Items where authors include "Gallone, G."

Article

Wright, C.F., Quaife, N.M., Ramos-Hernández, L. et al. (31 more authors) (2021) Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanisms. American Journal of Human Genetics, 108 (6). pp. 1083-1094. ISSN 0002-9297

Martin, H.C., Gardner, E.J., Samocha, K.E. et al. (13 more authors) (2021) The contribution of X-linked coding variation to severe developmental disorders. Nature Communications, 12. 627. ISSN 2041-1723

Kaplanis, J., Samocha, K.E., Wiel, L. et al. (30 more authors) (2020) Evidence for 28 genetic disorders discovered by combining healthcare and research data. Nature, 586 (7831). pp. 757-762. ISSN 0028-0836

Milazzo, M., Gallone, G., Marcello, E. et al. (4 more authors) (2020) Biodegradable polymeric micro/nano-structures with intrinsic antifouling/antimicrobial properties: relevance in damaged skin and other biomedical applications. Journal of Functional Biomaterials, 11 (3). 60.

Martin, H.C., Jones, W.D., McIntyre, R. et al. (37 more authors) (2018) Quantifying the contribution of recessive coding variation to developmental disorders. Science, 362 (6419). pp. 1161-1164. ISSN 0036-8075