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P. Evangelidou · SciRah

Researcher profile · Semantic Scholar

P. Evangelidou

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P. Evangelidou — researcher profile on SciRah

h-index: 7
Works: 23
Citations: 246

Most-cited papers

Fluorescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity
P. Patsalis, P. Evangelidou, Spyros Charalambous, C. Sismani
2004European Journal of Human Genetics63 citations
Semantic Scholar
Implementation of High Resolution Whole Genome Array CGH in the Prenatal Clinical Setting: Advantages, Challenges, and Review of the Literature
P. Evangelidou, Angelos Alexandrou, Maria Moutafi, M. Ioannides +6 more
2013BioMed Research International57 citations Open access
Semantic Scholar
Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations
P. Evangelidou, C. Sismani, M. Ioannides, C. Christodoulou +5 more
2010Molecular Cytogenetics51 citations Open access
Semantic Scholar
Partial MEF2C deletion in a Cypriot patient with severe intellectual disability and a jugular fossa malformation: Review of the literature
G. Tanteles, Angelos Alexandrou, P. Evangelidou, M. Gavatha +2 more
2015American Journal of Medical Genetics. Part A13 citations
Semantic Scholar
A Prenatally Ascertained De Novo Terminal Deletion of Chromosomal Bands 1q43q44 Associated with Multiple Congenital Abnormalities in a Female Fetus
C. Sismani, G. Christopoulou, Angelos Alexandrou, P. Evangelidou +3 more
2015Case Reports in Genetics9 citations Open access
Semantic Scholar
Fetal genetic factors in pregnancy loss: Insights from a meta-analysis and effectiveness of whole exome sequencing
Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou, Angelos Alexandrou +21 more
2025PLoS ONE8 citations Open access
Semantic Scholar
Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders
Chelsea Lowther, M. Mehrjouy, Ryan L. Collins, M. Bak +151 more
2022medRxiv8 citations Open access
Semantic Scholar
Sodium Channel Gene Variants in Fetuses with Abnormal Sonographic Findings: Expanding the Prenatal Phenotypic Spectrum of Sodium Channelopathies
Andrea Hadjipanteli, Athina Theodosiou, Ioannis Papaevripidou, P. Evangelidou +10 more
2024Genes7 citations Open access
Semantic Scholar
Investigating TNNC1 gene inheritance and clinical outcomes through a comprehensive familial study
Constantinos Patsalis, S. Kyriakou, M. Georgiadou, Lygia Ioannou +8 more
2024American Journal of Medical Genetics. Part A5 citations
Semantic Scholar
An unusual combination of an atypical maternally inherited novel 0.3Mb deletion in Williams-Beuren region and a de novo 22q11.21 microduplication in an infant with supravalvular aortic stenosis.
P. Evangelidou, L. Kousoulidou, Nicole Salameh, Angelos Alexandrou +7 more
2020European Journal of Medical Genetics5 citations
Semantic Scholar
Hereditary multiple exostoses caused by a chromosomal inversion removing part of EXT1 gene
Angelos Alexandrou, Nicole Salameh, Ioannis Papaevripidou, N. Nicolaou +7 more
2023Molecular Cytogenetics4 citations Open access
Semantic Scholar
De novo mosaic MECP2 mutation in a female with Rett syndrome
Angelos Alexandrou, Ioannis Papaevripidou, Ioanna Alexandrou, Athina Theodosiou +5 more
2019Clinical Case Reports4 citations Open access
Semantic Scholar
Two unrelated individuals carrying rare mosaic deletions in TCF4 gene
L. Kousoulidou, Angelos Alexandrou, Ioannis Papaevripidou, P. Evangelidou +3 more
2018American Journal of Medical Genetics. Part A4 citations Open access
Semantic Scholar
Mild Phenotype in a Patient with a De Novo 6.3 Mb Distal Deletion at 10q26.2q26.3
G. Tanteles, E. Nikolaou, Y. Christou, Angelos Alexandrou +4 more
2015Case Reports in Genetics4 citations Open access
Semantic Scholar
Identification of a novel, pathogenic CREBBP variant in a patient with Menke-Hennekam syndrome: a Case Report
Anna-Maria Anastasiou, Constantia Aristidou, Athina Theodosiou, L. Kousoulidou +7 more
2025Frontiers in Genetics3 citations Open access
Semantic Scholar
Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing
Constantia Aristidou, Athina Theodosiou, Angelos Alexandrou, Ioannis Papaevripidou +6 more
2022Genes2 citations Open access
Semantic Scholar
Hb A2 Episkopi – a novel δ-globin chain variant [HBD:c.428C>T] in a family of mixed Cypriot–Lebanese descent
C. Lederer, E. Pavlou, G. Tanteles, P. Evangelidou +6 more
2017Hematology1 citations Open access
Semantic Scholar
Discovery of Causative Genetic Variants in Patients with Congenital and/or Developmental Anomalies by Exome Sequencing
Athina Theodosiou, L. Kousoulidou, Ioannis Papaevripidou, Constantia Aristidou +14 more
2026Genes0 citations Open access
Semantic Scholar
Assessing concordance of genetic parameters between trophectoderm and inner cell mass in morphologically scored day-5 embryos via NGS
Nicole Salameh, Athina Theodosiou, L. Kousoulidou, Ioannis Papaevripidou +9 more
2026Reproduction and Fertility0 citations Open access
Semantic Scholar
Investigating the “Dark” Genome: First Report of Partington Syndrome in Cyprus
Constantia Aristidou, Athina Theodosiou, P. Antoniou, Angelos Alexandrou +13 more
2025Genes0 citations
Semantic Scholar
24. PREIMPLANTATION GENETIC TESTING FOR ANEUPLOIDIES WITH NGS ON MINISEQ. A RELIABLE ALTERNATIVE FOR SMALL LABORATORIES
Ioannis Papaevripidou, Angelos Alexandrou, E. Constantinou, Athina Theodosiou +2 more
2019Reproductive Biomedicine Online0 citations
Semantic Scholar
Genomic Arrays in Prenatal Diagnosis
P. Evangelidou, C. Sismani
20170 citations
Semantic Scholar
Erratum: Prenatal diagnosis of a de novo partial trisomy 10p12.1–12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH
S. Kitsiou-tzeli, C. Sismani, M. Karkaletsi, L. Florentin +6 more
20100 citations Open access
Semantic Scholar

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