Chiara Gnan

1.2k total citations
7 papers, 52 citations indexed

About

Chiara Gnan is a scholar working on Genetics, Genetics and Molecular Biology. According to data from OpenAlex, Chiara Gnan has authored 7 papers receiving a total of 52 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in Chiara Gnan's work include Genomic variations and chromosomal abnormalities (4 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Chiara Gnan is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Chiara Gnan collaborates with scholars based in Italy, Argentina and Slovenia. Chiara Gnan's co-authors include Daniela De Rocco, Felisa C. Molinas, Nora P. Goette, Paula G. Heller, Federica Baldan, Ana C. Glembotsky, Giuseppe Damante, Alessandra Franzoni, Rosana F. Marta and Alessandro Pecci and has published in prestigious journals such as International Journal of Pharmaceutics, Gene and Journal of Thrombosis and Haemostasis.

In The Last Decade

Chiara Gnan

6 papers receiving 52 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Chiara Gnan Italy	4	22	21	19	6	5	7	52
Aidan Thomas Canada	5	26 1.2×	19 0.9×	17 0.9×	3 0.5×	6 1.2×	7	56
Julia Obländer Germany	4	39 1.8×	31 1.5×	12 0.6×	6 1.0×	6 1.2×	10	66
Gudrun Goehring Germany	3	33 1.5×	19 0.9×	7 0.4×	3 0.5×	2 0.4×	7	40
Nhu Nguyen United States	4	21 1.0×	46 2.2×	17 0.9×	7 1.2×	2 0.4×	4	69
Daniel Hüebschmann Germany	3	15 0.7×	27 1.3×	9 0.5×	14 2.3×	5 1.0×	3	49
Peer Wünsche Germany	3	11 0.5×	38 1.8×	11 0.6×	13 2.2×	4 0.8×	3	45
Claire Searle United Kingdom	4	6 0.3×	28 1.3×	26 1.4×	4 0.7×	5 1.0×	8	66
Rossella Tita Italy	3	9 0.4×	37 1.8×	28 1.5×	4 0.7×	3 0.6×	7	60
Alissa Greenwald United States	2	10 0.5×	17 0.8×	5 0.3×	11 1.8×	5 1.0×	3	46
Christopher J. Yoon United States	5	19 0.9×	50 2.4×	9 0.5×	25 4.2×	4 0.8×	8	76

Countries citing papers authored by Chiara Gnan

Since Specialization

Citations

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

Fields of papers citing papers by Chiara Gnan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Gnan

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Gnan. A scholar is included among the top collaborators of Chiara Gnan 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 Chiara Gnan. Chiara Gnan 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.

Baldan, Federica, Chiara Gnan, Giuseppe Damante, et al.. (2024). Chromoanagenesis of chromosome 22 in a subject with obesity and borderline cognitive performance. Gene. 933. 148956–148956.

2.

Dapas, Barbara, Gabriele Pozzato, Sonia Zorzet, et al.. (2019). Effects of eEF1A1 targeting by aptamer/siRNA in chronic lymphocytic leukaemia cells. International Journal of Pharmaceutics. 574. 118895–118895. 13 indexed citations

3.

Baldan, Federica, et al.. (2018). Genomic Deletion Involving the <b><i>IMMP2L</i></b> Gene in Two Cases of Autism Spectrum Disorder. Cytogenetic and Genome Research. 154(4). 196–200. 11 indexed citations

4.

Lovrečić, Luca, Chiara Gnan, Federica Baldan, et al.. (2018). Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability. Molecular Cytogenetics. 11(1). 39–39. 3 indexed citations

5.

Gnan, Chiara, et al.. (2017). Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy. Molecular Syndromology. 8(2). 98–102. 1 indexed citations

6.

Sechi, Annalisa, et al.. (2016). Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings. Cytogenetic and Genome Research. 148(1). 14–18. 2 indexed citations

7.

Glembotsky, Ana C., Rosana F. Marta, Alessandro Pecci, et al.. (2012). International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country. Journal of Thrombosis and Haemostasis. 10(8). 1653–1661. 22 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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