Jörg Klepper

3.2k total citations
42 papers, 1.6k citations indexed

About

Jörg Klepper is a scholar working on Physiology, Clinical Biochemistry and Molecular Biology. According to data from OpenAlex, Jörg Klepper has authored 42 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Physiology, 23 papers in Clinical Biochemistry and 14 papers in Molecular Biology. Recurrent topics in Jörg Klepper's work include Diet and metabolism studies (24 papers), Metabolism and Genetic Disorders (23 papers) and Metabolism, Diabetes, and Cancer (9 papers). Jörg Klepper is often cited by papers focused on Diet and metabolism studies (24 papers), Metabolism and Genetic Disorders (23 papers) and Metabolism, Diabetes, and Cancer (9 papers). Jörg Klepper collaborates with scholars based in Germany, United States and Netherlands. Jörg Klepper's co-authors include Darryl C. De Vivo, Thomas Voit, Thomas Voït, Jorge Fischbarg, Kevin R. O’Driscoll, Juan Carlos Vera, Morris J. Birnbaum, Glen Seidner, Nancy B. Spinner and Jih‐I Yeh and has published in prestigious journals such as Nature Genetics, Biochemistry and Annals of Neurology.

In The Last Decade

Jörg Klepper

42 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
Jörg Klepper Germany 20 911 759 555 311 213 42 1.6k
Douglas S. Kerr United States 22 492 0.5× 1.1k 1.5× 969 1.7× 160 0.5× 143 0.7× 48 1.9k
Silvia Tortorelli United States 30 621 0.7× 1.1k 1.5× 1.0k 1.9× 97 0.3× 310 1.5× 70 2.3k
José E. Abdenur United States 24 446 0.5× 818 1.1× 978 1.8× 110 0.4× 325 1.5× 63 1.8k
Stephen D. Cederbaum United States 21 547 0.6× 1.1k 1.4× 793 1.4× 95 0.3× 134 0.6× 39 1.6k
Deborah Marsden United States 24 532 0.6× 1.2k 1.6× 854 1.5× 88 0.3× 269 1.3× 65 1.8k
Klary E. Niezen‐Koning Netherlands 22 930 1.0× 522 0.7× 709 1.3× 61 0.2× 163 0.8× 59 1.8k
Federica Deodato Italy 23 640 0.7× 608 0.8× 801 1.4× 48 0.2× 144 0.7× 55 1.7k
Birgit Assmann Germany 23 214 0.2× 789 1.0× 870 1.6× 76 0.2× 299 1.4× 51 1.7k
Wenjuan Qiu China 22 378 0.4× 606 0.8× 730 1.3× 114 0.4× 314 1.5× 146 1.5k
Lena Bezman United States 14 567 0.6× 746 1.0× 1.4k 2.5× 136 0.4× 81 0.4× 16 2.1k

Countries citing papers authored by Jörg Klepper

Since Specialization
Citations

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

Fields of papers citing papers by Jörg Klepper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jörg Klepper

