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Personalized Medicine|May 23, 2018
Thalassemia and its relevance to personalized medicineMarina Kleanthous, Marios PhylactidesCells|July 2, 2021
Therapy Development by Genome Editing of Hematopoietic Stem CellsLola Koniali, Carsten W Lederer, Marina KleanthousMolecular Diagnosis & Therapy|April 5, 2019
Rare Opportunities: CRISPR/Cas-Based Therapy Development for Rare Genetic DiseasesPanayiota Papasavva, Marina Kleanthous, Carsten W LedererMolecular Diagnosis & Therapy|April 5, 2019
Disruptive Technology: CRISPR/Cas-Based Tools and ApproachesPetros Patsali, Marina Kleanthous, Carsten W LedererClinical Biochemistry|July 18, 2009
Prenatal diagnosis of hemoglobin disorders: present and future strategiesCornelis L Harteveld, Marina Kleanthous, Joanne Traeger-SynodinosBMC Genomics|February 8, 2014
Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approachPavlos Fanis, Ioanna Kousiappa, Marios Phylactides, et al.Annals of the New York Academy of Sciences|October 8, 2008
Arrayed primer extension for the noninvasive prenatal diagnosis of beta-thalassemia based on detection of single nucleotide polymorphismsThessalia Papasavva, Ioannis Kalikas, Andreanni Kyrri, et al.International Journal of Molecular Sciences|March 1, 2020
Acid Ceramidase Depletion Impairs Neuronal Survival and Induces Morphological Defects in Neurites Associated with Altered Gene Transcription and Sphingolipid ContentKalia Kyriakou, Carsten W Lederer, Marina Kleanthous, et al.Hemoglobin|October 22, 2008
Molecular basis of thalassemia intermedia in IranMohammad T Akbari, Pantea Izadi, Mina Izadyar, et al.Veterinary Journal (London, England : 1997)|November 30, 2005
Novel polymorphisms at codons 146 and 151 in the prion protein gene of Cyprus goats, and their association with natural scrapiePenelope Papasavva-Stylianou, Marina Kleanthous, Pavlos Toumazos, et al.Pageof 8