Elisa Fermo

3.6k total citations
93 papers, 2.0k citations indexed

About

Elisa Fermo is a scholar working on Physiology, Hematology and Genetics. According to data from OpenAlex, Elisa Fermo has authored 93 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Physiology, 41 papers in Hematology and 37 papers in Genetics. Recurrent topics in Elisa Fermo's work include Erythrocyte Function and Pathophysiology (70 papers), Hemoglobinopathies and Related Disorders (25 papers) and Neonatal Health and Biochemistry (24 papers). Elisa Fermo is often cited by papers focused on Erythrocyte Function and Pathophysiology (70 papers), Hemoglobinopathies and Related Disorders (25 papers) and Neonatal Health and Biochemistry (24 papers). Elisa Fermo collaborates with scholars based in Italy, Netherlands and Germany. Elisa Fermo's co-authors include Paola Bianchi, Alberto Zanella, Cristina Vercellati, Wilma Barcellini, Giovanna Valentini, Anna Paola Marcello, Agostino Cortelezzi, Laurent R. Chiarelli, Alessandra Iurlo and Anna Zaninoni and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Elisa Fermo

88 papers receiving 2.0k citations

Peers

Countries citing papers authored by Elisa Fermo

Since Specialization

Citations

This map shows the geographic impact of Elisa Fermo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Elisa Fermo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elisa Fermo more than expected).

Fields of papers citing papers by Elisa Fermo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elisa Fermo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Elisa Fermo. The network helps show where Elisa Fermo may publish in the future.

