Fabiola Ceroni

7PUBLICATIONS
57CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseases
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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

|Aug 23, 2022
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.

Else Eising, Nazanin Mirza-Schreiber, Eveline L de Zeeuw

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Frequent Collaborators

6 joint publications

Nicola K Ragge

4 joint publications

Julie Plaisancié

3 joint publications

Elena V Semina

3 joint publications

Carmen Ayuso