Finelli Palma

Tenured Associate Professor
SSD
MED/03 - MEDICAL GENETICS
Competition sector
06/A1 - MEDICAL GENETICS

Contacts

Workplace

Via Zucchi, 18 - Istituto Auxologico Cusano
20095 CUSANO MILANINO (MI)

Via Fratelli Cervi, 93 - L.I.T.A. Segrate
20090 SEGRATE (MI)

Office phone number
02503 30361
University email address
Teaching - Programme courses

Postgraduate programmes

A.Y. 2019/2020
Postgraduate Schools - Medicine, Healthcare, Dental Medicine
A.Y. 2018/2019
Postgraduate Schools - Medicine, Healthcare, Dental Medicine
Research

Publications

Publications
  • SETD5 Gene Haploinsufficiency in Three Patients With Suspected KBG Syndrome / M. Crippa, I. Bestetti, S. Maitz, K. Weiss, A. Spano, M. Masciadri, S. Smithson, L. Larizza, K. Low, L. Cohen, P. Finelli. - In: FRONTIERS IN NEUROLOGY. - ISSN 1664-2295. - 11(2020 Jul 24), pp. 631.1-631.9.
  • Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency / R. Rossetti, I. Ferrari, I. Bestetti, S. Moleri, F. Brancati, L. Petrone, P. Finelli, L. Persani. - In: HUMAN MUTATION. - ISSN 1059-7794. - (2020). [Epub ahead of print]
  • Transcriptome Analysis of iPSC-Derived Neurons from Rubinstein-Taybi Patients Reveals Deficits in Neuronal Differentiation / L. Calzari, M. Barcella, V. Alari, D. Braga, R. Munoz-Viana, C. Barlassina, P. Finelli, C. Gervasini, A. Barco, S. Russo, L. Larizza. - In: MOLECULAR NEUROBIOLOGY. - ISSN 0893-7648. - 57:9(2020), pp. 3685-3701.
  • Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes / M. Crippa, M.T. Bonati, L. Calzari, C. Picinelli, C. Gervasini, A. Sironi, I. Bestetti, S. Guzzetti, S. Bellone, A. Selicorni, A. Mussa, A. Riccio, G.B. Ferrero, S. Russo, L. Larizza, P. Finelli. - In: FRONTIERS IN GENETICS. - ISSN 1664-8021. - 10(2019 Oct 15), pp. 955.1-955.13.
  • Generation of three iPSC lines (IAIi002, IAIi004, IAIi003) from Rubinstein-Taybi syndrome 1 patients carrying CREBBP non sense c.4435G>T, p.(Gly1479*) and c.3474G>A, p.(Trp1158*) and missense c.4627G>T, p.(Asp1543Tyr) mutations / V. Alari, S. Russo, D. Rovina, M. Garzo, M. Crippa, L. Calzari, C. Scalera, D. Concolino, E. Castiglioni, D. Giardino, E. Prosperi, P. Finelli, C. Gervasini, A. Gowran, L. Larizza. - In: STEM CELL RESEARCH. - ISSN 1873-5061. - 40(2019 Oct).