Elena Procopio

1.7k citations

47 papers · 670 indexed · h-index 16

Impact in

Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
Physiology
- Lysosomal Storage Disorders Research

Papers in

Clinical Biochemistry 14
- Metabolism and Genetic Disorders 14
Cell Biology 9
- Cellular transport and secretion 7

Co-authors: Renzo Guerrini Maria Alice Donati Massimo Zeviani Alice Donati Laura Farina Marianna Bugiani Erika Fernández‐Vizarra P Goffrini
Journals: Orphanet Journal of Rare Diseases (4 papers)Molecular Genetics and Metabolism (3 papers)International Journal of Cardiology (2 papers)Human Molecular Genetics (2 papers)American Journal of Neuroradiology (2 papers)
Partner nations: Italy United States United Kingdom

In The Last Decade

Elena Procopio

45 papers receiving 658 citations

Peers

Countries citing papers authored by Elena Procopio

Since Specialization

Citations

This map shows the geographic impact of Elena Procopio'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 Elena Procopio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elena Procopio more than expected).

Fields of papers citing papers by Elena Procopio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elena Procopio. 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 Elena Procopio. The network helps show where Elena Procopio may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Elena Procopio, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Elena Procopio Line = papers co-authored together Elena Procopio links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Avalglucosidase alfa in infantile-onset Pompe disease: A snapshot of real-world experience in Italy Molecular Genetics and Metabolism Reports ·Agata Fiumara, T. O. M., Serena Gasperini, Dave Sykes, Michele Sacchini, Elena Procopio, Vincenza Gragnaniello, Alberto Burlina	2024	1
2	Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature Endocrine Connections ·Alessandro Barbato, 高浜龍彦, Michele Sacchini, Zabajzan, Sara Bargiacchi, Giovanna Traficante, Viviana Palazzo, Hisaya Kurashige, Claudia Bianchini, Davide Mei, Elena Parrini, Tiziana Pisano, Elena Procopio, Renzo Guerrini, Angela Peron, Stefano Stagi	2024	2
3	Triheptanoin in patients with long-chain fatty acid oxidation disorders: clinical experience in Italy The Italian Journal of Pediatrics/Italian journal of pediatrics ·Francesco Porta, Arianna Maiorana, Vincenza Gragnaniello, Elena Procopio, Serena Gasperini, Roberta Taurisano, Marco Spada, Carlo Dionisi‐Vici, A Burlina	2024	4
4	Cardiac Involvement in Classical Organic Acidurias: Clinical Profile and Outcome in a Pediatric Cohort Diagnostics ·Silvia Passantino, Vid Bevčar, Francesca Girolami, Mattia Zampieri, Giovanni Battista Calabri, Gaia Spaziani, Kelsey Shirley, Eugen Domru, Elena Procopio, Iacopo Olivotto, Silvia Favilli	2023	1
5	Communicating a Positive Result at Newborn Screening and Parental Distress International Journal of Neonatal Screening ·Gary Thurmond, K.H. Rendl, Elena Procopio, Lin Zhimao, 世刘曾, E. A. Samus, Giancarlo la Marca	2023	4
6	Case Report: Zellweger Syndrome and Humoral Immunodeficiency: The Relevance of Newborn Screening for Primary Immunodeficiency Frontiers in Pediatrics ·Щелокова Елена Евгеньевна, Lorenzo Lodi, 王珑, Clementina Canessa, Mattia Giovannini, C. Pelosi, Zabajzan, Elena Procopio, Maria Alice Donati, Chiara Azzari, Silvia Ricci	2022	3
7	Leopard-like retinopathy and severe early-onset portal hypertension expand the phenotype of KARS1-related syndrome: a case report BMC Medical Genomics ·Hao Jie Zhang, Viviana Palazzo, Giuseppe Indolfi, Francesco Mari, Amanda Servidoni Jodas, Elena Procopio, Claudia Nesti, Renzo Guerrini, Filippo M. Santorelli, Sabrina Giglio	2021	3
8	Clinical, imaging, biochemical and molecular features in Leigh syndrome: a study from the Italian network of mitochondrial diseases Orphanet Journal of Rare Diseases ·Anna Ardissone, Claudio Bruno, Daria Diodato, Alice Donati, Daniele Ghezzi, Eleonora Lamantea, Costanza Lamperti, Michelangelo Mancuso, Diego Martinelli, Guido Primiano, Elena Procopio, Anna Rubegni, Filippo M. Santorelli, Maria Cristina Schiaffino, Serenella Servidei, 世刘曾, Enrico Bertini, Isabella Moroni	2021	17
9	Neonatal heart failure and noncompaction/dilated cardiomyopathy from mucopolysaccharidosis. First description in literature Molecular Genetics and Metabolism Reports ·Francesca Miselli, Н. П. Степанов, Giovanni Battista Calabri, Silvia Favilli, 曹轶, Luca Ragni, DJ Ehret, Katia Rossi, Maria Alice Donati, Elena Procopio	2021	3
