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
-
- Mitochondrial Function and Pathology 7
- Genomics and Phylogenetic Studies 6
- Metabolomics and Mass Spectrometry Studies 5
- Fungal and yeast genetics research 5
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- Metabolism and Genetic Disorders 13
- 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)Zhenglong Gu (1 shared paper)Xun Gu (1 shared paper)Wen‐Hsiung Li (1 shared paper)
- Journals
- Genetics in Medicine (4 papers)Nucleic Acids Research (3 papers)International Journal of Neonatal Screening (3 papers)Proceedings of the National Academy of Sciences (3 papers)Nature Genetics (2 papers)
- Partner nations
- United StatesGermanyNetherlands
In The Last Decade
Curt Scharfe
51 papers receiving 3.5k citations
Curt Scharfe's Hit Papers
Peers
Comparison fields: 5 of 143
- Clinical Biochemistry 301
- Molecular Biology 2.6k
- Genetics 891
- Aging 48
- Cell Biology 150
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 | Evolutionary Rate in the Protein Interaction Network Hit paper breakdown → | 2002 | 711 |
| 2 | Role of duplicate genes in genetic robustness against null mutations Hit paper breakdown → | 2003 | 699 |
| 3 | 2002 | 443 | |
| 4 | 2005 | 370 | |
| 5 | 2000 | 205 | |
| 6 | 2004 | 180 | |
| 7 | 2000 | 73 | |
| 8 | 2020 | 71 | |
| 9 | 2005 | 71 | |
| 10 | 2009 | 70 | |
| 11 | 2000 | 64 | |
| 12 | 2011 | 48 | |
| 13 | 2020 | 48 | |
| 14 | 2013 | 38 | |
| 15 | 2020 | 36 | |
| 16 | 2016 | 35 | |
| 17 | 2015 | 35 | |
| 18 | 2018 | 31 | |
| 19 | 2010 | 30 | |
| 20 | 2016 | 28 |
About Curt Scharfe
Curt Scharfe is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Rheumatology and Physiology, having authored 53 papers that have together received 3.6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (7 papers), Genomics and Rare Diseases (6 papers), Genomics and Phylogenetic Studies (6 papers), Metabolomics and Mass Spectrometry Studies (5 papers), Fungal and yeast genetics research (5 papers), Folate and B Vitamins Research (4 papers) and Forensic and Genetic Research (4 papers). The work is most often cited by research in Clinical Biochemistry (301 citations), Molecular Biology (2.6k citations), Genetics (891 citations), Aging (48 citations) and Cell Biology (150 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, Zhenglong Gu, Xun Gu, Wen‐Hsiung Li, Peter J. Oefner and Holger Prokisch. Their work appears in journals such as Genetics in Medicine, Nucleic Acids Research, International Journal of Neonatal Screening, Proceedings of the National Academy of Sciences and Nature 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.