Silvana Guerneri
Milan, Italy
Last Updated: 09/26/2026
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Found 30 publications
Positive predictive values and outcomes for uninformative cell-free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study).
Journal: Prenatal diagnosis
Published: August 05, 2022
Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome.
Journal: Prenatal diagnosis
Published: March 02, 2022
Correction to: Incidental finding of APC deletion in a child: double trouble or double chance? - a case report.
Journal: Italian journal of pediatrics
Published: September 15, 2021
The Core Stem Genes SOX2, POU5F1/OCT4, and NANOG Are Expressed in Human Parathyroid Tumors and Modulated by MEN1, YAP1, and β-catenin Pathways Activation.
Journal: Biomedicines
Published: April 10, 2021
Yes-Associated Protein 1 Is a Novel Calcium Sensing Receptor Target in Human Parathyroid Tumors.
Journal: International journal of molecular sciences
Published: December 24, 2020
Autism spectrum disorder and intellectual disability in an inherited 2q14.3 micro-deletion involving CNTNAP5.
Journal: American journal of medical genetics. Part A
Published: August 26, 2020
Cytogenetic study in primary myelofibrosis at diagnosis: Clinical and histological association and impact on survival according to WHO 2017 classification in an Italian multicenter series.
Journal: Hematological oncology
Published: July 29, 2020
Incidental finding of APC deletion in a child: double trouble or double chance? - a case report.
Journal: Italian journal of pediatrics
Published: July 02, 2020
Complex genomic alterations and intellectual disability: an interpretative challenge.
Journal: Journal of intellectual disability research : JIDR
Published: April 09, 2020
The Oncosuppressors MEN1 and CDC73 Are Involved in lncRNA Deregulation in Human Parathyroid Tumors.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: April 05, 2020
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: December 05, 2019
Small supernumerary marker chromosomes: A legacy of trisomy rescue?
Journal: Human mutation
Published: August 21, 2018
Last Updated: 09/26/2026