Wolfgang Sperl

11.0k total citations
204 papers, 6.2k citations indexed

About

Wolfgang Sperl is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Wolfgang Sperl has authored 204 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 128 papers in Molecular Biology, 97 papers in Clinical Biochemistry and 27 papers in Physiology. Recurrent topics in Wolfgang Sperl's work include Metabolism and Genetic Disorders (95 papers), Mitochondrial Function and Pathology (87 papers) and ATP Synthase and ATPases Research (32 papers). Wolfgang Sperl is often cited by papers focused on Metabolism and Genetic Disorders (95 papers), Mitochondrial Function and Pathology (87 papers) and ATP Synthase and ATPases Research (32 papers). Wolfgang Sperl collaborates with scholars based in Austria, Germany and Netherlands. Wolfgang Sperl's co-authors include Johannes A. Mayr, Barbara Kofler, René G. Feichtinger, Franz Zimmermann, Johannes Koch, Daniela Skladal, Holger Prokisch, Sepideh Aminzadeh-Gohari, Peter Freisinger and David Meierhofer and has published in prestigious journals such as Nature, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Wolfgang Sperl

198 papers receiving 6.1k citations

Peers

Wolfgang Sperl

PHYSI

GENET

Michael J. Bennett United States

Marinus Durán Netherlands

Fumio Endo Japan

Frédéric M. Vaz Netherlands

Anne Lombès France

Seiji Yamaguchi Japan

Andreas Schulze Germany

Arnold W. Strauss United States

Matthias R. Baumgartner Switzerland

Gerard T. Berry United States

Michael J. Bennett United States

Wolfgang Sperl

4.1k ×1.0

2.4k ×1.0

1.8k ×2.1

PHYSI

773 ×1.3

631 ×1.4

GENET

Citations per year, relative to Wolfgang Sperl Wolfgang Sperl (= 1×) peers Michael J. Bennett

Countries citing papers authored by Wolfgang Sperl

Since Specialization

Citations

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

Fields of papers citing papers by Wolfgang Sperl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wolfgang Sperl

This figure shows the co-authorship network connecting the top 25 collaborators of Wolfgang Sperl. A scholar is included among the top collaborators of Wolfgang Sperl 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 Wolfgang Sperl. Wolfgang Sperl 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

Schneider, Anna-Maria, Franz Zimmermann, Susanne M. Brunner, et al.. (2022). Expression of Oxidative Phosphorylation Complexes and Mitochondrial Mass in Pediatric and Adult Inflammatory Bowel Disease. Oxidative Medicine and Cellular Longevity. 2022(1). 9151169–9151169. 9 indexed citations

Schneider, Anna-Maria, Franz Zimmermann, René G. Feichtinger, et al.. (2020). Age-Related Deterioration of Mitochondrial Function in the Intestine. Oxidative Medicine and Cellular Longevity. 2020. 1–12. 15 indexed citations

Burlina, Alberto, Sebastian Tims, Francjan van Spronsen, et al.. (2018). The potential role of gut microbiota and its modulators in the management of propionic and methylmalonic acidemia. Expert Opinion on Orphan Drugs. 6(11). 683–692. 5 indexed citations

Feichtinger, René G., Daniel Neureiter, Silja Weßler, et al.. (2017). Oxidative Phosphorylation System in Gastric Carcinomas and Gastritis. Oxidative Medicine and Cellular Longevity. 2017(1). 1320241–1320241. 19 indexed citations

Morscher, Raphael J., Christian Rauscher, Wolfgang Sperl, & Olaf Rittinger. (2017). Seizures, enamel defects and psychomotor developmental delay: The first patient with Kohlschütter-Tönz syndrome caused by a ROGDI-gene deletion. Seizure. 50. 118–120. 5 indexed citations

Feichtinger, René G., Michaela Brunner‐Krainz, Bader Alhaddad, et al.. (2017). Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. Oxidative Medicine and Cellular Longevity. 2017(1). 7202589–7202589. 33 indexed citations

Koch, Johannes, Peter Freisinger, René G. Feichtinger, et al.. (2015). Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype. Orphanet Journal of Rare Diseases. 10(1). 40–40. 19 indexed citations

Mueller, Edith E., Susanne M. Brunner, Waltraud Eder, et al.. (2012). Mitochondrial Haplogroups and Control Region Polymorphisms in Age-Related Macular Degeneration: A Case-Control Study. PLoS ONE. 7(2). e30874–e30874. 56 indexed citations

Rogač, Mihael, Marija Meznarič, Massimo Zeviani, Wolfgang Sperl, & David Neubauer. (2011). Functional Outcome of Children With Mitochondrial Diseases. Pediatric Neurology. 44(5). 340–346. 8 indexed citations

10.

Mueller, Edith E., Waltraud Eder, Danijela Šantić, et al.. (2011). The Mitochondrial T16189C Polymorphism Is Associated with Coronary Artery Disease in Middle European Populations. PLoS ONE. 6(1). e16455–e16455. 63 indexed citations

11.

Mayr, Johannes A., David Meierhofer, Franz Zimmermann, et al.. (2008). Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma. Clinical Cancer Research. 14(8). 2270–2275. 128 indexed citations

12.

Meierhofer, David, et al.. (2006). Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis. 27(19). 3864–3868. 21 indexed citations

13.

Sperl, Wolfgang, Pavel Ješina, J Zeman, et al.. (2005). Isolated defects of mitochondrial ATP synthase: overview of 15 cases.. Journal of Inherited Metabolic Disease. 134–134. 1 indexed citations

14.

Sjarif, Damayanti Rusli, Johannes Kristian Ploos van Amstel, Wolfgang Sperl, et al.. (2004). Glycerol kinase deficiency: residual activity explained by reduced transcription and enzyme conformation. European Journal of Human Genetics. 12(6). 424–432. 12 indexed citations

15.

Sperl, Wolfgang, C. Murr, Daniela Skladal, et al.. (2000). Odd-numbered long-chain fatty acids in propionic acidaemia. European Journal of Pediatrics. 159(1-2). 54–58. 20 indexed citations

16.

Henry, Hugues, Jean‐Daniel Tissot, M. Markert, et al.. (1997). Microheterogeneity of serum glycoproteins and their liver precursors in patients with carbohydrate-deficient glycoprotein syndrome type I: Apparent deficiencies in clusterin and serum amyloid P. Journal of Laboratory and Clinical Medicine. 129(4). 412–421. 31 indexed citations

17.

Bongaerts, G.P.A., J.J.M. Tolboom, A.H.J. Naber, et al.. (1997). Role of bacteria in the pathogenesis of short bowel syndrome-associated D-lactic acidemia. Microbial Pathogenesis. 22(5). 285–293. 86 indexed citations

18.

Sperl, Wolfgang, et al.. (1995). Reversible hepatic veno-occlusive disease in an infant after consumption of pyrrolizidine-containing herbal tea. European Journal of Pediatrics. 154(2). 112–116. 64 indexed citations

19.

Sperl, Wolfgang, et al.. (1993). Measurement of Totally Activated Pyruvate Dehydrogenase Complex Activity in Human Muscle: Evaluation of a Useful Assay. PubMed. 47(1). 37–46. 25 indexed citations

20.

Sperl, Wolfgang, J. M. F. Trijbels, W. Ruitenbeek, et al.. (1992). Postnatal Development of Pyruvate Oxidation in Quadriceps Muscle of the Rat. Neonatology. 61(3). 188–200. 5 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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