Anna Ardissone

2.1k total citations
47 papers, 885 citations indexed

About

Anna Ardissone is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Anna Ardissone has authored 47 papers receiving a total of 885 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Anna Ardissone's work include Mitochondrial Function and Pathology (19 papers), Metabolism and Genetic Disorders (17 papers) and ATP Synthase and ATPases Research (10 papers). Anna Ardissone is often cited by papers focused on Mitochondrial Function and Pathology (19 papers), Metabolism and Genetic Disorders (17 papers) and ATP Synthase and ATPases Research (10 papers). Anna Ardissone collaborates with scholars based in Italy, United Kingdom and United States. Anna Ardissone's co-authors include Isabella Moroni, Daniele Ghezzi, Eleonora Lamantea, Andrea Legati, Barbara Garavaglia, Laura Farina, Massimo Zeviani, Alessia Nasca, Federica Invernizzi and Enrico Bertini and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Scientific Reports.

In The Last Decade

Anna Ardissone

47 papers receiving 878 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Anna Ardissone Italy 17 705 242 149 80 72 47 885
Daria Diodato Italy 18 868 1.2× 535 2.2× 89 0.6× 84 1.1× 48 0.7× 44 1.2k
Maria Chiara Meschini Italy 15 461 0.7× 242 1.0× 64 0.4× 91 1.1× 35 0.5× 23 637
Emil Ylikallio Finland 20 952 1.4× 346 1.4× 106 0.7× 287 3.6× 144 2.0× 37 1.2k
Inés García‐Consuegra Spain 15 591 0.8× 152 0.6× 136 0.9× 149 1.9× 99 1.4× 36 953
Sofía García United States 13 722 1.0× 239 1.0× 36 0.2× 64 0.8× 22 0.3× 18 839
Irene De Biase United States 16 644 0.9× 120 0.5× 86 0.6× 470 5.9× 87 1.2× 39 771
Albandary AlBakheet Saudi Arabia 13 360 0.5× 60 0.2× 132 0.9× 67 0.8× 24 0.3× 34 576
Albert Misko United States 10 584 0.8× 140 0.6× 19 0.1× 264 3.3× 100 1.4× 15 818
Fabiana Fattori Italy 15 550 0.8× 94 0.4× 59 0.4× 173 2.2× 21 0.3× 47 691
Fabio Acquaviva Italy 17 592 0.8× 36 0.1× 197 1.3× 382 4.8× 83 1.2× 25 842

Countries citing papers authored by Anna Ardissone

Since Specialization
Citations

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

Fields of papers citing papers by Anna Ardissone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Ardissone

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

All Works

20 of 20 papers shown
1.
Burlina, Alessandro P., Anna Ardissone, Alberto Burlina, et al.. (2025). Arginase 1 deficiency: a treatable form of spastic paraplegia. Neurological Sciences. 46(9). 4219–4228. 2 indexed citations
2.
Invernizzi, Federica, Andrea Legati, Nadia Zanetti, et al.. (2023). NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia. Genes. 14(7). 1393–1393. 3 indexed citations
3.
Moroni, Isabella, et al.. (2023). Nutritional status of children affected by X‐linked adrenoleukodystrophy. Journal of Human Nutrition and Dietetics. 36(4). 1316–1326. 1 indexed citations
4.
Ardissone, Anna, Costanza Lamperti, Valeria Tiranti, et al.. (2023). Phenotyping mitochondrial DNA‐related diseases in childhood: A cohort study of 150 patients. European Journal of Neurology. 30(7). 2079–2091. 7 indexed citations
5.
Moroni, Isabella, Federica Rachele Danti, Davide Pareyson, et al.. (2022). Validation of the Italian version of the pediatric CMT quality of life outcome measure. Journal of the Peripheral Nervous System. 27(2). 127–130. 4 indexed citations
6.
Brémovà-Ertl, Tatiana, Larry A. Abel, Mark Walterfang, et al.. (2021). A cross‐sectional, prospective ocular motor study in 72 patients with Niemann‐Pick disease type C. European Journal of Neurology. 28(9). 3040–3050. 9 indexed citations
7.
Ardissone, Anna, Claudio Bruno, Daria Diodato, et al.. (2021). Clinical, imaging, biochemical and molecular features in Leigh syndrome: a study from the Italian network of mitochondrial diseases. Orphanet Journal of Rare Diseases. 16(1). 413–413. 17 indexed citations
8.
Nicita, Francesco, Silvia Masnada, Roberta Battini, et al.. (2021). Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patients. Molecular Genetics and Metabolism. 134(4). 353–358. 6 indexed citations
9.
Esposito, Silvia, Marco Moscatelli, Claudio Caccia, et al.. (2020). Teaching NeuroImages: Symmetrical abnormalities of the globi pallidi in succinic semialdehyde dehydrogenase deficiency. Neurology. 95(16). e2316–e2317. 2 indexed citations
10.
Caciotti, Anna, Elena Procopio, Rita Fischetto, et al.. (2019). Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content. Scientific Reports. 9(1). 17684–17684. 9 indexed citations
11.
Tatton‐Brown, Katrina, Chey Loveday, Shawn Yost, et al.. (2017). Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability. The American Journal of Human Genetics. 100(5). 725–736. 128 indexed citations
12.
Legati, Andrea, Aurelio Reyes, Alessia Nasca, et al.. (2016). New genes and pathomechanisms in mitochondrial disorders unraveled by NGS technologies. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857(8). 1326–1335. 71 indexed citations
13.
Torraco, Alessandra, Anna Ardissone, Federica Invernizzi, et al.. (2016). Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes. Journal of Neurology. 264(1). 102–111. 34 indexed citations
14.
Ardissone, Anna, et al.. (2016). Intrafamilial phenotypic variability in Andersen–Tawil syndrome: A diagnostic challenge in a potentially treatable condition. Neuromuscular Disorders. 27(3). 294–297. 15 indexed citations
15.
Ardissone, Anna, Tiziana Granata, Andrea Legati, et al.. (2015). Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of Literature. JIMD Reports. 22. 115–120. 13 indexed citations
16.
Ardissone, Anna, Eleonora Lamantea, Federica Invernizzi, et al.. (2014). Mitochondrial Diseases in Childhood. Current Molecular Medicine. 14(8). 1069–1078. 2 indexed citations
17.
Invernizzi, Federica, Anna Ardissone, Eleonora Lamantea, et al.. (2014). Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations. Frontiers in Genetics. 5. 412–412. 40 indexed citations
18.
Ardissone, Anna, Eleonora Lamantea, Cristina Dallabona, et al.. (2014). A Novel Homozygous YARS2 Mutation in Two Italian Siblings and a Review of Literature. JIMD Reports. 20. 95–101. 13 indexed citations
19.
Saredi, S., Sara Gibertini, Anna Ardissone, et al.. (2013). A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation. European Journal of Paediatric Neurology. 18(3). 404–408. 14 indexed citations
20.
Saredi, S., Anna Ardissone, Alessandra Ruggieri, et al.. (2012). Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease. Journal of the Neurological Sciences. 318(1-2). 45–50. 20 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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