Kurt Ullrich

7.7k total citations
166 papers, 5.5k citations indexed

About

Kurt Ullrich is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Kurt Ullrich has authored 166 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Clinical Biochemistry, 77 papers in Molecular Biology and 65 papers in Physiology. Recurrent topics in Kurt Ullrich's work include Metabolism and Genetic Disorders (83 papers), Lysosomal Storage Disorders Research (44 papers) and Mitochondrial Function and Pathology (38 papers). Kurt Ullrich is often cited by papers focused on Metabolism and Genetic Disorders (83 papers), Lysosomal Storage Disorders Research (44 papers) and Mitochondrial Function and Pathology (38 papers). Kurt Ullrich collaborates with scholars based in Germany, United States and United Kingdom. Kurt Ullrich's co-authors include James V. Leonard, Gepke Visser, Philippe Labrune, J. Weglage, Jan Peter Rake, Gerrit Smit, Kurt Von Figura, Thomas Braulke, Harald E. Möller and Peter Smit and has published in prestigious journals such as The Lancet, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Kurt Ullrich

162 papers receiving 5.3k citations

Peers

Countries citing papers authored by Kurt Ullrich

Since Specialization

Citations

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

Fields of papers citing papers by Kurt Ullrich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kurt Ullrich

This figure shows the co-authorship network connecting the top 25 collaborators of Kurt Ullrich. A scholar is included among the top collaborators of Kurt Ullrich 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 Kurt Ullrich. Kurt Ullrich 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	Gain-of-function variants in CLCN7 cause hypopigmentation and lysosomal storage disease 2024 ·Journal of Biological Chemistry ·(unknown), (unknown), Kurt Ullrich, Simona Murko, Tatjana Bierhals, (unknown), (unknown), (unknown), René Santer, Thomas J. Jentsch	5
2	Glutaric Aciduria Type 1 Metabolites Impair the Succinate Transport from Astrocytic to Neuronal Cells 2011 ·Journal of Biological Chemistry ·(unknown), Britta Keyser, David M. Koeller, Kurt Ullrich, Thomas Braulke, Chris Mühlhausen	59
3	Transport and distribution of 3-hydroxyglutaric acid before and during induced encephalopathic crises in a mouse model of glutaric aciduria type 1 2008 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Britta Keyser, Markus Glatzel, (unknown), (unknown), Zoltán Lukács, Stefan Kölker, Sven W. Sauer, Nicole Muschol, (unknown), Joachim Thiem, Stephen I. Goodman, David M. Koeller, Kurt Ullrich, Thomas Braulke, Chris Mühlhausen	27
4	The Mutation p.Ser298Pro in the sulphamidase gene (SGSH) is associated with a slowly progressive clinical phenotype in mucopolysaccharidosis type IIIA (Sanfilippo A Syndrome) 2008 ·Human Mutation ·(unknown), (unknown), Andreas Gal, Cordula Steglich, Chris Mühlhausen, Kurt Ullrich, Thomas Braulke, Nicole Muschol	31
5	Mutational analysis in longest known survivor of mucopolysaccharidosis type VII 2003 ·Human Genetics ·Stephan Storch, (unknown), Rafiqul Islam, Kurt Ullrich, William S. Sly, Thomas Braulke	11
6	Glycogen storage disease type I: diagnosis, management, clinical course and outcome. Results of the European Study on Glycogen Storage Disease Type I (ESGSD I) 2002 ·European Journal of Pediatrics ·Jan Peter Rake, Gepke Visser, Philippe Labrune, James V. Leonard, Kurt Ullrich, Peter Smit	251
7	Upregulation of respiratory chain enzymes in guanidinoacetate methyltransferase deficiency 2000 ·Journal of Inherited Metabolic Disease ·Anibh M. Das, Kurt Ullrich, Dirk Isbrandt	5
8	Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls 2000 ·European Journal of Pediatrics ·Anibh M. Das, Ralph Fingerhut, Ronald J. A. Wanders, Kurt Ullrich	54
9	Localization of receptors for endocytosis of lysosomal enzymes on different brain cells 1998 ·Journal of Inherited Metabolic Disease ·(unknown), B. Flott‐Rahmel, Volkmar Gieselmann, (unknown), (unknown), Kurt Ullrich	4
10	A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype 1998 ·The American Journal of Human Genetics ·Per Guldberg, Françoise Rey, Johannes Zschocke, Valentino Romano, Baudouin François, L. Michiels, Kurt Ullrich, Georg F. Hoffmann, Peter Burgard, Hildgund Schmidt, Concetta Meli, Enrica Riva, Irma Dianzani, Alberto Ponzone, Jean Rey, Flemming Güttler	278
11	In vivo NMR spectroscopy in patients with phenylketonuria: Clinical significance of interindividual differences in brain phenylalanine concentrations 1998 ·Journal of Inherited Metabolic Disease ·J. Weglage, Harald E. Möller, Dirk Wiedermann, (unknown), Johannes Zschocke, Kurt Ullrich	34
12	Magnetic resonance imaging and proton spectroscopy in PKU 1995 ·Max Planck Institute for Plasma Physics ·Kurt Ullrich, B. Fünders, J. Weglage, (unknown), (unknown), Harald E. Möller, Ulrich Bick, Gerhard Schuierer, Alexander Ludolph	4
13	In vivo study of brain metabolism in galactosemia by1H and31P magnetic resonance spectroscopy 1995 ·European Journal of Pediatrics ·Harald E. Möller, Kurt Ullrich, Peter Vermathen, Gerhard Schuierer, Hans-Georg Koch	13
14	Screening for lysosomal disorders 1994 ·European Journal of Pediatrics ·Kurt Ullrich	101
15	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
16	Psychological and social findings in adolescents with phenylketonuria 1992 ·European Journal of Pediatrics ·J. Weglage, B. Fünders, B. Wilken, Daniel Schubert, E. Schmidt, Peter Burgard, Kurt Ullrich	65
17	Recurrent nonsense mutation in exon 7 of the phenylalanine hydroxylase gene 1991 ·Human Genetics ·Bernd Dworniczak, Luba Kalaydjieva, C. Aulehla‐Scholz, Kurt Ullrich, Ivo Kremensky, (unknown), J. Horst	14
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	[Aspartylglucosaminuria. Clinical description of 2 German patients]. 1989 ·PubMed ·(unknown), H. Schmidt, A Sewell, J. Weglage, (unknown), Kurt Ullrich	2
20	Phenylketonuria: distribution of DNA diagnostic patterns in German families 1988 ·Human Genetics ·C. Aulehla‐Scholz, Matthias Vorgerd, (unknown), D. Leupold, (unknown), Kurt Ullrich, K. Olek, J. Horst	40

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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