Andreina Bordoni
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Mitochondrial Function and Pathology 42
- ATP Synthase and ATPases Research 15
- RNA modifications and cancer 7
-
- Metabolism and Genetic Disorders 31
- Co-authors
- Giacomo P. Comi (65 shared papers)Nereo Bresolin (57 shared papers)Maurizio Moggio (34 shared papers)Monica Sciacco (25 shared papers)Francesco Fortunato (17 shared papers)G. Scarlato (14 shared papers)Stefania Corti (28 shared papers)Roberto Del Bo (15 shared papers)
- Journals
- Journal of the Neurological Sciences (12 papers)Neurology (6 papers)Journal of Neurology (5 papers)Annals of Neurology (3 papers)Human Molecular Genetics (3 papers)
- Partner nations
- ItalyGreeceUnited Kingdom
In The Last Decade
Andreina Bordoni
73 papers receiving 2.7k citations
Peers
Comparison fields: 5 of 91
- Clinical Biochemistry 896
- Genetics 387
- Molecular Biology 2.0k
- Neurology 395
- Cellular and Molecular Neuroscience 364
Countries citing papers authored by Andreina Bordoni
This map shows the geographic impact of Andreina Bordoni'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 Andreina Bordoni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreina Bordoni more than expected).
Fields of papers citing papers by Andreina Bordoni
This network shows the impact of papers produced by Andreina Bordoni. 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 Andreina Bordoni. The network helps show where Andreina Bordoni may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreina Bordoni, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 230 | |
| 2 | 1998 | 208 | |
| 3 | Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease. | 1990 | 129 |
| 4 | 2010 | 121 | |
| 5 | 2008 | 120 | |
| 6 | 2009 | 120 | |
| 7 | 2001 | 105 | |
| 8 | 1998 | 93 | |
| 9 | 2002 | 86 | |
| 10 | 2005 | 82 | |
| 11 | 2003 | 82 | |
| 12 | 2001 | 81 | |
| 13 | 2004 | 65 | |
| 14 | 2003 | 64 | |
| 15 | 2006 | 55 | |
| 16 | 2003 | 53 | |
| 17 | 2016 | 52 | |
| 18 | 2012 | 48 | |
| 19 | 2005 | 47 | |
| 20 | 2007 | 43 |
About Andreina Bordoni
Andreina Bordoni is a scholar working on Molecular Biology, Clinical Biochemistry, Physiology, Rheumatology and Genetics, having authored 73 papers that have together received 2.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (42 papers), Metabolism and Genetic Disorders (31 papers), ATP Synthase and ATPases Research (15 papers), Lysosomal Storage Disorders Research (8 papers), Glycogen Storage Diseases and Myoclonus (8 papers), Neurogenetic and Muscular Disorders Research (7 papers), RNA modifications and cancer (7 papers) and Genetic Neurodegenerative Diseases (6 papers). The work is most often cited by research in Clinical Biochemistry (896 citations), Genetics (387 citations), Molecular Biology (2.0k citations), Neurology (395 citations) and Cellular and Molecular Neuroscience (364 citations). Andreina Bordoni has collaborated with scholars based in Italy, Greece and United Kingdom. Frequent co-authors include Giacomo P. Comi, Nereo Bresolin, Maurizio Moggio, Monica Sciacco, Francesco Fortunato, G. Scarlato, Stefania Corti, Roberto Del Bo, A. Prelle and Massimo Zeviani. Their work appears in journals such as Journal of the Neurological Sciences, Neurology, Journal of Neurology, Annals of Neurology and Human Molecular Genetics.
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.