LabCompass

Alayne P. Meyer

Medicine · The Ohio State University

Early career · publishing since 2019Rising activity

Publications

15

Citations

78

Est. group size

Recurring co-author estimate

Active years

8

Publishing since 2019

Research summary
AI-generated

Alayne P. Meyer's research focuses on genetic causes of neuromuscular and muscle-related disorders in children, including muscular dystrophies, myopathies, and inherited nerve conditions. The work combines clinical observation, genetic testing (such as exome sequencing), and case studies to identify disease-causing gene variants and describe how these conditions progress over time. This research aims to improve diagnosis and understanding of rare pediatric neuromuscular diseases.

Pediatric neuromuscular disordersGenetic diagnosis of muscle diseaseMuscular dystrophy phenotypes and progressionRare disease case studies and gene variant discoveryNeurogenetic and neurodevelopmental conditions

Publication output has grown over the last decade, rising from little to no output before 2019 to a more active and fairly steady pace of about 2-4 papers per year since 2022.

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

Publication cadence
Publications per year over the last 10 years — averaging 2.6/year recently
17182019: 1 publication192020: 1 publication20212022: 2 publications222023: 4 publications4232024: 2 publications242025: 4 publications4252026: 1 publication26
Publishes in
  • Journal of Neuromuscular Diseases×3
  • Neuromuscular Disorders×2
  • medRxiv×2
  • Frontiers in Neurology×1
  • Journal of Medical Genetics×1
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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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