Eric W. Klee

10.9k total citations
178 papers, 4.0k citations indexed

About

Eric W. Klee is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Eric W. Klee has authored 178 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Molecular Biology, 72 papers in Genetics and 26 papers in Cancer Research. Recurrent topics in Eric W. Klee's work include Genomics and Rare Diseases (40 papers), Cancer Genomics and Diagnostics (18 papers) and Genetic factors in colorectal cancer (16 papers). Eric W. Klee is often cited by papers focused on Genomics and Rare Diseases (40 papers), Cancer Genomics and Diagnostics (18 papers) and Genetic factors in colorectal cancer (16 papers). Eric W. Klee collaborates with scholars based in United States, Germany and Canada. Eric W. Klee's co-authors include George G. Klee, Margot A. Cousin, Gavin R. Oliver, Lynda B.M. Ellis, Stephen C. Ekker, Steven N. Hart, Filippo Pinto e Vairo, Matthew J. Ferber, Patrick R. Blackburn and Paldeep S. Atwal and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Journal of Clinical Oncology.

In The Last Decade

Eric W. Klee

168 papers receiving 3.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Eric W. Klee United States 34 2.1k 1.0k 652 422 416 178 4.0k
Weizhong Chang United States 14 2.3k 1.1× 1.1k 1.1× 752 1.2× 363 0.9× 198 0.5× 30 4.4k
Zhiao Shi United States 18 2.9k 1.4× 636 0.6× 931 1.4× 516 1.2× 208 0.5× 35 4.9k
Inbar Plaschkes Israel 17 3.1k 1.5× 705 0.7× 670 1.0× 403 1.0× 180 0.4× 30 5.2k
Cecilia Lindskog Sweden 29 2.3k 1.1× 568 0.6× 615 0.9× 497 1.2× 186 0.4× 95 4.3k
Mark J. Cowley Australia 36 2.1k 1.0× 698 0.7× 709 1.1× 268 0.6× 174 0.4× 108 3.7k
Michal Twik Israel 8 2.8k 1.4× 706 0.7× 682 1.0× 390 0.9× 154 0.4× 8 4.8k
Neil R. Clark United States 16 3.6k 1.7× 555 0.6× 846 1.3× 443 1.0× 363 0.9× 27 5.7k
Simon Fishilevich Israel 10 2.5k 1.2× 625 0.6× 622 1.0× 382 0.9× 152 0.4× 12 4.5k
Edward Y. Chen United States 12 3.4k 1.7× 567 0.6× 830 1.3× 442 1.0× 290 0.7× 15 5.5k
Mikhail G. Dozmorov United States 36 2.2k 1.0× 494 0.5× 708 1.1× 363 0.9× 178 0.4× 153 4.0k

