S. Toma

Two Novel Mutations (HBG1: c.-250C>T and HBG2: c.-250C>T) Associated With Hereditary Persistence of Fetal Hemoglobin

S. Thein, B. Clark, S. Toma, 2014, Hemoglobin.

The molecular characterization of Beta globin gene in thalassemia patients reveals rare and a novel mutations in Pakistani population.

Humaira Yasmeen, Letizia Foroni, Shahida Hasnain, 2016, European journal of medical genetics.

8 – Molecular and Cytogenetic Analysis

L. Foroni, G. Gerrard, A. Reid, 2017 .

The Association of Gilbert's Syndrome with Hyperbilirubinaemia Occurring on Any of Imatinib, Dasatinib and Nilotinib in Patients with Chronic Myeloid Leukaemia (CML)

L. Foroni, S. Hing, J. Apperley, 2015 .

The cytological features of NPM1‐mutated acute myeloid leukemia

B. Bain, J. Pavlů, S. Toma, 2015, American journal of hematology.