U. Wendel

7.8k total citations
200 papers, 5.1k citations indexed

About

U. Wendel is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, U. Wendel has authored 200 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 150 papers in Clinical Biochemistry, 93 papers in Molecular Biology and 46 papers in Rheumatology. Recurrent topics in U. Wendel's work include Metabolism and Genetic Disorders (150 papers), Mitochondrial Function and Pathology (35 papers) and Amino Acid Enzymes and Metabolism (30 papers). U. Wendel is often cited by papers focused on Metabolism and Genetic Disorders (150 papers), Mitochondrial Function and Pathology (35 papers) and Amino Acid Enzymes and Metabolism (30 papers). U. Wendel collaborates with scholars based in Germany, Netherlands and United States. U. Wendel's co-authors include Peter Schadewaldt, H. J. Bremer, Hildegard Przyrembel, Ute Spiekerkoetter, Ertan Mayatepek, U. Langenbeck, Bernd Schwahn, Kurt Ullrich, Éva Simon and Peter Burgard and has published in prestigious journals such as The Lancet, Brain and Neurology.

In The Last Decade

U. Wendel

198 papers receiving 4.9k citations

Peers

Countries citing papers authored by U. Wendel

Since Specialization

Citations

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

Fields of papers citing papers by U. Wendel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of U. Wendel

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

#	Work	Indexed citations
1	Clinical and molecular characterization of five patients with succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency 2011 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Toshiyuki Fukao, Jörn Oliver Sass, Petri Kursula, Eva Thimm, U. Wendel, Can Fıçıcıoğlu, Kamel Monastiri, Nathalie Guffon, Ivo Barić, M. T. Zabot, Naomi Kondo	26
2	Safety and efficacy of 22 weeks of treatment with sapropterin dihydrochloride in patients with phenylketonuria 2008 ·American Journal of Medical Genetics Part A ·Phillip Lee, Eileen P. Treacy, Eric Crombez, Melissa Wasserstein, Lewis Waber, Jon A. Wolff, U. Wendel, Alex Dorenbaum, Judith D. Bebchuk, Heidi Christ‐Schmidt, Margretta R. Seashore, Marcello Giovannini, Barbara K. Burton, Andrew A. M. Morris	79
3	Cystic renal dysplasia as a leading sign of inherited metabolic disease 2007 ·Pediatric Nephrology ·Felix Distelmaier, Markus Vogel, Ute Spiekerkötter, Klaus Gempel, Dirk Klee, Stefan Braunstein, (unknown), Ertan Mayatepek, U. Wendel, Bernd Schwahn	8
4	Acute Neuronopathic Gaucher Disease Complicated by Fatal Gastrointestinal Bleeding 2006 ·Neuropediatrics ·(unknown), Bernd Schwahn, Christiane B. Knobbe‐Thomsen, (unknown), Martin Blohm, Ertan Mayatepek, U. Wendel	7
5	Pitfalls of neonatal screening for very-long-chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometry 2006 ·The Journal of Pediatrics ·(unknown), (unknown), Martina Mueller, U. Wendel, Ertan Mayatepek, Arnold W. Strauss, Ronald J. A. Wanders, Ute Spiekerkoetter	49
6	[Inborn errors of metabolism (IEM) in adults. A new challenge to internal medicine (Part 2)]. 2005 ·PubMed ·Martin Schwarz, U. Wendel	14
7	Erwachsene mit angeborenen Stoffwechselkrankheiten 2005 ·Medizinische Klinik ·Martin Schwarz, U. Wendel	4
8	MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency 2003 ·The Journal of Pediatrics ·Ute Spiekerkoetter, Bin Sun, Thomas H. Zytkovicz, Ronald J. A. Wanders, Arnold W. Strauss, U. Wendel	94
9	Odd-numbered long-chain fatty acids in propionic acidaemia 2000 ·European Journal of Pediatrics ·Wolfgang Sperl, C. Murr, Daniela Skladal, Jörn Oliver Sass, Terttu Suormala, R. Baumgartner, U. Wendel	20
10	Molecular analysis in glycogen storage disease 1non-A: DHPLC detection of the highly prevalent exon 8 mutations of theG6PT1 gene in German patients 2000 ·Human Mutation ·René Santer, Johannes Rischewski, (unknown), Martina Kinner, U. Wendel, J. Schaub, Reinhard Schneppenheim	23
11	Treatment and molecular analysis of neonatal carnitine palmitoyltransferase II deficiency. 1999 ·Pediatric Research ·Jan Smeıtınk, B. A. Semmekrot, (unknown), H.R. Scholte, Lambertus P. van den Heuvel, Carla Costa, U. Wendel, W. Ruitenbeek, (unknown), (unknown), (unknown), Jennifer Jager, (unknown), (unknown), R. C. A. Sengers, C. Jakobs, J. M. F. Trijbels	2
12	β-Trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brain 1999 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·(unknown), (unknown), J.G.N. de Jong, Jan A. M. Smeitink, (unknown), Godfried H.J. Boers, Harald S. Conradt, U. Wendel, Ron A. Wevers	28
13	Pregnancy in a woman with maple syrup urine disease 1998 ·Journal of Inherited Metabolic Disease ·(unknown), (unknown), U. Wendel	26
14	White matter abnormalities in patients with treated hyperphenylalaninaemia: Magnetic resonance relaxometry and proton spectroscopy findings 1993 ·European Journal of Pediatrics ·Ulrich Bick, Kurt Ullrich, (unknown), Harald E. Möller, Gerhard Schuierer, Albert C. Ludolph, C. Oberwittler, J. Weglage, U. Wendel	86
15	Intellectual performance of children with maple syrup urine disease 1993 ·European Journal of Pediatrics ·(unknown), (unknown), U. Wendel	42
16	Neonatal screening for maple syrup urine disease by an enzyme-mediated colorimetric method 1993 ·Clinica Chimica Acta ·U. Wendel, (unknown), Werner Hummel	8
17	Development of height and weight in children with diabetes mellitus: Report on two prospective multicentre studies, one cross-sectional, one longitudinal 1992 ·European Journal of Pediatrics ·A. Thon, E. Heinze, (unknown), Reinhard W. Holl, H. Schmidt, Sibylle Koletzko, U. Wendel, (unknown)	56
18	Six-year follow up of phenylalanine intakes and plasma phenylalanine concentrations 1990 ·European Journal of Pediatrics ·U. Wendel, Kurt Ullrich, Hildgund Schmidt, (unknown)	20
19	Analysis of the fatty acid composition of erythrocyte phospholipids by a base catalysed transesterification method — prevention of formation of dimethylacetals 1988 ·Clinica Chimica Acta ·M. D. Laryea, (unknown), (unknown), U. Wendel	18
20	Szintigraphische Diagnostik multipler Phaochromozytome im Kindesalter mit 131I-m-Benzylguanidin 1984 ·Monatsschrift Kinderheilkunde ·Sibylle Koletzko, (unknown), U. Wendel, Berthold Koletzko, I. Lombeck, H. J. Bremer	1

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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