W. Lehnert

4.0k total citations
98 papers, 2.9k citations indexed

About

W. Lehnert is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, W. Lehnert has authored 98 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Clinical Biochemistry, 59 papers in Molecular Biology and 18 papers in Biochemistry. Recurrent topics in W. Lehnert's work include Metabolism and Genetic Disorders (70 papers), Mitochondrial Function and Pathology (22 papers) and Biochemical and Molecular Research (18 papers). W. Lehnert is often cited by papers focused on Metabolism and Genetic Disorders (70 papers), Mitochondrial Function and Pathology (22 papers) and Biochemical and Molecular Research (18 papers). W. Lehnert collaborates with scholars based in Germany, United States and Netherlands. W. Lehnert's co-authors include Regina Ensenauer, Dieter Hunkler, H. Niederhoff, U. Wendel, Friedrich K. Trefz, K. Michael Gibson, Georg F. Hoffmann, N. B�hm, Wolfgang Sperl and E. R. Baumgartner and has published in prestigious journals such as PEDIATRICS, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

W. Lehnert

96 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
W. Lehnert Germany 29 1.7k 1.5k 510 331 318 98 2.9k
David S. Duch United States 25 1.2k 0.7× 461 0.3× 548 1.1× 287 0.9× 342 1.1× 62 2.6k
Alessandro P. Burlina Italy 33 1.1k 0.6× 823 0.6× 434 0.9× 195 0.6× 1.9k 6.0× 113 3.3k
R. Franchi‐Gazzola Italy 25 892 0.5× 304 0.2× 323 0.6× 590 1.8× 164 0.5× 42 2.0k
R. Potashnik Israel 25 741 0.4× 167 0.1× 144 0.3× 377 1.1× 785 2.5× 48 2.2k
Jianfei Jiang United States 29 2.9k 1.7× 214 0.1× 187 0.4× 234 0.7× 437 1.4× 46 3.9k
Klaus D. Schnackerz Germany 28 1.3k 0.8× 154 0.1× 76 0.1× 406 1.2× 244 0.8× 99 2.2k
Kazuyoshi Ikeda Japan 25 808 0.5× 1.1k 0.7× 169 0.3× 83 0.3× 464 1.5× 64 2.2k
Tomiko Kuhara Japan 26 1.0k 0.6× 855 0.6× 20 0.0× 282 0.9× 274 0.9× 98 1.8k
Luciana Hannibal Germany 27 1.3k 0.7× 294 0.2× 64 0.1× 112 0.3× 430 1.4× 97 2.3k
Detcho A. Stoyanovsky United States 31 2.0k 1.1× 105 0.1× 322 0.6× 441 1.3× 777 2.4× 75 3.4k

Countries citing papers authored by W. Lehnert

Since Specialization
Citations

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

Fields of papers citing papers by W. Lehnert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of W. Lehnert

This figure shows the co-authorship network connecting the top 25 collaborators of W. Lehnert. A scholar is included among the top collaborators of W. Lehnert 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 W. Lehnert. W. Lehnert 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.
Grünert, Sarah C., U. Wendel, Martin Lindner, et al.. (2012). Clinical and neurocognitive outcome in symptomatic isovaleric acidemia. Orphanet Journal of Rare Diseases. 7(1). 9–9. 60 indexed citations
2.
Mühlendahl, K. E. von, W. Lehnert, & E. Mönch. (2008). Medium-Chain-Acyl-CoA-Dehydrogenase(MCAD)-Defekt: Akute zerebrale Episoden und nicht-ketotische Hypoglykämien bei Kindern. DMW - Deutsche Medizinische Wochenschrift. 115(33). 1235–1238. 1 indexed citations
3.
Sass, Jörn Oliver, Regina Ensenauer, Wulf Röschinger, et al.. (2007). 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: Functional and molecular studies on a defect in isoleucine catabolism. Molecular Genetics and Metabolism. 93(1). 30–35. 35 indexed citations
4.
Ensenauer, Regina, T Thiel, Karl Otfried Schwab, et al.. (2004). Guanidinoacetate methyltransferase deficiency: differences of creatine uptake in human brain and muscle. Molecular Genetics and Metabolism. 82(3). 208–213. 43 indexed citations
5.
6.
IJlst, Lodewijk, Ference J. Loupatty, Jos P.N. Ruiter, et al.. (2002). 3-Methylglutaconic Aciduria Type I Is Caused by Mutations in AUH. The American Journal of Human Genetics. 71(6). 1463–1466. 57 indexed citations
7.
Ensenauer, Regina, H. Niederhoff, Jos P.N. Ruiter, et al.. (2002). Clinical variability in 3‐hydroxy‐2‐methylbutyryl‐coa dehydrogenase deficiency. Annals of Neurology. 51(5). 656–659. 49 indexed citations
8.
9.
Lehnert, W., et al.. (1999). Long-term follow up of a new case of hawkinsinuria. European Journal of Pediatrics. 158(7). 578–582. 11 indexed citations
10.
Steen, Chloé B., E. R. Baumgartner, M. Durán, et al.. (1999). Metabolic stroke in isolated 3-methylcrotonyl-CoA carboxylase deficiency. European Journal of Pediatrics. 158(9). 730–733. 18 indexed citations
11.
Sewell, A, J. Herwig, Inka Wiegratz, et al.. (1998). Mitochondrial acetoacetyl‐CoA thiolase (β‐ketothiolase) deficiency and pregnancy. Journal of Inherited Metabolic Disease. 21(4). 441–442. 20 indexed citations
12.
Suormala, Terttu, Brian Fowler, C. Jakobs, et al.. (1998). Late-onset holocarboxylase synthetase-deficiency: pre- and post-natal diagnosis and evaluation of effectiveness of antenatal biotin therapy. European Journal of Pediatrics. 157(7). 570–575. 26 indexed citations
13.
Sperl, Wolfgang, Ralf Geiger, W. Lehnert, & William J. Rhead. (1997). Stridor as the major presenting symptom in riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency. European Journal of Pediatrics. 156(10). 800–802. 8 indexed citations
14.
Matern, Dietrich, H. H. Seydewitz, W. Lehnert, et al.. (1996). Primary treatment of propionic acidemia complicated by acute thiamine deficiency. The Journal of Pediatrics. 129(5). 758–760. 12 indexed citations
15.
Lehnert, W., et al.. (1996). Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency: Long-term outcome in a case with neonatal onset. European Journal of Pediatrics. 155(7). 568–572. 16 indexed citations
16.
Corydon, Morten J., N. Gregersen, W. Lehnert, et al.. (1996). Ethylmalonic Aciduria Is Associated with an Amino Acid Variant of Short Chain Acyl-Coenzyme A Dehydrogenase. Pediatric Research. 39(6). 1059–1066. 82 indexed citations
17.
Lehnert, W.. (1994). Long-term results of selective screening for inborn errors of metabolism. European Journal of Pediatrics. 153(S1). S9–S13. 41 indexed citations
18.
Lehnert, W., Wolfgang Sperl, Terttu Suormala, & E. R. Baumgartner. (1994). Propionic acidaemia: clinical, biochemical and therapeutic aspects. European Journal of Pediatrics. 153(S1). S68–S80. 89 indexed citations
19.
Barth, P. G., Georg F. Hoffmann, J. Jaeken, et al.. (1992). L‐2‐hydroxyglutaric acidemia: A novel inherited neurometabolic disease. Annals of Neurology. 32(1). 66–71. 119 indexed citations
20.
Gibson, K. Michael, William L. Nyhan, L. Sweetman, et al.. (1988). 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal. European Journal of Pediatrics. 148(1). 76–82. 21 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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