Anna Baroncini

1.2k total citations
29 papers, 458 citations indexed

About

Anna Baroncini is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Anna Baroncini has authored 29 papers receiving a total of 458 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 10 papers in Pediatrics, Perinatology and Child Health and 6 papers in Molecular Biology. Recurrent topics in Anna Baroncini's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and BRCA gene mutations in cancer (6 papers). Anna Baroncini is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and BRCA gene mutations in cancer (6 papers). Anna Baroncini collaborates with scholars based in Italy, India and Germany. Anna Baroncini's co-authors include Antonino Forabosco, Orsetta Zuffardi, Elisa Calzolari, Roberto Giorda, María Clara Bonaglia, Francesca Rivieri, Gianni Astolfi, Maria Elisabetta Raggi, Elena Rossi and G Cocchi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genome Research and The American Journal of Human Genetics.

In The Last Decade

Anna Baroncini

28 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Baroncini Italy 13 256 149 128 101 64 29 458
Moira Blyth United Kingdom 12 162 0.6× 139 0.9× 51 0.4× 28 0.3× 68 1.1× 22 379
Emmanouil Manolakos Greece 15 342 1.3× 181 1.2× 312 2.4× 102 1.0× 24 0.4× 70 642
Takeki Hirano Japan 14 238 0.9× 170 1.1× 92 0.7× 29 0.3× 66 1.0× 28 549
Birsen Karaman Türkiye 12 157 0.6× 180 1.2× 57 0.4× 32 0.3× 44 0.7× 58 345
Claire Turner United Kingdom 13 414 1.6× 304 2.0× 183 1.4× 31 0.3× 19 0.3× 14 578
Alida C. Knegt Netherlands 14 257 1.0× 271 1.8× 232 1.8× 37 0.4× 47 0.7× 35 652
I. López Pajares Spain 12 316 1.2× 286 1.9× 106 0.8× 94 0.9× 64 1.0× 27 493
Daniele De Brasi Italy 14 256 1.0× 224 1.5× 86 0.7× 48 0.5× 43 0.7× 44 478
Barbara Delle Chiaie Belgium 7 251 1.0× 195 1.3× 136 1.1× 38 0.4× 48 0.8× 10 423
Bruno Donadille France 15 354 1.4× 602 4.0× 94 0.7× 28 0.3× 43 0.7× 35 968

Countries citing papers authored by Anna Baroncini

Since Specialization
Citations

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

Fields of papers citing papers by Anna Baroncini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Baroncini

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Baroncini. A scholar is included among the top collaborators of Anna Baroncini 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 Anna Baroncini. Anna Baroncini 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.
Astolfi, Gianni, Stefania Bigoni, Anna Baroncini, et al.. (2022). Prenatal genetic counselling: issues and perspectives for pre-conceptional health care in Emilia Romagna (Northern Italy). SHILAP Revista de lepidopterología. 11(2).
2.
Baroncini, Anna, Olga Calabrese, Marco Colotto, et al.. (2022). Knowledge and attitude of general pratictioners towards direct-to-consumer genomic tests: a survey conducted in Italy. SHILAP Revista de lepidopterología. 12(4). 2 indexed citations
3.
Baroncini, Anna, Francesca Torricelli, Guido Cocchi, & Giovanni Corsello. (2022). Survey of Italian Pediatricians on awareness, experiences and beliefs regarding direct-to-consumer genetic testing in minors. SHILAP Revista de lepidopterología. 16(1). 1 indexed citations
4.
Baldasseroni, Samuele, Alessandra Pratesi, Francesco Orso, et al.. (2020). Role of Frailty on Risk Stratification in Cardiac Surgery and Procedures. Advances in experimental medicine and biology. 1216. 99–113. 11 indexed citations
5.
Baldasseroni, Samuele, Alessandra Pratesi, Pierluigi Stefàno, et al.. (2020). Pre-operative physical performance as a predictor of in-hospital outcomes in older patients undergoing elective cardiac surgery. European Journal of Internal Medicine. 84. 80–87. 14 indexed citations
6.
Baroncini, Anna, et al.. (2013). 8q12 microduplication including CHD7: clinical report on a new patient with Duane retraction syndrome type 3. Molecular Cytogenetics. 6(1). 49–49. 5 indexed citations
7.
Sun, Yu, Rowida Almomani, Emmelien Aten, et al.. (2010). Terminal Osseous Dysplasia Is Caused by a Single Recurrent Mutation in the FLNA Gene. The American Journal of Human Genetics. 87(1). 146–153. 45 indexed citations
8.
Floridia, Giovanna, Vincenzo Falbo, Federica Censi, et al.. (2008). The Italian External Quality Assessment Scheme in Classical Cytogenetics: Four Years of Activity. Public Health Genomics. 11(5). 295–303. 3 indexed citations
9.
Giorda, Roberto, María Clara Bonaglia, Anna Baroncini, et al.. (2008). Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1). European Journal of Human Genetics. 16(8). 897–905. 26 indexed citations
10.
Bonaglia, María Clara, Roberto Giorda, Silvana Beri, et al.. (2008). Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversion. European Journal of Human Genetics. 17(4). 426–433. 12 indexed citations
11.
Compadretti, Giacomo Ceroni, Ignazio Tasca, Anna Baroncini, & Maria Carla Pittalis. (2007). Nasal Abnormalities in the 9p Deletion Syndrome. Archives of Otolaryngology - Head and Neck Surgery. 133(10). 1054–1054. 1 indexed citations
12.
Baroncini, Anna, et al.. (2006). Terminal osseous dysplasia with pigmentary defects: Clinical description of a new family. American Journal of Medical Genetics Part A. 143A(1). 51–57. 12 indexed citations
13.
Calzolari, Elisa & Anna Baroncini. (2005). International Cooperation and Networking in Genetic Health Care Provision: Issues Arising from the Genetic Services Plan for the Emilia-Romagna Region, Italy. Public Health Genomics. 8(2). 122–129. 3 indexed citations
14.
Baroncini, Anna, Francesca Rivieri, Gianfranco Croci, et al.. (2005). FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. European Journal of Medical Genetics. 48(4). 388–396. 16 indexed citations
15.
Calzolari, Elisa, Giampaolo Garani, G Cocchi, et al.. (2003). Congenital heart defects: 15 years of experience of the Emilia-Romagna Registry (Italy). European Journal of Epidemiology. 18(8). 773–780. 73 indexed citations
16.
Bonaglia, María Clara, Roberto Giorda, Maria Elisabetta Raggi, et al.. (2000). Inverted duplications are recurrent rearrangements always associated with a distal deletion: description of a new case involving 2q. European Journal of Human Genetics. 8(8). 597–603. 53 indexed citations
17.
Caramia, G, et al.. (1990). Ring chromosome 7: Report of the fifth case. European Journal of Pediatrics. 149(7). 475–476. 13 indexed citations
18.
Baroncini, Anna, et al.. (1990). Distal 12p deletion in a stillborn infant. American Journal of Medical Genetics. 36(3). 358–360. 19 indexed citations
19.
Forabosco, Antonino, Anna Baroncini, Leda Dalprà, et al.. (1988). The phenotype of partial dup(7q) reconsidered: a report of five new cases. Clinical Genetics. 34(1). 48–59. 34 indexed citations
20.
Lenzini, Elisabetta, et al.. (1980). [The syndrome of trisomy 9p and presentation of 2 new cases].. PubMed. 71(1013). 347–8. 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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