Publications by authors named "Giulia Melloni"

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Correlation Between Angular Position and Pathological Changes in Impacted Lower Third Molars: A Systematic Review and Meta-Analysis.
Shaniko Kaleci, Pierantonio Bellini, Giacomo Setti, Giulia Melloni, Matilde Ruozzi

Dent J (Basel)· March 2025

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Case report: Deciphering the clinical significance of a novel partial exon 10 duplication in a patient with triple-negative breast cancer.
Alice Faversani, Debora Manuelli, Davide Barteselli, Giulia Melloni, Carlo Santaniello

Front Oncol· February 2025

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Characterization of a New Variant in Probably Involved in Adams-Oliver Syndrome in a Family with a Variable Phenotypic Spectrum.
Carlo Santaniello, Alice Faversani, Luigi Corsaro, Giulia Melloni, Silvia Motta

Genes (Basel)· April 2024

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Simultaneous Detection of , , , and Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients.
Donatella Bianchessi, Maria Cristina Ibba, Veronica Saletti, Stefania Blasa, Tiziana Langella, Giulia Melloni

Genes (Basel)· June 2020

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Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent Cohort.
Giulia Melloni, Marica Eoli, Claudia Cesaretti, Donatella Bianchessi, Maria Cristina Ibba

Cancers (Basel)· November 2019

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Chiari I malformation in defined genetic syndromes in children: are there common pathways?
Veronica Saletti, Ilaria Viganò, Giulia Melloni, Chiara Pantaleoni, Ignazio Gaspare Vetrano

Childs Nerv Syst· October 2019

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Correction: The absence that makes the difference: choroidal abnormalities in Legius syndrome.
Arianna Tucci, Veronica Saletti, Francesca Menni, Claudia Cesaretti, Giulietta Scuvera, Giulia Melloni

J Hum Genet· March 2018

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The absence that makes the difference: choroidal abnormalities in Legius syndrome.
Arianna Tucci, Veronica Saletti, Francesca Menni, Claudia Cesaretti, Giulietta Scuvera, Giulia Melloni

J Hum Genet· November 2017

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Delineating the Mosaic Trisomy 15 Phenotype Using a Serendipitous Mechanism as a Clue.
Federica Natacci, Giulia Melloni, Francesca Motta, Rosamaria Silipigni, Fabio Doniselli

Cytogenet Genome Res· March 2016

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Prenatal phenotype of Nager syndrome and Rodriguez syndrome: variable expression of the same entity?
Simone Gana, Barbara Gentilin, Vera Bianchi, Sonia Gorla, Florinda Ceriani, Giulia Melloni

Clin Dysmorphol· October 2013

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Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
Fergus J Couch, Xianshu Wang, Lesley McGuffog, Andrew Lee, Curtis Olswold, Giulia Melloni

PLoS Genet· June 2013

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Neurofibromatosis type 1 and pregnancy: maternal complications and attitudes about prenatal diagnosis.
Claudia Cesaretti, Giulia Melloni, Donatella Quagliarini, Roberto Fogliani, Barbara Zaina

Am J Med Genet A· February 2013

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Choroidal abnormalities detected by near-infrared reflectance imaging as a new diagnostic criterion for neurofibromatosis 1.
Francesco Viola, Edoardo Villani, Federica Natacci, Angelo Selicorni, Giulia Melloni

Ophthalmology· February 2012

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Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations.
Claudia Cesaretti, Barbara Gentilin, Vera Bianchi, Giulia Melloni, Michela Bonaguro

Clin Dysmorphol· October 2011

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