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Giuliana Longo

Observed names: G Longo, Longo, Giuliana
ORCID: 0009-0008-1750-8587
Observed ORCID: 0009-0008-1750-8587
OpenAlex ID: A5031989206
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: significant association of twelve variants
2017 · Raffaella Cascella, Claudia Strafella, et al. · Oncotarget · 38
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HFE gene variants and iron-induced oxygen radical generation in idiopathic pulmonary fibrosis
2014 · Federica Sangiuolo, Ermanno Puxeddu, et al. · European Respiratory Journal · 38
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Assessing individual risk for AMD with genetic counseling, family history, and genetic testing
2017 · R Cascella, C Strafella, et al. · Eye · 22
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Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience
2019 · Liliana Mannucci, Serena Luciano, et al. · Clinica Chimica Acta · 15
Pharmacogenomics of Multifactorial Diseases: A Focus on Psoriatic Arthritis
2016 · Raffaella Cascella, Claudia Strafella, et al. · Pharmacogenomics · 15
Investigating the “Fetal Side” in Recurrent Pregnancy Loss: Reliability of Cell-Free DNA Testing in Detecting Chromosomal Abnormalities of Miscarriage Tissue
2023 · Silvia D’Ippolito, Giuliana Longo, et al. · Journal of Clinical Medicine · 14
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Effects of Simulated Microgravity on Wild Type and Marfan hiPSCs-Derived Embryoid Bodies
2021 · Paola Spitalieri, Mario Marini, et al. · Cellular and Molecular Bioengineering · 8
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Hb-M "Hyde Park": a de novo mutation, identified by mass spectrometry and DNA analysis.
1992 · B Rotoli, A Camera, et al. · PubMed · 7
Implementing the Risk Stratification and Clinical Management of Breast Cancer Families Using Polygenic Risk Score Evaluation: A Pilot Study
2024 · Barbara Rizzacasa, Vanessa Nicolì, et al. · Journal of Personalized Medicine · 4
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A Cultural Comparison of Dream Content, Mood and Waking Day Anxiety between Italians and Canadians
2013 · DeCicco, Teresa L, Zanasi, Marco, et al. · International journal of dream research · 4
Genotype–phenotype correlation of F484L mutation in three Italian families with Thomsen myotonia
2016 · Marco Cassone, Valentina Ferradini, et al. · Muscle & Nerve · 3
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry
2016 · Adalgisa Pietropolli, Maria Vittoria Capogna, et al. · Human Genomics · 3
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Clinical impact of the TPM1 p.Tyr221Cys variant causing hypertrophic cardiomyopathy
2025 · Alessio Marinelli, Giuliana Longo, et al. · Genes & Diseases · 2
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations
2015 · Raffaella Cascella, Claudia Strafella, et al. · Electrophoresis · 2
Beyond the linear genome: how reference bias threatens preventive medicine and geroscience
2026 · Gyula Richárd Nagy, Gyöngyi Munkácsy, et al. · GeroScience
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Additional file 2: of Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry
2016 · Pietropolli, Adalgisa, Capogna, Maria, et al. · Figshare
Additional file 1: Table S1. of Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry
2016 · Pietropolli, Adalgisa, Capogna, Maria, et al. · Figshare
Natural transmission and widening of a Y chromosome microdeletion involving the deleted in azoospermia gene
2000 · Garofalo, Aldo E. Calogero, et al.
Works count: 18
Citation count: 175
H-index: 7
I10-index: 6
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