FM
Francesco Manna
astro-ph.IManemiaC15ORF41CDA (I–III)functional characterization of proteinsgenetic testingMutationMutation, Missense[(177)Lu] Lu-PSMA-I&Tactivin receptor II ligand trap
On Valency
published · living versionsW_7x987qsc·v1 · currentpublished
DAMEWARE: A web cyberinfrastructure for astrophysical data mining
with Massimo Brescia, Stefano Cavuoti, Giuseppe Longo, Alfonso Nocella +12
1 version
Preprints & journals
26 papers in the corpus · 2010–2026[177Lu] Lu-PSMA-I&T for prostate cancer radioligand therapy: A radiopharmacy's journey from synthesis to cost-effectiveness.42696922 · Aurilio, Michela, Maisto, Costantina, Morisco, Anna et al.2026 · 0 citationsApplied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine. 2026;238:112855
Exposure Time Dependence of Operators' Head Entrance Air Kerma in Interventional Radiology Measured by TLD-100H Chips.40573552 · Mottareale, Rocco, Manna, Francesco, Carmosino, Patrizio Antonio et al.2025 · 2 citationsSensors (Basel, Switzerland). 2025;25(12)
Use of Thermoluminescence Dosimetry for QA in High-Dose-Rate Skin Surface Brachytherapy with Custom-Flap Applicator.37050652 · Manna, Francesco, Pugliese, Mariagabriella, Buonanno, Francesca et al.2023 · 2 citationsSensors (Basel, Switzerland). 2023;23(7)
Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene.32720728 · Russo, Roberta, Marra, Roberta, Andolfo, Immacolata et al.2020 · 14 citationsAmerican journal of hematology. 2020;95(11):1423-1426
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.32848870 · Russo, Roberta, Marra, Roberta, Andolfo, Immacolata et al.2020 · 1 citationFrontiers in physiology. 2020;11:940
RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.32759740 · De Rosa, Gianluca, Andolfo, Immacolata, Marra, Roberta et al.2021 · 21 citationsInternational journal of molecular sciences. 2020;21(15)
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus.33256393 · Andolfo, Immacolata, Martone, Stefania, Ribersani, Michela et al.2021 · 9 citationsHaematologica. 2020;105(12):2883-2886
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma.32336043 · Andolfo, Immacolata, Lasorsa, Vito A, Manna, Francesco et al.2021 · 8 citationsJournal of cellular and molecular medicine. 2020;24(11):6459-6471
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway.31737919 · Andolfo, Immacolata, Rosato, Barbara Eleni, Manna, Francesco et al.2020 · 62 citationsAmerican journal of hematology. 2020;95(2):188-197
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant.31400017 · Andolfo, Immacolata, Rosato, Barbara Eleni, Marra, Roberta et al.2020 · 25 citationsAmerican journal of hematology. 2019;94(11):1227-1235
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein.31191338 · Russo, Roberta, Marra, Roberta, Andolfo, Immacolata et al.2020 · 28 citationsFrontiers in physiology. 2019;10:621
PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells.30930797 · Andolfo, Immacolata, De Rosa, Gianluca, Errichiello, Edoardo et al.2020 · 42 citationsFrontiers in physiology. 2019;10:258
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.30187933 · Andolfo, Immacolata, Russo, Roberta, Rosato, Barbara Eleni et al.2019 · 63 citationsAmerican journal of hematology. 2018;93(12):1509-1517
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias.29396846 · Russo, Roberta, Andolfo, Immacolata, Manna, Francesco et al.2019 · 158 citationsAmerican journal of hematology. 2018;93(5):672-682
PIEZO1-R1864H rare variant accounts for a genetic phenotype-modifier role in dehydrated hereditary stomatocytosis.29191841 · Andolfo, Immacolata, Manna, Francesco, De Rosa, Gianluca et al.2019 · 25 citationsHaematologica. 2018;103(3):e94-e97
Kinome expression profiling of human neuroblastoma tumors identifies potential drug targets for ultra high-risk patients.28968651 · Russo, Roberta, Cimmino, Flora, Pezone, Lucia et al.2017 · 23 citationsCarcinogenesis. 2017;38(10):1011-1020
Data demonstrating the role of peroxiredoxin 2 as important anti-oxidant system in lung homeostasis.29034295 · Federti, Enrica, Matte, Alessandro, Ghigo, Alessandra et al.2020 · 0 citationsData in brief. 2017;15:376-381
Peroxiredoxin-2 plays a pivotal role as multimodal cytoprotector in the early phase of pulmonary hypertension.28801243 · Federti, Enrica, Matté, Alessandro, Ghigo, Alessandra et al.2018 · 33 citationsFree radical biology & medicine. 2017;112:376-386
Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis.28699249 · Al-Riyami, Arwa Z, Iolascon, Achille, Al-Zadjali, Shoaib et al.2017 · 8 citationsAmerican journal of hematology. 2017;92(10):E607-E609
GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II.28550189 · Russo, Roberta, Andolfo, Immacolata, Gambale, Antonella et al.2018 · 19 citationsHaematologica. 2017;102(9):e371-e374
Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II.27540014 · Russo, Roberta, Andolfo, Immacolata, Manna, Francesco et al.2018 · 30 citationsBlood. 2016;128(14):1899-1902
Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemia.27151991 · Andolfo, Immacolata, Russo, Roberta, Manna, Francesco et al.2017 · 41 citationsHaematologica. 2016;101(8):909-17
DAMEWARE - Data Mining & Exploration Web Application Resource1603.00720v2 · Massimo Brescia, Stefano Cavuoti, Francesco Esposito et al.2016 · 1 citationarXiv
Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).26178367 · Andolfo, Immacolata, Russo, Roberta, Manna, Francesco et al.2015 · 99 citationsAmerican journal of hematology. 2015;90(10):921-6
DAMEWARE: A web cyberinfrastructure for astrophysical data mining1406.3538v1 · Massimo Brescia, Stefano Cavuoti, Giuseppe Longo et al.2014 · 18 citationsarXivon Valency
DAME: A Web Oriented Infrastructure for Scientific Data Mining & Exploration1010.4843v2 · Massimo Brescia, Giuseppe Longo, George S. Djorgovski et al.2010 · 4 citationsarXiv
Career total: 32 works. 26 are in this corpus.
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