Megan A Waldrop

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 9

Top Topics

Top Venues

American journal of medical genetics. Part A

Neurology. Clinical practice

Pediatric pulmonology

This page only lists publications with an associated author ORCID identifier.

Publications

Mary K Schroth, Jennifer Deans, Kapil Arya, Diana Castro, Darryl C De Vivo, Melissa A Gibbons, Cristian Ionita, Nancy L Kuntz, Arpita Lakhotia, Erin Neil Knierbein, Mariacristina Scoto, Thomas Sejersen, Laurent Servais, Cuixia Tian, Megan A Waldrop, Juan Francisco Vázquez Costa
Spinal Muscular Atrophy Update in Best Practices: Recommendations for Diagnosis Considerations. Neurology. Clinical practice 14 (4) (2024)
Mary K Schroth, Jennifer Deans, Kapil Arya, Diana Castro, Darryl C De Vivo, Melissa A Gibbons, Cristian Ionita, Nancy L Kuntz, Arpita Lakhotia, Erin Neil Knierbein, Mariacristina Scoto, Thomas Sejersen, Laurent Servais, Cuixia Tian, Megan A Waldrop, Juan Francisco Vázquez Costa
Spinal Muscular Atrophy Update in Best Practices: Recommendations for Diagnosis Considerations. Neurology. Clinical practice 14 (4) (2024)
Megan A Waldrop, Steven A Moore, Katherine D Mathews, Benjamin W Darbro, Livja Medne, Richard Finkel, Anne M Connolly, Thomas O Crawford, Daniel Drachman, Nicolas Wein, Ali A Habib, Monika A Krzesniak-Swinarska, Craig M Zaidman, James J Collins, Manu Jokela, Bjarne Udd, John W Day, Gloria Ortiz-Guerrero, Jeff Statland, Russell J Butterfield, Diane M Dunn, Robert B Weiss, Kevin M Flanigan
Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophy. Human mutation 43 (4) (2022)
Alberto Andrea Zambon, Megan A Waldrop, Roxane Alles, Robert B Weiss, Sara Conroy, Melissa Moore-Clingenpeel, Previtali Stefano Carlo, Kevin M Flanigan, null null
Phenotypic Spectrum of Dystrophinopathy Due to Duchenne Muscular Dystrophy Exon 2 Duplications. Neurology 98 (7) (2021)
Daniel C Koboldt, Megan A Waldrop, Richard K Wilson, Kevin M Flanigan
The Genotypic and Phenotypic Spectrum of BICD2 Variants in Spinal Muscular Atrophy. Annals of neurology 87 (4) (2020)
Nicolas J Abreu, Megan A Waldrop
Overview of gene therapy in spinal muscular atrophy and Duchenne muscular dystrophy. Pediatric pulmonology 56 (4) (2020)
Nicolas J Abreu, Daniel C Koboldt, Julie M Gastier-Foster, Ashita Dave-Wala, Kevin M Flanigan, Megan A Waldrop
Homozygous variants in AMPD2 and COL11A1 lead to a complex phenotype of pontocerebellar hypoplasia type 9 and Stickler syndrome type 2. American journal of medical genetics. Part A 182 (3) (2019)
Megan A Waldrop, Felecia Gumienny, Daniel Boue, Emily de Los Reyes, Richard Shell, Robert B Weiss, Kevin M Flanigan
Low-level expression of EPG5 leads to an attenuated Vici syndrome phenotype. American journal of medical genetics. Part A 176 (5) (2019)
Shen Gu, Chun-An Chen, Jill A Rosenfeld, Heidi Cope, Nathalie Launay, Kevin M Flanigan, Megan A Waldrop, Rachel Schrader, Jane Juusola, Ozlem Goker-Alpan, Aubrey Milunsky, Agatha Schlüter, Mónica Troncoso, Aurora Pujol, Queenie K-G Tan, Christian Patrick Schaaf, Linyan Meng
Truncating variants in UBAP1 associated with childhood-onset nonsyndromic hereditary spastic paraplegia. Human mutation 41 (3) (2019)