Emily Perry

18.3k citations
7 papers · 703 · 1 hit paper · h-index 5

Impact in

  • Genetics top 10%
    • Genetic Associations and Epidemiology
    • Genetic Mapping and Diversity in Plants and Animals
    • Genomics and Rare Diseases
    • Plant Molecular Biology Research
    • Plant nutrient uptake and metabolism
    • Chromosomal and Genetic Variations

Papers in

    • Genomics and Phylogenetic Studies 5
    • Epigenetics and DNA Methylation 1
    • Genomics and Chromatin Dynamics 1
    • Genomics and Rare Diseases 4
    • Genetic Associations and Epidemiology 3
    • Genomic variations and chromosomal abnormalities 1

Emily Perry

7 papers receiving 700 citations

Emily Perry's Hit Papers

The International Genome Sample Resource (IGSR) collection of open human genomic variation resources 2019 · 215 citations
2150+2+4Years since publication50100150200

Peers

Emily Perry
Comparison fields: 5 of 104
  • Genetics 231
  • Plant Science 229
  • Molecular Biology 387
  • Cancer Research 72
  • Endocrinology 11
Replace Christophe Van Neste with:
Christophe Van Neste Belgium
Ke Gong China
Yiming Yu China
Stephanie L. Chissoe United States
Eugene Bolotin United States
Shu Tadaka Japan
Hideaki Konno Japan
Prashant K. Srivastava United Kingdom
Rebecca B. Katzman United States
Michael Snaith Sweden
Emily Perry relative to Christophe Van Neste Belgium Christophe Van Neste's profile →
Citations per field
00.5×3.0×
Christophe Van Neste · 1×
Citations per year

Countries citing papers authored by Emily Perry

Since Specialization
Citations

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

Fields of papers citing papers by Emily Perry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

7 of 7 papers shown
#Work
1 2016278
2
The International Genome Sample Resource (IGSR) collection of open human genomic variation resources
Hit paper breakdown →
2019215
3 2016158
4 202135
5 201813
6 20213
7 20181

About Emily Perry

Emily Perry is a scholar working on Molecular Biology, Genetics, Plant Science, Cancer Research and Infectious Diseases, having authored 7 papers that have together received 703 indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (5 papers), Genomics and Rare Diseases (4 papers), Genetic Associations and Epidemiology (3 papers), Epigenetics and DNA Methylation (1 paper), Genomics and Chromatin Dynamics (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Cancer Genomics and Diagnostics (1 paper) and Plant Virus Research Studies (1 paper). The work is most often cited by research in Genetics (231 citations), Plant Science (229 citations), Molecular Biology (387 citations), Cancer Research (72 citations) and Endocrinology (11 citations). Emily Perry has collaborated with scholars based in United Kingdom, Austria and Canada. Frequent co-authors include Paul Flicek, Ernesto Lowy, Susan Fairley, D. Staines, Dan Bolser, Paul Kersey, Laura Clarke, Anne-Marie Tassé, Xiangqun Zheng-Bradley and Ian Streeter. Their work appears in journals such as Nucleic Acids Research, Genome biology, Human Mutation, Molecular Genetics & Genomic Medicine and Methods in molecular biology.

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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