IthaGenes: An Interactive Database for Haemoglobin Variations and EpidemiologyPetros Kountouris, Marina Kleanthous, Carsten W. Lederer et al.|PLoS ONE|2014Cited by 261
Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemiaThessalia Papasavva, Marina Kleanthous, Wilfred F. J. van IJcken et al.|European Journal of Human Genetics|2013Cited by 55
The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective studyPetros Kountouris, Soteroula Christou, Michael Hadjigavriel et al.|Scientific Reports|2016Cited by 48
The International Hemoglobinopathy Research Network (<scp>INHERENT</scp>): An international initiative to study the role of genetic modifiers in hemoglobinopathiesPetros Kountouris, Marina Kleanthous, Coralea Stephanou et al.|American Journal of Hematology|2021Cited by 39
Adapting the ACMG/AMP variant classification framework: A perspective from the ClinGen Hemoglobinopathy Variant Curation Expert PanelPetros Kountouris, Coralea Stephanou, Carsten W. Lederer et al.|Human Mutation|2021Cited by 38