Stephan Rust

8.4k total citations · 1 hit paper
63 papers, 3.9k citations indexed

About

Stephan Rust is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Stephan Rust has authored 63 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 19 papers in Surgery and 12 papers in Genetics. Recurrent topics in Stephan Rust's work include Cholesterol and Lipid Metabolism (13 papers), Glycosylation and Glycoproteins Research (12 papers) and Metabolism and Genetic Disorders (9 papers). Stephan Rust is often cited by papers focused on Cholesterol and Lipid Metabolism (13 papers), Glycosylation and Glycoproteins Research (12 papers) and Metabolism and Genetic Disorders (9 papers). Stephan Rust collaborates with scholars based in Germany, Japan and Switzerland. Stephan Rust's co-authors include Gerd Assmann, Harald Funke, Marie Rosier, Patrice Denèfle, H. Bryan Brewer, José Manuel Fernández‐Real, Jean‐François Deleuze, Jean‐Charles Piette, Nicolas Duverger and Zahir Amoura and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Stephan Rust

60 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1

1999 1.2k citations Stephan Rust, Marie Rosier et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephan Rust Germany	30	2.0k	1.9k	1.0k	558	436	63	3.9k
Masataka Kudo Japan	40	1.8k 0.9×	1.1k 0.6×	311 0.3×	395 0.7×	1.0k 2.4×	128	4.9k
Seijiro Mori Japan	31	2.5k 1.2×	540 0.3×	567 0.6×	319 0.6×	480 1.1×	137	4.5k
Anélia Horvath United States	33	1.4k 0.7×	1.1k 0.6×	700 0.7×	587 1.1×	867 2.0×	100	3.3k
Michelle Olive United States	29	2.7k 1.4×	580 0.3×	382 0.4×	404 0.7×	219 0.5×	43	4.2k
Elizabeth J. Galbreath United States	20	2.6k 1.3×	571 0.3×	479 0.5×	226 0.4×	423 1.0×	46	4.1k
Karen Schwartz United States	25	1.8k 0.9×	1.4k 0.7×	577 0.6×	437 0.8×	312 0.7×	54	3.5k
Vardiella Meiner Israel	31	1.1k 0.6×	1.1k 0.6×	301 0.3×	285 0.5×	276 0.6×	128	3.2k
Miklós Tóth Hungary	31	763 0.4×	1.3k 0.7×	492 0.5×	439 0.8×	914 2.1×	162	3.1k
Kàroly Rácz Hungary	28	1.1k 0.5×	725 0.4×	345 0.3×	760 1.4×	1.0k 2.3×	162	2.9k
Janete M. Cerutti Brazil	32	1.3k 0.7×	773 0.4×	687 0.7×	454 0.8×	2.1k 4.7×	102	3.7k

Countries citing papers authored by Stephan Rust

Since Specialization

Citations

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

Fields of papers citing papers by Stephan Rust

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephan Rust

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Rust. A scholar is included among the top collaborators of Stephan Rust 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 Stephan Rust. Stephan Rust is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Iuso, Arcangela, Janine Reunert, Marianne Grüneberg, et al.. (2024). Expanding the genetic and clinical spectrum of SLC25A42‐associated disorders and testing of pantothenic acid to improve CoA level in vitro. JIMD Reports. 65(6). 417–425.

Reunert, Janine, Lambert van den Heuvel, Richard J. Rodenburg, et al.. (2021). Severe Form of ßIV-Spectrin Deficiency With Mitochondrial Dysfunction and Cardiomyopathy—A Case Report. Frontiers in Neurology. 12. 643805–643805. 5 indexed citations

Marquardt, Thorsten, Vladimı́r Bzdúch, Stephan Rust, et al.. (2020). SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation. Molecular Genetics and Metabolism Reports. 25. 100636–100636. 5 indexed citations

Park, Julien H., Janine Reunert, Michael L. McCormick, et al.. (2019). SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosis. Brain. 142(8). 2230–2237. 62 indexed citations

Park, Julien H., Marianne Grüneberg, Stephan Rust, et al.. (2017). Limitations of galactose therapy in phosphoglucomutase 1 deficiency. Molecular Genetics and Metabolism Reports. 13. 33–40. 27 indexed citations

