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Giulia Melloni

Observed names: G. Melloni, Melloni Giulia, Melloni, Giulia
Observed institutions: University of Milan, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, IFOM, Centro Diagnostico Italiano, Fondazione IRCCS Istituto Nazionale dei Tumori, Fondazione IRCCS Istituto Neurologico Carlo Besta
ORCID: 0000-0002-8894-4449
Observed ORCID: 0000-0002-8894-4449
OpenAlex ID: A5062539462
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
2013 · Fergus J. Couch, Xianshu Wang, et al. · PLoS Genetics · 381
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Choroidal Abnormalities Detected by Near-Infrared Reflectance Imaging as a New Diagnostic Criterion for Neurofibromatosis 1
2011 · Francesco Viola, Edoardo Villani, et al. · Ophthalmology · 163
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Neurofibromatosis type 1 and pregnancy: Maternal complications and attitudes about prenatal diagnosis
2013 · Claudia Cesaretti, Giulia Melloni, et al. · American Journal of Medical Genetics Part A · 28
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Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort
2019 · Giulia Melloni, Marica Eoli, et al. · Cancers · 27
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Chiari I malformation in defined genetic syndromes in children: are there common pathways?
2019 · Veronica Saletti, Ilaria Viganò, et al. · Child s Nervous System · 21
Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients
2020 · Donatella Bianchessi, Maria Cristina Ibba, et al. · Genes · 16
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The absence that makes the difference: choroidal abnormalities in Legius syndrome
2017 · Arianna Tucci, Veronica Saletti, et al. · Journal of Human Genetics · 10
Occurrence of complete arhinia in two siblings with a clinical picture of Treacher Collins syndrome negative for TCOF1, POLR1D and POLR1C mutations
2011 · Claudia Cesaretti, Barbara Gentilin, et al. · Clinical Dysmorphology · 8
Delineating the Mosaic Trisomy 15 Phenotype Using a Serendipitous Mechanism as a Clue
2015 · Federica Natacci, Giulia Melloni, et al. · Cytogenetic and Genome Research · 6
Prenatal phenotype of Nager syndrome and Rodriguez syndrome: variable expression of the same entity?
2013 · Simone Gana, Barbara Gentilin, et al. · Clinical Dysmorphology · 6
Characterization of a New Variant in ARHGAP31 Probably Involved in Adams–Oliver Syndrome in a Family with a Variable Phenotypic Spectrum
2024 · Carlo Santaniello, Alice Faversani, et al. · Genes · 3
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Correction: The absence that makes the difference: choroidal abnormalities in Legius syndrome
2018 · Arianna Tucci, Veronica Saletti, et al. · Journal of Human Genetics · 2
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Case report: Deciphering the clinical significance of a novel partial BRCA1 exon 10 duplication in a patient with triple-negative breast cancer
2025 · Alice Faversani, Debora Manuelli, et al. · Frontiers in Oncology
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Bone Loss Associated with Extraction of Impacted Third Molars: A Literature Review and Meta-Analysis
2025 · Shaniko Kaleci, Pierantonio Bellini, et al. · Journal of Surgery and Medical Case Reports
A novel mutation in FHL1 gene causing hypertrophic cardiomyopathy associated with myopathy
2017 · R. Petillo, P. D'Ambrosio, et al. · Neuromuscular Disorders
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk
2013 · Fergus J. Couch, Xianshu Wang, et al. · Newcastle University ePrints (Newcastle Univesity)
Allotrapianti Di Polmone Sinistro Nel Maiale. Tecnica Di Valutazione Funzionale Secondo Cooper
1991 · Alessandro Baisi, Piero Zannini, et al. · Der Chirurg
Works count: 19
Citation count: 671
H-index: 8
I10-index: 7
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