Michalis Georgiou

15PUBLICATIONS
46CO-AUTHORS
Optical technologyGene expression (incl. microarray and other genome-wide approaches)Vision scienceGene mappingNeurogenetics
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Publications (15)

|Jul 09, 2025
Quantification of Optical Coherence Tomography Features in >3500 Patients with Inherited Retinal Disease Reveals Novel Genotype-Phenotype Associations.

William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei

|Apr 08, 2024
Quantification of Fundus Autofluorescence Features in a Molecularly Characterized Cohort of More Than 3500 Inherited Retinal Disease Patients from the United Kingdom.

William Woof, Thales A C de Guimarães, Saoud Al-Khuzaei

|Oct 18, 2023
KCNV2-associated retinopathy: genotype-phenotype correlations - KCNV2 study group report 3.

Thales A C de Guimaraes, Michalis Georgiou, Anthony G Robson

|Jul 26, 2023
Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British family.

Vanita Berry, Alexander Ionides, Michalis Georgiou

|Sep 26, 2022
Inherited causes of combined vision and hearing loss: clinical features and molecular genetics.

Thales Antonio Cabral de Guimaraes, Elizabeth Arram, Ahmed F Shakarchi

|Nov 26, 2021
Functional evaluation in inherited retinal disease.

Malena Daich Varela, Michalis Georgiou, Shaima A Hashem

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Frequent Collaborators

8 joint publications

Thales Antonio Cabral de Guimaraes

6 joint publications

Malena Daich Varela

3 joint publications

Yu Fujinami-Yokokawa

3 joint publications

Nikolas Pontikos