Manuela Volta
Impact in
- Molecular Biology top 5%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- Cancer-related gene regulation
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genetic Associations and Epidemiology
Papers in
-
- Epigenetics and DNA Methylation 3
- Pluripotent Stem Cells Research 2
- Genomics and Chromatin Dynamics 2
- RNA modifications and cancer 2
-
- Amyotrophic Lateral Sclerosis Research 2
- Co-authors
- Katie Lunnon (3 shared papers)Leonard C. Schalkwyk (3 shared papers)Jonathan Mill (3 shared papers)Ruth Pidsley (2 shared papers)Chloe C. Y. Wong (1 shared paper)Claire Troakes (2 shared papers)Aleksandar Milosavljevic (1 shared paper)Safa Al‐Sarraj (1 shared paper)
- Journals
- Genomics (3 papers)Antioxidants and Redox Signaling (1 paper)Haemophilia (1 paper)The Journal of Immunology (1 paper)Biochemical and Biophysical Research Communications (1 paper)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Manuela Volta
16 papers receiving 2.0k citations
Manuela Volta's Hit Papers
Peers
Comparison fields: 5 of 100
- Molecular Biology 1.4k
- Genetics 435
- Biological Psychiatry 35
- Pediatrics, Perinatology and Child Health 205
- Developmental Neuroscience 42
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 | 698 |
| 2 | Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood Hit paper breakdown → | 2012 | 536 |
| 3 | 1997 | 299 | |
| 4 | 2008 | 168 | |
| 5 | 2001 | 72 | |
| 6 | 2012 | 56 | |
| 7 | 1999 | 39 | |
| 8 | 1998 | 34 | |
| 9 | 2016 | 25 | |
| 10 | 1999 | 25 | |
| 11 | 2004 | 24 | |
| 12 | 2010 | 19 | |
| 13 | 2009 | 17 | |
| 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 Molecular Biology, Neurology, Cell Biology, Genetics and Clinical Biochemistry, having authored 16 papers that have together received 2.0k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (3 papers), Amyotrophic Lateral Sclerosis Research (2 papers), Metabolism and Genetic Disorders (2 papers), Pluripotent Stem Cells Research (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genomics and Chromatin Dynamics (2 papers), Proteoglycans and glycosaminoglycans research (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Molecular Biology (1.4k citations), Genetics (435 citations), Biological Psychiatry (35 citations), Pediatrics, Perinatology and Child Health (205 citations) and Developmental Neuroscience (42 citations). Manuela Volta has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Katie Lunnon, Leonard C. Schalkwyk, Jonathan Mill, Ruth Pidsley, Chloe C. Y. Wong, Claire Troakes, Aleksandar Milosavljevic, Safa Al‐Sarraj, Matthew N Davies and Abhishek Dixit. Their work appears in journals such as Genomics, Antioxidants and Redox Signaling, Haemophilia, The Journal of Immunology and Biochemical and Biophysical Research Communications.
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.