• 4 Citations
  • 1 h-Index
20172019
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Fingerprint Dive into the research topics where Emilia Stellacci is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 2 Similar Profiles
Intellectual Disability Medicine & Life Sciences
Zinc Fingers Medicine & Life Sciences
Organoids Medicine & Life Sciences
Mutation Medicine & Life Sciences
Regenerative Medicine Medicine & Life Sciences
Germ-Line Mutation Medicine & Life Sciences
Guanosine Triphosphate Medicine & Life Sciences
Transducers Medicine & Life Sciences

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Research Output 2017 2019

  • 4 Citations
  • 1 h-Index
  • 4 Article

Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases

Grassi, L., Alfonsi, R., Francescangeli, F., Signore, M., De Angelis, M. L., Addario, A., Costantini, M., Flex, E., Ciolfi, A., Pizzi, S., Bruselles, A., Pallocca, M., Simone, G., Haoui, M., Falchi, M., Milella, M., Sentinelli, S., Di Matteo, P., Stellacci, E., Gallucci, M. & 4 others, Muto, G., Tartaglia, M., De Maria, R. & Bonci, D., Feb 27 2019, In : Cell death & disease. 10, 3, p. 201

Research output: Contribution to journalArticle

Organoids
Regenerative Medicine
Kidney
Kidney Neoplasms
Neoplasms

Clinical and functional characterization of two novel ZBTB20 mutations causing Primrose syndrome

Stellacci, E., Steindl, K., Joset, P., Mercurio, L., Anselmi, M., Cecchetti, S., Gogoll, L., Zweier, M., Hackenberg, A., Bocchinfuso, G., Stella, L., Tartaglia, M. & Rauch, A., 2018, In : Human Mutation. 39, 7, p. 959-964 6 p.

Research output: Contribution to journalArticle

Zinc Fingers
Mutation
Megalencephaly
Amino Acid Substitution
Protein C

Clinical and functional characterization of two novel ZBTB20 mutations causing Primrose syndrome

Stellacci, E., Steindl, K., Joset, P., Mercurio, L., Anselmi, M., Cecchetti, S., Gogoll, L., Zweier, M., Hackenberg, A., Bocchinfuso, G., Stella, L., Tartaglia, M. & Rauch, A., Jul 2018, In : Human Mutation. 39, 7, p. 959-964 6 p.

Research output: Contribution to journalArticle

Zinc Fingers
Mutation
Megalencephaly
Amino Acid Substitution
Protein C
4 Citations (Scopus)

Aberrant HRAS transcript processing underlies a distinctive phenotype within the RASopathy clinical spectrum

Pantaleoni, F., Lev, D., Cirstea, I. C., Motta, M., Lepri, F. R., Bottero, L., Cecchetti, S., Linger, I., Paolacci, S., Flex, E., Novelli, A., Carè, A., Ahmadian, M. R., Stellacci, E. & Tartaglia, M., Jul 2017, In : Human Mutation. 38, 7, p. 798-804 7 p.

Research output: Contribution to journalArticle

Germ-Line Mutation
Guanosine Triphosphate
Transducers
Growth and Development
Intellectual Disability