Nicola Ragge

7PUBLICATIONS
19CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesCancer genetics
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (7)

|Apr 07, 2026
Variants in the CxxC domain of the epigenetic regulator KDM2B support its role in developmental eye anomalies.

Fabiola Ceroni, Linda M Reis, Fiona Watkins

|Apr 29, 2025
GJA8-associated developmental eye disorders: a new multicentre study highlights mutational hotspots and genotype-phenotype correlations.

Solomon S Merepa, Linda M Reis, Alejandra Damián

|Oct 25, 2024
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development.

Fabiola Ceroni, Munevver B Cicekdal, Richard Holt

|Mar 30, 2023
Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia.

Yesim Kesim, Fabiola Ceroni, Alejandra Damián

|Oct 07, 2022
Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia.

Fabiola Ceroni, Daniel Osborne, Samuel Clokie

|Jul 06, 2018
Expanding the phenotype of the X-linked BCOR microphthalmia syndromes.

Nicola Ragge, Bertrand Isidor, Pierre Bitoun

Pageof 2

Frequent Collaborators

6 joint publications

Fabiola Ceroni

4 joint publications

Julie Plaisancié

3 joint publications

Alejandra Damián

3 joint publications

Carmen Ayuso