Robert Steinfeld

4.9k total citations
56 papers, 2.8k citations indexed

About

Robert Steinfeld is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, Robert Steinfeld has authored 56 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 23 papers in Physiology and 13 papers in Cell Biology. Recurrent topics in Robert Steinfeld's work include Lysosomal Storage Disorders Research (19 papers), Metabolism and Genetic Disorders (9 papers) and Cellular transport and secretion (9 papers). Robert Steinfeld is often cited by papers focused on Lysosomal Storage Disorders Research (19 papers), Metabolism and Genetic Disorders (9 papers) and Cellular transport and secretion (9 papers). Robert Steinfeld collaborates with scholars based in Germany, Switzerland and United States. Robert Steinfeld's co-authors include Jutta Gärtner, Gregory David, Herman Van den Berghe, Marcel Grapp, Alfried Kohlschütter, R. Kraetzner, Kurt Ullrich, Michaela Schweizer, Wolfgang Brück and Zoltán Lukács and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Robert Steinfeld

56 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
Robert Steinfeld Germany 29 1.6k 820 655 472 418 56 2.8k
Maja Di Rocco Italy 34 1.5k 1.0× 1.2k 1.4× 498 0.8× 778 1.6× 254 0.6× 147 3.6k
Yoko Aoki Japan 36 2.9k 1.8× 254 0.3× 562 0.9× 762 1.6× 408 1.0× 170 4.8k
Kenji E. Orii Japan 29 851 0.5× 1.4k 1.7× 269 0.4× 332 0.7× 317 0.8× 71 2.4k
Luisa Bonafé Switzerland 36 1.8k 1.1× 311 0.4× 378 0.6× 502 1.1× 723 1.7× 97 3.5k
Philippe M. Campeau Canada 33 1.8k 1.2× 369 0.5× 298 0.5× 231 0.5× 191 0.5× 123 3.3k
Muriel I. Kaiser‐Kupfer United States 41 2.0k 1.2× 291 0.4× 620 0.9× 330 0.7× 350 0.8× 103 4.9k
Frans W. Verheijen Netherlands 25 850 0.5× 722 0.9× 477 0.7× 173 0.4× 95 0.2× 47 1.8k
Roseline Froissart France 27 804 0.5× 2.1k 2.5× 657 1.0× 646 1.4× 185 0.4× 90 2.8k
M. Elleder Czechia 32 1.4k 0.9× 2.7k 3.3× 1.1k 1.7× 628 1.3× 246 0.6× 194 4.1k
Jaana Tyynelä Finland 31 1.4k 0.9× 1.7k 2.0× 1.1k 1.7× 213 0.5× 106 0.3× 63 3.1k

