Christodoulos Christodoulou

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

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

Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method

Lieselot Deleye, Dieter De Coninck, Christodoulos Christodoulou et al. · Scientific Reports · 2015 · 51 citations · Full text

Life Sciences, Biology, Genetics +16

Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts

Lieselot Deleye, Annelies Dheedene, Dieter De Coninck et al. · Fertility and Sterility · 2015 · 46 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation

George Koumbaris, Hariklia Hatzisevastou-Loukidou, Angelos Alexandrou et al. · Human Molecular Genetics · 2011 · 38 citations

Life Sciences, Genetics, Molecular Genetics +17