Raffaella Meneveri

2.1k total citations
64 papers, 1.6k citations indexed

About

Raffaella Meneveri is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Raffaella Meneveri has authored 64 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 13 papers in Genetics and 11 papers in Immunology. Recurrent topics in Raffaella Meneveri's work include Chromosomal and Genetic Variations (11 papers), RNA and protein synthesis mechanisms (7 papers) and Genomics and Chromatin Dynamics (7 papers). Raffaella Meneveri is often cited by papers focused on Chromosomal and Genetic Variations (11 papers), RNA and protein synthesis mechanisms (7 papers) and Genomics and Chromatin Dynamics (7 papers). Raffaella Meneveri collaborates with scholars based in Italy, Germany and United States. Raffaella Meneveri's co-authors include Enrico Ginelli, Donatella Barisani, Anna Marozzi, A Agresti, Silvia Brunelli, C. De Santis, Walter Vegetti, Emanuela Manfredini, Leda Dalprà and Lucia Lopalco and has published in prestigious journals such as The Journal of Experimental Medicine, The Journal of Cell Biology and The Journal of Immunology.

In The Last Decade

Raffaella Meneveri

64 papers receiving 1.6k citations

Peers

Raffaella Meneveri
Debbie Watson Australia
Ralph M. Bunte United States
Bernard Conrad Switzerland
Nancy A. Hong United States
Philip A. Robinson United Kingdom
Raffaella Meneveri
Citations per year, relative to Raffaella Meneveri Raffaella Meneveri (= 1×) peers Florence Bernex

Countries citing papers authored by Raffaella Meneveri

Since Specialization
Citations

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

Fields of papers citing papers by Raffaella Meneveri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raffaella Meneveri

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

All Works

20 of 20 papers shown
1.
Sala, Elisa, Geeta G. Sharma, Maria Gemelli, et al.. (2024). New pan-ALK inhibitor-resistant EML4::ALK mutations detected by liquid biopsy in lung cancer patients. npj Precision Oncology. 8(1). 29–29. 3 indexed citations
2.
Tombetti, Enrico, Raffaella Meneveri, Mario Tirone, et al.. (2019). Macrophages Guard Endothelial Lineage by Hindering Endothelial-to-Mesenchymal Transition: Implications for the Pathogenesis of Systemic Sclerosis. The Journal of Immunology. 203(1). 247–258. 12 indexed citations
3.
Dinelli, Marco, et al.. (2015). miRNA-regulated gene expression differs in celiac disease patients according to the age of presentation. Genes & Nutrition. 10(5). 482–482. 44 indexed citations
4.
Giussani, Marta, Maria Francesca Cardone, Beatrice Bodega, Enrico Ginelli, & Raffaella Meneveri. (2012). Evolutionary history of linked D4Z4 and Beta satellite clusters at the FSHD locus (4q35). Genomics. 100(5). 289–296. 4 indexed citations
5.
Barisani, Donatella, Sara Galimberti, Raffaella Mariani, et al.. (2008). Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload. Journal of Hepatology. 49(1). 123–133. 84 indexed citations
6.
Bodega, Beatrice, Maria Francesca Cardone, Mariano Rocchi, et al.. (2006). The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution. Genomics. 88(5). 564–571. 5 indexed citations
7.
Barisani, Donatella, et al.. (2006). IL-10 polymorphisms are associated with early-onset celiac disease and severe mucosal damage in patients of Caucasian origin. Genetics in Medicine. 8(3). 169–174. 25 indexed citations
8.
Marozzi, Anna, Diego Fornasari, Roberta Benfante, et al.. (2003). Genomic organization and transcription of the human retinol dehydrogenase 10 (RDH10) gene. FEBS Letters. 554(1-2). 59–66. 9 indexed citations
9.
Barisani, Donatella, et al.. (2001). Duodenal expression of a putative stimulator of Fe transport and transferrin receptor in anemia and hemochromatosis. Gastroenterology. 120(6). 1404–1411. 1 indexed citations
10.
Barisani, Donatella, Dario Conte, Antonina Parafioriti, Elisabetta Armiraglio, & Raffaella Meneveri. (2001). Duodenal expression of a putative stimulator of Fe transport and transferrin receptor in anemia and hemochromatosis. Gastroenterology. 120(6). 1404–1411. 15 indexed citations
11.
Marozzi, Anna, Walter Vegetti, Emanuela Manfredini, et al.. (2000). Association between idiopathic premature ovarian failure and fragile X premutation. Human Reproduction. 15(1). 197–202. 105 indexed citations
12.
Bassi, Carla A., Ivana Magnani, Nicoletta Sacchi, et al.. (2000). Molecular structure and evolution of DNA sequences located at the alpha satellite boundary of chromosome 20. Gene. 256(1-2). 43–50. 6 indexed citations
13.
Rainaldi, Giuseppe, et al.. (1998). Absence of mutations in the highest mutability region of the p-53 gene in tumour-derived CHEF18 Chinese hamster cells. Mutagenesis. 13(2). 153–155. 5 indexed citations
14.
Molteni, Elena, A Agresti, Raffaella Meneveri, et al.. (1996). Molecular Characterization of a Variant of Proviral Bovine Leukaemia Virus (BLV). Journal of Veterinary Medicine Series B. 43(1-10). 201–211. 23 indexed citations
15.
Agresti, A, W. Ponti, Mara Rocchi, et al.. (1993). Use of polymerase chain reaction to diagnose bovine leukemia virus infection in calves at birth. American Journal of Veterinary Research. 54(3). 373–378. 41 indexed citations
16.
Marozzi, Anna, Raffaella Meneveri, Giuseppe Bunone, et al.. (1993). Expression of β2m‐Free HLA Class I Heavy Chains in Neuroblastoma Cell Lines. Scandinavian Journal of Immunology. 37(6). 661–667. 24 indexed citations
17.
Lopalco, Lucia, C. De Santis, Raffaella Meneveri, et al.. (1993). Human immunodeficiency virus type 1 gp120 C5 region mimics the HLA class I α1 peptide‐binding domain. European Journal of Immunology. 23(8). 2016–2021. 51 indexed citations
18.
Meneveri, Raffaella, A Agresti, Anna Marozzi, et al.. (1993). Molecular organization and chromosomal location of human GC-rich heterochromatic blocks. Gene. 123(2). 227–234. 31 indexed citations
19.
Grassi, Fabio, Raffaella Meneveri, Martin Gullberg, et al.. (1991). Human immunodeficiency virus type 1 gp120 mimics a hidden monomorphic epitope borne by class I major histocompatibility complex heavy chains.. The Journal of Experimental Medicine. 174(1). 53–62. 94 indexed citations
20.
Meneveri, Raffaella, et al.. (1988). Development of a Salmonella-specific biotinylated DNA probe for rapid routine identification of Salmonella. Molecular and Cellular Probes. 2(4). 271–279. 32 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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