Judith Armstrong-Moron

19PUBLICATIONS
74CO-AUTHORS
Multimodal analysis and synthesisPsychological methodology, design and analysisEpigenetics (incl. genome methylation and epigenomics)Medical mycologyGene and molecular therapy
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (19)

|Oct 08, 2026
Systematic Review of Females With Intellectual Disability and MECP2 Duplication.

|May 27, 2026
DDX3X Syndrome: Clinical, Neuroimaging, AI-Assisted Facial Profiling and Genotype-Phenotype Correlations.

|Aug 28, 2025
Unveiling the Spectrum: Clinical and Molecular Insights from a Spanish Pediatric Cohort with Hypermobility Disorders and Ehlers-Danlos Syndrome.

David Foz Felipe, Dídac Casas-Alba, Sara H Sadok

|Jan 11, 2025
MECP2 Duplication Syndrome: AI-Based Diagnosis, Severity Scale Development and Correlation with Clinical and Molecular Variables.

Lourdes Vega-Hanna, Dídac Casas-Alba, Sol Balsells

|May 15, 2024
Multi-omics in MECP2 duplication syndrome patients and carriers.

Ainhoa Pascual-Alonso, Clara Xiol, Dmitrii Smirnov

|Mar 07, 2024
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies.

Daniel Brooks, Elizabeth Burke, Sukyeong Lee

Pageof 4

Frequent Collaborators

6 joint publications

Antonio F Martínez-Monseny

4 joint publications

Mar O'Callaghan

3 joint publications

Dídac Casas-Alba

2 joint publications

Francesc Palau