• Developmental Genetics of Haemoglobin & Thalassaemia

Borg, J., Patrinos, G.P., Felice, A.E., and Philipsen, S. 2011, "Erythroid phenotypes associated with KLF1 mutations", Hematologia, vol. 96, no. 5, pp. 635-638.

Giardine, B., Borg, J., Higgs, D.R., Peterson, K.R., Philipsen, S., Maglott, D., Singleton, B.K., Anstee, D.J., Basak, A.N., Clark, B., Costa, F.C., Faustino, P., Fedosyuk, H., Felice, A.E., Francina, A., Galanello, R., Gallivan, M.V., Georgitsi, M., Gibbons, R.J., Giordano, P.C., Harteveld, C.L., Hoyer, J.D., Jarvis, M., Joly, P., Kanavakis, E., Kollia, P., Menzel, S., Miller, W., Moradkhani, K., Old, J., Papachatzopoulou, A., Papadakis, M.N., Papadopoulos. P., Pavlovic ,S,. Perseu, L., Radmilovic, M., Riemer, C., Satta, S., Schrijver, I., Stojiljkovic, M., Thein, S.L., Traeger-Synodinos, J., Tully, R., Wada, T., Waye, J.S., Wiemann, C., Zukic, B., Chui, D.H., Wajcman, H., Hardison, R.C., Patrinos, G.P. 2011, "Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.", Nature Genetics, vol. 43, no. 4, pp. 295-301.

Borg, J., Papadopoulos, P., Georgitsi, M., Gutiérrez, L., Grech, G., Fanis, P., Phylactides, M., Verkerk A.J., van der Spek, P.J., Scerri, C.A., Cassar, W., Galdies, R., van Ijcken, W., Ozgür, Z., Gillemans, N., Hou, J,, Bugeja, M., Grosveld, F,G., von Lindern, M., Felice, A,E., Patrinos, G,P., Philipsen, S. 2010, "Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.", Nature Genetics, vol. 42, no. 9, pp. 801-805.

Capelli, C., Redhead, N., Romano, V., Calì, F., Lefranc, G., Delague, V., Megarbane, A., Felice, A.E., Pascali, V.L., Neophytou, P.I., Poulli, Z., Novelletto, A., Malaspina, P., Terrenato, L., Berebbi, A., Fellous, M., Thomas, M.G., Goldstein, D.B. 2006, "Population structure in the Mediterranean basin: a Y chromosome perspective.", Annals of Human Genetics, vol. 70 (pt 2), no. 207, pp. 225.

Neville, R.R.G., Parascandalo, R., Attard Montalto, S., Farrugia, R., and Felice, A.E. 2005, "A Congenital Dopa Responsive Motor Disorder: a Maltese Variant due to Sepiapterin Reductase Deficiency", Brain, vol. 128, pp. 2291-2296.

Scerri, C.A., Abela, W., Galdies, R, Pizzuto, M., Grech, J.L., and Felice, A.E. 1993, "The beta + IVS, I-NT no. 6 (T --> C) thalassaemia in heterozygotes with an associated Hb Valletta or Hb S heterozygosity in homozygotes from Malta. ", British Journal o Haematology, vol. 83, no. 4, pp. 669-671.

Felice, A.E., Cleek, M.P., McKie, K., McKie, V., and Huisman T.H.J. 1984, "The rare a-Thalassemia-1 of Blacks is a za-Thalassemia with Deletion of all a and z Globin Genes.", Blood, vol. 63, pp. 1253-1257.

Felice, A.E., Abraham, E.C., Miller, A., Stallings, M., and Huisman, TH.J. 1978, "Is the Trimodality of Hb Leslie (a2 b2 131 Gln O) in Heterozygotes the Result of a Variable Number of Active a-Chain Genes? Evidence for Post-Translational Control of Hemoglobin Synthesis.", American Journal of Hematology, vol. 5, pp. 1-9.

Altay, G., Garver, F., Bannister, W.H., Grech, J.L., Felice, A.E., and Huisman, T.H.J. 1977, "Detection and Quantitation of the Fetal Hemoglobin Variant Hb F Malta-1 in Adults.", Biomedical Genetics, vol. 9-10, pp. 915-923.

Huisman, T.H.J., Schroeder, W.A., Felice, A.E., Powars, D. and Ringelhann, B. 1977, "An Anomaly in the g Chain Heterogeneity of the Newborn.", Nature, vol. 265, pp. 63.

• PHB5030 - Molecular Biology and Genetics