Paola Riva

3.2k total citations
98 papers, 2.3k citations indexed

About

Paola Riva is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Paola Riva has authored 98 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 25 papers in Genetics and 21 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Paola Riva's work include Neurofibromatosis and Schwannoma Cases (19 papers), Genomic variations and chromosomal abnormalities (16 papers) and Sarcoma Diagnosis and Treatment (16 papers). Paola Riva is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (19 papers), Genomic variations and chromosomal abnormalities (16 papers) and Sarcoma Diagnosis and Treatment (16 papers). Paola Riva collaborates with scholars based in Italy, United States and Malaysia. Paola Riva's co-authors include Marco Venturin, Lidia Larizza, Antonia Ratti, Silvia Moncini, G. Franceschi, N. Riva, Pietro Mortini, M. Casi, Monica Miozzo and Nicola Boari and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Cancer.

In The Last Decade

Paola Riva

95 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paola Riva Italy 27 1.1k 537 385 382 358 98 2.3k
Hideo Takeshima Japan 25 765 0.7× 219 0.4× 317 0.8× 180 0.5× 117 0.3× 123 2.3k
D C Brown United Kingdom 17 620 0.6× 205 0.4× 385 1.0× 116 0.3× 92 0.3× 31 2.0k
James O’Sullivan United Kingdom 22 1.4k 1.3× 166 0.3× 111 0.3× 510 1.3× 66 0.2× 40 2.0k
Ann Johnsson Sweden 7 1.6k 1.4× 341 0.6× 236 0.6× 410 1.1× 201 0.6× 7 2.6k
Nino Sorgente United States 31 1.1k 1.0× 286 0.5× 102 0.3× 136 0.4× 881 2.5× 72 2.6k
Yoshitaka Ohnishi Japan 31 1.3k 1.2× 291 0.5× 173 0.4× 293 0.8× 1.4k 4.0× 128 3.4k
Bret C. Mobley United States 23 727 0.7× 193 0.4× 333 0.9× 56 0.1× 87 0.2× 67 1.7k
Božo Krušlin Croatia 24 689 0.6× 273 0.5× 488 1.3× 90 0.2× 66 0.2× 158 1.7k
Patrizia Gugliotta Italy 23 561 0.5× 403 0.8× 187 0.5× 158 0.4× 224 0.6× 38 2.0k
Aya Shinozaki‐Ushiku Japan 26 836 0.8× 532 1.0× 637 1.7× 97 0.3× 122 0.3× 134 2.5k

Countries citing papers authored by Paola Riva

Since Specialization
Citations

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

Fields of papers citing papers by Paola Riva

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paola Riva

This figure shows the co-authorship network connecting the top 25 collaborators of Paola Riva. A scholar is included among the top collaborators of Paola Riva 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 Paola Riva. Paola Riva 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
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Capitanio, Daniele, et al.. (2023). Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes. International Journal of Molecular Sciences. 24(4). 4035–4035. 1 indexed citations
4.
Paterra, Rosina, Paola Bettinaglio, Eleonora Mangano, et al.. (2022). A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort. Cancers. 15(1). 59–59. 3 indexed citations
5.
Eoli, Marica, Rosina Paterra, Serena Redaelli, et al.. (2022). Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes. International Journal of Molecular Sciences. 23(17). 10017–10017. 1 indexed citations
6.
Redaelli, Serena, Donatella Conconi, Nicoletta Villa, et al.. (2020). Instability of Short Arm of Acrocentric Chromosomes: Lesson from Non-Acrocentric Satellited Chromosomes. Report of 24 Unrelated Cases. International Journal of Molecular Sciences. 21(10). 3431–3431. 2 indexed citations
7.
Ferrari, Luca, Eleonora Mangano, Maria Teresa Bonati, et al.. (2020). Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?. European Journal of Human Genetics. 28(10). 1432–1445. 12 indexed citations
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Riva, Paola, Antonia Ratti, & Marco Venturin. (2016). The Long Non-Coding RNAs in Neurodegenerative Diseases: Novel Mechanisms of Pathogenesis. Current Alzheimer Research. 13(11). 1219–1231. 252 indexed citations
10.
Moncini, Silvia, Mariangela Cisternino, Ilaria Morella, et al.. (2010). Noonan syndrome associated with both a new Jnk‐activating familial SOS1 and a de novo RAF1 mutations. American Journal of Medical Genetics Part A. 152A(9). 2176–2184. 14 indexed citations
11.
Rossi, Elena, Mariluce Riegel, Jole Messa, et al.. (2007). Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation. Journal of Medical Genetics. 45(3). 147–154. 83 indexed citations
12.
Bodega, Beatrice, Maria Francesca Cardone, Stefan Müller, et al.. (2007). Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2). BMC Evolutionary Biology. 7(1). 39–39. 9 indexed citations
13.
Gervasini, Cristina, Francesca Orzan, Angela Bentivegna, et al.. (2004). Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions. Human Genetics. 115(1). 69–80. 31 indexed citations
14.
Goetz, Claudia, et al.. (2003). Locoregional radioimmunotherapy in selected patients with malignant glioma: experiences, side effects and survival times. Journal of Neuro-Oncology. 62(3). 321–328. 40 indexed citations
15.
Riva, Paola, Marco Venturin, Paolo Guarnieri, et al.. (2002). Genotype-phenotype correlation in patients with NF1 microdeletion syndrome: identification of candidate genes for mental retardation. The American Journal of Human Genetics. 71(4). 308–308.
16.
Bentivegna, Angela, Marco Venturin, Cristina Gervasini, et al.. (2001). Identification of duplicated genes in 17q11.2 using FISH on stretched chromosomes and DNA fibers. Human Genetics. 109(1). 48–54. 6 indexed citations
17.
Riva, Paola, Lucia Corrado, Patrizia Colapietro, & Lidia Larizza. (1999). A rapid and simple method for the generation of locus-specific probes for fish analysis. 4(1). 16–20. 8 indexed citations
18.
Bettio, Daniela, et al.. (1996). Isochromosome 15q of Maternal Origin in a Prader-Willi Patient with Pituitary Adenoma. Acta geneticae medicae et gemellologiae twin research. 45(1-2). 213–216. 7 indexed citations
19.
Czuczman, M. S., Michael J. Blend, Paola Riva, et al.. (1994). RADIOIMMUNOTHERAPY OF B-CELL LYMPHOMAS WITH IODINE-131-LABELED LL2 MONOCLONAL ANTIBODY. Journal of Immunotherapy. 16(2). 160–160. 4 indexed citations
20.
Seccamani, E., et al.. (1991). A new enzymatic method gives F(ab)2 suitable for 99mTc labeling and use in immunoscintigraphy. International Journal of Radiation Applications and Instrumentation Part B Nuclear Medicine and Biology. 18(1). 19–25. 1 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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