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Immacolata Andolfo

ResearcherID Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 20

Top Venues

American journal of hematology

Blood advances

Genes

British journal of haematology

Università degli Studi di Napoli Federico II

Università degli Studi di Napoli Federico II (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Università degli Studi di Napoli Federico II Dec 31o 2007 - Jan 1o 2009

Italy

Graduated fellow :: Department of Biochemistry and Medical Biotechnologies

Education History

Università degli Studi di Napoli Federico II - May 16o 2017

Italy

PHD :: Dep. Molecular Medicine and Medical biotchnologies

Publications

Valeria Maria Pinto, Roberta Russo, Sabrina Quintino, Barbara Eleni Rosato, Roberta Marra, Federica Del Giudice, Massimo Mogni, Massimo Maffei, Achille Iolascon, Gian Luca Forni, Immacolata Andolfo
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers. American journal of hematology (2023)
Immacolata Andolfo, Vittoria Monaco, Flora Cozzolino, Barbara Eleni Rosato, Roberta Marra, Vincenza Cerbone, Valeria Maria Pinto, Gian Luca Forni, Sule Unal, Achille Iolascon, Maria Monti, Roberta Russo
Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations. Blood advances (2023)
Valeria Maria Pinto, Roberta Russo, Sabrina Quintino, Barbara Eleni Rosato, Roberta Marra, Federica Del Giudice, Massimo Mogni, Massimo Maffei, Achille Iolascon, Gian Luca Forni, Immacolata Andolfo
Coinheritance of PIEZO1 variants and multi-locus red blood cell defects account for the symptomatic phenotype in beta-thalassemia carriers. American journal of hematology (2023)
Immacolata Andolfo, Vittoria Monaco, Flora Cozzolino, Barbara Eleni Rosato, Roberta Marra, Vincenza Cerbone, Valeria Maria Pinto, Gian Luca Forni, Sule Unal, Achille Iolascon, Maria Monti, Roberta Russo
Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations. Blood advances (2023)
Noémi B A Roy, Lydie Da Costa, Roberta Russo, Paola Bianchi, Maria Del Mar Mañú-Pereira, Elisa Fermo, Immacolata Andolfo, Barnaby Clark, Melanie Proven, Mayka Sanchez, Richard van Wijk, Bert van der Zwaag, Mark Layton, David C Rees, Achille Iolascon, null null
The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper. British journal of haematology 198 (3) (2022)
Achille Iolascon, Paola Bianchi, Immacolata Andolfo, Roberta Russo, Wilma Barcellini, Elisa Fermo, Gergely Toldi, Stefano Ghirardello, Davis Rees, Richard Van Wijk, Antonis Kattamis, Patrick G Gallagher, Noemi Roy, Ali T Taher, Razan Mohty, Andreas Kulozik, Lucia De Franceschi, Antonella Gambale, Mariane De Montalembert, Gian Luca Forni, Cornelis L Harteveld, Josef Prchal, null null
Recommendations for diagnosis and treatment of methemoglobinemia. American journal of hematology 96 (12) (2021)
Roberta Russo, Immacolata Andolfo, Vito Alessandro Lasorsa, Sueva Cantalupo, Roberta Marra, Giulia Frisso, Pasquale Abete, Gian Marco Cassese, Giuseppe Servillo, Gabriella Esposito, Gentile Ivan, Carmelo Piscopo, Matteo Della Monica, Giuseppe Fiorentino, Giuseppe Russo, Pellegrino Cerino, Carlo Buonerba, Bianca Maria Pierri, Massimo Zollo, Achille Iolascon, Mario Capasso
The TNFRSF13C H159Y Variant Is Associated with Severe COVID-19: A Retrospective Study of 500 Patients from Southern Italy. Genes 12 (6) (2021)
Immacolata Andolfo, Seth L Alper, Achille Iolascon
Nobel prize in physiology or medicine 2021, receptors for temperature and touch: Implications for hematology. American journal of hematology (2021)
