Fiorella Gurrieri

5.7k citations
88 papers · 2.4k indexed · h-index 27
Topics
Genomic variations and chromosomal abnormalities (23 papers)Genetics and Neurodevelopmental Disorders (17 papers)Genetic Syndromes and Imprinting (12 papers)
Partner nations
ItalyUnited StatesCanada

In The Last Decade

Fiorella Gurrieri

85 papers receiving 2.3k citations

Peers

Fiorella Gurrieri
Comparison fields: 5 of 102
  • Molecular Biology 1.4k
  • Genetics 1.3k
  • Pediatrics, Perinatology and Child Health 345
  • Cognitive Neuroscience 290
  • Developmental Biology 219
Replace Angelo Selicorni with:
Angelo Selicorni Italy
Carlos A. Bacino United States
Donatella Milani Italy
Cédric Le Caignec France
Benoı̂t Arveiler France
Anne Moncla France
Maureen Bocian United States
Jeffrey W. Innis United States
M. W. Partington Canada
Hans G. Dauwerse Netherlands
Fiorella Gurrieri relative to Angelo Selicorni Italy Angelo Selicorni's profile →
Citations per field
00.5×1.5×2.4×
Angelo Selicorni · 1×
Citations per year

Countries citing papers authored by Fiorella Gurrieri

Since Specialization
Citations

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

Fields of papers citing papers by Fiorella Gurrieri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fiorella Gurrieri

This figure shows the co-authorship network connecting the top 25 collaborators of Fiorella Gurrieri. A scholar is included among the top collaborators of Fiorella Gurrieri 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 Fiorella Gurrieri. Fiorella Gurrieri 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
#WorkIndexed citations
1 0
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3 5
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7 10
8 5
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10 34
11 178
12 36
13 176
14 21
15 17
16 1
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P63 mutations in the EEC, Hay-Wells, ADULT syndromes and in split hand/foot malformation reveals a genotype-phenotype correlation.
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18 135
19 2
20 7

About Fiorella Gurrieri

Fiorella Gurrieri is a scholar working on Developmental Biology, Genetics and Molecular Biology, having authored 88 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Genetic Syndromes and Imprinting (12 papers). The work is most often cited by research in Developmental Biology (219 citations), Genetics (1.3k citations) and Molecular Biology (1.4k citations). Fiorella Gurrieri has collaborated with scholars based in Italy, United States and Canada. Frequent co-authors include Giovanni Neri, Charles E. Schwartz, Eugenio Sangiorgi, David B. Everman, Angela E. Lin, Ginevra Zanni, Helga V. Toriello, Marcella Zollino, Maurizio Genuardi and Brunella Franco. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

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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