Fabiola Ceroni

Discovery of 42 genome-wide significant loci associated with dyslexia

Catherine Doust, Pierre Fontanillas, Else Eising et al. · Nature Genetics · 2022 · 140 citations · Full text

Life Sciences, Genetics, Psychology +17

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 et al. · Proceedings of the National Academy of Sciences · 2022 · 133 citations · Full text

Life Sciences, Genetics, Behavioral Genetics +16

A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder

Elena Bacchelli, Fabiola Ceroni, Dalila Pinto et al. · Journal of Neurodevelopmental Disorders · 2014 · 58 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies

Ddd Study, Fabiola Ceroni, Domingo Aguilera‐Garcia et al. · Human Genetics · 2018 · 57 citations · Full text

Medicine, Genetics, Ophthalmology +14

De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies

Richard Holt, Rodrigo Young, Berta Crespo et al. · The American Journal of Human Genetics · 2019 · 57 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17