Robert Steinfeld
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Physiology top 2%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
Papers in
-
- Glycosylation and Glycoproteins Research 5
- Mitochondrial Function and Pathology 5
- RNA regulation and disease 4
- Physiology 22
- Lysosomal Storage Disorders Research 18
- Co-authors
- Jutta Gärtner (17 shared papers)Herman Van den Berghe (1 shared paper)Gregory David (1 shared paper)Marcel Grapp (6 shared papers)Alfried Kohlschütter (9 shared papers)R. Kraetzner (3 shared papers)Kurt Ullrich (6 shared papers)Michaela Schweizer (2 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (4 papers)Neuropediatrics (3 papers)The American Journal of Human Genetics (3 papers)Human Mutation (3 papers)Neurology (2 papers)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Robert Steinfeld
58 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 107
- Clinical Biochemistry 388
- Physiology 192
- Cell Biology 623
- Physiology 848
- Rheumatology 451
Countries citing papers authored by Robert Steinfeld
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
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-authors
The 25 scholars most cited alongside Robert Steinfeld, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 303 | |
| 2 | 2013 | 265 | |
| 3 | 1996 | 245 | |
| 4 | 2006 | 238 | |
| 5 | 2009 | 207 | |
| 6 | 2002 | 134 | |
| 7 | 2009 | 116 | |
| 8 | 2012 | 95 | |
| 9 | 1997 | 90 | |
| 10 | 2014 | 85 | |
| 11 | 1999 | 84 | |
| 12 | 1997 | 71 | |
| 13 | 2011 | 69 | |
| 14 | 2019 | 67 | |
| 15 | 2011 | 61 | |
| 16 | Lysosome-mediated apoptosis is associated with cathepsin D-specific processing of bid at Phe24, Trp48, and Phe183. | 2012 | 55 |
| 17 | 2014 | 51 | |
| 18 | 2009 | 50 | |
| 19 | 2003 | 44 | |
| 20 | 2008 | 41 |
About Robert Steinfeld
Robert Steinfeld is a scholar working on Molecular Biology, Physiology, Rheumatology, Cell Biology and Clinical Biochemistry, having authored 58 papers that have together received 3.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (18 papers), Folate and B Vitamins Research (11 papers), Metabolism and Genetic Disorders (9 papers), Cellular transport and secretion (8 papers), Glycosylation and Glycoproteins Research (5 papers), Mitochondrial Function and Pathology (5 papers), Fetal and Pediatric Neurological Disorders (4 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Clinical Biochemistry (388 citations), Physiology (192 citations), Cell Biology (623 citations), Physiology (848 citations) and Rheumatology (451 citations). Robert Steinfeld has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include Jutta Gärtner, Herman Van den Berghe, Gregory David, Marcel Grapp, Alfried Kohlschütter, R. Kraetzner, Kurt Ullrich, Michaela Schweizer, Wolfgang Brück and Merle Hillebrand. Their work appears in journals such as Journal of Inherited Metabolic Disease, Neuropediatrics, The American Journal of Human Genetics, Human Mutation and Neurology.
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.