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%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
Papers in
-
- Epigenetics and DNA Methylation 3
- RNA modifications and cancer 3
- Genomics and Chromatin Dynamics 2
- Genetics 5
- Genetic Syndromes and Imprinting 3
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Co-authors
- Jonathan 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)Matthew N Davies (1 shared paper)R. Alan Harris (1 shared paper)
- Journals
- Genomics (3 papers)Nature Genetics (1 paper)PLoS Biology (1 paper)BMC Genomics (1 paper)Journal of Neuroscience (1 paper)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Manuela Volta
16 papers receiving 1.9k citations
Manuela Volta's Hit Papers
Peers
Comparison fields: 5 of 102
- Molecular Biology 1.5k
- Genetics 523
- Biological Psychiatry 41
- Pediatrics, Perinatology and Child Health 256
- Developmental Neuroscience 45
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 | 671 |
| 2 | Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood Hit paper breakdown → | 2012 | 494 |
| 3 | 1997 | 283 | |
| 4 | 2008 | 167 | |
| 5 | 2001 | 65 | |
| 6 | 2012 | 55 | |
| 7 | 1999 | 38 | |
| 8 | 1998 | 33 | |
| 9 | 1999 | 25 | |
| 10 | 2016 | 24 | |
| 11 | 2004 | 20 | |
| 12 | 2010 | 18 | |
| 13 | 2009 | 16 | |
| 14 | 1994 | 10 | |
| 15 | Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type II. | 1992 | 2 |
| 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, Genetics, Neurology, Cell Biology and Genetics, having authored 16 papers that have together received 1.9k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (3 papers), Genetic Syndromes and Imprinting (3 papers), RNA modifications and cancer (3 papers), Metabolism and Genetic Disorders (2 papers), Amyotrophic Lateral Sclerosis Research (2 papers), Genomics and Chromatin Dynamics (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers) and Proteoglycans and glycosaminoglycans research (2 papers). The work is most often cited by research in Molecular Biology (1.5k citations), Genetics (523 citations), Biological Psychiatry (41 citations), Pediatrics, Perinatology and Child Health (256 citations) and Developmental Neuroscience (45 citations). Manuela Volta has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Jonathan Mill, Leonard C. Schalkwyk, Katie Lunnon, Ruth Pidsley, Chloe C. Y. Wong, Claire Troakes, Matthew N Davies, R. Alan Harris, Safa Al‐Sarraj and Richard Dobson. Their work appears in journals such as Genomics, Nature Genetics, PLoS Biology, BMC Genomics and Journal of Neuroscience.
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.