Countries citing papers authored by Eric W. Klee

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Eric W. Klee

This figure shows the co-authorship network connecting the top 25 collaborators of Eric W. Klee. A scholar is included among the top collaborators of Eric W. Klee 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 Eric W. Klee. Eric W. Klee 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.
Tian, Shulan, Garrett Jenkinson, Huihuang Yan, et al.. (2025). UNISOM: Unified Somatic Calling and Machine Learning-based Classification Enhance the Discovery of CHIP. Genomics Proteomics & Bioinformatics. 23(2).
2.
Vairo, Filippo Pinto e, Michael T. Zimmermann, Salomão Dória Jorge, et al.. (2025). Discovery of a MET-driven monogenic cause of steatotic liver disease. Hepatology. 82(6). 1512–1522.
3.
Blake, Emily J., et al.. (2024). Expanding Upon Genomics in Rare Diseases: Epigenomic Insights. International Journal of Molecular Sciences. 26(1). 135–135. 1 indexed citations
4.
Walsh, Jesse R., Guangchao Sun, Jayson Hardcastle, et al.. (2024). A supervised learning method for classifying methylation disorders. BMC Bioinformatics. 25(1). 1 indexed citations
5.
Paldino, Alessia, Jan Verheijen, John R. Giudicessi, et al.. (2024). Prevalence, Penetrance, and Phenotypic Manifestation of Cardiomyopathy-Associated Genetic Variants in the General Population: Insights from a Mayo Clinic Biobank Study. Mayo Clinic Proceedings. 99(11). 1732–1743. 1 indexed citations
6.
Schwarz, Falko, Eric W. Klee, Philipp Schenk, et al.. (2023). Impact of Anxiety During Hospitalization on the Clinical Outcome of Patients With Osteoporotic Thoracolumbar Vertebral Fracture. Global Spine Journal. 15(2). 417–424. 2 indexed citations
7.
Guéguen, Naïg, Valérie Desquiret‐Dumas, Eric W. Klee, et al.. (2022). Expanding the phenotype of DNAJC30 associated Leigh syndrome. Clinical Genetics. 102(5). 438–443. 6 indexed citations
8.
Macke, Erica L., Joel A. Morales‐Rosado, Sarah K. Macklin‐Mantia, et al.. (2022). Functional validation of a novel AAAS variant in an atypical presentation of Allgrove syndrome. Molecular Genetics & Genomic Medicine. 10(7). e1966–e1966. 1 indexed citations
9.
Thompson, Kevin J., Roberto A. Leon‐Ferre, Jason P. Sinnwell, et al.. (2022). Luminal androgen receptor breast cancer subtype and investigation of the microenvironment and neoadjuvant chemotherapy response. NAR Cancer. 4(2). zcac018–zcac018. 26 indexed citations
10.
Jenkinson, Garrett, Ross A. Aleff, Christopher A. Hilker, et al.. (2021). Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing. Journal of Molecular Diagnostics. 23(12). 1732–1740. 10 indexed citations
11.
Macke, Erica L., Joel A. Morales‐Rosado, Aditi Gupta, et al.. (2020). A novel missense variant and multiexon deletion causing a delayed presentation of xeroderma pigmentosum, group C. Molecular Case Studies. 6(4). a005165–a005165. 1 indexed citations
12.
Marshall, Christian R., Shimul Chowdhury, Ryan J. Taft, et al.. (2020). Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease. npj Genomic Medicine. 5(1). 47–47. 85 indexed citations
13.
Mangaonkar, Abhishek A., Alejandro Ferrer, Filippo Pinto e Vairo, et al.. (2019). Clinical Applications and Utility of a Precision Medicine Approach for Patients With Unexplained Cytopenias. Mayo Clinic Proceedings. 94(9). 1753–1768. 12 indexed citations
14.
Kaiwar, Charu, Sarah Macklin, Jennifer Gass, et al.. (2017). Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1. Hereditary Cancer in Clinical Practice. 15(1). 10–10. 1 indexed citations
15.
Conboy, Erin, Filippo Pinto e Vairo, Darrel Waggoner, et al.. (2017). Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation. SHILAP Revista de lepidopterología. 2017. 1–4. 13 indexed citations
16.
Blackburn, Patrick R., Duygu Selcen, Jennifer Gass, et al.. (2017). Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1. Molecular Genetics & Genomic Medicine. 5(3). 295–302. 4 indexed citations
17.
Morales‐Rosado, Joel A., Margot A. Cousin, Jon O. Ebbert, & Eric W. Klee. (2015). A Critical Review of Repurposing Apomorphine for Smoking Cessation. Assay and Drug Development Technologies. 13(10). 612–622. 6 indexed citations
18.
Mahapatra, Saswati, Eric W. Klee, Charles Y.F. Young, et al.. (2012). Global Methylation Profiling for Risk Prediction of Prostate Cancer. Clinical Cancer Research. 18(10). 2882–2895. 100 indexed citations
19.
Kosari, Farhad, C. Dilara Savci‐Heijink, Craig Spiro, et al.. (2008). Identification of Prognostic Biomarkers for Prostate Cancer. Clinical Cancer Research. 14(6). 1734–1743. 52 indexed citations
20.
Klee, Eric W.. (2008). The Zebrafish Secretome. Zebrafish. 5(2). 131–138. 13 indexed citations

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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