Cristina Cuoco

1.3k total citations
38 papers, 647 citations indexed

About

Cristina Cuoco is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Cristina Cuoco has authored 38 papers receiving a total of 647 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 19 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in Cristina Cuoco's work include Genomic variations and chromosomal abnormalities (26 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Chromosomal and Genetic Variations (6 papers). Cristina Cuoco is often cited by papers focused on Genomic variations and chromosomal abnormalities (26 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Chromosomal and Genetic Variations (6 papers). Cristina Cuoco collaborates with scholars based in Italy, Switzerland and Germany. Cristina Cuoco's co-authors include Giorgio Gimelli, Elisa Tassano, P Maraschio, Patrizia Ronchetto, Claudio Romano, L. Tiepolo, Stefania Gimelli, Orsetta Zuffardi, M. Fraccaro and Marisol Mirabelli-Badenier and has published in prestigious journals such as PLoS ONE, Gene and Human Genetics.

In The Last Decade

Cristina Cuoco

38 papers receiving 594 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cristina Cuoco Italy 15 396 275 214 89 87 38 647
Joe J. Hoo United States 20 510 1.3× 388 1.4× 196 0.9× 206 2.3× 93 1.1× 54 900
Courtney Sebold United States 16 437 1.1× 216 0.8× 141 0.7× 97 1.1× 52 0.6× 27 616
Vanna Pecile Italy 17 499 1.3× 443 1.6× 175 0.8× 112 1.3× 70 0.8× 54 825
Roel Hordijk Netherlands 15 520 1.3× 409 1.5× 184 0.9× 100 1.1× 73 0.8× 22 739
Sophia Kitsiou‐Tzeli Greece 16 407 1.0× 422 1.5× 77 0.4× 69 0.8× 49 0.6× 39 656
Brigitte Benzacken France 20 737 1.9× 462 1.7× 426 2.0× 156 1.8× 57 0.7× 61 1.3k
Martine Doco‐Fenzy France 15 302 0.8× 349 1.3× 80 0.4× 70 0.8× 47 0.5× 29 690
Alina T. Midro Poland 16 575 1.5× 436 1.6× 244 1.1× 192 2.2× 36 0.4× 74 943
Sylvie Jaillard France 16 397 1.0× 435 1.6× 148 0.7× 44 0.5× 48 0.6× 54 802
Sara Loddo Italy 13 402 1.0× 277 1.0× 123 0.6× 59 0.7× 37 0.4× 39 639

Countries citing papers authored by Cristina Cuoco

Since Specialization
Citations

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

Fields of papers citing papers by Cristina Cuoco

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cristina Cuoco

This figure shows the co-authorship network connecting the top 25 collaborators of Cristina Cuoco. A scholar is included among the top collaborators of Cristina Cuoco 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 Cristina Cuoco. Cristina Cuoco 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.
Tassano, Elisa, et al.. (2016). Interstitial 11q24 deletion: a new case and review of the literature. Journal of Applied Genetics. 57(3). 357–362. 6 indexed citations
2.
Tassano, Elisa, Vidhya Jagannathan, Cord Drögemüller, et al.. (2015). Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion. American Journal of Medical Genetics Part A. 167(3). 537–544. 26 indexed citations
3.
Cuoco, Cristina, et al.. (2015). Hypogonadotropic hypogonadism in a trisomy X carrier: phenotype description and genotype correlation. Gynecological Endocrinology. 32(1). 14–17. 1 indexed citations
4.
5.
Tassano, Elisa, Marisol Mirabelli-Badenier, Edvige Veneselli, et al.. (2015). Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion. Molecular Cytogenetics. 8(1). 31–31. 14 indexed citations
6.
Tassano, Elisa, et al.. (2015). Clinical and molecular delineation of a 16p13.2p13.13 microduplication. European Journal of Medical Genetics. 58(3). 194–198. 5 indexed citations
7.
Severino, Mariasavina, Andrea Accogli, Giorgio Gimelli, et al.. (2015). Clinico-radiological and molecular characterization of a child with ring chromosome 2 presenting growth failure, microcephaly, kidney and brain malformations. Molecular Cytogenetics. 8(1). 17–17. 15 indexed citations
8.
Tassano, Elisa, Andrea Accogli, Marco Pavanello, et al.. (2015). Interstitial 9p24.3 deletion involving only DOCK8 and KANK1 genes in two patients with non-overlapping phenotypic traits. European Journal of Medical Genetics. 59(1). 20–25. 11 indexed citations
9.
10.
Tassano, Elisa, et al.. (2014). Phenotypic and genetic characterization of a patient with a de novo interstitial 14q24.1q24.3 deletion. Molecular Cytogenetics. 7(1). 49–49. 4 indexed citations
11.
Gimelli, Stefania, Valeria Capra, Maja Di Rocco, et al.. (2014). Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders. Molecular Cytogenetics. 7(1). 54–54. 25 indexed citations
12.
Capra, Valeria, Samantha Mascelli, Maria Luisa Garrè, et al.. (2013). Parental Imbalances Involving Chromosomes 15q and 22q May Predispose to the Formation of De Novo Pathogenic Microdeletions and Microduplications in the Offspring. PLoS ONE. 8(3). e57910–e57910. 5 indexed citations
13.
14.
Baglietto, M. G., Gianluca Caridi, Giorgio Gimelli, et al.. (2013). RORB gene and 9q21.13 microdeletion: Report on a patient with epilepsy and mild intellectual disability. European Journal of Medical Genetics. 57(1). 44–46. 31 indexed citations
15.
Gimelli, Stefania, Cristina Cuoco, Patrizia Ronchetto, Giorgio Gimelli, & Elisa Tassano. (2013). Interstitial deletion 14q31.1q31.3 transmitted from a mother to her daughter, both with features of hemifacial microsomia. Journal of Applied Genetics. 54(3). 361–365. 9 indexed citations
16.
Tassano, Elisa, Roberto Valli, Concetta Micalizzi, et al.. (2012). New recurrent chromosome change in pediatric therapy-related myelodysplastic syndrome: unbalanced translocation 1/6 with cryptic duplication of short arm of chromosome 6. Leukemia & lymphoma. 53(12). 2434–2438. 1 indexed citations
17.
Tassano, Elisa, et al.. (2011). Monosomal complex karyotype in pediatric mixed phenotype acute leukemia. Cancer Genetics. 204(9). 507–511. 2 indexed citations
18.
Cuoco, Cristina, Patrizia Ronchetto, Stefania Gimelli, et al.. (2011). Microarray based analysis of an inherited terminal 3p26.3 deletion, containing only the CHL1 gene, from a normal father to his two affected children. Orphanet Journal of Rare Diseases. 6(1). 12–12. 42 indexed citations
19.
Mignon‐Ravix, Cécile, D. Depétris, Judith Luciani, et al.. (2007). Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations. European Journal of Human Genetics. 15(4). 432–440. 38 indexed citations
20.
Buscaglia, M, F Dambrosio, Silvana Guerneri, et al.. (1990). Genetic amniocentesis: 505 cases performed before the sixteenth week of gestation. Prenatal Diagnosis. 10(6). 359–364. 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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