MLC1 cause folding defects. Human Molecular Genetics. 17(23). 3728–3739. 52 indexed citations
10.
Mathis, Stéphane, Gert C. Scheper, Nicole Baumann, et al.. (2008). The ovarioleukodystrophy. Clinical Neurology and Neurosurgery. 110(10). 1035–1037. 18 indexed citations
11.
Boor, Ilja, Wouter Kamphorst, Paul van der Valk, et al.. (2007). MLC1 is associated with the Dystrophin-Glycoprotein Complex at astrocytic endfeet. Acta Neuropathologica. 114(4). 403–410. 47 indexed citations
12.
Scheper, Gert C., Christopher G. Proud, & Marjo S. van der Knaap. (2006). Defective translation initiation causes vanishing of cerebral white matter. Trends in Molecular Medicine. 12(4). 159–166. 32 indexed citations
13.
Seidl, Rainer, et al.. (2005). Fright is a provoking factor in vanishing white matter disease. Annals of Neurology. 57(4). 560–563. 36 indexed citations
14.
Waisfisz, Quinten, Wouter Kamphorst, Cees B.M. Oudejans, et al.. (2005). MLC1: A Novel Protein in Distal Astroglial Processes. Journal of Neuropathology & Experimental Neurology. 64(5). 412–419. 81 indexed citations
15.
Kollenburg, Barbara van, Adri A.M. Thomas, Carola G.M. van Berkel, et al.. (2005). Regulation of protein synthesis in lymphoblasts from vanishing white matter patients. Neurobiology of Disease. 21(3). 496–504. 42 indexed citations
16.
Jurkiewicz, Elżbieta, Hanna Mierzewska, Monika Bekiesińska‐Figatowska, et al.. (2005). MRI of a family with leukoencephalypathy with vanishing white matter. Pediatric Radiology. 35(10). 1027–1030. 3 indexed citations
17.
Knaap, Marjo S. van der, Carola G.M. van Berkel, Jochen Herms, et al.. (2003). eIF2B-Related Disorders: Antenatal Onset and Involvement of Multiple Organs. The American Journal of Human Genetics. 73(5). 1199–1207. 114 indexed citations
18.
Scheper, Gert C., et al.. (2002). Phosphorylation of Eukaryotic Initiation Factor 4E Markedly Reduces Its Affinity for Capped mRNA. Journal of Biological Chemistry. 277(5). 3303–3309. 211 indexed citations
19.
Karim, Muhammad Manjurul, John M.X. Hughes, Jim Warwicker, et al.. (2001). A Quantitative Molecular Model for Modulation of Mammalian Translation by the eIF4E-binding Protein 1. Journal of Biological Chemistry. 276(23). 20750–20757. 68 indexed citations
20.
Kleijn, Miranda, Gavin I. Welsh, Gert C. Scheper, et al.. (1998). Nerve and Epidermal Growth Factor Induce Protein Synthesis and eIF2B Activation in PC12 Cells. Journal of Biological Chemistry. 273(10). 5536–5541. 54 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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