Maddalena Allegretta

Activating mutations in the NT5C2 nucleotidase gene drive chemotherapy resistance in relapsed ALL

A. Ferrando, R. Rabadán, T. Palomero, 2013, Nature Medicine.

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.

T. Palomero, V. D’Agati, H. Kim, 2011, Kidney international.

Recurrent mutations in epigenetic regulators, RHOA and FYN kinase in peripheral T cell lymphomas

I. Lossos, E. Campo, A. Ferrando, 2014, Nature Genetics.

Point mutation E1099K in MMSET/NSD2 enhances its methyltranferase activity and leads to altered global chromatin methylation in lymphoid malignancies

N. Kelleher, J. Licht, A. Melnick, 2014, Leukemia.