Eric W. Klee

10.9k citations

178 papers · 4.0k indexed · h-index 34

Impact in

Cancer Research top 2%
- Cancer Genomics and Diagnostics
Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities

Papers in

Genetics 72
- Genomics and Rare Diseases 40
- Genetics and Neurodevelopmental Disorders 14
- Genomic variations and chromosomal abnormalities 12
Cancer Research 26
- Cancer Genomics and Diagnostics 18

Co-authors: 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
Journals: Molecular Case Studies (8 papers)Clinical Chemistry (8 papers)European Journal of Human Genetics (5 papers)Mayo Clinic Proceedings (5 papers)BMC Bioinformatics (5 papers)
Partner nations: United States Germany Canada

In The Last Decade

Eric W. Klee

168 papers receiving 3.9k citations

Peers

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-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.

Border = papers with Eric W. Klee Line = papers co-authored together Eric W. Klee links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Discovery of a MET-driven monogenic cause of steatotic liver disease Hepatology ·Filippo Pinto e Vairo, Michael T. Zimmermann, Jessica B. Wagenknecht, Salomão Dória Jorge, Shulan Tian, Robert A. Vierkant, Anthony C. Luehrs, Thiago M. de Assuncao, Angela Mathison, Paldeep S. Atwal, Yang Cao, Alina M. Allen, Eric W. Klee, Raúl Urrutia, Konstantinos N. Lazaridis	2025	0
2	UNISOM: Unified Somatic Calling and Machine Learning-based Classification Enhance the Discovery of CHIP Genomics Proteomics & Bioinformatics ·Shulan Tian, Garrett Jenkinson, Alejandro Tiana Ferrer, Huihuang Yan, Joel A. Morales‐Rosado, Kevin L. Wang, Terra L. Lasho, Benjamin B. Yan, Saurabh Baheti, Janet E. Olson, Linda B. Baughn, Wei Ding, Susan L. Slager, Mrinal M. Patnaik, Konstantinos N. Lazaridis, Eric W. Klee	2025	0
3	A supervised learning method for classifying methylation disorders BMC Bioinformatics ·Jesse R. Walsh, Guangchao Sun, Jagadheshwar Balan, Jayson Hardcastle, Jason Vollenweider, Calvin R. Jerde, Kandelaria M. Rumilla, Christy Koellner, Alaa Koleilat, Linda Hasadsri, Benjamin R. Kipp, Garrett Jenkinson, Eric W. Klee	2024	1
4	Expanding Upon Genomics in Rare Diseases: Epigenomic Insights International Journal of Molecular Sciences ·Jia W. Tan, Emily J. Blake, Joseph Farris, Eric W. Klee	2024	1
5	Prevalence, Penetrance, and Phenotypic Manifestation of Cardiomyopathy-Associated Genetic Variants in the General Population: Insights from a Mayo Clinic Biobank Study Mayo Clinic Proceedings ·Marta Figueiral, Alessia Paldino, Matheus Vernet Machado Bressan Wilke, Joseph Farris, Jan Verheijen, John R. Giudicessi, Michael J. Ackerman, Janet E. Olson, Jennifer Arroyo, Rory J. Olson, Eric W. Klee, Naveen L. Pereira	2024	1
6	Impact of Anxiety During Hospitalization on the Clinical Outcome of Patients With Osteoporotic Thoracolumbar Vertebral Fracture Global Spine Journal ·Falko Schwarz, Eric W. Klee, Philipp Schenk, S. Katscher, Klaus John Schnake, Martin Bäumlein, V. Zimmermann, Gregor Schmeiser, Michael Scherer, Michael Müller, Kai Sprengel, Ulrich Spiegl, Georg Osterhoff, Simon Schramm, Holger Siekmann, A. Franck, Max J. Scheyerer, Bernhard Ullrich, (unknown)	2023	2
7	Expanding the phenotype of DNAJC30 ‐ associated Leigh syndrome Clinical Genetics ·Marta Zawadzka, Magdalena Krygier, Małgorzata Pawłowicz, Matheus Vernet Machado Bressan Wilke, Karolina Rutkowska, Naïg Guéguen, Valérie Desquiret‐Dumas, Eric W. Klee, Lisa A. Schimmenti, Jarosław Sławek, Vincent Procaccio, Rafał Płoski, Maria Mazurkiewicz‐Bełdzińska	2022	6
8	Functional validation of a novel AAAS variant in an atypical presentation of Allgrove syndrome Molecular Genetics & Genomic Medicine ·Erica L. Macke, Joel A. Morales‐Rosado, Sarah K. Macklin‐Mantia, Christopher T. Schmitz, Björn Oskarsson, Eric W. Klee, Klaas J. Wierenga	2022	1
9	Luminal androgen receptor breast cancer subtype and investigation of the microenvironment and neoadjuvant chemotherapy response NAR Cancer ·Kevin J. Thompson, Roberto A. Leon‐Ferre, Jason P. Sinnwell, David Zahrieh, Vera J. Suman, Filho Otto Metzger, Sarah Asad, Daniel G. Stover, Lisa A. Carey, William M. Sikov, James N. Ingle, Minetta C. Liu, Jodi M. Carter, Eric W. Klee, Richard M. Weinshilboum, Judy C. Boughey, Liewei Wang, Fergus J. Couch, Matthew P. Goetz, Krishna R. Kalari	2022	26
