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Paola Granata

Observed names: Granata P., Granata Paola, Granata, Paola, P Granata, P. Granata
ORCID: 0000-0001-7620-4163
Observed ORCID: 0000-0001-7620-4163
OpenAlex ID: A5008698644
De novo balanced chromosome rearrangements in prenatal diagnosis
2009 · Daniela Giardino, Cecilia Corti, et al. · Prenatal Diagnosis · 141
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Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories
2005 · Leda Dalprà, Daniela Giardino, et al. · Genetics in Medicine · 105
Cytogenetic analysis reveals clonal proliferation of smooth muscle cells in atherosclerotic plaques
1991 · R. Casalone, P. Granata, et al. · Human Genetics · 78
Gene Set Enrichment Analysis of Interaction Networks Weighted by Node Centrality
2021 · Alessandra Zito, Marta Lualdi, et al. · Frontiers in Genetics · 62
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Correlation between cytogenetic and histopathological findings in 65 human meningiomas
1990 · R. Casalone, P. Simi, et al. · Cancer Genetics and Cytogenetics · 59
Large T antigen coding sequences of two DNA tumor viruses, BK and SV40, and nonrandom chromosome changes in two glioblastoma cell lines
1996 · M. Tognon, R. Casalone, et al. · Cancer Genetics and Cytogenetics · 50
Recessive cancer genes in meningiomas? An analysis of 31 cases
1987 · R. Casalone, P. Granata, et al. · Cancer Genetics and Cytogenetics · 42
Cerebral germ cell tumor and XXY karyotype
1994 · R. Casalone, R. Righi, et al. · Cancer Genetics and Cytogenetics · 24
Cytogenetic and interphase cytogenetic analyses reveal chromosome instability but no clonal trisomy 8 in dupuytren contracture
1997 · R. Casalone, D. Mazzola, et al. · Cancer Genetics and Cytogenetics · 21
Nonrandom chromosome changes in Kaposi sarcoma
2001 · R. Casalone, A. Albini, et al. · Cancer Genetics and Cytogenetics · 16
Cytogenetic and Interphase FISH Analyses of 73 Basal Cell and Three Squamous Cell Carcinomas
2000 · Rosario Casalone, Daniela Mazzola, et al. · Cancer Genetics and Cytogenetics · 16
Cytogenetic findings in echographically defined blighted ovum abortions.
1993 · E Minelli, C Buchi, et al. · PubMed · 16
Chromosome changes in benign prostatic hyperplasia and their significance in the origin of prostatic carcinoma
1993 · R. Casalone, P. Portentoso, et al. · Cancer Genetics and Cytogenetics · 13
Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches
2022 · Paola Granata, Dario Cocciadiferro, et al. · Frontiers in Genetics · 12
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Molecular cytogenetics, RFLP analysis and clinical characterization of a de novo trisomy 10p case
2000 · Paola Granata, Daniel Mazzola, et al. · Annales de Génétique · 12
A new acute myeloid leukemia case with STAT5B-RARA gene fusion due to 17q21.2 interstitial deletion
2016 · Chiara Pessina, Claudia Basilico, et al. · Leukemia & lymphoma/Leukemia and lymphoma · 10
Unveiling genetic insights: Array-CGH and WES discoveries in a cohort of 122 children with essential autism spectrum disorder
2024 · Paola Granata, Alessandra Zito, et al. · BMC Genomics · 8
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Clonal chromosome changes in renal carcinoma do not correlate with clinical stages and histopathologic grades
1992 · P. Granata, P. Portentoso, et al. · Cancer Genetics and Cytogenetics · 8
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate
2019 · Ilaria Catusi, Maria Paola Recalcati, et al. · Molecular Genetics & Genomic Medicine · 7
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Clonal chromosome changes in non-neoplastic ureters
1995 · R. Casalone, E. Minelli, et al. · Cancer Genetics and Cytogenetics · 4
Koolen-de Vries Syndrome: Preliminary Observations of Topiramate Efficacy
2021 · Piccinelli Paolo, Ferri Matteo, et al. · Child Neurology Open · 3
Chromosome changes in lymphocytes of patients with scleroderma.
1995 · R Casalone, P Granata, et al. · PubMed · 2
Partial Trisomy 13 and Partial Monosomy 8 Mosaicism Secondary to an Unbalanced De Novo Translocation
2013 · Giovanni Baranello, Claudia Cesaretti, et al. · Journal of Child Neurology · 1
Trisomy 6 in direct preparation of basal cell carcinoma (BBC)
1996 · R. Casalone, R. Righi, et al. · Cancer Genetics and Cytogenetics · 1
The p.Gly130Val mutation in the GJB2 gene: A familiar case of autosomal dominant non-syndromic hearing loss
2019 · Adelaide Bussini, Rossana Righi, et al. · International Journal of Pediatric Otorhinolaryngology
Works count: 38
Citation count: 711
H-index: 13
I10-index: 16
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