Marcello Bellusci

422 total citations
18 papers, 177 citations indexed

About

Marcello Bellusci is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marcello Bellusci has authored 18 papers receiving a total of 177 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marcello Bellusci's work include Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (5 papers) and Coenzyme Q10 studies and effects (3 papers). Marcello Bellusci is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (5 papers) and Coenzyme Q10 studies and effects (3 papers). Marcello Bellusci collaborates with scholars based in Spain, Italy and United Kingdom. Marcello Bellusci's co-authors include Luca De Palma, Federico Vigevano, Nicola Specchio, Marina Trivisano, Nicola Pietrafusa, Elena Martín‐Hernández, María Elena Rodríguez‐García, Francisco Martı́nez-Azorı́n, Miguel A. Martı́n and Chun‐An Chen and has published in prestigious journals such as Epilepsia, Human Mutation and The Pediatric Infectious Disease Journal.

In The Last Decade

Marcello Bellusci

16 papers receiving 174 citations

Peers

Marcello Bellusci

GENET

PHYSI

RHEUM

Elisenda Cortès‐Saladelafont Spain

Àngels García Cazorla Spain

Laura A. Tseng Netherlands

Marianna Pezzella Italy

Berit Woldseth Norway

K. Vande Kerckhove Belgium

James R. Bonham United Kingdom

Omar Hikmat Norway

Clarisa Maxit Argentina

C. Whitehouse United Kingdom

Elisenda Cortès‐Saladelafont Spain

Marcello Bellusci

99 ×1.3

111 ×2.5

47 ×1.3

GENET

47 ×1.3

PHYSI

15 ×0.5

RHEUM

Citations per year, relative to Marcello Bellusci Marcello Bellusci (= 1×) peers Elisenda Cortès‐Saladelafont

Countries citing papers authored by Marcello Bellusci

Since Specialization

Citations

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

Fields of papers citing papers by Marcello Bellusci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcello Bellusci

This figure shows the co-authorship network connecting the top 25 collaborators of Marcello Bellusci. A scholar is included among the top collaborators of Marcello Bellusci 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 Marcello Bellusci. Marcello Bellusci is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Reinson, Karit, Marcello Bellusci, Julien H. Park, et al.. (2024). Current global vitamin and cofactor prescribing practices for primary mitochondrial diseases: Results of a European reference network survey. Journal of Inherited Metabolic Disease. 48(1). e12805–e12805. 2 indexed citations

Prasuhn, Jannik, Lucia Laugwitz, Cheuk‐Wing Fung, et al.. (2023). Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders. Antioxidants. 12(3). 718–718. 6 indexed citations

Alcaide, Patricia, Leticia Gutierrez, Fátima Leal, et al.. (2022). Lymphocyte Medium-Chain Acyl-CoA Dehydrogenase Activity and Its Potential as a Diagnostic Confirmation Tool in Newborn Screening Cases. Journal of Clinical Medicine. 11(10). 2933–2933.

Martín‐Rivada, Álvaro, Pedro Ruiz‐Sala, Rosa Navarrete, et al.. (2022). Diagnosis of inborn errors of metabolism within the expanded newborn screening in the Madrid region. JIMD Reports. 63(2). 146–161. 17 indexed citations

Martín‐Rivada, Álvaro, Elena Martín‐Hernández, Ana Moráis López, et al.. (2022). Newborn screening for propionic, methylmalonic acidemia and vitamin B12 deficiency. Analysis of 588,793 newborns. Journal of Pediatric Endocrinology and Metabolism. 35(10). 1223–1231. 12 indexed citations

Rodríguez‐García, María Elena, Marcello Bellusci, Ana Martı́nez de Aragón, et al.. (2022). First splicing variant in HECW2 with an autosomal recessive pattern of inheritance and associated with NDHSAL. Human Mutation. 43(10). 1361–1367. 1 indexed citations

Bellusci, Marcello, et al.. (2021). The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call. Genes. 12(10). 1590–1590. 8 indexed citations

Rodríguez‐García, María Elena, et al.. (2021). New subtype of PCH1C caused by novel EXOSC8 variants in a 16-year-old Spanish patient. Neuromuscular Disorders. 31(8). 773–782. 1 indexed citations

Bellusci, Marcello, María Teresa García‐Silva, Ana Martı́nez de Aragón, & Miguel A. Martı́n. (2021). Distal phalangeal erythema in an infant with biallelic PDSS1 mutations: Expanding the phenotype of primary Coenzyme Q₁₀ deficiency. JIMD Reports. 62(1). 3–5. 7 indexed citations

10.

Gijón, Manuel, Marcello Bellusci, Antoni Noguera‐Julián, et al.. (2020). Pediatric Community-Acquired Bone and Joint Staphylococcus Aureus Infections In Europe. The Pediatric Infectious Disease Journal. 39(6). e73–e76. 10 indexed citations

11.

Rodríguez‐García, María Elena, et al.. (2019). A novel de novo MTOR gain-of-function variant in a patient with Smith-Kingsmore syndrome and Antiphospholipid syndrome. European Journal of Human Genetics. 27(9). 1369–1378. 9 indexed citations

12.

Pietrafusa, Nicola, Marina Trivisano, Luca De Palma, et al.. (2019). Paediatric Status Epilepticus: identification of prognostic factors using the new ILAE classification. Epilepsy & Behavior. 101. 106745–106745.

13.

Specchio, Nicola, Nicola Pietrafusa, Marcello Bellusci, et al.. (2019). Pediatric status epilepticus: Identification of prognostic factors using the new ILAE classification after 5 years of follow‐up. Epilepsia. 60(12). 2486–2498. 14 indexed citations

14.

Martín‐Hernández, Elena, María Elena Rodríguez‐García, Chun‐An Chen, et al.. (2018). Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation. Journal of Human Genetics. 63(4). 525–528. 22 indexed citations

15.

Specchio, Nicola, Marcello Bellusci, Nicola Pietrafusa, et al.. (2017). Photosensitivity is an early marker of neuronal ceroid lipofuscinosis type 2 disease. Epilepsia. 58(8). 1380–1388. 41 indexed citations

16.

Bellusci, Marcello, Pilar Quijada‐Fraile, Elena Martín‐Hernández, et al.. (2017). Carnitine palmitoyltransferase 1A deficiency: abnormal muscle biopsy findings in a child presenting with Reye's syndrome. Journal of Inherited Metabolic Disease. 40(5). 751–752. 4 indexed citations

17.

Bellusci, Marcello, et al.. (2016). Acute Liver Failure. Pediatric Emergency Care. 34(6). 409–412. 17 indexed citations

18.

Perseghin, Paolo, C. L. Balduini, G. Piccolo, et al.. (1985). Guillain-Barré syndrome with autoimmune hemolytic anemia following acute viral hepatitis. Neurological Sciences. 6(4). 447–450. 6 indexed citations

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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