Devon E. Bonner

3.1k citations
75 papers · 2.0k · h-index 24

Impact in

  • Genetics top 2%
    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
  • Aging top 10%

Papers in

    • Genomics and Rare Diseases 18
    • Genomic variations and chromosomal abnormalities 8
    • BRCA gene mutations in cancer 8
    • Genetics and Neurodevelopmental Disorders 7
    • RNA Research and Splicing 8
    • RNA modifications and cancer 5

Devon E. Bonner

68 papers receiving 2.0k citations

Peers

Devon E. Bonner
Comparison fields: 5 of 103
  • Genetics 923
  • Aging 31
  • Cancer Research 180
  • Molecular Biology 843
  • Physiology 39
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Citations per field
00.5×1.5×2×2.5×
David R. Murdock · 1×
Citations per year

Countries citing papers authored by Devon E. Bonner

Since Specialization
Citations

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

Fields of papers citing papers by Devon E. Bonner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Devon E. Bonner. 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 Devon E. Bonner. The network helps show where Devon E. Bonner may publish in the future.

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 75 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2019240
2 2017231
3 2015101
4 201884
5 201880
6 201578
7 201976
8 202372
9 201870
10 201953
11 202050
12 202149
13 201948
14 202144
15 201942
16 202042
17 201940
18 202235
19 201333
20 202032

About Devon E. Bonner

Devon E. Bonner is a scholar working on Genetics, Molecular Biology, Genetics, Cell Biology and Cancer Research, having authored 75 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (18 papers), Genomic variations and chromosomal abnormalities (8 papers), RNA Research and Splicing (8 papers), BRCA gene mutations in cancer (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Cellular transport and secretion (6 papers), RNA modifications and cancer (5 papers) and Cancer Genomics and Diagnostics (4 papers). The work is most often cited by research in Genetics (923 citations), Aging (31 citations), Cancer Research (180 citations), Molecular Biology (843 citations) and Physiology (39 citations). Devon E. Bonner has collaborated with scholars based in United States, Canada and France. Frequent co-authors include Tuya Pal, Susan Thomas Vadaparampil, Deborah L. Cragun, Jongphil Kim, Courtney C Lewis, Anne E. Weidner, Steven Alexander Narod, Mohammad Reza Akbari, Álvaro N.A. Monteiro and Catherine Phelan. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Brain, Proceedings of the National Academy of Sciences and Orphanet Journal of Rare Diseases.

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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