Serena Corsini
Bologna, 40131, Italy
Last Updated: 09/26/2026
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Found 10 publications
A Novel Pathogenic Large Duplication in EXT1 Identified in a Family with Multiple Osteochondromas.
Journal: Genes
Published: July 26, 2024
Osteogenesis imperfecta: a cross-sectional study of skeletal and extraskeletal features in a large cohort of Italian patients.
Journal: Frontiers in endocrinology
Published: September 22, 2023
A novel patient-derived immortalised cell line of myxofibrosarcoma: a tool for preclinical drugs testing and the generation of near-patient models.
Journal: BMC cancer
Published: July 12, 2023
An Easy-to-Use Approach to Detect CNV From Targeted NGS Data: Identification of a Novel Pathogenic Variant in MO Disease.
Journal: Frontiers in endocrinology
Published: February 11, 2022
Preanalytical DNA assessment for downstream applications: How to optimize the management of human biospecimens to support molecular diagnosis-An experimental study.
Journal: Journal of clinical laboratory analysis
Published: February 11, 2022
The Rizzoli Multiple Osteochondromas Classification revised: describing the phenotype to improve clinical practice.
Journal: American journal of medical genetics. Part A
Published: February 23, 2021
Structural Features of Heparan Sulfate from Multiple Osteochondromas and Chondrosarcomas.
Journal: Molecules (Basel, Switzerland)
Published: October 29, 2018
Genotype-phenotype correlation study in 364 osteogenesis imperfecta Italian patients.
Journal: European journal of human genetics : EJHG
Published: May 04, 2018
Evaluation of TP53 Pro72Arg and MDM2 SNP285-SNP309 polymorphisms in an Italian cohort of LFS suggestive patients lacking identifiable TP53 germline mutations.
Journal: Familial cancer
Published: March 10, 2016
Influence of the immunogenetic KIR and HLA systems on long-term renal transplant outcome.
Journal: Annals of transplantation
Published: November 14, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026