Anna Rubegni

1.4k total citations
47 papers, 493 citations indexed

About

Anna Rubegni is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Anna Rubegni has authored 47 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 16 papers in Cellular and Molecular Neuroscience and 13 papers in Clinical Biochemistry. Recurrent topics in Anna Rubegni's work include Mitochondrial Function and Pathology (22 papers), Metabolism and Genetic Disorders (13 papers) and ATP Synthase and ATPases Research (10 papers). Anna Rubegni is often cited by papers focused on Mitochondrial Function and Pathology (22 papers), Metabolism and Genetic Disorders (13 papers) and ATP Synthase and ATPases Research (10 papers). Anna Rubegni collaborates with scholars based in Italy, France and Greece. Anna Rubegni's co-authors include Filippo M. Santorelli, Alessandra Tessa, Claudia Nesti, Roberta Battini, Claudio Bruno, Antonio Federico, Chiara Fiorillo, Guja Astrea, Carlo Minetti and Denise Cassandrini and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and International Journal of Molecular Sciences.

In The Last Decade

Anna Rubegni

44 papers receiving 489 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 Rubegni Italy 15 329 132 110 83 76 47 493
Foudil Lamari France 14 257 0.8× 80 0.6× 95 0.9× 78 0.9× 43 0.6× 28 582
Stephanie Kleinle Germany 17 587 1.8× 117 0.9× 292 2.7× 56 0.7× 50 0.7× 27 772
Davor Ivankovic United Kingdom 5 510 1.6× 99 0.8× 92 0.8× 28 0.3× 18 0.2× 5 729
Nathan A. Bihlmeyer United States 7 361 1.1× 89 0.7× 74 0.7× 136 1.6× 16 0.2× 8 615
Anja Kahl United States 9 235 0.7× 83 0.6× 41 0.4× 49 0.6× 28 0.4× 15 450
В. С. Сухоруков Russia 8 251 0.8× 68 0.5× 23 0.2× 19 0.2× 27 0.4× 81 379
Hyang-Sook Kim South Korea 11 222 0.7× 150 1.1× 9 0.1× 67 0.8× 38 0.5× 26 366
Ndidi-Ese Uzor United States 9 246 0.7× 53 0.4× 21 0.2× 51 0.6× 58 0.8× 11 439
Ese Mudanohwo United Kingdom 7 340 1.0× 184 1.4× 165 1.5× 63 0.8× 56 0.7× 10 495
Kirsty Greenwood United Kingdom 8 266 0.8× 149 1.1× 72 0.7× 75 0.9× 13 0.2× 9 503

Countries citing papers authored by Anna Rubegni

Since Specialization
Citations

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

Fields of papers citing papers by Anna Rubegni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Rubegni

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Rubegni. A scholar is included among the top collaborators of Anna Rubegni 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 Rubegni. Anna Rubegni 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.
Falco, Alessandro De, Anna Rubegni, Stefano Pagano, et al.. (2025). Impact of SDHA Mutations on Yeast Growth and Mitochondrial Function. Case Study Linking Genetic Findings to Clinical Phenotypes. Clinical Genetics. 108(3). 323–328.
2.
Orsini, Alessandro, Elisa Costa, Andrea Santangelo, et al.. (2023). Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature. Genes. 14(7). 1363–1363. 3 indexed citations
3.
Romano, Alessandro, Stefano Doccini, Rosa Pasquariello, et al.. (2023). Novel COX11 Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and Saccharomyces cerevisiae. International Journal of Molecular Sciences. 24(23). 16636–16636. 4 indexed citations
4.
Calderisi, Marco, et al.. (2022). Automatic Recognition of Ragged Red Fibers in Muscle Biopsy from Patients with Mitochondrial Disorders. Healthcare. 10(3). 574–574. 2 indexed citations
5.
Magno, Silvia, Giovanni Ceccarini, Andrea Barison, et al.. (2021). Partial Lipodystrophy and LMNA p.R545H Variant. Journal of Clinical Medicine. 10(5). 1142–1142. 3 indexed citations
6.
Nesti, Claudia, Anna Rubegni, Stefano Doccini, et al.. (2021). Bi‐allelic variants in MDH2: Expanding the clinical phenotype. Clinical Genetics. 101(2). 260–264. 7 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.
Scala, Marcello, Giorgia Brigati, Chiara Fiorillo, et al.. (2019). Novel homozygous TSFM pathogenic variant associated with encephalocardiomyopathy with sensorineural hearing loss and peculiar neuroradiologic findings. Neurogenetics. 20(3). 165–172. 7 indexed citations
9.
Filosto, Massimiliano, Stefano Cotti Piccinelli, Costanza Lamperti, et al.. (2019). Muscle pain in mitochondrial diseases: a picture from the Italian network. Journal of Neurology. 266(4). 953–959. 6 indexed citations
10.
Nesti, Claudia, et al.. (2019). Complex multisystem phenotype associated with the mitochondrial DNA m.5522G>A mutation. Neurological Sciences. 40(8). 1705–1708. 4 indexed citations
11.
Moro, Francesca, et al.. (2018). Autophagic vacuolar myopathy caused by a CLN3 mutation. A case report. Neuromuscular Disorders. 29(1). 67–69. 2 indexed citations
12.
Mari, Francesco, Beatrice Berti, Alessandro Romano, et al.. (2018). Clinical and neuroimaging features of autosomal recessive spastic paraplegia 35 (SPG35): case reports, new mutations, and brief literature review. Neurogenetics. 19(2). 123–130. 17 indexed citations
13.
Cassandrini, Denise, Rosanna Trovato, Anna Rubegni, et al.. (2017). Congenital myopathies: clinical phenotypes and new diagnostic tools. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 43(1). 101–101. 70 indexed citations
14.
Rubegni, Anna, Carla Battisti, Alessandra Tessa, et al.. (2017). SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing. Journal of the Neurological Sciences. 375. 198–202. 15 indexed citations
15.
Seitun, Sara, Anna Rubegni, Claudia Nesti, et al.. (2016). MELAS Syndrome with Cardiac Involvement: A Multimodality Imaging Approach. Case Reports in Cardiology. 2016. 1–4. 8 indexed citations
16.
Astrea, Guja, Antonio Petrucci, Denise Cassandrini, et al.. (2016). Myoimaging in the NGS era: the discovery of a novel mutation in MYH7 in a family with distal myopathy and core-like features – a case report. BMC Medical Genetics. 17(1). 25–25. 5 indexed citations
17.
Nesti, Claudia, Maria Chiara Meschini, Brigitte Meunier, et al.. (2015). Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy. Human Molecular Genetics. 24(11). 3248–3256. 14 indexed citations
18.
Rubegni, Anna, Elena Cardaioli, Paola Da Pozzo, et al.. (2014). A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia. Journal of the Neurological Sciences. 338(1-2). 232–234. 3 indexed citations
19.
Cardaioli, Elena, Edoardo Malfatti, Carla Battisti, et al.. (2012). Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation. Journal of the Neurological Sciences. 321(1-2). 92–95. 5 indexed citations
20.
Cardaioli, Elena, Paola Da Pozzo, Edoardo Malfatti, et al.. (2008). Chronic progressive external ophthalmoplegia: A new heteroplasmic tRNALeu(CUN) mutation of mitochondrial DNA. Journal of the Neurological Sciences. 272(1-2). 106–109. 16 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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