Roberta Serrani

<i>FOXC2</i>disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function

Daniela Tavian, Sara Missaglia, Paolo Enrico Maltese et al. · Oncotarget · 2016 · 40 citations · Full text

Increasing evidence of hereditary lymphedema caused by <i>CELSR1</i> loss‐of‐function variants

Paolo Enrico Maltese, Sandro Michelini, Maurizio Ricci et al. · American Journal of Medical Genetics Part A · 2019 · 38 citations

Clinical and genetic study of 46 Italian patients with primary lymphedema.

Sandro Michelini, D. Degiorgio, Marina Cestari et al. · PubMed · 2012 · 27 citations

Genetics, Pathology, Molecular Genetics +16

TIE1 as a Candidate Gene for Lymphatic Malformations with or without Lymphedema

Sandro Michelini, Maurizio Ricci, Dominika Vešelényiová et al. · International Journal of Molecular Sciences · 2020 · 21 citations · Full text

The Impact of Lifestyle Interventions in High-Risk Early Breast Cancer Patients: A Modeling Approach from a Single Institution Experience

Mirco Pistelli, Valentina Natalucci, Laura Scortichini et al. · Cancers · 2021 · 17 citations · Full text