10	Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing Journal of Molecular Diagnostics ·Aruna Rangan, Molly S. Hein, Garrett Jenkinson, Tejaswi Koganti, Ross A. Aleff, Christopher A. Hilker, Joseph H. Blommel, Tavanna R. Porter, Kenneth C. Swanson, Patrick A. Lundquist, Phuong L. Nguyen, Min Shi, Rong He, David S. Viswanatha, Jin Jen, Eric W. Klee, Benjamin R. Kipp, James D. Hoyer, Eric D. Wieben, Jennifer L. Oliveira	2021	10
11	A novel missense variant and multiexon deletion causing a delayed presentation of xeroderma pigmentosum, group C Molecular Case Studies ·Erica L. Macke, Joel A. Morales‐Rosado, Aditi Gupta, Christopher T. Schmitz, Teresa Kruisselbrink, Brendan C. Lanpher, Eric W. Klee	2020	1
12	Clinical Applications and Utility of a Precision Medicine Approach for Patients With Unexplained Cytopenias Mayo Clinic Proceedings ·Abhishek A. Mangaonkar, Alejandro Ferrer, Filippo Pinto e Vairo, Margot A. Cousin, Ryan J. Kuisle, Naseema Gangat, William J. Hogan, Mark R. Litzow, Tammy M. McAllister, Eric W. Klee, Konstantinos N. Lazaridis, A. Keith Stewart, Mrinal M. Patnaik	2019	12
13	Protein modeling and clinical description of a novel in‐frame GLB1 deletion causing GM1 gangliosidosis type II Molecular Genetics & Genomic Medicine ·John E. Richter, Michael T. Zimmermann, Patrick R. Blackburn, Ahmed N. Mohammad, Eric W. Klee, Laura Pollard, Colleen Macmurdo, Paldeep S. Atwal, Thomas R. Caulfield	2018	4
14	Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation SHILAP Revista de lepidopterología ·Erin Conboy, Filippo Pinto e Vairo, Darrel Waggoner, Carole Ober, Soma Das, Radhika Dhamija, Eric W. Klee, Pavel N. Pichurin	2017	13
15	Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1 Hereditary Cancer in Clinical Practice ·Charu Kaiwar, Sarah Macklin, Jennifer Gass, Jessica L. Jackson, Eric W. Klee, Stephanie L. Hines, John Stauffer, Paldeep S. Atwal	2017	1
16	Novel Pathogenic Variant in TGFBR2 Confirmed by Molecular Modeling Is a Rare Cause of Loeys-Dietz Syndrome SHILAP Revista de lepidopterología ·Michael T. Zimmermann, Raúl Urrutia, Patrick R. Blackburn, Margot A. Cousin, Nicole J. Boczek, Eric W. Klee, Colleen Macmurdo, Paldeep S. Atwal	2017	3
17	A Critical Review of Repurposing Apomorphine for Smoking Cessation Assay and Drug Development Technologies ·Joel A. Morales‐Rosado, Margot A. Cousin, Jon O. Ebbert, Eric W. Klee	2015	6
18	Global Methylation Profiling for Risk Prediction of Prostate Cancer Clinical Cancer Research ·Saswati Mahapatra, Eric W. Klee, Charles Y.F. Young, Zhifu Sun, Rafael E. Jiménez, George G. Klee, Donald J. Tindall, Krishna Vanaja Donkena	2012	100
19	Identification of Prognostic Biomarkers for Prostate Cancer Clinical Cancer Research ·Farhad Kosari, Jan Marie A. Munz, C. Dilara Savci‐Heijink, Craig Spiro, Eric W. Klee, Dagmar Marie Kube, Lori S. Tillmans, Jeff Slezak, R. Jeffrey Karnes, John C. Cheville, George Vasmatzis	2008	52
20	The Zebrafish Secretome Zebrafish ·Eric W. Klee	2008	13

About Eric W. Klee

Eric W. Klee is a scholar working on Genetics, Cancer Research, Molecular Biology, Pathology and Forensic Medicine and Genetics, having authored 178 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (40 papers), Cancer Genomics and Diagnostics (18 papers), Genetic factors in colorectal cancer (16 papers), Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Phylogenetic Studies (13 papers), Epigenetics and DNA Methylation (13 papers), Genomic variations and chromosomal abnormalities (12 papers) and Molecular Biology Techniques and Applications (10 papers). The work is most often cited by research in Cancer Research (652 citations), Genetics (1.0k citations), Molecular Biology (2.1k citations), Clinical Biochemistry (178 citations) and Cell Biology (416 citations). Eric W. Klee has collaborated with scholars based in United States, Germany and Canada. Frequent 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 Olga P. Bondar. Their work appears in journals such as Molecular Case Studies, Clinical Chemistry, European Journal of Human Genetics, Mayo Clinic Proceedings and BMC Bioinformatics.

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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