Park, Julien H., Manfred Fobker, Barbara Fiedler, et al.. (2017). SLC39A8 deficiency: biochemical correction and major clinical improvement by manganese therapy. Genetics in Medicine. 20(2). 259–268. 57 indexed citations

Reunert, Janine, et al.. (2015). Rapid Diagnosis of 83 Patients with Niemann Pick Type C Disease and Related Cholesterol Transport Disorders by Cholestantriol Screening. EBioMedicine. 4. 170–175. 53 indexed citations

Grüneberg, Marianne, Janine Reunert, Julien H. Park, et al.. (2015). TMEM165 Deficiency: Postnatal Changes in Glycosylation. JIMD Reports. 26. 21–29. 23 indexed citations

Arjona, Francisco J., Jeroen H. F. de Baaij, Karl P. Schlingmann, et al.. (2014). CNNM2 Mutations Cause Impaired Brain Development and Seizures in Patients with Hypomagnesemia. PLoS Genetics. 10(4). e1004267–e1004267. 92 indexed citations

10.

Park, Julien H., Yoshinao Wada, Stephan Rust, et al.. (2014). Transferrin variants: Pitfalls in the diagnostics of Congenital disorders of glycosylation. Clinical Biochemistry. 48(1-2). 11–13. 23 indexed citations

11.

Kannenberg, Frank, Kerstin Gorzelniak, Kathrin Jäger, et al.. (2013). Characterization of Cholesterol Homeostasis in Telomerase-immortalized Tangier Disease Fibroblasts Reveals Marked Phenotype Variability. Journal of Biological Chemistry. 288(52). 36936–36947. 9 indexed citations

12.

Muntoni, Sa., Heiko Wiebusch, Stephan Rust, et al.. (2012). Heterozygosity for lysosomal acid lipase E8SJM mutation and serum lipid concentrations. Nutrition Metabolism and Cardiovascular Diseases. 23(8). 732–736. 25 indexed citations

13.

Peden, John F., Stefan Lorkowski, Anuj Goel, et al.. (2007). Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Human Molecular Genetics. 17(6). 806–814. 389 indexed citations

14.

Nofer, Jerzy–Roch, Martin F. Brodde, Eberhard Morgenstern, et al.. (2004). Impaired Platelet Activation in Familial High Density Lipoprotein Deficiency (Tangier Disease). Journal of Biological Chemistry. 279(32). 34032–34037. 48 indexed citations

15.

Schlüter, Bernhard, Michael Erren, Heiko Schotte, et al.. (2002). The mutagenically separated polymerase chain reaction is a rapid and reliable method for genotyping of the tumour necrosis factor-α promoter polymorphism (−308 G/A). Clinica Chimica Acta. 320(1-2). 135–138. 11 indexed citations

16.

Schlüter, Bernhard, Michael Erren, Heiko Schotte, et al.. (2002). Effect of the interleukin-6 promoter polymorphism (−174 G/C) on the incidence and outcome of sepsis. Critical Care Medicine. 30(1). 32–37. 143 indexed citations

17.

Engel, Thomas, Stefan Lorkowski, Aloys Lueken, et al.. (2001). The Human ABCG4 Gene Is Regulated by Oxysterols and Retinoids in Monocyte-Derived Macrophages. Biochemical and Biophysical Research Communications. 288(2). 483–488. 83 indexed citations

18.

Utech, Markus, et al.. (2001). Accumulation of RhoA, RhoB, RhoG, and Rac1 in Fibroblasts from Tangier Disease Subjects Suggests a Regulatory Role of Rho Family Proteins in Cholesterol Efflux. Biochemical and Biophysical Research Communications. 280(1). 229–236. 32 indexed citations

19.

Lorkowski, Stefan, Stephan Rust, Thomas Engel, et al.. (2001). Genomic Sequence and Structure of the Human ABCG1 (ABC8) Gene. Biochemical and Biophysical Research Communications. 280(1). 121–131. 55 indexed citations

20.

Rust, Stephan, Marie Rosier, Harald Funke, et al.. (1999). Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nature Genetics. 22(4). 352–355. 1189 indexed citations breakdown →

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.

Explore authors with similar magnitude of impact