Curt Scharfe
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Molecular Biology top 2%
- Bioinformatics and Genomic Networks
- Mitochondrial Function and Pathology
- Genomics and Phylogenetic Studies
- Fungal and yeast genetics research
- RNA and protein synthesis mechanisms
- Microbial Metabolic Engineering and Bioproduction
Papers in
-
- Genomics and Phylogenetic Studies 7
- Mitochondrial Function and Pathology 7
- Fungal and yeast genetics research 5
- Metabolomics and Mass Spectrometry Studies 5
- Genetics 15
- Genomics and Rare Diseases 7
- Co-authors
- Lars M. Steinmetz (6 shared papers)Ronald W. Davis (14 shared papers)Marcus W. Feldman (2 shared papers)Aaron E. Hirsh (1 shared paper)Hunter B. Fraser (1 shared paper)Xun Gu (1 shared paper)Wen‐Hsiung Li (1 shared paper)Zhenglong Gu (1 shared paper)
- Journals
- Genetics in Medicine (4 papers)Nucleic Acids Research (3 papers)Proceedings of the National Academy of Sciences (3 papers)International Journal of Neonatal Screening (3 papers)Forensic Science International Genetics (2 papers)
- Partner nations
- United StatesGermanyNetherlands
In The Last Decade
Curt Scharfe
50 papers receiving 3.4k citations
Curt Scharfe's Hit Papers
Peers
Comparison fields: 5 of 144
- Clinical Biochemistry 309
- Molecular Biology 2.7k
- Genetics 917
- Aging 48
- Cell Biology 155
Countries citing papers authored by Curt Scharfe
This map shows the geographic impact of Curt Scharfe'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 Curt Scharfe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Curt Scharfe more than expected).
Fields of papers citing papers by Curt Scharfe
This network shows the impact of papers produced by Curt Scharfe. 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 Curt Scharfe. The network helps show where Curt Scharfe may publish in the future.
Co-authors
The 25 scholars most cited alongside Curt Scharfe, 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 53 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Role of duplicate genes in genetic robustness against null mutations Hit paper breakdown → | 2003 | 676 |
| 2 | Evolutionary Rate in the Protein Interaction Network Hit paper breakdown → | 2002 | 667 |
| 3 | 2002 | 433 | |
| 4 | 2005 | 356 | |
| 5 | 2000 | 187 | |
| 6 | 2004 | 176 | |
| 7 | 2005 | 70 | |
| 8 | 2000 | 70 | |
| 9 | 2020 | 69 | |
| 10 | 2009 | 64 | |
| 11 | 2000 | 63 | |
| 12 | 2011 | 47 | |
| 13 | 2020 | 45 | |
| 14 | 2013 | 38 | |
| 15 | 2016 | 34 | |
| 16 | 2015 | 33 | |
| 17 | 2020 | 31 | |
| 18 | 2018 | 29 | |
| 19 | 2016 | 27 | |
| 20 | 2010 | 27 |
About Curt Scharfe
Curt Scharfe is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Rheumatology and Physiology, having authored 53 papers that have together received 3.5k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (12 papers), Genomics and Phylogenetic Studies (7 papers), Mitochondrial Function and Pathology (7 papers), Genomics and Rare Diseases (7 papers), Fungal and yeast genetics research (5 papers), Diet and metabolism studies (5 papers), Metabolomics and Mass Spectrometry Studies (5 papers) and Folate and B Vitamins Research (5 papers). The work is most often cited by research in Clinical Biochemistry (309 citations), Molecular Biology (2.7k citations), Genetics (917 citations), Aging (48 citations) and Cell Biology (155 citations). Curt Scharfe has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include Lars M. Steinmetz, Ronald W. Davis, Marcus W. Feldman, Aaron E. Hirsh, Hunter B. Fraser, Xun Gu, Wen‐Hsiung Li, Zhenglong Gu, Peter J. Oefner and Holger Prokisch. Their work appears in journals such as Genetics in Medicine, Nucleic Acids Research, Proceedings of the National Academy of Sciences, International Journal of Neonatal Screening and Forensic Science International Genetics.
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.