Eric W. Klee
Impact in
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Epigenetics and DNA Methylation 11
- Genomics and Phylogenetic Studies 8
- Molecular Biology Techniques and Applications 8
- Genetics 65
- Genomics and Rare Diseases 38
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 9
- Co-authors
- George G. Klee (11 shared papers)Margot A. Cousin (34 shared papers)Gavin R. Oliver (19 shared papers)Matthew J. Ferber (8 shared papers)Stephen C. Ekker (9 shared papers)Steven N. Hart (4 shared papers)Lynda B.M. Ellis (4 shared papers)Filippo Pinto e Vairo (18 shared papers)
- Journals
- Molecular Case Studies (8 papers)Clinical Chemistry (8 papers)European Journal of Human Genetics (5 papers)Mayo Clinic Proceedings (5 papers)Journal of Molecular Diagnostics (5 papers)
- Partner nations
- United StatesGermanyNetherlands
In The Last Decade
Eric W. Klee
170 papers receiving 4.0k citations
Peers
Comparison fields: 5 of 149
- Cancer Research 523
- Genetics 914
- Clinical Biochemistry 165
- Molecular Biology 1.7k
- Cell Biology 383
Countries citing papers authored by Eric W. Klee
This map shows the geographic impact of Eric W. Klee'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 Eric W. Klee with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric W. Klee more than expected).
Fields of papers citing papers by Eric W. Klee
This network shows the impact of papers produced by Eric W. Klee. 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 Eric W. Klee. The network helps show where Eric W. Klee may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric W. Klee, 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 180 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 272 | |
| 2 | 2017 | 164 | |
| 3 | 2016 | 160 | |
| 4 | 2019 | 143 | |
| 5 | 2012 | 136 | |
| 6 | 2009 | 135 | |
| 7 | 2018 | 118 | |
| 8 | 2007 | 107 | |
| 9 | 2011 | 103 | |
| 10 | 2012 | 100 | |
| 11 | 2020 | 89 | |
| 12 | 2014 | 88 | |
| 13 | 2015 | 85 | |
| 14 | 2008 | 70 | |
| 15 | 2006 | 68 | |
| 16 | 2008 | 65 | |
| 17 | 2005 | 64 | |
| 18 | 2011 | 60 | |
| 19 | 2011 | 54 | |
| 20 | 2014 | 53 |
About Eric W. Klee
Eric W. Klee is a scholar working on Molecular Biology, Genetics, Cancer Research, Pulmonary and Respiratory Medicine and Pathology and Forensic Medicine, having authored 180 papers that have together received 4.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (38 papers), Cancer Genomics and Diagnostics (14 papers), Genetic factors in colorectal cancer (13 papers), Epigenetics and DNA Methylation (11 papers), Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (9 papers), Genomics and Phylogenetic Studies (8 papers) and Molecular Biology Techniques and Applications (8 papers). The work is most often cited by research in Cancer Research (523 citations), Genetics (914 citations), Clinical Biochemistry (165 citations), Molecular Biology (1.7k citations) and Cell Biology (383 citations). Eric W. Klee has collaborated with scholars based in United States, Germany and Netherlands. Frequent co-authors include George G. Klee, Margot A. Cousin, Gavin R. Oliver, Matthew J. Ferber, Stephen C. Ekker, Steven N. Hart, Lynda B.M. Ellis, Filippo Pinto e Vairo, Patrick R. Blackburn and Paldeep S. Atwal. Their work appears in journals such as Molecular Case Studies, Clinical Chemistry, European Journal of Human Genetics, Mayo Clinic Proceedings and Journal of Molecular Diagnostics.
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.