Petros Kountouris

17PUBLICATIONS
69CO-AUTHORS
Gene and molecular therapyHaematologyMajor global burdens of diseaseGene mappingGene expression (incl. microarray and other genome-wide approaches)
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Publications (17)

|Aug 07, 2026
Modifying quality and equity of care: emerging roles of genetic disease modifiers in β-hemoglobinopathies.

|Jul 04, 2026
Undetectable Hydroxyurea Levels in the Majority of Sickle Cell Disease Patients, Especially in Young Children.

|May 13, 2026
Mapping Current and Emerging Laboratory Techniques for Haemoglobinopathy Carrier Detection and Prevention: A Narrative Review from the HELIOS Action.

|Feb 27, 2026
Special Issue "Genetic Modifiers of Hemoglobinopathies: Recent Advances and Future Directions".

Carsten W Lederer, Alex E Felice, Petros Kountouris

|Jan 29, 2026
Mapping diagnostic practices in hemoglobinopathies: a cross-country HELIOS COST Action study.

Coralea Stephanou, Sotiroula Chatzimatthaiou, Petros Kountouris

|Jan 25, 2025
Non-Invasive Determination of the Paternal Inheritance in Pregnancies at Risk for β-Thalassaemia by Analyzing Cell-Free Fetal DNA Using Targeted Next-Generation Sequencing.

Stefania Byrou, Rutger W W Brouwer, Marios Tomazou

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Frequent Collaborators

8 joint publications

Coralea Stephanou

6 joint publications

Carsten Werner Lederer

5 joint publications

Joanne Traeger-Synodinos

4 joint publications

Stella Tamana