Paola Evangelidou

6PUBLICATIONS
8CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesCell and nuclear division
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Publications (6)

|Aug 27, 2026
Discovery of Causative Genetic Variants in Patients with Congenital and/or Developmental Anomalies by Exome Sequencing.

|Oct 29, 2025
Investigating the "Dark" Genome: First Report of Partington Syndrome in Cyprus.

Constantia Aristidou, Athina Theodosiou, Pavlos Antoniou

|Feb 25, 2025
Fetal genetic factors in pregnancy loss: Insights from a meta-analysis and effectiveness of whole exome sequencing.

Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou

|Jan 23, 2024
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies.

Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou

|Jan 21, 2023
Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing.

Constantia Aristidou, Athina Theodosiou, Angelos Alexandrou

|Feb 28, 2015
A prenatally ascertained de novo terminal deletion of chromosomal bands 1q43q44 associated with multiple congenital abnormalities in a female fetus.

Carolina Sismani, Georgia Christopoulou, Angelos Alexandrou

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Frequent Collaborators

6 joint publications

Carolina Sismani

2 joint publications

Andrea Hadjipanteli

2 joint publications

Athina Theodosiou

2 joint publications

Marios Tomazou