C. Zoi

Switch in X-inactivation in a JAK2 V617F-negative case of polycythemia vera with two acquired X-autosome translocations.

K. Zoi, G. Pantelias, K. Manola, 2007, Leukemia research.

Frequent Inactivating Mutations of TET2 and CBL Are Associated with Acquired Uniparental Disomy in Atypical Chronic Myeloid Leukemia and Related Disorders.

W. Vainchenker, A. Chase, K. Zoi, 2009 .

Increased CD177 (PRV1) expression in thalassaemia and the underlying erythropoietic activity

K. Zoi, E. Terpos, D. Loukopoulos, 2008, British journal of haematology.

The severity of FIP1L1–PDGFRA-positive chronic eosinophilic leukaemia is associated with polymorphic variation at the IL5RA locus

C. Preudhomme, K. Zoi, A. Reiter, 2007, Leukemia.

Management of Hypereosinophilic Syndrome: A Prospective Study in the Era of Molecular Genetics

S. Giannouli, I. Dahabreh, K. Zoi, 2007, Medicine.

Mutations in exon 12 of JAK2 are mainly found in JAK2 V617F‐negative polycythaemia vera patients

W. Vainchenker, P. Fenaux, L. Scott, 2008, British journal of haematology.

Is JAK2 V617F mutation more than a diagnostic index? A meta-analysis of clinical outcomes in essential thrombocythemia.

S. Giannouli, I. Dahabreh, K. Zoi, 2009, Leukemia research.

Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders.

D. Oscier, A. Jones, A. Chase, 2005, Blood.

Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders.

D. Oscier, A. Jones, A. Chase, 2005, Blood.

Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms.

A. Hall, D. Oscier, A. Jones, 2008, Blood.

No evidence for increased prevalence of JAK2 V617F in women with a history of recurrent miscarriage

S. Giannouli, I. Dahabreh, A. Jones, 2008, British journal of haematology.

Widespread occurrence of the JAK 2 V 617 F mutation in chronic myeloproliferative disorders

D. Oscier, A. Jones, A. Chase, 2005 .

Correlation of single nucleotide polymorphisms in the promoter region of the ANXA5 (annexin A5) gene with recurrent miscarriages in women of Greek origin

K. Zoi, A. Pouliakis, M. Voulgarelis, 2018, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.