LabCompass
Established · publishing since 1991

Publications

339

Citations

20,667

Est. group size

~2

Recurring co-author estimate

Active years

36

Publishing since 1991

Research summary
AI-generated

Rabi Tawil's research focuses on facioscapulohumeral muscular dystrophy (FSHD) and related neuromuscular diseases, combining clinical trials, imaging, and molecular biology approaches to understand disease progression and identify biomarkers. Work includes testing new drugs (like losmapimod), developing muscle imaging techniques (electrical impedance myography, MRI, 3D modeling), and studying the genetic and epigenetic mechanisms (such as SMCHD1 and DUX4 gene activation) underlying muscle degeneration.

Facioscapulohumeral muscular dystrophy (FSHD)Neuromuscular disease clinical trialsMuscle imaging and biomarkersEpigenetics and gene regulation in muscle diseaseDuchenne muscular dystrophy and related muscle disorders

Publication output was higher around 2017 but has declined and stabilized at a lower, steady level of roughly 9-10 papers per year over the past several years.

Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026

Publication cadence
Publications per year over the last 10 years — averaging 9.8/year recently
2017: 49 publications49172018: 19 publications182019: 13 publications192020: 18 publications202021: 18 publications212022: 17 publications222023: 9 publications232024: 10 publications242025: 10 publications252026: 3 publications26
Recent publications
Publishes in
  • Figshare×38
  • Neuromuscular Disorders×25
  • Neurology×17
  • Muscle & Nerve×14
  • Human Molecular Genetics×11
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This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.

Last updated Jul 19, 2026.

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