Linda M Reis

12PUBLICATIONS
38CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Aerospace structuresDevelopmental genetics (incl. sex determination)Hypersonic propulsion and hypersonic aerothermodynamics
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Publications (12)

|Sep 26, 2026
Guillouet-Gordon Syndrome With Severe Microtia in an Infant With a Homozygous Variant in MED16.

|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

|Jan 08, 2025
Novel Intragenic and Genomic Variants Highlight the Phenotypic Variability in HCCS-Related Disease.

Linda M Reis, Donald Basel, Pierre Bitoun

|Oct 28, 2023
Alternative Genetic Diagnoses in Axenfeld-Rieger Syndrome Spectrum.

Linda M Reis, David J Amor, Raad A Haddad

|Aug 29, 2023
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.

Henry Oppermann, Elia Marcos-Grañeda, Linnea A Weiss

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Frequent Collaborators

12 joint publications

Elena V Semina

2 joint publications

Samuel Thompson

2 joint publications

Nicola K Ragge

2 joint publications

Fabiola Ceroni