Publications:  Miss Angelica Gualtieri

Giri D, Vignola ML, Gualtieri A, Scagliotti V, McNamara P, Peak M, Didi M, Gaston-Massuet C et al.(2017). Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endodermderived organ abnormalities. Human Molecular Genetics vol. 26, (22) 4315-4326.

Gaston-Massuet C, McCabe MJ, Scagliotti V, Young RM, Carreno G, Gregory LC, Jayakody SA, Pozzi S et al.(2016). Transcription factor 7-like 1 is involved in hypothalamo-pituitary axis development in mice and humans. Proceedings of the National Academy of Sciences of the United States of America vol. 113, (5) E548-E557.

Avagliano L, Doi P, Tosi D, Scagliotti V, Gualtieri A, Gaston-Massuet C, Pistocchi A, Gallina A et al.(2016). Cell death and cell proliferation in human spina bifida. Birth Defects Research Part A - Clinical and Molecular Teratology vol. 106, (2) 104-113.

Scagliotti V, Avagliano L, Gualtieri A, Graziola F, Doi P, Chalker J, Righini A, Korbonits M et al.(2016). Histopathology and molecular characterisation of intrauterine-diagnosed congenital craniopharyngioma. Pituitary vol. 19, (1) 50-56.

McCabe MJ, Hu Y, Gregory LC, Gaston-Massuet C, Alatzoglou KS, Saldanha JW, Gualtieri A, Thankamony A et al.(2015). Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD). Molecular and Cellular Endocrinology vol. 417, 63-72.