Manuela Volta
Impact in
- Molecular Biology top 5%
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- Developmental Neuroscience top 5%
- Neurogenesis and neuroplasticity mechanisms
Papers in
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- Congenital limb and hand anomalies 2
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- Neurofibromatosis and Schwannoma Cases 2
- Co-authors
- Jonathan S. Mill (3 shared papers)Leonard C. Schalkwyk (3 shared papers)Katie Lunnon (3 shared papers)Ruth Pidsley (2 shared papers)Chloe C. Y. Wong (1 shared paper)Claire Troakes (2 shared papers)Abhishek Dixit (1 shared paper)Simon Lovestone (1 shared paper)
- Journals
- Genomics (3 papers)Antioxidants and Redox Signaling (1 paper)BMC Genomics (1 paper)Nature Neuroscience (1 paper)Epigenetics (1 paper)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Manuela Volta
16 papers receiving 2.6k citations
Manuela Volta's Hit Papers
Peers
Comparison fields: 5 of 88
- Molecular Biology 1.6k
- Developmental Neuroscience 77
- Psychiatry and Mental health 255
- Behavioral Neuroscience 35
- Neurology 156
Countries citing papers authored by Manuela Volta
This map shows the geographic impact of Manuela Volta'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 Manuela Volta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Manuela Volta more than expected).
Fields of papers citing papers by Manuela Volta
This network shows the impact of papers produced by Manuela Volta. 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 Manuela Volta. The network helps show where Manuela Volta may publish in the future.
Co-authors
The 25 scholars most cited alongside Manuela Volta, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | A data-driven approach to preprocessing Illumina 450K methylation array data Hit paper breakdown → | 2013 | 835 |
| 2 | 2012 | 559 | |
| 3 | Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease Hit paper breakdown → | 2014 | 462 |
| 4 | 1997 | 313 | |
| 5 | 2008 | 165 | |
| 6 | 2001 | 72 | |
| 7 | 2012 | 58 | |
| 8 | 1999 | 37 | |
| 9 | 1998 | 34 | |
| 10 | 1999 | 25 | |
| 11 | 2016 | 25 | |
| 12 | 2004 | 24 | |
| 13 | 2009 | 16 | |
| 14 | 1994 | 11 | |
| 15 | Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type II. | 1992 | 3 |
| 16 | A defect of midline development, Opitz syndrome, is due to mutations in a novel RING finger gene on Xp22 | 1997 | 1 |
About Manuela Volta
Manuela Volta is a scholar working on Developmental Biology, Neurology, Clinical Biochemistry, Molecular Biology and Genetics, having authored 16 papers that have together received 2.6k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (4 papers), Pluripotent Stem Cells Research (2 papers), Congenital limb and hand anomalies (2 papers), Metabolism and Genetic Disorders (2 papers), Genomics and Rare Diseases (2 papers), Neurofibromatosis and Schwannoma Cases (2 papers), Proteoglycans and glycosaminoglycans research (1 paper) and Alzheimer's disease research and treatments (1 paper). The work is most often cited by research in Molecular Biology (1.6k citations), Developmental Neuroscience (77 citations), Psychiatry and Mental health (255 citations), Behavioral Neuroscience (35 citations) and Neurology (156 citations). Manuela Volta has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Jonathan S. Mill, Leonard C. Schalkwyk, Katie Lunnon, Ruth Pidsley, Chloe C. Y. Wong, Claire Troakes, Abhishek Dixit, Simon Lovestone, Cristian Coarfa and Ronald Alan Harris. Their work appears in journals such as Genomics, Antioxidants and Redox Signaling, BMC Genomics, Nature Neuroscience and Epigenetics.
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.