Ornella Rondinone

A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability: a case report

S. Orcesi, D. Milani, M. Miozzo, 2020, Italian Journal of Pediatrics.

Extensive Placental Methylation Profiling in Normal Pregnancies

E. Ferrazzi, S. Bosari, D. Gentilini, 2021, International journal of molecular sciences.

Pitfalls of whole exome sequencing in undefined clinical conditions with a suspected genetic etiology

G. Scuvera, M. Bedeschi, D. Milani, 2022, Genes & Genomics.

Differential glycosylation of collagen modulates lung cancer stem cell subsets through β1 integrin‐mediated interactions

F. Nicotra, G. Sozzi, F. Andriani, 2020, Cancer science.

MMP1 drives tumor progression in large cell carcinoma of the lung through fibroblast senescence.

J. Alcaraz, D. Radisky, P. Gascón, 2021, Cancer letters.

Case report: Chorea and cognitive decline in a young woman: instrumental and genetic assessment of a case originally diagnosed as multiple sclerosis

P. Vitali, C. Pappone, Clemente Dato, 2023, Frontiers in Genetics.

The Genetic Basis, Lung Involvement, and Therapeutic Options in Niemann–Pick Disease: A Comprehensive Review

M. Mondoni, Ornella Rondinone, Sabrina Mira, 2024, Biomolecules.