Countries citing papers authored by Robert Steinfeld

Since Specialization
Citations

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

Fields of papers citing papers by Robert Steinfeld

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robert Steinfeld

This figure shows the co-authorship network connecting the top 25 collaborators of Robert Steinfeld. A scholar is included among the top collaborators of Robert Steinfeld 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 Robert Steinfeld. Robert Steinfeld 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.
Dreha‐Kulaczewski, Steffi, Prativa Sahoo, Peter Dechent, et al.. (2024). Folate receptor α deficiency – Myelin‐sensitive MRI as a reliable biomarker to monitor the efficacy and long‐term outcome of a new therapeutic approach. Journal of Inherited Metabolic Disease. 47(2). 387–403. 2 indexed citations
2.
Korinthenberg, Rudolf, Janbernd Kirschner, Matthias Eckenweiler, et al.. (2021). Alpers- and MNGIE-like disease with disturbed CSF folate transport and an unusual mode of genetic transmission of POLG mutations: a case report. 1(1). 2 indexed citations
3.
Cao, Xuanye, Annika Wolf, Sung‐Eun Kim, et al.. (2020). CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression. Journal of Medical Genetics. 58(7). 484–494. 18 indexed citations
4.
Bölsterli, Bigna K., et al.. (2020). Pontocerebellar Hypoplasia: a Pattern Recognition Approach. The Cerebellum. 19(4). 569–582. 25 indexed citations
5.
Yambire, King Faisal, Lorena Fernández-Mosquera, Robert Steinfeld, et al.. (2019). Mitochondrial biogenesis is transcriptionally repressed in lysosomal lipid storage diseases. eLife. 8. 63 indexed citations
6.
Ohlenbusch, Andreas, Klaus Jung, Robert Steinfeld, Jutta Gärtner, & Matthias Kettwig. (2017). Cathepsin D Polymorphism C224T in Childhood-Onset Neurodegenerative Disorders: No Impact for Childhood Dementia. Journal of Pediatric Genetics. 7(1). 14–18. 2 indexed citations
7.
Sidhu, Navdeep Singh, Kevin Pröpper, Stefan Becker, et al.. (2014). Structure of sulfamidase provides insight into the molecular pathology of mucopolysaccharidosis IIIA. Acta Crystallographica Section D Biological Crystallography. 70(5). 1321–1335. 30 indexed citations
8.
Grapp, Marcel, Tarja Linnankivi, Philip A. Wolf, et al.. (2012). Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiency. Brain. 135(7). 2022–2031. 90 indexed citations
9.
Banka, Siddharth, Henk J. Blom, John H. Walter, et al.. (2011). Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency. The American Journal of Human Genetics. 88(2). 216–225. 57 indexed citations
10.
Blau, Nenad, et al.. (2011). Cerebral folate deficiency: A neurometabolic syndrome?. Molecular Genetics and Metabolism. 104(3). 369–372. 29 indexed citations
11.
Steinfeld, Robert. (2010). Diagnostik und Therapie der neuronalen Zeroidlipofuszinosen aus Sicht des Neuropädiaters. Der Ophthalmologe. 107(7). 616–620. 1 indexed citations
12.
Feldhammer, Matthew, Stéphanie Durand, Lenka Mrázová, et al.. (2009). Sanfilippo syndrome type C: mutation spectrum in the heparan sulfate acetyl-CoA: α-glucosaminide N-acetyltransferase (HGSNAT) gene. Human Mutation. 30(6). 918–925. 45 indexed citations
13.
Grapp, Marcel, et al.. (2009). Novel CLN8 mutations confirm the clinical and ethnic diversity of late infantile neuronal ceroid lipofuscinosis. Clinical Genetics. 77(1). 79–85. 27 indexed citations
14.
Schlotawa, Lars, Robert Steinfeld, Kurt Von Figura, Thomas Dierks, & Jutta Gärtner. (2007). Molecular analysis ofSUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Human Mutation. 29(1). 205–205. 35 indexed citations
15.
Steinfeld, Robert, Merle Hillebrand, R. Kraetzner, et al.. (2006). Cathepsin D Deficiency Is Associated with a Human Neurodegenerative Disorder. The American Journal of Human Genetics. 78(6). 988–998. 222 indexed citations
16.
Steinfeld, Robert, Alfried Kohlschütter, Johannes Zschocke, et al.. (2002). Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations. European Journal of Pediatrics. 161(7). 403–405. 29 indexed citations
17.
Steinfeld, Robert, Peter Heim, Kerstin B. Meyer, et al.. (2002). Late infantile neuronal ceroid lipofuscinosis: Quantitative description of the clinical course in patients with CLN2 mutations. American Journal of Medical Genetics. 112(4). 347–354. 123 indexed citations
18.
Veugelers, Mark, et al.. (1997). Characterization of Glypican-5 and Chromosomal Localization of HumanGPC5,a New Member of the Glypican Gene Family. Genomics. 40(1). 24–30. 87 indexed citations
19.
Steinfeld, Robert, Herman Van den Berghe, & Gregory David. (1996). Stimulation of fibroblast growth factor receptor-1 occupancy and signaling by cell surface-associated syndecans and glypican.. The Journal of Cell Biology. 133(2). 405–416. 235 indexed citations
20.

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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