Publications by authors named "Stefania Byrou"

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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, Stella Tamana, Petros Kountouris

Int J Mol Sci· January 2025

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Case report: Rethinking NGS analysis in diagnosing Diamond-Blackfan anemia syndrome.
Panayiota L Papasavva, Konstantinos Kaouranis, Stefania Byrou, Constantina G Constantinou, Iacovou Efrosini

Front Genet· November 2024

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Optimized Droplet Digital PCR Assay on Cell-Free DNA Samples for Non-Invasive Prenatal Diagnosis: Application to Beta-Thalassemia.
Constantina G Constantinou, Eleni Karitzi, Stefania Byrou, Coralea Stephanou, Kyriaki Michailidou

Clin Chem· July 2022

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Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of β-thalassaemia.
Stefania Byrou, G Mike Makrigiorgos, Agathoklis Christofides, Ioannis Kallikas, Thessalia Papasavva

PLoS One· January 2019

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Evidence of digenic inheritance in autoinflammation-associated genes.
Vassos Neocleous, Stefania Byrou, Meropi Toumba, Constantina Costi, Christos Shammas

J Genet· December 2016

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Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation.
Christos Shammas, Stefania Byrou, Marie M Phelan, Meropi Toumba, Charilaos Stylianou

Hormones (Athens)· April 2016

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