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Author

Francesco Libotte

ORCID: 0000-0001-9050-324X
Observed ORCID: 0000-0001-9050-324X
OpenAlex ID: A5104097745
Pallister–Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis
2016 · Francesco Libotte, Domenico Bizzoco, et al. · Taiwanese Journal of Obstetrics and Gynecology · 13
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Agnathia-Otocephaly Complex Due to a De Novo Deletion in the OTX2 Gene
2022 · Marco Fabiani, Francesco Libotte, et al. · Genes · 7
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Prenatal Diagnosis by Trio Clinical Exome Sequencing: Single Center Experience
2024 · Katia Margiotti, Marco Fabiani, et al. · Current Issues in Molecular Biology · 6
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A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findings
2015 · Francesco Libotte · Journal of Prenatal Medicine · 6
Digenic Origin of Difference of Sex Development in a Patient Harbouring DHX37 and MAMLD1 Variants
2024 · Katia Margiotti, Francesco Libotte, et al. · Case Reports in Pediatrics · 5
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Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound Examinations
2020 · Francesco Libotte, Sonia Lorena Carpineto, et al. · Journal of Medicine and Life · 4
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De novo 3q13.13q21.2 interstitial deletion and paternal 12p13.3 microdeletion in a fetus with dysplasia of the corpus callosum and ventriculomegaly: A case report
2023 · Francesco Libotte, Marco Fabiani, et al. · Experimental and Therapeutic Medicine · 3
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Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication
2021 · Francesco Libotte, Marco Fabiani, et al. · Genes · 3
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Synergistic Induction of Apoptosis in Multiple Myeloma Cells by Simultaneous Inhibition of the Raf/MEK/ERK and BCL-2 Pathways
2008 · Maria Rosaria Ricciardi, Michele Milella, et al. · Blood · 2
A Case Report of 10q24.32 Microduplication Associated with Split Hand/Foot Malformation (SHFM) in Prenatal Diagnosis
2024 · Marco Fabiani, Katia Margiotti, et al. · Fetal and Pediatric Pathology · 1
Development of Mek inhibition (MEK-I)-Based Therapeutic Strategies in Acute Myeloid Leukemia (AML)
2008 · Michele Milella, Maria Rosaria Ricciardi, et al. · Blood · 1
Extended Non‐Invasive Prenatal Testing for Chromosomal and Monogenic Disorders by Cell‐Free DNA Sequencing: A Blinded Comparison With Amniocentesis
2026 · Alvaro Mesoraca, Katia Margiotti, et al. · Prenatal Diagnosis
Prenatal Diagnosis and Genotype-Phenotype Correlation in 8q21.11 Microdeletion Syndrome: A Case Report
2026 · Francesco Libotte, Katia Margiotti, et al. · International Medical Case Reports Journal
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Pathogenic KCNH2 variant in monozygotic twins with speech delay and lower risk type 2 long QT syndrome
2025 · Katia Margiotti, Marco Fabiani, et al. · Neurogenetics
Correction: Uniparental disomy (UPD) exclusion in embryos following Preimplantation Genetic Testing for Structural Rearrangements (PGT-SR)
2025 · Marco Fabiani, Katia Margiotti, et al. · Journal of Assisted Reproduction and Genetics
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Uniparental disomy (UPD) exclusion in embryos following Preimplantation Genetic Testing for Structural Rearrangements (PGT-SR)
2024 · Marco Fabiani, Katia Margiotti, et al. · Journal of Assisted Reproduction and Genetics
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Multiple Strategies Based on MEK, mTOR and BCL-2 Signal Transduction Inhibition in Acute Lymphoblastic Leukemia (ALL)
2008 · Maria Rosaria Ricciardi, Samantha Decandia, et al. · Blood
BCL-2/BCL-XL Inhibition in Smoldering Multiple Myeloma CD138+ Cells: Functional Effects and Protein Expression Levels
2008 · Francesco Libotte, Maria Rosaria Ricciardi, et al. · Blood
Works count: 19
Citation count: 52
H-index: 5
I10-index: 1
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