Linda M Reis
11PUBLICATIONS
37CO-AUTHORS
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Publications (11)
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|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
|Mar 29, 2025
Displacement of distant regulatory elements of FOXC1 as a potential human disease mechanism.Jesús-José Ferre-Fernández, Linda M Reis, Elena V Semina
|Jan 08, 2025
Novel Intragenic and Genomic Variants Highlight the Phenotypic Variability in HCCS-Related Disease.Linda M Reis, Donald Basel, Pierre Bitoun
|Oct 25, 2024
Further Evidence for a Possible Role for ZFHX4 in Human Ocular Development and Disease.Linda M Reis, Gerald W Zaidman, Samuel Thompson
|Oct 28, 2023
Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum.Linda M Reis, David J Amor, Raad A Haddad
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Frequent Collaborators
11 joint publications
Elena V Semina
2 joint publications
Samuel Thompson
2 joint publications
Nicola K Ragge
2 joint publications
Fabiola Ceroni
1 joint publications
Jeffrey C Murray
1 joint publications
Henry Oppermann
1 joint publications
Elia Marcos-Grañeda
1 joint publications
Anne Marie Jelsig
1 joint publications
Jacob S Martin
1 joint publications
Alistair T Pagnamenta
