Lorella Valletta

1.2k total citations
9 papers, 460 citations indexed

About

Lorella Valletta is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Lorella Valletta has authored 9 papers receiving a total of 460 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Lorella Valletta's work include Glioma Diagnosis and Treatment (5 papers), Neurological diseases and metabolism (2 papers) and Epigenetics and DNA Methylation (2 papers). Lorella Valletta is often cited by papers focused on Glioma Diagnosis and Treatment (5 papers), Neurological diseases and metabolism (2 papers) and Epigenetics and DNA Methylation (2 papers). Lorella Valletta collaborates with scholars based in Italy, United Kingdom and Germany. Lorella Valletta's co-authors include Gaetano Finocchiaro, Maria Grazia Bruzzone, Bianca Pollo, Valeria Tiranti, Marica Eoli, Donatella Bianchessi, Antonio Silvani, A. Boiardi, Giovanni Broggi and Tiziana De Simone and has published in prestigious journals such as Neurology, Clinical Cancer Research and International Journal of Cancer.

In The Last Decade

Lorella Valletta

9 papers receiving 452 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lorella Valletta Italy	8	254	251	99	91	71	9	460
Lorena Bissola Italy	6	167 0.7×	244 1.0×	123 1.2×	42 0.5×	61 0.9×	6	357
Klazien S. Bosch Netherlands	7	224 0.9×	213 0.8×	174 1.8×	11 0.1×	34 0.5×	8	456
Scott Ryall Canada	11	230 0.9×	455 1.8×	110 1.1×	7 0.1×	53 0.7×	25	619
Meng Dong China	9	266 1.0×	57 0.2×	164 1.7×	10 0.1×	43 0.6×	23	404
David W. Ellison United Kingdom	9	825 3.2×	415 1.7×	142 1.4×	38 0.4×	18 0.3×	9	1.1k
Karen Beets Belgium	5	241 0.9×	43 0.2×	37 0.4×	8 0.1×	30 0.4×	6	379
Hamda Al Thawadi Qatar	5	291 1.1×	60 0.2×	141 1.4×	26 0.3×	6 0.1×	6	464
Dario Balestra Italy	16	505 2.0×	118 0.5×	16 0.2×	33 0.4×	9 0.1×	33	634
Rosina Paterra Italy	11	215 0.8×	363 1.4×	141 1.4×	3 0.0×	92 1.3×	25	551

Countries citing papers authored by Lorella Valletta

Since Specialization

Citations

This map shows the geographic impact of Lorella Valletta'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 Lorella Valletta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lorella Valletta more than expected).

Fields of papers citing papers by Lorella Valletta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lorella Valletta. 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 Lorella Valletta. The network helps show where Lorella Valletta may publish in the future.

Co-authorship network of co-authors of Lorella Valletta

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

All Works

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9 of 9 papers shown

Carecchio, Miryam, Marina Picillo, Lorella Valletta, et al.. (2017). Rare causes of early-onset dystonia-parkinsonism with cognitive impairment: a de novo PSEN-1 mutation. Neurogenetics. 18(3). 175–178. 14 indexed citations

Pellegatta, Serena, Lorella Valletta, Cristina Corbetta, et al.. (2015). Effective immuno-targeting of the IDH1 mutation R132H in a murine model of intracranial glioma. Acta Neuropathologica Communications. 3(1). 4–4. 100 indexed citations

Venco, Paola, Sabrina Dusi, Lorella Valletta, & Valeria Tiranti. (2014). Alteration of the coenzyme A biosynthetic pathway in neurodegeneration with brain iron accumulation syndromes. Biochemical Society Transactions. 42(4). 1069–1074. 22 indexed citations

Menghi, Francesca, Francesca Orzan, Marica Eoli, et al.. (2011). DNA Microarray Analysis Identifies CKS2 and LEPR as Potential Markers of Meningioma Recurrence. The Oncologist. 16(10). 1440–1450. 21 indexed citations

Bruzzone, Maria Grazia, Marica Eoli, Valeria Cuccarini, et al.. (2009). Genetic signature of adult gliomas and correlation with MRI features. Expert Review of Molecular Diagnostics. 9(7). 709–720. 15 indexed citations

Eoli, Marica, Francesca Menghi, Maria Grazia Bruzzone, et al.. (2007). Methylation of O6-Methylguanine DNA Methyltransferase and Loss of Heterozygosity on 19q and/or 17p Are Overlapping Features of Secondary Glioblastomas with Prolonged Survival. Clinical Cancer Research. 13(9). 2606–2613. 134 indexed citations

Eoli, Marica, Lorena Bissola, Maria Grazia Bruzzone, et al.. (2006). Reclassification of oligoastrocytomas by loss of heterozygosity studies. International Journal of Cancer. 119(1). 84–90. 34 indexed citations

Eoli, Marica, Antonio Silvani, Bianca Pollo, et al.. (2006). Molecular markers of gliomas: a clinical approach. Neurological Research. 28(5). 538–541. 6 indexed citations

Agostino, A., Lorella Valletta, Patrick F. Chinnery, et al.. (2003). Mutations of ANT1 , Twinkle , and POLG1 in sporadic progressive external ophthalmoplegia (PEO). Neurology. 60(8). 1354–1356. 114 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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