Francesca Marta Elli

7PUBLICATIONS
16CO-AUTHORS
Predictive and prognostic markersEpigenetics (incl. genome methylation and epigenomics)Medical and biological physics not elsewhere classifiedMedical biochemistry - proteins and peptides (incl. medical proteomics)Liquid biopsies
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Publications (7)

|May 13, 2026
Parathyroid hormone, FGF23, and bone turnover markers in CKD and PTH deficiency or resistance: associations with aortic and ectopic calcifications.

|Dec 13, 2021
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly.

Francesca Marta Elli, Deborah Mattinzoli, Camilla Lucca

|Feb 23, 2019
FGF23 and Fetuin-A Interaction and Mesenchymal Osteogenic Transformation.

Deborah Mattinzoli, Masami Ikehata, Koji Tsugawa

|Jan 09, 2019
Association of GNAS imprinting defects and deletions of chromosome 2 in two patients: clues explaining phenotypic heterogeneity in pseudohypoparathyroidism type 1B/iPPSD3.

F M Elli, L deSanctis, M A Maffini

|Jul 01, 2018
Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement.

Giovanna Mantovani, Murat Bastepe, David Monk

|Feb 16, 2018
Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases.

Francesca Marta Elli, Paolo Bordogna, Maura Arosio

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Frequent Collaborators

2 joint publications

Masami Ikehata

2 joint publications

Carlo M Alfieri

1 joint publications

Mattinzoli Deborah

1 joint publications

Molinari Paolo