Ekkehard Wilichowski

3.3k total citations
51 papers, 1.2k citations indexed

About

Ekkehard Wilichowski is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Ekkehard Wilichowski has authored 51 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 21 papers in Clinical Biochemistry and 8 papers in Genetics. Recurrent topics in Ekkehard Wilichowski's work include Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (21 papers) and ATP Synthase and ATPases Research (6 papers). Ekkehard Wilichowski is often cited by papers focused on Mitochondrial Function and Pathology (25 papers), Metabolism and Genetic Disorders (21 papers) and ATP Synthase and ATPases Research (6 papers). Ekkehard Wilichowski collaborates with scholars based in Germany, Switzerland and Austria. Ekkehard Wilichowski's co-authors include F. Hanefeld, Jens Frahm, R. Rüchel, B. Kruse, U. Holzbach, Eric A. Schon, Yingying Tang, Elke Hobbiebrunken, Michael P. King and Edgar Davidson and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Annals of Neurology.

In The Last Decade

Ekkehard Wilichowski

50 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ekkehard Wilichowski Germany 21 865 384 123 117 104 51 1.2k
Mitsunobu Shimadzu Japan 22 812 0.9× 370 1.0× 195 1.6× 176 1.5× 87 0.8× 43 1.7k
Caterina Garone Italy 21 1.3k 1.5× 641 1.7× 182 1.5× 78 0.7× 42 0.4× 45 1.7k
Pirjo Isohanni Finland 22 1.4k 1.6× 812 2.1× 179 1.5× 116 1.0× 68 0.7× 45 1.7k
Christine Barnérias France 20 704 0.8× 236 0.6× 283 2.3× 113 1.0× 156 1.5× 73 1.4k
Alberto Blázquez Spain 18 750 0.9× 323 0.8× 141 1.1× 129 1.1× 45 0.4× 50 1.1k
Charissa A. Dyer United States 22 799 0.9× 237 0.6× 52 0.4× 209 1.8× 190 1.8× 46 1.4k
Paule Frachon France 16 1.4k 1.7× 567 1.5× 99 0.8× 151 1.3× 108 1.0× 23 1.7k
Katsuo Sugita Japan 22 790 0.9× 105 0.3× 268 2.2× 136 1.2× 71 0.7× 101 1.6k
Ana Fernández‐Marmiesse Spain 17 460 0.5× 233 0.6× 219 1.8× 144 1.2× 43 0.4× 33 842
Parayil Sankaran Bindu India 19 386 0.4× 177 0.5× 80 0.7× 170 1.5× 77 0.7× 92 1.1k

Countries citing papers authored by Ekkehard Wilichowski

Since Specialization
Citations

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

Fields of papers citing papers by Ekkehard Wilichowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ekkehard Wilichowski. 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 Ekkehard Wilichowski. The network helps show where Ekkehard Wilichowski may publish in the future.

