Klaus Gempel

2.4k total citations
30 papers, 1.5k citations indexed

About

Klaus Gempel is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Klaus Gempel has authored 30 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 11 papers in Physiology. Recurrent topics in Klaus Gempel's work include Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (11 papers) and Diet and metabolism studies (7 papers). Klaus Gempel is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Mitochondrial Function and Pathology (11 papers) and Diet and metabolism studies (7 papers). Klaus Gempel collaborates with scholars based in Germany, United States and Switzerland. Klaus Gempel's co-authors include Klaus-Dieter Gerbitz, Dieter Brdiczka, Rita Horváth, Hanns Lochmüller, Benedikt Schoser, D. Pongratz, Matthias Bauer, Wolfgang Müller‐Felber, Peter Schneiderat and Ali Naini and has published in prestigious journals such as Biomaterials, Journal of Molecular Biology and Brain.

In The Last Decade

Klaus Gempel

27 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Klaus Gempel Germany 17 825 569 451 315 190 30 1.5k
María Antònia Vilaseca Spain 20 639 0.8× 652 1.1× 269 0.6× 251 0.8× 151 0.8× 45 1.1k
Mark Korson United States 19 553 0.7× 616 1.1× 243 0.5× 200 0.6× 121 0.6× 38 1.1k
Henk Overmars Netherlands 21 886 1.1× 497 0.9× 236 0.5× 44 0.1× 104 0.5× 33 1.5k
Naruji Sugiyama Japan 18 843 1.0× 1.0k 1.8× 366 0.8× 168 0.5× 131 0.7× 61 1.4k
S. Krywawych United Kingdom 16 465 0.6× 335 0.6× 284 0.6× 93 0.3× 61 0.3× 32 1.2k
Michinori Ito Japan 19 483 0.6× 524 0.9× 361 0.8× 67 0.2× 224 1.2× 51 1.3k
Akash K. George United States 19 395 0.5× 57 0.1× 132 0.3× 161 0.5× 162 0.9× 46 844
Yoshio Takasato Japan 18 203 0.2× 77 0.1× 99 0.2× 116 0.4× 100 0.5× 80 1.4k
Mirjam Langeveld Netherlands 23 612 0.7× 156 0.3× 872 1.9× 176 0.6× 49 0.3× 78 1.5k
Tomomi Matsuura Japan 18 805 1.0× 49 0.1× 125 0.3× 70 0.2× 84 0.4× 56 1.4k

Countries citing papers authored by Klaus Gempel

Since Specialization
Citations

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

Fields of papers citing papers by Klaus Gempel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Klaus Gempel

