Lorella Caffi

535 total citations
7 papers, 203 citations indexed

About

Lorella Caffi is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Cell Biology. According to data from OpenAlex, Lorella Caffi has authored 7 papers receiving a total of 203 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Cell Biology. Recurrent topics in Lorella Caffi's work include RNA regulation and disease (2 papers), Infant Development and Preterm Care (2 papers) and Caveolin-1 and cellular processes (2 papers). Lorella Caffi is often cited by papers focused on RNA regulation and disease (2 papers), Infant Development and Preterm Care (2 papers) and Caveolin-1 and cellular processes (2 papers). Lorella Caffi collaborates with scholars based in Italy, United Kingdom and United States. Lorella Caffi's co-authors include Simona Orcesi, Elisa Fazzi, G Rondini, G. Lanzi, Maria Luisa Bianchi, Flavia Blàsevich, Sabrina Maestrini, Lucía Morandi, Isabella Moroni and Cinzia Bragato and has published in prestigious journals such as Clinical Genetics, American Journal of Medical Genetics Part A and Neuropediatrics.

In The Last Decade

Lorella Caffi

7 papers receiving 202 citations

Peers

Lorella Caffi

MB

PPCH

GENET

DB

PRM

Anne Chun‐Hui Tsai United States

Mary K. Bofinger United States

Suliman Khan Pakistan

Angelika Köhler Germany

Raoul C. M. Hennekam Netherlands

Tomohiko Nakata Japan

J A Hurst United Kingdom

Elke Hobbiebrunken Germany

Conneally Pm United States

Seiichi Sugama Japan

Anne Chun‐Hui Tsai United States

Lorella Caffi

126 ×1.6

MB

47 ×0.8

PPCH

117 ×2.7

GENET

32 ×0.9

DB

8 ×0.2

PRM

Citations per year, relative to Lorella Caffi Lorella Caffi (= 1×) peers Anne Chun‐Hui Tsai

Countries citing papers authored by Lorella Caffi

Since Specialization

Citations

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

Fields of papers citing papers by Lorella Caffi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lorella Caffi

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

All Works

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7 of 7 papers shown

1.

D’Antiga, Lorenzo, et al.. (2021). The Conundrum of Cognitive Dysfunction in Children With Portal Hypertension: The Experience of Bergamo, Italy. Journal of Clinical and Experimental Hepatology. 12(2). 723–724. 2 indexed citations

2.

Pezzani, Lidia, Daniela Marchetti, Anna Cereda, et al.. (2018). Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy. American Journal of Medical Genetics Part A. 176(12). 2867–2871. 24 indexed citations

3.

Tonduti, Davide, Anna Pichiecchio, Annalisa Vetro, et al.. (2015). A novel mutation in COL4A1 gene: A possible cause of early postnatal cerebrovascular events. American Journal of Medical Genetics Part A. 167(4). 810–815. 8 indexed citations

4.

Negri, Gloria, Donatella Milani, Francesca Forzano, et al.. (2014). Clinical and molecular characterization of Rubinstein‐Taybi syndrome patients carrying distinct novel mutations of the EP300 gene. Clinical Genetics. 87(2). 148–154. 60 indexed citations

5.

Ardissone, Anna, Cinzia Bragato, Lorella Caffi, et al.. (2013). Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy. BMC Medical Genetics. 14(1). 89–89. 42 indexed citations

6.

Fazzi, Elisa, et al.. (2006). A questionnaire on sleep behaviour in the first years of life: preliminary results from a normative sample.. PubMed. 21(3). 151–8. 9 indexed citations

7.

Fazzi, Elisa, et al.. (1994). Neurodevelopmental Outcome at 5-7 Years in Preterm Infants with Periventricular Leukomalacia. Neuropediatrics. 25(3). 134–139. 58 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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