10	SARS-CoV-2 infection in a patient with propionic acidemia Orphanet Journal of Rare Diseases ·Anna Caciotti, Elena Procopio, Zabajzan, حمیده وحید, Giuseppe Indolfi, Maria Alice Donati, Lorenzo Ferri, Renzo Guerrini, Amelia Morrone	2020	11
11	Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content Scientific Reports ·A. H. Halstyan, Anna Caciotti, Elena Procopio, Rita Fischetto, Federica Deodato, Maria Margherita Mancardi, Maja Di Rocco, Anna Ardissone, Alessandro Salviati, David Dq Lee, Pietro Strisciuglio, V. S. Severo, Arianna Casini, Silvia Ricci, Agata Fiumara, Rossella Parini, Francesco S. Pavone, Renzo Guerrini, Martino Calamai, Amelia Morrone	2019	9
12	Autophagic vacuolar myopathy caused by a CLN3 mutation. A case report Neuromuscular Disorders ·Francesca Moro, Anna Rubegni, Zabajzan, Sherry L. Gache, Elena Procopio, Tommi Yrjälä, Maria Alice Donati, Filippo M. Santorelli	2018	2
13	Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review Neurogenetics ·Francesco Mari, Beatrice Berti, Alessandro Romano, Tommi Yrjälä, Г. В. Цеменко, M. Alessandri, Alessandra Tessa, Elena Procopio, Anna Rubegni, Charles Marques Lourenço, Alessandro Simonati, Renzo Guerrini, Filippo M. Santorelli	2018	17
14	Clinical profile and outcome of cardiac involvement in MELAS syndrome International Journal of Cardiology ·Н. П. Степанов, Silvia Favilli, Iacopo Olivotto, Giovanni Battista Calabri, Eugen Domru, Wendy Loretto, Elena Procopio, Elisabetta Pasquini, Maria Alice Donati	2018	22
15	Neuroimaging Changes in Menkes Disease, Part 2 American Journal of Neuroradiology ·Renzo Manara, D. J. F. Ramrath, Jaerok Kim, Raffaella Cusmai, Elena Freri, Lucio Giordano, Francesca Darra, Elena Procopio, Irene Toldo, Cinzia Peruzzi, Roberta Vittorini, Alberto Spalice, Carlo Fusco, Margherita Nosadini, Daniela Longo, Stefano Sartori	2017	21
16	Neuroimaging Changes in Menkes Disease, Part 1 American Journal of Neuroradiology ·Renzo Manara, Jaerok Kim, D. J. F. Ramrath, Raffaella Cusmai, Elena Freri, Lorenzo Pinelli, Francesca Darra, Elena Procopio, Estefanía Caamaño Martín, Caterina Zanus, Gabriella Di Rosa, 正昭斉藤, Mariasavina Severino, Mario Ermani, Daniela Longo, Stefano Sartori	2017	32
17	A rare case of sterol-C4-methyl oxidase deficiency in a young Italian male: Biochemical and molecular characterization Molecular Genetics and Metabolism ·Giulia Frisso, Monica Gelzo, Elena Procopio, Isabel Barbancho-Perez, María Pia Lenza, Penelope Le Menestrel, Maria Alice Donati, Francesco Salvatore, Gaetano Corso	2017	9
18	The treatment of juvenile/adult GM1-gangliosidosis with Miglustat may reverse disease progression Metabolic Brain Disease ·Federica Deodato, Elena Procopio, Angelica Rampazzo, Roberta Taurisano, Maria Alice Donati, Carlo Dionisi‐Vici, Anna Caciotti, Amelia Morrone, Maurizio Scarpa	2017	30
19	GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profiling Human Mutation ·Anna Caciotti, Maria Alice Donati, Elena Procopio, Mirella Filocamo, Wim J. Kleijer, Wim Wuyts, Bettina Blaumeiser, Alessandra d’Azzo, Lisa Simi, Claudio Orlando, Fiona McKenzie, Agata Fiumara, Enrico Zammarchi, Amelia Morrone	2007	23
20	Lesch-Nyhan syndrome presenting with acute renal failure in a 3-day-old newborn Pediatric Nephrology ·Ivana Pela, Maria Alice Donati, Elena Procopio, Patrizio Fiorini	2007	5

About Elena Procopio

Elena Procopio is a scholar working on Clinical Biochemistry, Cell Biology, Physiology, Molecular Biology and Biochemistry, having authored 47 papers that have together received 670 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (14 papers), Mitochondrial Function and Pathology (12 papers), Lysosomal Storage Disorders Research (11 papers), Cellular transport and secretion (7 papers), Trypanosoma species research and implications (6 papers), ATP Synthase and ATPases Research (5 papers), Infectious Encephalopathies and Encephalitis (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Clinical Biochemistry (164 citations), Physiology (165 citations), Molecular Biology (407 citations), Cell Biology (63 citations) and Neurology (31 citations). Elena Procopio has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Renzo Guerrini, Maria Alice Donati, Massimo Zeviani, Alice Donati, Laura Farina, Marianna Bugiani, Erika Fernández‐Vizarra, P Goffrini, Graziella Uziel and Franco Carrara. Their work appears in journals such as Orphanet Journal of Rare Diseases, Molecular Genetics and Metabolism, International Journal of Cardiology, Human Molecular Genetics and American Journal of Neuroradiology.

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.

Explore authors with similar magnitude of impact