Stephen Meader

2.9k citations
11 papers · 497 · h-index 10

Impact in

  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genetic diversity and population structure
    • Genomics and Phylogenetic Studies
    • RNA and protein synthesis mechanisms
    • Genomics and Chromatin Dynamics

Papers in

    • Genomic variations and chromosomal abnormalities 4
    • Genomics and Rare Diseases 3
    • Genetic diversity and population structure 3
    • Genetics and Neurodevelopmental Disorders 2
    • Genomics and Phylogenetic Studies 6
    • RNA and protein synthesis mechanisms 2

Stephen Meader

11 papers receiving 487 citations

Peers

Stephen Meader
Comparison fields: 5 of 68
  • Genetics 286
  • Molecular Biology 352
  • Cancer Research 61
  • Plant Science 90
  • Cognitive Neuroscience 42
Replace Debashish U. Menon with:
Debashish U. Menon United States
Kerrie Nichol Edamura Canada
Patrick Landback United States
Sarah Smith United Kingdom
Nastassia Gobet Switzerland
Mark Fell United Kingdom
Atteeq U. Rehman United States
Will Nash United Kingdom
David A. Largaespada United States
Roya Hosseini United States
Stephen Meader relative to Debashish U. Menon United States Debashish U. Menon's profile →
Citations per field
00.5×2.6×
Debashish U. Menon · 1×
Citations per year

Countries citing papers authored by Stephen Meader

Since Specialization
Citations

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

Fields of papers citing papers by Stephen Meader

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

11 of 11 papers shown
#Work
1 2014137
2 201379
3 201073
4 201342
5 201539
6 201039
7 201335
8 201418
9 201116
10 201512
11 20087

About Stephen Meader

Stephen Meader is a scholar working on Genetics, Molecular Biology, Plant Science, Ecology, Evolution, Behavior and Systematics and Cognitive Neuroscience, having authored 11 papers that have together received 497 indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Chromosomal and Genetic Variations (3 papers), Genetic diversity and population structure (3 papers), RNA and protein synthesis mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Animal Behavior and Reproduction (2 papers). The work is most often cited by research in Genetics (286 citations), Molecular Biology (352 citations), Cancer Research (61 citations), Plant Science (90 citations) and Cognitive Neuroscience (42 citations). Stephen Meader has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Chris P. Ponting, Gerton Lunter, Chris M. Rands, Caleb Webber, Frantisek Honti, Julia Steinberg, Devin P. Locke, LaDeana W. Hillier, Rolph Pfundt and Jayne Y. Hehir‐Kwa. Their work appears in journals such as PLoS Genetics, Genome Research, Human Mutation, BMC Genomics and PLoS Computational 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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