Co-authorship network of co-authors of Elisa Fermo

This figure shows the co-authorship network connecting the top 25 collaborators of Elisa Fermo. A scholar is included among the top collaborators of Elisa Fermo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Elisa Fermo. Elisa Fermo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Not-So-Rare Defects of RBC Lipidic Composition: Four New Cases of Flippase Deficiency Due to ATP11C Mutations 2025 ·International Journal of Molecular Sciences ·Elisa Fermo, Elena Trombetta, Anna Paola Marcello, Cristina Vercellati, Giulia Ferrari, Anna Zaninoni, Valentina Brancaleoni, Elena Di Pierro, (unknown), (unknown), Bruno Fattizzo, Tommaso Casini, Paola Corti, Paola Bianchi	0
2	Diagnosis of Diamond-Blackfan anemia in adulthood: case series and review of the literature 2024 ·Orphanet Journal of Rare Diseases ·(unknown), Paola Bianchi, Elisa Fermo, Wilma Barcellini, Bruno Fattizzo	1
3	Toward the Creation of Diagnostic Algorithms for Congenital Hemolytic Anemia Using Advanced Parameters from Modern Hematology Analyzers 2024 ·Blood ·Paola Bianchi, (unknown), Cristina Vercellati, Elisa Fermo, (unknown), Anna Paola Marcello, Anna Zaninoni, Nadia Mirra, (unknown), (unknown), (unknown), Francesco Passamonti, Wilma Barcellini, Matteo Vidali, (unknown)	0
4	Pathological and genomic features of myeloproliferative neoplasms associated with splanchnic vein thrombosis in a single-center cohort 2023 ·Annals of Hematology ·Daniele Cattaneo, Cristina Bucelli, Alfredo Marchetti, Marta Lionetti, Elisa Fermo, (unknown), (unknown), Akihiro Maeda, (unknown), Massimo Primignani, Dario Consonni, Umberto Gianelli, Antonino Neri, Luca Baldini, Niccolò Bolli, Alessandra Iurlo	9
5	Biochemical and Metabolomic Analysis of Glycolytic Activity in Red Blood Cells from Low-Risk Myelodysplastic Syndromes (LR-MDS) Patients and in-Vitro Effect of the Pyruvate Kinase Activator AG-946 2023 ·Blood ·Bruno Fattizzo, Cristina Vercellati, Anna Paola Marcello, (unknown), Megan Wind‐Rotolo, (unknown), Marcella Bonanomi, Daniela Gaglio, (unknown), Elisa Fermo, Paola Bianchi, Anna Zaninoni, Wilma Barcellini	2
6	Six novel variants in the PKLR gene associated with pyruvate kinase deficiency in Argentinian patients 2021 ·Clinical Biochemistry ·(unknown), Carolina Pepe, Lucas A. Defelipe, (unknown), (unknown), (unknown), (unknown), (unknown), Diego Fernández-Rodríguez, (unknown), (unknown), Adrián G. Turjanski, Paola Bianchi, Elisa Fermo, (unknown)	6
7	Red blood cell phenotyping from 3D confocal images using artificial neural networks 2021 ·PLoS Computational Biology ·Greta Simionato, (unknown), (unknown), Paola Bianchi, Elisa Fermo, Richard van Wijk, (unknown), Christian Wagner, Lars Kaestner, (unknown)	25
8	Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo 2019 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Bartholomew P. Roland, (unknown), (unknown), (unknown), (unknown), Tien‐Chien Chang, (unknown), Paola Bianchi, Elisa Fermo, Bianca Maria Ricerca, Luca Tortorolo, Jerry Vockley, Andrew P. VanDemark, Michael J. Palladino	15
9	Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases 2019 ·Frontiers in Physiology ·Elisa Fermo, Cristina Vercellati, Anna Paola Marcello, Anna Zaninoni, Selin Aytaç, Mualla Çetin, (unknown), Maddalena Casale, Sabrina Paci, Alberto Zanella, Wilma Barcellini, Paola Bianchi	21
10	The Role of New Technologies in Myeloproliferative Neoplasms 2019 ·Frontiers in Oncology ·Giuseppe A. Palumbo, Stefania Stella, Maria Stella Pennisi, (unknown), Elisa Fermo, Sonia Fabris, Daniele Cattaneo, Alessandra Iurlo	35
11	Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients 2018 ·Frontiers in Physiology ·Anna Zaninoni, Elisa Fermo, Cristina Vercellati, Dario Consonni, Anna Paola Marcello, Alberto Zanella, Agostino Cortelezzi, Wilma Barcellini, Paola Bianchi	58
12	Chromosome 7q31.1 deletion in myeloid neoplasms 2013 ·Human Pathology ·P. Tripputi, Paola Bianchi, Elisa Fermo, (unknown), Alberto Zanella	3
13	A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: Molecular and functional characterization 2012 ·Molecular Genetics and Metabolism ·Elisa Fermo, Paola Bianchi, Laurent R. Chiarelli, Maristella Maggi, (unknown), Cristina Vercellati, Anna Paola Marcello, Wilma Barcellini, Agostino Cortelezzi, Giovanna Valentini, Alberto Zanella	27
14	Molecular Insights on Pathogenic Effects of Mutations Causing Phosphoglycerate Kinase Deficiency 2012 ·PLoS ONE ·Laurent R. Chiarelli, (unknown), Paola Bianchi, Elisa Fermo, Alberto Zanella, Alessandro Galizzi, Giovanna Valentini	63
15	Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics 2011 ·Haematologica ·Paola Bianchi, Elisa Fermo, Cristina Vercellati, Anna Paola Marcello, Laura Porretti, Agostino Cortelezzi, Wilma Barcellini, Andréa Zanella	125
16	RAS Mutations Contribute to Evolution of Chronic Myelomonocytic Leukemia to the Proliferative Variant 2010 ·Clinical Cancer Research ·Clara Ricci, Elisa Fermo, Stefania Corti, Mauro Molteni, (unknown), Agostino Cortelezzi, Giorgio La Nasa, Miloslav Beran, Francesco Onida	99
17	CDAII presenting as hydrops foetalis: Molecular characterization of two cases 2010 ·Blood Cells Molecules and Diseases ·Elisa Fermo, Paola Bianchi, Lucia Dora Notarangelo, (unknown), Cristina Vercellati, Anna Paola Marcello, Carla Boschetti, Wilma Barcellini, Alberto Zanella	23
18	Molecular basis of pyrimidine 5′-nucleotidase deficiency caused by 3 newly identified missense mutations (c.187T>C, c.469G>C and c.740T>C) and a tabulation of known mutations 2007 ·Blood Cells Molecules and Diseases ·Laurent R. Chiarelli, (unknown), Alessandro Galizzi, Elisa Fermo, Alberto Zanella, Giovanna Valentini	6
19	A new variant of adenylate kinase (delG138) associated with severe hemolytic anemia 2004 ·Blood Cells Molecules and Diseases ·Elisa Fermo, Paola Bianchi, Cristina Vercellati, (unknown), Anna Paola Marcello, (unknown), Alberto Zanella	6
20	Molecular characterization of six unrelated Italian patients affected by pyrimidine 5′‐nucleotidase deficiency 2003 ·British Journal of Haematology ·Paola Bianchi, Elisa Fermo, Fiorella Alfinito, Cristina Vercellati, Mariangiola Baserga, (unknown), (unknown), Bruno Rotoli, (unknown)	18

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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