Roberta Russo (R Russo)

ResearcherID Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 39

Top Venues

American journal of hematology

Genes

International journal of molecular sciences

Blood advances

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

Italy

Researcher in tenure track :: Medicina Molecolare e Biotecnologie Mediche

Università degli Studi di Napoli Federico II

Italy

Cooperation contract :: Medicina Molecolare e Biotecnologie Mediche

Università degli Studi di Napoli Federico II

Italy

Research Fellow :: Medicina Molecolare e Biotecnologie Mediche

CEINGE Biotecnologie Avanzate Sca r l

Italy

Cooperation contract

Università degli Studi di Napoli Federico II

Italy

Graduated fellow :: Biochimica e Biotecnologie Mediche

Università degli Studi di Napoli Federico II

Italy

Cooperation contract :: Endocrinologia Clinica Molecolare e Oncologia

Seconda Università degli Studi di Napoli

Italy

Graduated fellow :: Medicina- Chirurgia Clinica e Sperimentale Internisti "F.Magrassi e A.Lanzara"

CEINGE Biotecnologie Avanzate Sca r l

Italy

Cooperation contract

Education History

Università degli Studi di Napoli Federico II Oct 01 2013 - May 03 2016

Italy

PHD :: Medicina Molecolare e Biotecnologie Mediche

Publications

Roberta Russo, Achille Iolascon, Immacolata Andolfo, Roberta Marra, Barbara Eleni Rosato
Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias. International journal of laboratory hematology (2024)
Roberta Marra, Antonella Nostroso, Barbara Eleni Rosato, Federica Maria Esposito, Vanessa D'Onofrio, Anthony Iscaro, Antonella Gambale, Barbara Bruschi, Paola Coccia, Antonella Poloni, Sule Unal, Alberto Romano, Achille Iolascon, Immacolata Andolfo, Roberta Russo
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients. American journal of hematology 99 (8) (2024)
Achille Iolascon, Immacolata Andolfo, Roberta Russo, Mayka Sanchez, Fabiana Busti, Dorine Swinkels, Patricia Aguilar Martinez, Rayan Bou-Fakhredin, Martina U Muckenthaler, Sule Unal, Graça Porto, Tomas Ganz, Antonis Kattamis, Lucia De Franceschi, Maria Domenica Cappellini, Malcolm G Munro, Ali Taher, null null
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia. HemaSphere 8 (7) (2024)
Achille Iolascon, Immacolata Andolfo, Roberta Russo, Mayka Sanchez, Fabiana Busti, Dorine Swinkels, Patricia Aguilar Martinez, Rayan Bou-Fakhredin, Martina U Muckenthaler, Sule Unal, Graça Porto, Tomas Ganz, Antonis Kattamis, Lucia De Franceschi, Maria Domenica Cappellini, Malcolm G Munro, Ali Taher, null null
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia. HemaSphere 8 (7) (2024)
Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Roberta Russo, Achille Iolascon, Immacolata Andolfo, Roberta Marra, Barbara Eleni Rosato
Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias. International journal of laboratory hematology 46 (4) (2024)
Roberta Marra, Antonella Nostroso, Barbara Eleni Rosato, Federica Maria Esposito, Vanessa D'Onofrio, Anthony Iscaro, Antonella Gambale, Barbara Bruschi, Paola Coccia, Antonella Poloni, Sule Unal, Alberto Romano, Achille Iolascon, Immacolata Andolfo, Roberta Russo
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients. American journal of hematology (2024)
Roberta Marra, Antonella Nostroso, Barbara Eleni Rosato, Federica Maria Esposito, Vanessa D'Onofrio, Anthony Iscaro, Antonella Gambale, Barbara Bruschi, Paola Coccia, Antonella Poloni, Sule Unal, Alberto Romano, Achille Iolascon, Immacolata Andolfo, Roberta Russo
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patients. American journal of hematology 99 (8) (2024)
Enrico Attardi, Immacolata Andolfo, Roberta Russo, Lucia Tiberi, Marco Gabriele Raddi, Barbara Eleni Rosato, Roberta Marra, Daniela Formicola, Federica Del Giudice, Alice Brogi, Angela Consagra, Cristina Amato, Alessandro Sanna, Rosangela Artuso, Achille Iolascon, Valeria Santini
PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes. American journal of hematology 98 (4) (2023)
Enrico Attardi, Immacolata Andolfo, Roberta Russo, Lucia Tiberi, Marco Gabriele Raddi, Barbara Eleni Rosato, Roberta Marra, Daniela Formicola, Federica Del Giudice, Alice Brogi, Angela Consagra, Cristina Amato, Alessandro Sanna, Rosangela Artuso, Achille Iolascon, Valeria Santini
PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes. American journal of hematology 98 (4) (2023)
E Attardi, I Andolfo, Roberta Russo, L Tiberi, M G Raddi, B E Rosato, R Marra, D Formicola, F Del Giudice, A Brogi, A Consagra, C Amato, Alessandro Sanna, R Artuso, A Iolascon, Valeria Santini
PIEZO1 mutations impact on early clinical manifestations of Myelodysplastic Syndromes. American journal of hematology (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)
Enrico Attardi, Immacolata Andolfo, Roberta Russo, Lucia Tiberi, Marco Gabriele Raddi, Barbara Eleni Rosato, Roberta Marra, Daniela Formicola, Federica Del Giudice, Alice Brogi, Angela Consagra, Cristina Amato, Alessandro Sanna, Rosangela Artuso, Achille Iolascon, Valeria Santini
PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes. American journal of hematology (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)
Enrico Attardi, Immacolata Andolfo, Roberta Russo, Lucia Tiberi, Marco Gabriele Raddi, Barbara Eleni Rosato, Roberta Marra, Daniela Formicola, Federica Del Giudice, Alice Brogi, Angela Consagra, Cristina Amato, Alessandro Sanna, Rosangela Artuso, Achille Iolascon, Valeria Santini
PIEZO1 mutations impact on early clinical manifestations of myelodysplastic syndromes. American journal of hematology 98 (4) (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)
Immacolata Andolfo, Roberta Russo
Novel Insights and Future Perspective in Iron Metabolism and Anemia. Metabolites 12 (2) (2022)
Barbara Eleni Rosato, Roberta Marra, Vanessa D'Onofrio, Federica Del Giudice, Simone Della Monica, Achille Iolascon, Immacolata Andolfo, Roberta Russo
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells. International journal of molecular sciences 23 (3) (2022)
Sueva Cantalupo, Vito Alessandro Lasorsa, Roberta Russo, Immacolata Andolfo, Giuseppe D'Alterio, Barbara Eleni Rosato, Giulia Frisso, Pasquale Abete, Gian Marco Cassese, Giuseppe Servillo, Ivan Gentile, Carmelo Piscopo, Matteo Della Monica, Giuseppe Fiorentino, Giuseppe Russo, Pellegrino Cerino, Carlo Buonerba, Bianca Maria Pierri, Massimo Zollo, Achille Iolascon, Mario Capasso
Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19. International journal of molecular sciences 22 (10) (2021)
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)
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)
Gianluca De Rosa, Immacolata Andolfo, Roberta Marra, Francesco Manna, Barbara Eleni Rosato, Achille Iolascon, Roberta Russo
RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway. International journal of molecular sciences 21 (15) (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)
Immacolata Andolfo, Roberta Russo, Antonella Gambale, Achille Iolascon
Hereditary stomatocytosis: An underdiagnosed condition. American journal of hematology 93 (1) (2017)
Arwa Z Al-Riyami, Achille Iolascon, Shoaib Al-Zadjali, Immacolata Andolfo, Sahima Al-Mammari, Francesco Manna, AbdulHakim Al Rawas, May-Jean King, Roberta Russo
Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis. American journal of hematology 92 (10) (2017)
Roberta Russo, Immacolata Andolfo, Francesco Manna, Gianluca De Rosa, Luigia De Falco, Antonella Gambale, Mariasole Bruno, Alessandro Mattè, Paolo Ricchi, Domenico Girelli, Lucia De Franceschi, Achille Iolascon
Increased levels of ERFE-encoding FAM132B in patients with congenital dyserythropoietic anemia type II. Blood 128 (14) (2016)

Roberta Russo.css-eqlu8i{font-size:small;padding-left:4px;} (R Russo)

Publication Activity (10 Years)

Top Topics

Top Venues

Roberta Russo (R Russo)