Tracey Willis

2.1k citations
51 papers · 638 · h-index 14

Impact in

  • Genetics top 10%
    • Neurogenetic and Muscular Disorders Research
    • Genetics and Neurodevelopmental Disorders
    • Genetic Neurodegenerative Diseases
    • Hereditary Neurological Disorders

Papers in

    • Muscle Physiology and Disorders 20
    • RNA modifications and cancer 4
    • Neurogenetic and Muscular Disorders Research 19
    • Genetics and Neurodevelopmental Disorders 3

Tracey Willis

44 papers receiving 629 citations

Peers

Tracey Willis
Comparison fields: 5 of 57
  • Genetics 100
  • Cellular and Molecular Neuroscience 133
  • Molecular Biology 340
  • Cardiology and Cardiovascular Medicine 95
  • Physiology 90
Replace Satoshi Kuru with:
Satoshi Kuru Japan
Robert‐Yves Carlier France
Elisabetta Iannaccone Italy
K. Eger Germany
C. Sewry United Kingdom
Matthew Wicklund United States
Terumi Murakami Japan
Ziad Rifai United States
Paola D′Ambrosio Italy
Matt Parton United Kingdom
Tracey Willis relative to Satoshi Kuru Japan Satoshi Kuru's profile →
Citations per field
00.5×1.5×2×2.4×
Satoshi Kuru · 1×
Citations per year

Countries citing papers authored by Tracey Willis

Since Specialization
Citations

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

Fields of papers citing papers by Tracey Willis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2013149
2 201477
3 201652
4 201738
5 201929
6 200728
7 200927
8 201625
9 202123
10 202021
11 201318
12 201818
13 201918
14 201614
15 201911
16 201810
17 20188
18 20128
19 20207
20 20246

About Tracey Willis

Tracey Willis is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Surgery and Neurology, having authored 51 papers that have together received 638 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (20 papers), Neurogenetic and Muscular Disorders Research (19 papers), Genetic Neurodegenerative Diseases (5 papers), Amyotrophic Lateral Sclerosis Research (4 papers), Hereditary Neurological Disorders (4 papers), Cardiomyopathy and Myosin Studies (4 papers), RNA modifications and cancer (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (100 citations), Cellular and Molecular Neuroscience (133 citations), Molecular Biology (340 citations), Cardiology and Cardiovascular Medicine (95 citations) and Physiology (90 citations). Tracey Willis has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include Volker Straub, Hanns Lochmüller, Kieren G. Hollingsworth, Michelle Eagle, Kate Bushby, John Vissing, John S. Thornton, Jean‐Yves Hogrel, Pierre G. Carlier and Tanya Stojkovic. Their work appears in journals such as Neuromuscular Disorders, PLoS ONE, Journal of Neuromuscular Diseases, BMJ Supportive & Palliative Care and Journal of Neurology.

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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