Beata Piovesan

Hereditary haemorrhagic telangiectasia: mutation detection, test sensitivity and novel mutations

H. Ozçelik, S. Savas, E. Zhang, 2006, Journal of Medical Genetics.

Detection of mosaic RB1 mutations in families with retinoblastoma

B. Gallie, R. Clark, Katherine Zhang, 2009, Human mutation.

Identification of clinically relevant mosaicism in type I hereditary haemorrhagic telangiectasia

B. Gallie, D. Rushlow, B. Piovesan, 2011, Journal of Medical Genetics.

Loss of RB1 induces non-proliferative retinoma: increasing genomic instability correlates with progression to retinoblastoma.

T. Corson, B. Gallie, W. Halliday, 2008, Human molecular genetics.

Molecular analysis distinguishes metastatic disease from second cancers in patients with retinoblastoma.

T. Corson, B. Gallie, B. Argiropoulos, 2016, Cancer genetics.