Author

Julia M. Gable

RTI InternationalORCID 0000-0002-8564-9460Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Allan L. ReissiD· 1 shared Amy A. LightbodyiD· 1 shared Amy EsleriD· 1 shared Amy L. Talboy· 1 shared Andrea Lynne GropmaniD· 1 shared Angel Wang· 1 shared Anjali SadhwaniiD· 1 shared Anne WheeleriD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Allan L. ReissORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Assessment of adaptive functioning in Angelman syndrome using the Vineland Adaptive Behavior Scales, Third Edition

Sarah Nelson Potter, Julia Zhang, Batsheva Friedman, Julia M. Gable, Nadia Ali, Rene L. Barbieri‐Welge, Ayala Ben-Tall, Kelly E. Caravella, Margaret DeRamus, Dea Garic, M. MacKay, Kara Murias, Sarika U. Peters, Kimberly Smyth, Jane Summers, , Anjali Sadhwani

This study tracks adaptive functioning in Angelman syndrome using Vineland-3, finding slower growth in deletion subtypes and parallel developmental trajectories across subtypes.

medRxiv · Jun 22, 2026 · PreprintGenetic & Genomic Medicine

Latent class analysis identifies distinctive behavioral subtypes in children with fragile X syndrome

Walter E. Kaufmann, Melissa Raspa, Carla Bann, Julia M. Gable, Holly K. Harris, Dejan B. Budimirovic, Reymundo Lozano, Elizabeth Berry‐Kravis, Milen T. Velinov, Amy L. Talboy, Stephanie L. Sherman, Marcy Schuster, Nicole R. Tartaglia, Robyn A. Filipink, Deborah Barbouth, , Stephanie M. Morris

The paper uses latent class analysis to identify distinct behavioral subtypes in children with fragile X syndrome, revealing clinically meaningful groups with unique cognitive and behavioral profiles.

Journal of Autism and Developmental Disorders · Nov 28, 2022Peer-reviewedGenetic & Genomic Medicine