Jennifer Harrow

55.4k citations
61 papers · 6.1k indexed · 2 hit papers · h-index 35

Impact in

    • Cancer-related molecular mechanisms research
    • RNA modifications and cancer
    • RNA and protein synthesis mechanisms
    • Genomics and Phylogenetic Studies
    • RNA Research and Splicing
    • CRISPR and Genetic Engineering
    • Genomics and Chromatin Dynamics

Papers in

    • Scientific Computing and Data Management 7
    • Genomics and Phylogenetic Studies 29
    • RNA and protein synthesis mechanisms 22
    • RNA modifications and cancer 13
    • RNA Research and Splicing 8
    • Genomics and Chromatin Dynamics 6
    • Machine Learning in Bioinformatics 5

Jennifer Harrow

59 papers receiving 6.0k citations

Hit Papers

Introducing the FAIR Principles for research software 2022 · 175 citations
17520112026201620214008001.2k

Peers

Jennifer Harrow
Comparison fields: 5 of 179
  • Cancer Research 1.2k
  • Molecular Biology 4.5k
  • Genetics 908
  • Information Systems and Management 191
  • Sensory Systems 117
Replace Donna Maglott with:
Donna Maglott United States
Anthony Philippakis United States
Michael L. Metzker United States
Brad Chapman United States
Peter A.C. ’t Hoen Netherlands
Michael Brudno Canada
Laura Elnitski United States
Charles W. Sugnet United States
Cathy Riemer United States
Krishna M. Roskin United States
Jennifer Harrow relative to Donna Maglott United States Donna Maglott's profile →
Citations per field
00.5×2.5×
Donna Maglott · 1×
Citations per year

Countries citing papers authored by Jennifer Harrow

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Harrow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown
#Work
1 20250
2
Introducing the FAIR Principles for research software
Hit paper breakdown →
2022175
3 2019150
4 2015120
5 201426
6 2013341
7 201342
8 2013471
9 201242
10 201122
11 2011101
12 201143
13 20101
14 2010134
15 200969
16 200937
17 2007216
18 2007164
19 2006240
20 2006100

About Jennifer Harrow

Jennifer Harrow is a scholar working on Information Systems and Management, Molecular Biology, Cancer Research, Genetics and Spectroscopy, having authored 61 papers that have together received 6.1k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (29 papers), RNA and protein synthesis mechanisms (22 papers), RNA modifications and cancer (13 papers), RNA Research and Splicing (8 papers), Cancer-related molecular mechanisms research (7 papers), Scientific Computing and Data Management (7 papers), Genomics and Chromatin Dynamics (6 papers) and Machine Learning in Bioinformatics (5 papers). The work is most often cited by research in Cancer Research (1.2k citations), Molecular Biology (4.5k citations), Genetics (908 citations), Information Systems and Management (191 citations) and Sensory Systems (117 citations). Jennifer Harrow has collaborated with scholars based in United Kingdom, United States and Spain. Frequent co-authors include Adam Frankish, Tim Hubbard, Roderic Guigó, Jonathan M. Mudge, Alexandre Reymond, Paul Bertone, Pär G. Engström, James Gilbert, Mark Thomas and Josep F. Abril. Their work appears in journals such as Genome biology, Database, BMC Genomics, Genome Research and Nature Communications.

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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