Publications
15
Citations
78
Est. group size
—
Recurring co-author estimate
Active years
8
Publishing since 2019
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.
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
- Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy
Genetics in Medicine · 2025
- A prospective observational study assessing the functional disease progression of LGMDR4, betasarcoglycan-related limb girdle muscular dystrophy
Journal of Neuromuscular Diseases · 2025
- Three Siblings With an Attenuated Presentation of Perlman Syndrome: A Case Report and Literature Review
Molecular Genetics & Genomic Medicine · 2025
- Gross motor delays in infants and young boys with Duchenne muscular dystrophy
Journal of Neuromuscular Diseases · 2024
- Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features
medRxiv · 2024
- Continued safety and long-term effectiveness of onasemnogene abeparvovec in Ohio
Neuromuscular Disorders · 2023
- Neuromuscular and cardiovascular phenotypes in paediatric titinopathies: a multisite retrospective study
Journal of Medical Genetics · 2023
- Exome sequencing in the pediatric neuromuscular clinic leads to more frequent diagnosis of both neuromuscular and neurodevelopmental conditions
Muscle & Nerve · 2023
- Pathogenic missense variants altering codon 336 of <i>GARS1</i> lead to divergent dominant phenotypes
Human Mutation · 2022
- A missense, loss-of-function<i>YARS1</i>variant in a patient with proximal-predominant motor neuropathy
Molecular Case Studies · 2022
- Journal of Neuromuscular Diseases×3
- Neuromuscular Disorders×2
- medRxiv×2
- Frontiers in Neurology×1
- Journal of Medical Genetics×1
- W. David Arnold
Medicine · The Ohio State University
- Megan A. Waldrop
Medicine · The Ohio State University
- Kelly Rich
Medicine · The Ohio State University
- Amy Bartlett
Medicine · The Ohio State University
- Stephen J. Kolb
Medicine · The Ohio State University
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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