This figure shows the co-authorship network connecting the top 25 collaborators of Klaus Gempel. A scholar is included among the top collaborators of Klaus Gempel 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 Klaus Gempel. Klaus Gempel 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.
Prestel, Jürgen, Klaus Gempel, Till Hauser, et al.. (2008). Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation. Journal of Neurology. 255(5). 643–648. 26 indexed citations
2.
Pauli, Silke, Thomas Vogl, Wolfgang Höhne, et al.. (2008). Investigation of citrullinemia type I variants by in vitro expression studies. Human Mutation. 29(10). 1222–1227. 35 indexed citations
3.
Distelmaier, Felix, Markus Vogel, Ute Spiekerkötter, et al.. (2007). Cystic renal dysplasia as a leading sign of inherited metabolic disease. Pediatric Nephrology. 22(12). 2119–2124. 8 indexed citations
4.
Müller‐Felber, Wolfgang, Rita Horváth, Klaus Gempel, et al.. (2007). Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients. Neuromuscular Disorders. 17(9-10). 698–706. 193 indexed citations
5.
Gempel, Klaus, Haluk Topaloğlu, Beril Talim, et al.. (2007). The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. Brain. 130(8). 2037–2044. 231 indexed citations
6.
Schoser, Benedikt, Josef Müller‐Höcker, Rita Horváth, et al.. (2007). Adult‐onset glycogen storage disease type 2: clinico‐pathological phenotype revisited. Neuropathology and Applied Neurobiology. 33(5). 544–559. 55 indexed citations
7.
Bissé, Emmanuel, Thomas Epting, Rima Obeid, et al.. (2007). Clinical validation of a new blood collection tube for the accuracy of total homocysteine measurement by different methods. Clinical Biochemistry. 40(9-10). 739–743.
8.
Busch, Raymonde, et al.. (2006). Monitoring of Ketogenic Diet for Carnitine Metabolites by Subcutaneous Microdialysis. Pediatric Research. 60(1). 93–96. 17 indexed citations
9.
Freisinger, Peter, Erwin Lankes, Klaus Gempel, et al.. (2006). Hepatocerebral Mitochondrial DNA Depletion Syndrome Caused by Deoxyguanosine Kinase (DGUOK) Mutations. Archives of Neurology. 63(8). 1129–1129. 89 indexed citations
10.
Gempel, Klaus, et al.. (2006). Asymptomatischer Carnitinmangel unter ketogener Diät bei Patienten mit pharmakoresistenten Epilepsien. Klinische Pädiatrie. 218(5). 260–263. 4 indexed citations
11.
Burghaus, Lothar, et al.. (2005). Glykogenose Typ II (M. Pompe). Der Nervenarzt. 77(2). 181–186. 12 indexed citations
12.
Eyer, Florian, Norbert Felgenhauer, Klaus Gempel, et al.. (2005). Acute Valproate Poisoning. Journal of Clinical Psychopharmacology. 25(4). 376–380. 60 indexed citations
13.
Reichl, Franz‐Xaver, Jürgen Durner, Juergen Manhart, et al.. (2002). Biological clearance of HEMA in guinea pigs. Biomaterials. 23(10). 2135–2141. 13 indexed citations
14.
Gempel, Klaus, et al.. (2002). Tandem Mass Spectrometric Assay for the Determination of Carnitine Palmitoyltransferase II Activity in Muscle Tissue. Analytical Biochemistry. 302(2). 246–251. 8 indexed citations
15.
Gempel, Klaus, et al.. (2001). "Adult" form of muscular carnitine palmitoyltransferase II deficiency: manifestation in a 2-year-old child. European Journal of Pediatrics. 160(9). 548–551. 16 indexed citations
16.
Gempel, Klaus, Klaus-Dieter Gerbitz, Bruno Casetta, & Matthias Bauer. (2000). Rapid Determination of Total Homocysteine in Blood Spots by Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry. Clinical Chemistry. 46(1). 122–123. 48 indexed citations
17.
Bauer, Matthias, Klaus Gempel, Andreas S. Reichert, et al.. (1999). Genetic and structural characterization of the human mitochondrial inner membrane translocase 1 1Edited by J. Karn. Journal of Molecular Biology. 289(1). 69–82. 95 indexed citations
18.
Burwinkel, Barbara, Joachim Kreuder, Susanne Schweitzer, et al.. (1999). Carnitine Transporter OCTN2 Mutations in Systemic Primary Carnitine Deficiency: A Novel Arg169Gln Mutation and a Recurrent Arg282ter Mutation Associated with an Unconventional Splicing Abnormality. Biochemical and Biophysical Research Communications. 261(2). 484–487. 51 indexed citations
19.
Gerbitz, Klaus-Dieter, Klaus Gempel, & Dieter Brdiczka. (1996). Mitochondria and Diabetes: Genetic, Biochemical, and Clinical Implications of the Cellular Energy Circuit. Diabetes. 45(2). 113–126. 233 indexed citations
20.
Gempel, Klaus, Klaus-Dieter Gerbitz, B. Olgemöller, & E. Schleicher. (1993). In-Vitro Carboxymethylation of Low Density Lipoprotein Alters its Metabolism Via the High-Affinity Receptor. Hormone and Metabolic Research. 25(5). 250–252. 14 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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