Paolo Moi

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia

Gonçalo R. Abecasis, Stuart H. Orkin, Ramaiah Nagaraja, 2008, Proceedings of the National Academy of Sciences.

Towards the genetic treatment of β-thalassemia: new disease models, new vectors, new cells

Michel Sadelain, M. Sadelain, P. Moi, 2008, Haematologica.

Chromosomal localization of the human NF-E2 family of bZIP transcription factors by fluorescence in situ hybridization

Y. Kan, P. Moi, J. Chan, 1995, Human Genetics.

KLF1 gene mutations cause borderline HbA(2).

P. Moi, A. Cao, R. Galanello, 2011, Blood.