Judith Armstrong-Moron

18PUBLICATIONS

68CO-AUTHORS

Psychological methodology, design and analysisEpigenetics (incl. genome methylation and epigenomics)Medical mycologyGene and molecular therapyMedical infection agents (incl. prions)

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Publications (18)

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|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

<i>MECP2</i> 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

|Jan 21, 2023

Global Impairment of Immediate-Early Genes Expression in Rett Syndrome Models and Patients Linked to Myelination Defects.

Paolo Petazzi, Olga Caridad Jorge-Torres, Antonio Gomez

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Frequent Collaborators

5 joint publications

Antonio F Martínez-Monseny

Dídac Casas-Alba

Mar O'Callaghan

Francesc Palau

Soledad Alcántara

Àngels García-Cazorla

A Bachiller

A Tost

Maria L Couce

A López-Sala

Frequent Collaborators

5 joint publications

Antonio F Martínez-Monseny

3 joint publications

Dídac Casas-Alba

3 joint publications

Mar O'Callaghan

2 joint publications

Francesc Palau