This figure shows the co-authorship network connecting the top 25 collaborators of Jörg Klepper. A scholar is included among the top collaborators of Jörg Klepper 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 Jörg Klepper. Jörg Klepper 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.
Vill, Katharina, Wolfgang Müller‐Felber, Dieter Gläser, et al.. (2018). SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy. Human Genetics. 137(11-12). 911–919. 15 indexed citations
2.
Herbst, Martin, Roel P. Gazendam, Julie Sawalle‐Belohradsky, et al.. (2015). Chronic Candida albicans Meningitis in a 4-Year-Old Girl with a Homozygous Mutation in the CARD9 Gene (Q295X). The Pediatric Infectious Disease Journal. 34(9). 999–1002. 44 indexed citations
3.
Klepper, Jörg, et al.. (2009). Autosomal Recessive Inheritance of GLUT1 Deficiency Syndrome. Neuropediatrics. 40(5). 207–210. 46 indexed citations
4.
Bağcı, Soyhan, Johannes Zschocke, G. F. Hoffmann, et al.. (2009). Pyridoxal phosphate-dependent neonatal epileptic encephalopathy. BMJ Case Reports. 2009. bcr1120081247–bcr1120081247. 6 indexed citations
5.
Klepper, Jörg. (2008). Glucose transporter deficiency syndrome (GLUT1DS) and the ketogenic diet. Epilepsia. 49(s8). 46–49. 104 indexed citations
6.
Rauchenzauner, Markus, et al.. (2008). The Ketogenic Diet in Children with Glut1 Deficiency Syndrome and Epilepsy. The Journal of Pediatrics. 153(5). 716–718. 16 indexed citations
7.
Klepper, Jörg, et al.. (2007). Expect the unexpected: favourable outcome in Munchausen by proxy syndrome. European Journal of Pediatrics. 167(9). 1085–1088. 10 indexed citations
8.
Klepper, Jörg, Hans Scheffer, B. Leiendecker, et al.. (2005). Seizure Control and Acceptance of the Ketogenic Diet in GLUT1 Deficiency Syndrome: A 2- to 5-Year Follow-Up of 15 Children Enrolled Prospectively. Neuropediatrics. 36(5). 302–308. 109 indexed citations
9.
Klepper, Jörg, et al.. (2004). Effects of the ketogenic diet in the glucose transporter 1 deficiency syndrome. Prostaglandins Leukotrienes and Essential Fatty Acids. 70(3). 321–327. 88 indexed citations
10.
Klepper, Jörg. (2004). Impaired glucose transport into the brain: the expanding spectrum of glucose transporter type 1 deficiency syndrome. Current Opinion in Neurology. 17(2). 193–196. 33 indexed citations
11.
Klepper, Jörg, Anne Flörcken, Jorge Fischbarg, & Thomas Voït. (2003). Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro. European Journal of Pediatrics. 162(2). 84–89. 36 indexed citations
12.
Lange, Peter, et al.. (2003). Functional consequences of an in vivo mutation in exon 10 of the human GLUT1 gene. FEBS Letters. 555(2). 274–278. 9 indexed citations
13.
Willemsen, Michèl A.A.P., et al.. (2003). Neuroglycopenia in normoglycaemic patients, and the potential benefit of ketosis. Diabetic Medicine. 20(6). 481–482. 2 indexed citations
14.
Klepper, Jörg, Jörg Schaper, Gordana Raca, et al.. (2003). Progressive dystonia in a 12-year-old boy. European Journal of Paediatric Neurology. 7(2). 85–88. 4 indexed citations
15.
Klepper, Jörg & Thomas Voit. (2002). Facilitated glucose transporter protein type 1 (GLUT1) deficiency syndrome: impaired glucose transport into brain – a review. European Journal of Pediatrics. 161(6). 295–304. 121 indexed citations
16.
Wallot, Michael, Jörg Klepper, Philippe Clapuyt, et al.. (2002). Repeated detection of gas in the portal vein after liver transplantation: A sign of EBV‐associated post‐transplant lymphoproliferation?. Pediatric Transplantation. 6(4). 332–336. 4 indexed citations
17.
Klepper, Jörg. (2001). Autosomal dominant transmission of GLUT1 deficiency. Human Molecular Genetics. 10(1). 63–68. 77 indexed citations
18.
Klepper, Jörg, et al.. (2001). Functional consequences of the autosomal dominant G272A mutation in the human GLUT1 gene. FEBS Letters. 498(1). 104–109. 15 indexed citations
19.
Klepper, Jörg, Jorge Fischbarg, Juan Carlos Vera, Dong Wang, & Darryl C. De Vivo. (1999). GLUT1-Deficiency: Barbiturates Potentiate Haploinsufficiency in Vitro. Pediatric Research. 46(6). 677–677. 58 indexed citations
20.
Seidner, Glen, Jih‐I Yeh, Kevin R. O’Driscoll, et al.. (1998). GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier. Nature Genetics. 18(2). 188–191. 294 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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