Franca Bernardi

953 total citations
13 papers, 367 citations indexed

About

Franca Bernardi is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Franca Bernardi has authored 13 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Plant Science and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Franca Bernardi's work include Chromosomal and Genetic Variations (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Franca Bernardi is often cited by papers focused on Chromosomal and Genetic Variations (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Franca Bernardi collaborates with scholars based in Italy, Canada and Portugal. Franca Bernardi's co-authors include Orsetta Zuffardi, Cesare Danesino, P Maraschio, Elena Rossi, Giovanna Floridia, Antonella Minelli, Laura Papi, Massimiliano Casali, G Chiumello and Ivana Magnani and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Human Reproduction and Journal of Medical Genetics.

In The Last Decade

Franca Bernardi

13 papers receiving 347 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Franca Bernardi Italy 10 246 128 116 93 37 13 367
Philip N. Mowrey United States 11 232 0.9× 88 0.7× 162 1.4× 134 1.4× 34 0.9× 22 436
G. Bourrouillou France 14 398 1.6× 95 0.7× 279 2.4× 146 1.6× 36 1.0× 40 587
M.‐J. Le Bris France 13 262 1.1× 117 0.9× 102 0.9× 164 1.8× 48 1.3× 21 422
P Colombiès France 12 150 0.6× 75 0.6× 127 1.1× 93 1.0× 121 3.3× 64 438
M.H. Breuning Netherlands 8 157 0.6× 77 0.6× 219 1.9× 43 0.5× 34 0.9× 13 385
G. R. Stalder Switzerland 12 256 1.0× 87 0.7× 146 1.3× 98 1.1× 34 0.9× 21 387
Bogdan Kałużewski Poland 13 200 0.8× 88 0.7× 200 1.7× 67 0.7× 6 0.2× 59 407
R Elles United Kingdom 11 302 1.2× 78 0.6× 318 2.7× 75 0.8× 16 0.4× 21 530
Jack H. Jung Canada 13 208 0.8× 61 0.5× 218 1.9× 83 0.9× 6 0.2× 19 411
Berta Santesson Sweden 12 171 0.7× 82 0.6× 160 1.4× 78 0.8× 12 0.3× 23 410

Countries citing papers authored by Franca Bernardi

Since Specialization
Citations

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

Fields of papers citing papers by Franca Bernardi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Franca Bernardi

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

All Works

13 of 13 papers shown
1.
Dardano, Angela, Elisa Danese, Maria Vittoria Davì, et al.. (2009). Chromosome Translocation Frequency after Radioiodine Thyroid Remnant Ablation: A Comparison between Recombinant Human Thyrotropin Stimulation and Prolonged Levothyroxine Withdrawal. The Journal of Clinical Endocrinology & Metabolism. 94(9). 3472–3476. 30 indexed citations
2.
Rizzolio, Flavio, Tiziano Pramparo, Cinzia Sala, et al.. (2004). A susceptibility gene for premature ovarian failure (POF) maps to proximal Xq28. European Journal of Human Genetics. 12(10). 829–834. 30 indexed citations
3.
Maserati, Emanuela, Fabrizio Vinante, Franco Locatelli, et al.. (2001). Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15–20% of cases. Genes Chromosomes and Cancer. 33(1). 93–97. 60 indexed citations
4.
Giglio, Sabrina, Giulia Arrigo, Gian Paolo Dagrada, et al.. (2000). Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements. European Journal of Human Genetics. 8(1). 63–70. 26 indexed citations
5.
Maraschio, P, et al.. (1996). An analysis of Xq deletions. Human Genetics. 97(3). 375–381. 33 indexed citations
6.
Trabetti, Elisabetta, Roberta Galavotti, Elisabetta Zardini, et al.. (1993). The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphisms. Molecular and Cellular Probes. 7(4). 325–329. 10 indexed citations
7.
Minelli, Antonella, Giovanna Floridia, Elena Rossi, et al.. (1993). D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Human Genetics. 92(4). 391–396. 25 indexed citations
8.
Calzolari, Elisa, et al.. (1993). Characterization of a deleted Y chromosome in a male with Turner stigmata. Clinical Genetics. 43(1). 16–22. 8 indexed citations
9.
Rossi, Elena, Giovanna Floridia, Massimiliano Casali, et al.. (1993). Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.. Journal of Medical Genetics. 30(11). 926–931. 61 indexed citations
10.
Volinia, Stefano, P. Patracchini, Masayuki Otsu, et al.. (1992). Chromosomal localization of human p85 alpha, a subunit of phosphatidylinositol 3-kinase, and its homologue p85 beta.. PubMed. 7(4). 789–93. 15 indexed citations
11.
Bernardi, Franca, et al.. (1986). Reproductive failure and parental chromosome abnormalities. Human Reproduction. 1(2). 99–102. 6 indexed citations
12.
Maraschio, P, Orsetta Zuffardi, Franca Bernardi, et al.. (1981). Preferential maternal derivation in inv dup(15). Human Genetics. 57(4). 345–350. 58 indexed citations
13.
Zamboni, Giuseppe, et al.. (1980). Agenesis of the corpus callosum with mosaicism 46,XY/47,XY, extra ring chromosome.. Journal of Medical Genetics. 17(1). 59–61. 5 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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