Marios Ioannides

Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype

Carolina Sismani, Sofia Kitsiou‐Tzeli, Marios Ioannides et al. · Molecular Cytogenetics · 2008 · 124 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Bisulfite Conversion of DNA: Performance Comparison of Different Kits and Methylation Quantitation of Epigenetic Biomarkers that Have the Potential to Be Used in Non-Invasive Prenatal Testing

Chrysanthia A. Leontiou, Michael D. Hadjidaniel, Petros Mina et al. · PLoS ONE · 2015 · 97 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion

Sofia Kitsiou‐Tzeli, Carolina Sismani, Marios Ioannides et al. · European Journal of Medical Genetics · 2006 · 63 citations

Life Sciences, Genetics, Molecular Genetics +16

Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex

George Koumbaris, Elena Kypri, Kyriakos Tsangaras et al. · Clinical Chemistry · 2016 · 53 citations · Full text

Medicine, Genetics, Obstetrics +17

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations

Paola Evangelidou, Carolina Sismani, Marios Ioannides et al. · Molecular Cytogenetics · 2010 · 51 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17