Manuela Volta

3.4k total citations · 2 hit papers
16 papers, 1.9k citations indexed

About

Manuela Volta is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Manuela Volta has authored 16 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Neurology. Recurrent topics in Manuela Volta's work include Genetic Syndromes and Imprinting (3 papers), Epigenetics and DNA Methylation (3 papers) and RNA modifications and cancer (3 papers). Manuela Volta is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Epigenetics and DNA Methylation (3 papers) and RNA modifications and cancer (3 papers). Manuela Volta collaborates with scholars based in Italy, United Kingdom and United States. Manuela Volta's co-authors include Leonard C. Schalkwyk, Jonathan Mill, Katie Lunnon, Ruth Pidsley, Chloe C. Y. Wong, Claire Troakes, Abhishek Dixit, Simon Lovestone, Safa Al‐Sarraj and Cristian Coarfa and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and The Journal of Immunology.

In The Last Decade

Manuela Volta

16 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A data-driven approach to preprocessing Illumina 450K methylation array data

2013 671 citations Ruth Pidsley, Chloe C. Y. Wong et al. BMC Genomics profile →
Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood

2012 494 citations Matthew N Davies, Manuela Volta et al. Genome biology profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Manuela Volta Italy	13	1.5k	523	256	147	131	16	1.9k
Bronwyn Kerr United Kingdom	32	1.6k 1.1×	1.3k 2.5×	399 1.6×	221 1.5×	128 1.0×	67	3.2k
Mark Corbett Australia	24	1.4k 0.9×	715 1.4×	428 1.7×	76 0.5×	190 1.5×	72	2.5k
Jillian S. Parboosingh Canada	29	936 0.6×	617 1.2×	306 1.2×	58 0.4×	142 1.1×	85	2.0k
Paulo Alberto Otto Brazil	25	885 0.6×	825 1.6×	183 0.7×	76 0.5×	64 0.5×	130	1.9k
Susan Moore United Kingdom	20	873 0.6×	716 1.4×	297 1.2×	204 1.4×	89 0.7×	30	2.0k
Cynthia M. Powell United States	28	953 0.7×	1.2k 2.2×	536 2.1×	66 0.4×	86 0.7×	79	2.5k
Donatella Milani Italy	24	1.3k 0.9×	994 1.9×	180 0.7×	78 0.5×	67 0.5×	118	2.1k
Caroline Brain United Kingdom	25	814 0.6×	538 1.0×	214 0.8×	54 0.4×	63 0.5×	62	2.2k
Myka L. Estes United States	16	600 0.4×	235 0.4×	262 1.0×	370 2.5×	97 0.7×	24	2.1k
Garry L. Warne Australia	32	1.3k 0.9×	1.1k 2.0×	340 1.3×	81 0.6×	49 0.4×	109	2.9k

Countries citing papers authored by Manuela Volta

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Manuela Volta

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Volta. A scholar is included among the top collaborators of Manuela Volta 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 Manuela Volta. Manuela Volta is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Marzi, Sarah J., Emma L. Meaburn, Emma Dempster, et al.. (2016). Tissue-specific patterns of allelically-skewed DNA methylation. Epigenetics. 11(1). 24–35. 24 indexed citations

Pidsley, Ruth, Chloe C. Y. Wong, Manuela Volta, et al.. (2013). A data-driven approach to preprocessing Illumina 450K methylation array data. BMC Genomics. 14(1). 293–293. 671 indexed citations breakdown →

Capitanio, Daniele, Michele Vasso, Antonia Ratti, et al.. (2012). Molecular Signatures of Amyotrophic Lateral Sclerosis Disease Progression in Hind and Forelimb Muscles of an SOD1 ^G93A Mouse Model. Antioxidants and Redox Signaling. 17(10). 1333–1350. 55 indexed citations

Davies, Matthew N, Manuela Volta, Ruth Pidsley, et al.. (2012). Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood. Genome biology. 13(6). R43–R43. 494 indexed citations breakdown →

Riccardi, Federica, Davide Martorana, Gianna Franca Rivolta, et al.. (2010). Spectrum of F8 gene mutations in haemophilia A patients from a region of Italy: identification of 23 new mutations. Haemophilia. 16(5). 791–800. 18 indexed citations

Volta, Manuela, Stefano Calza, Anne M. Roberts, & Roland G. Roberts. (2009). Characterisation of the interaction between syndecan-2, neurofibromin and CASK: Dependence of interaction on syndecan dimerization. Biochemical and Biophysical Research Communications. 391(2). 1216–1221. 16 indexed citations

Johnson, Rory, Galih Kunarso, Kandhadayar G. Srinivasan, et al.. (2008). REST Regulates Distinct Transcriptional Networks in Embryonic and Neural Stem Cells. PLoS Biology. 6(10). e256–e256. 167 indexed citations

Cova, Lidia, Antonia Ratti, Manuela Volta, et al.. (2004). Stem Cell Therapy for Neurodegenerative Diseases: The Issue of Transdifferentiation. Stem Cells and Development. 13(1). 121–131. 20 indexed citations

Hsueh, Yi‐Ping, Anne M. Roberts, Manuela Volta, Morgan Sheng, & Roland G. Roberts. (2001). Bipartite Interaction between Neurofibromatosis Type I Protein (Neurofibromin) and Syndecan Transmembrane Heparan Sulfate Proteoglycans. Journal of Neuroscience. 21(11). 3764–3770. 65 indexed citations

10.

Prakash, Siddharth K., Ignatia B. Van den Veyver, Brunella Franco, et al.. (1999). Characterization of a Novel Chromo Domain Gene in Xp22.3 with Homology to Drosophila msl-3. Genomics. 59(1). 77–84. 25 indexed citations

11.

Volta, Manuela, Alessandro Bulfone, Elena Rossi, et al.. (1999). Identification and Characterization of CDS2, a Mammalian Homolog of theDrosophilaCDP-diacylglycerol Synthase Gene. Genomics. 55(1). 68–77. 38 indexed citations

12.

Yu, Weiming, Elisa Soprana, Manuela Volta, et al.. (1998). Soluble CD141–152 Confers Responsiveness to Both Lipoarabinomannan and Lipopolysaccharide in a Novel HL-60 Cell Bioassay. The Journal of Immunology. 161(8). 4244–4251. 33 indexed citations

13.

Quaderi, Nandita, Susann Schweiger, Karin Gaudenz, et al.. (1997). Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nature Genetics. 17(3). 285–291. 283 indexed citations

14.

Quaderi, Nandita, Susann Schweiger, Karin Gaudenz, et al.. (1997). A defect of midline development, Opitz syndrome, is due to mutations in a novel RING finger gene on Xp22. 17. 285–291. 1 indexed citations

15.

Antonacci, Rachele, Irma Colombo, Nicoletta Archidiacono, et al.. (1994). Assignment of the Gene Encoding the β-Subunit of the Electron-Transfer Flavoprotein (ETFB) to Human Chromosome 19q13.3. Genomics. 19(1). 177–179. 10 indexed citations

16.

Colombo, Irma, Stefano DiDonato, Manuela Volta, et al.. (1992). Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type II.. PubMed. 375. 561–6. 2 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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