Feliciano J Ramos

13PUBLICATIONS
76CO-AUTHORS
NeonatologyEpigenetics (incl. genome methylation and epigenomics)Infant and child healthGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseases
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Publications (13)

|Sep 26, 2026
Is the Loss of Previously Acquired Skills a Feature of PACS1-, PACS2- and WDR37-Related Syndromes? A Systematized Narrative Review.

|Mar 30, 2026
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.

Ilaria Parenti, Alina Hesters, Marta Gil-Salvador

|Feb 27, 2026
Assessing Quality of Life in PACS1 Syndrome Using the KidsLife Scale from Mothers' and Fathers' Perspectives.

Julia Del Rincón, Laura Trujillano, Cristina Lucia-Campos

|Aug 28, 2025
AI-Based Facial Phenotyping Supports a Shared Molecular Axis in PACS1-, PACS2-, and WDR37-Related Syndromes.

Julia Del Rincón, Marta Gil-Salvador, Cristina Lucia-Campos

|Sep 28, 2023
Snijders Blok-Campeau Syndrome: Description of 20 Additional Individuals with Variants in CHD3 and Literature Review.

Patricia Pascual, Jair Tenorio-Castano, Cyril Mignot

|Jun 28, 2023
Heart Disease Characterization and Myocardial Strain Analysis in Patients with PACS1 Neurodevelopmental Disorder.

Ana Latorre-Pellicer, Laura Trujillano, Julia Del Rincón

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Frequent Collaborators

9 joint publications

Juan Pié Juste

8 joint publications

Ana Latorre-Pellicer

8 joint publications

Beatriz Puisac

7 joint publications

María Arnedo