Fabiola Ceroni

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Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia

R. Holt, P. Calvas, N. Chassaing, 2019, Human Genetics.

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

Luciana Rodrigues da Silva, R. Holt, P. Calvas, 2018, Human Genetics.

Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia

P. Calvas, N. Chassaing, D. Bax, 2023, European Journal of Human Genetics.

New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders

R. Holt, D. Gerrelli, D. Bax, 2017, Scientific Reports.

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

Timothy C. Bates, Till F. M. Andlauer, C. Francks, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Timothy C. Bates, Till F. M. Andlauer, C. Francks, 2021 .

A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma

D. Pinto, A. Pagnamenta, E. Maestrini, 2014, Autism research : official journal of the International Society for Autism Research.

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

Stephen W. Wilson, R. Holt, E. van Binsbergen, 2019, American journal of human genetics.

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Timothy C. Bates, Till F. M. Andlauer, C. Francks, 2022, Translational Psychiatry.

Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation

Dušica Filipović Đurđević, Laura E. Covill, D. Newbury, 2016, Scientific Reports.

Genome-wide analysis identifies a role for common copy number variants in specific language impairment

William W. Cohen, Gillian Baird, A Pickles, 2015, European Journal of Human Genetics.

Genome-wide analysis identi fi es a role for common copy number variants in speci fi c language impairment

G. Baird, P. Bolton, J. Knight, 2015 .

Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility

E. Bacchelli, E. Maestrini, A. Posar, 2022, Frontiers in Psychiatry.

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

D. Pinto, E. Bacchelli, A. Battaglia, 2014, Journal of Neurodevelopmental Disorders.

The Genetics of Specific Language Impairment (SLI)

D. Newbury, R. Nudel, F. Ceroni, 2015 .

The Genetics of Specific Language Impairment

D. Newbury, R. Nudel, F. Ceroni, 2018 .