Marianna Caterino, Michele Costanzo, Roberta Fedele, Armando Cevenini, Monica Gelzo, Alessandro Di Minno, Immacolata Andolfo, Mario Capasso, Roberta Russo, Anna Annunziata, Cecilia Calabrese, Giuseppe Fiorentino, Maurizio D'Abbraccio, Chiara Dell'Isola, Francesco Maria Fusco, Roberto Parrella, Gabriella Fabbrocini, Gentile Ivan, Giuseppe Castaldo, Margherita Ruoppolo
The Serum Metabolome of Moderate and Severe COVID-19 Patients Reflects Possible Liver Alterations Involving Carbon and Nitrogen Metabolism. International journal of molecular sciences 22 (17) (2021)
Immacolata Andolfo, Stefania Martone, Barbara Eleni Rosato, Roberta Marra, Antonella Gambale, Gian Luca Forni, Valeria Maria Pinto, Magnus Göransson, Vasiliki Papadopoulou, Mathilde Gavillet, Mohsen S Elalfy, Antonella Panarelli, Giovanna Tomaiuolo, Achille Iolascon, Roberta Russo
Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients. Genes 12 (7) (2021)
Immacolata Andolfo, Vito A Lasorsa, Francesco Manna, Barbara E Rosato, Daniela Formicola, Achille Iolascon, Mario Capasso
Kinome multigenic panel identified novel druggable EPHB4-V871I somatic variant in high-risk neuroblastoma. Journal of cellular and molecular medicine 24 (11) (2020)
Roberta Russo, Roberta Marra, Immacolata Andolfo, Francesco Manna, Gianluca De Rosa, Barbara Eleni Rosato, Kottayam Radhakrishnan, Michael Fahey, Achille Iolascon
Uridine treatment normalizes the congenital dyserythropoietic anemia type II-like hematological phenotype in a patient with homozygous mutation in the CAD gene. American journal of hematology 95 (11) (2020)
Immacolata Andolfo, Barbara Eleni Rosato, Francesco Manna, Gianluca De Rosa, Roberta Marra, Antonella Gambale, Domenico Girelli, Roberta Russo, Achille Iolascon
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathway. American journal of hematology 95 (2) (2019)
Achille Iolascon, Immacolata Andolfo, Roberta Russo
Advances in understanding the pathogenesis of red cell membrane disorders. British journal of haematology 187 (1) (2019)
Antonella Gambale, Roberta Russo, Immacolata Andolfo, Lucia Quaglietta, Gianluca De Rosa, Valentina Contestabile, Lucia De Martino, Rita Genesio, Piero Pignataro, Sabrina Rita Giglio, Mario Capasso, Rosanna Parasole, Barbara Pasini, Achille Iolascon
Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition. Clinical genetics 96 (4) (2019)
Immacolata Andolfo, Barbara Eleni Rosato, Roberta Marra, Gianluca De Rosa, Francesco Manna, Antonella Gambale, Achille Iolascon, Roberta Russo
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variant. American journal of hematology 94 (11) (2019)
Immacolata Andolfo, Roberta Russo, Barbara Eleni Rosato, Francesco Manna, Antonella Gambale, Carlo Brugnara, Achille Iolascon
Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients. American journal of hematology 93 (12) (2018)
Roberta Russo, Immacolata Andolfo, Francesco Manna, Antonella Gambale, Roberta Marra, Barbara Eleni Rosato, Paola Caforio, Valeria Pinto, Piero Pignataro, Kottayam Radhakrishnan, Sule Unal, Giovanna Tomaiuolo, Gian Luca Forni, Achille Iolascon
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemias. American journal of hematology 93 (5) (2018)
Alessandro Matte, Antonio Recchiuti, Enrica Federti, Bérengère Koehl, Thomas Mintz, Wassim El Nemer, Pierre-Louis Tharaux, Valentine Brousse, Immacolata Andolfo, Alessia Lamolinara, Olga Weinberg, Angela Siciliano, Paul C Norris, Ian R Riley, Achille Iolascon, Charles Nicholas Serhan, Carlo Brugnara, Lucia De Franceschi
Resolution of sickle cell disease-associated inflammation and tissue damage with 17R-resolvin D1. Blood 133 (3) (2018)
Immacolata Andolfo, Roberta Russo, Antonella Gambale, Achille Iolascon
Hereditary stomatocytosis: An underdiagnosed condition. American journal of hematology 93 (1) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Immacolata Andolfo