Co-authorship network of co-authors of Ekkehard Wilichowski

This figure shows the co-authorship network connecting the top 25 collaborators of Ekkehard Wilichowski. A scholar is included among the top collaborators of Ekkehard Wilichowski 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 Ekkehard Wilichowski. Ekkehard Wilichowski 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.
Park, Yohan, Saskia B. Wortmann, Adam C. Gunning, et al.. (2021). Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes. Genome Medicine. 13(1). 55–55. 20 indexed citations
2.
Baumer, Alessandra, et al.. (2014). Microcephalic osteodysplastic primordial dwarfism type II (MOPD II) with multiple vascular complications misdiagnosed as Dubowitz syndrome. European Journal of Pediatrics. 173(9). 1253–1256. 12 indexed citations
3.
Stettner, Georg M., Carlo Viscomi, Massimo Zeviani, Ekkehard Wilichowski, & Mathias Dutschmann. (2010). Hypoxic and hypercapnic challenges unveil respiratory vulnerability of Surf1 knockout mice, an animal model of Leigh syndrome. Mitochondrion. 11(3). 413–420. 7 indexed citations
4.
Auber, Bernd, Barbara Zoll, Peter Burfeind, et al.. (2009). Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation. Molecular Cytogenetics. 2(1). 10–10. 7 indexed citations
5.
Rostásy, K., et al.. (2008). Distinct inflammatory properties of late-activated macrophages in inflammatory myopathies.. PubMed. 27. 49–53. 16 indexed citations
6.
Antonická, Hana, et al.. (2006). Maternal Segmental Disomy in Leigh Syndrome with Cytochrome c Oxidase Deficiency Caused by Homozygous SURF1 Mutation. Neuropediatrics. 37(2). 88–94. 13 indexed citations
7.
Zavadáková, Petra, Brian Fowler, Terttu Suormala, et al.. (2005). cblEType of homocystinuria due to methionine synthase reductase deficiency: Functional correction by minigene expression. Human Mutation. 25(3). 239–247. 33 indexed citations
8.
Jerkic, Silvija‐Pera, et al.. (2005). Colorectal cancer in two pre-teenage siblings with familial adenomatous polyposis. European Journal of Pediatrics. 164(5). 306–310. 23 indexed citations
9.
Groeschel, Samuel, Knut Brockmann, Peter Dechent, et al.. (2005). Magnetic Resonance Imaging and Proton Magnetic Resonance Spectroscopy of Megalencephaly and Dilated Virchow-Robin Spaces. Pediatric Neurology. 34(1). 35–40. 9 indexed citations
10.
Joussen, A.M., et al.. (2003). Retinopathie als Leitbefund einer Mitochondriopathie ohne externe Ophthalmoplegie. Der Ophthalmologe. 100(3). 234–237. 2 indexed citations
11.
Hobbiebrunken, Elke, et al.. (2003). Effectiveness of creatine monohydrate in mitochondrial encephalomyopathies. Pediatric Neurology. 28(1). 53–58. 49 indexed citations
12.
Zwirner, Petra & Ekkehard Wilichowski. (2001). Progressive Sensorineural Hearing Loss in Children With Mitochondrial Encephalomyopathies. The Laryngoscope. 111(3). 515–521. 31 indexed citations
13.
Tang, Yingying, et al.. (2000). Rearrangements of Human Mitochondrial DNA (mtDNA): New Insights into the Regulation of mtDNA Copy Number and Gene Expression. Molecular Biology of the Cell. 11(4). 1471–1485. 102 indexed citations
14.
Wilichowski, Ekkehard, GC Korenke, H.‐J. Christen, et al.. (1997). Medikamentöse und diätetische Therapie der mitochondrialen Zytopathien des Kindesalters *. Monatsschrift Kinderheilkunde. 145(1). 5–19. 1 indexed citations
15.
Beetz, Rolf, Patrick Zorowka, W Schönberger, et al.. (1997). Hypoparathyreoidismus und Innenohrschwerhörigkeit. Monatsschrift Kinderheilkunde. 145(4). 347–352. 4 indexed citations
16.
Wilichowski, Ekkehard, H.‐J. Christen, Holger Schiffmann, Walter Schulz‐Schaeffer, & W. Behrens‐Baumann. (1996). Fatal Pseudallescheria boydii panencephalitis in a child after near-drowning. The Pediatric Infectious Disease Journal. 15(4). 365–370. 26 indexed citations
17.
Korenke, GC, Ekkehard Wilichowski, D. H. Hunneman, et al.. (1996). Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype. Annals of Neurology. 40(2). 254–257. 83 indexed citations
18.
Wilichowski, Ekkehard, et al.. (1994). Deletion screening of mitochondrial DNA via multiprimer DNA amplification. Molecular and Cellular Probes. 8(1). 45–49. 8 indexed citations
19.
20.
Wendel, U., Ekkehard Wilichowski, J. Schmidtke, & C. Bachmann. (1988). DNA analysis of ornithine transcarbamylase deficiency. European Journal of Pediatrics. 147(4). 368–371. 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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