Alayne P Meyer

6PUBLICATIONS
13CO-AUTHORS
Gene mappingNeurology and neuromuscular diseasesAutonomic nervous systemGene expression (incl. microarray and other genome-wide approaches)
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Publications (6)

|Jul 24, 2025
Three Siblings With an Attenuated Presentation of Perlman Syndrome: A Case Report and Literature Review.

Alayne P Meyer, Daniel C Koboldt, Swetha Ramadesikan

|May 13, 2025
A prospective observational study assessing the functional disease progression of LGMDR4, betasarcoglycan-related limb girdle muscular dystrophy.

Megan A Iammarino, Natalie F Reash, Kiana Shannon

|Dec 05, 2023
Neuromuscular and cardiovascular phenotypes in paediatric titinopathies: a multisite retrospective study.

Alayne P Meyer, Cara L Barnett, Katherine Myers

|Oct 04, 2023
Exome sequencing in the pediatric neuromuscular clinic leads to more frequent diagnosis of both neuromuscular and neurodevelopmental conditions.

Alayne P Meyer, Jianing Ma, Guy Brock

|Oct 28, 2022
A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy.

Megan E Forrest, Alayne P Meyer, Stephanie M Laureano Figueroa

|Mar 25, 2022
Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes.

Alayne P Meyer, Megan E Forrest, Stefan Nicolau

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Frequent Collaborators

2 joint publications

Anthony Antonellis

2 joint publications

Marco L Leung

1 joint publications

Megan A Iammarino

1 joint publications

Natalie F Reash