Edward Fox

6.3k citations
94 papers · 4.1k indexed · 1 hit paper · h-index 32

Edward Fox

92 papers receiving 4.0k citations

Hit Papers

Detection of ultra-rare mutations by next-generation sequ...7272012202620162021200400600

Peers

Edward Fox
Comparison fields: 5 of 135
  • Cancer Research 1.3k
  • Hematology 646
  • Pathology and Forensic Medicine 748
  • Molecular Biology 2.1k
  • Genetics 321
Replace Domenico Delia with:
Domenico Delia Italy
Mark A. Dawson Australia
Karen Blyth United Kingdom
Cristina Montagna United States
Janet Plescia United States
Young E. Whang United States
Patricia J.T.A. Groenen Netherlands
Beric R. Henderson Australia
Juan M. Zapata United States
Keith R. Loeb United States
Edward Fox relative to Domenico Delia Italy Domenico Delia's profile →
Citations per field
00.5×
Domenico Delia · 1×
Citations per year

Countries citing papers authored by Edward Fox

Since Specialization
Citations

This map shows the geographic impact of Edward Fox'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 Edward Fox with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edward Fox more than expected).

Fields of papers citing papers by Edward Fox

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward Fox. 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 Edward Fox. The network helps show where Edward Fox may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Edward Fox, 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 Edward Fox Line = papers co-authored together Edward Fox links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 202313
2 202215
3 20201
4 2015110
5 201517
6 201528
7 20152
8 2014314
9 201410
10 2014135
11 20134
12
Detection of ultra-rare mutations by next-generation sequencingbreakdown →
2012727
13 201153
14 201138
15 201012
16 201053
17 200841
18 200652
19 200549
20
Identification and characterization of a novel activating mutation of the FLT3 tyrosine kinase in AML
20043

About Edward Fox

Edward Fox is a scholar working on Genetics, Hematology, Radiology, Nuclear Medicine and Imaging, Cancer Research and Immunology, having authored 94 papers that have together received 4.1k indexed citations. Recurring topics across this work include Monoclonal and Polyclonal Antibodies Research (20 papers), Chronic Lymphocytic Leukemia Research (16 papers), Cancer Genomics and Diagnostics (13 papers), Acute Myeloid Leukemia Research (9 papers), Acute Lymphoblastic Leukemia research (9 papers), Immunotherapy and Immune Responses (8 papers), DNA Repair Mechanisms (7 papers) and Glycosylation and Glycoproteins Research (7 papers). The work is most often cited by research in Cancer Research (1.3k citations), Hematology (646 citations), Pathology and Forensic Medicine (748 citations), Molecular Biology (2.1k citations) and Genetics (321 citations). Edward Fox has collaborated with scholars based in United States, Ireland and Germany. Frequent co-authors include Lawrence A. Loeb, Jesse J. Salk, Scott R. Kennedy, Michael W. Schmitt, Joseph B. Hiatt, Kate S. Reid-Bayliss, Marc J. Prindle, Eun Hyun Ahn, Jacintha O’Sullivan and Jiang-Cheng Shen. Their work appears in journals such as Neurology, Blood, Proceedings of the National Academy of Sciences, The Journal of Immunology and Cancer Research.

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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