Francesca Antonacci

8.4k total citations · 2 hit papers
45 papers, 3.4k citations indexed

About

Francesca Antonacci is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Francesca Antonacci has authored 45 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 28 papers in Genetics and 26 papers in Plant Science. Recurrent topics in Francesca Antonacci's work include Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (26 papers) and Genomics and Phylogenetic Studies (11 papers). Francesca Antonacci is often cited by papers focused on Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (26 papers) and Genomics and Phylogenetic Studies (11 papers). Francesca Antonacci collaborates with scholars based in United States, Italy and Spain. Francesca Antonacci's co-authors include Evan E. Eichler, Maika Malig, Peter H. Sudmant, Can Alkan, Jacob O. Kitzman, Jeffrey M. Kidd, Mario Ventura, Tomàs Marquès‐Bonet, Fereydoun Hormozdiari and Megan Y. Dennis and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Francesca Antonacci

39 papers receiving 3.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Personalized copy number and segmental duplication maps using next-generation sequencing

2009 505 citations Can Alkan, Jeffrey M. Kidd et al. Nature Genetics profile →
Resolving the complexity of the human genome using single-molecule sequencing

2014 499 citations Mark Chaisson, John Huddleston et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Francesca Antonacci United States	24	2.3k	1.9k	1.3k	315	173	45	3.4k
Peter H. Sudmant United States	24	2.1k 0.9×	1.6k 0.9×	777 0.6×	409 1.3×	132 0.8×	47	3.2k
Maika Malig United States	28	3.2k 1.4×	2.4k 1.3×	1.7k 1.3×	496 1.6×	208 1.2×	33	4.8k
Devin P. Locke United States	18	1.8k 0.8×	2.1k 1.1×	1.1k 0.9×	350 1.1×	201 1.2×	19	3.1k
Donald F. Conrad United States	27	1.8k 0.8×	2.5k 1.3×	640 0.5×	297 0.9×	243 1.4×	70	3.6k
W. James Kent United States	19	4.1k 1.7×	1.3k 0.7×	1.1k 0.9×	790 2.5×	85 0.5×	21	5.0k
Cathy Riemer United States	15	3.0k 1.3×	1.1k 0.6×	757 0.6×	342 1.1×	227 1.3×	25	4.7k
Mario Ventura Italy	41	3.4k 1.4×	3.0k 1.6×	2.7k 2.2×	280 0.9×	395 2.3×	96	5.2k
Alexej Abyzov United States	30	3.2k 1.3×	1.9k 1.0×	595 0.5×	820 2.6×	129 0.7×	68	4.4k
Ines Hellmann Germany	26	3.9k 1.7×	2.3k 1.2×	775 0.6×	504 1.6×	208 1.2×	34	5.5k
Laura Elnitski United States	30	3.9k 1.7×	1.2k 0.7×	898 0.7×	602 1.9×	60 0.3×	75	5.0k

Countries citing papers authored by Francesca Antonacci

Since Specialization

Citations

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

Fields of papers citing papers by Francesca Antonacci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Antonacci

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

All Works

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20 of 20 papers shown

L’Abbate, Alberto, David Porubský, Claudia Rita Catacchio, et al.. (2023). Structural Variation Evolution at the 15q11-q13 Disease-Associated Locus. International Journal of Molecular Sciences. 24(21). 15818–15818. 4 indexed citations

Mercuri, Ludovica, Alberto L’Abbate, Pietro D’Addabbo, et al.. (2022). A high-resolution map of small-scale inversions in the gibbon genome. Genome Research. 32(10). 1941–1951. 5 indexed citations

Antonacci, Francesca, et al.. (2020). Una scuola sulla soglia, tra vita e istituzione. BOA (University of Milano-Bicocca). 30. 76–86. 1 indexed citations

Maggiolini, Flavia Angela Maria, Ashley D. Sanders, Colin J. Shew, et al.. (2020). Single-cell strand sequencing of a macaque genome reveals multiple nested inversions and breakpoint reuse during primate evolution. Genome Research. 30(11). 1680–1693. 11 indexed citations

Hsieh, PingHsun, Mitchell R. Vollger, Vy Dang, et al.. (2019). Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes. Science. 366(6463). 51 indexed citations

Catacchio, Claudia Rita, Flavia Angela Maria Maggiolini, Pietro D’Addabbo, et al.. (2018). Inversion variants in human and primate genomes. Genome Research. 28(6). 910–920. 27 indexed citations

Antonacci, Francesca, et al.. (2017). IN MIGRANTS’ SHOES. A GAME TO RAISE AWARENESS AND SUPPORT LONG-LASTING LEARNING. SHILAP Revista de lepidopterología. 25(1). 55–68. 1 indexed citations

Chiatante, Giorgia, Mattia Miroballo, Joyce Tang, et al.. (2017). Discovery of large genomic inversions using long range information. BMC Genomics. 18(1). 65–65. 12 indexed citations

Huddleston, John, Swati Ranade, Maika Malig, et al.. (2014). Reconstructing complex regions of genomes using long-read sequencing technology. Genome Research. 24(4). 688–696. 179 indexed citations

10.

Sudmant, Peter H., John Huddleston, Claudia Rita Catacchio, et al.. (2013). Evolution and diversity of copy number variation in the great ape lineage. Genome Research. 23(9). 1373–1382. 106 indexed citations

11.

Giannuzzi, Giuliana, John Huddleston, Francesca Antonacci, et al.. (2013). Hominoid fission of chromosome 14/15 and the role of segmental duplications. Genome Research. 23(11). 1763–1773. 10 indexed citations

12.

Hurlé, Belén, Tomàs Marquès‐Bonet, Francesca Antonacci, et al.. (2011). Lineage-specific evolution of the vertebrate Otopetringene family revealed by comparative genomic analyses. BMC Evolutionary Biology. 11(1). 23–23. 16 indexed citations

13.

Fieuw, Annelies, Candy Kumps, Alexander Schramm, et al.. (2011). Identification of a novel recurrent 1q42.2‐1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas. International Journal of Cancer. 130(11). 2599–2606. 34 indexed citations

14.

Alkan, Can, Maria Francesca Cardone, Claudia Rita Catacchio, et al.. (2010). Genome-wide characterization of centromeric satellites from multiple mammalian genomes. Genome Research. 21(1). 137–145. 69 indexed citations

15.

Mefford, Heather C, Francesca Antonacci, Jesse Tsai, et al.. (2010). Copy number variation analysis in single‐suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis. American Journal of Medical Genetics Part A. 152A(9). 2203–2210. 59 indexed citations

16.

Kidd, Jeffrey M., Nick Sampas, Francesca Antonacci, et al.. (2010). Characterization of missing human genome sequences and copy-number polymorphic insertions. Nature Methods. 7(5). 365–371. 97 indexed citations

17.

Smith, Jeramiah J., Francesca Antonacci, Evan E. Eichler, & Chris T. Amemiya. (2009). Programmed loss of millions of base pairs from a vertebrate genome. Proceedings of the National Academy of Sciences. 106(27). 11212–11217. 106 indexed citations

18.

Antonacci, Francesca, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, et al.. (2009). Characterization of six human disease-associated inversion polymorphisms. Human Molecular Genetics. 18(14). 2555–2566. 94 indexed citations

19.

Bekpen, Cemalettin, Tomàs Marquès‐Bonet, Can Alkan, et al.. (2009). Death and Resurrection of the Human IRGM Gene. PLoS Genetics. 5(3). e1000403–e1000403. 82 indexed citations

20.

Zody, Michael C., Zhaoshi Jiang, Hon‐Chung Fung, et al.. (2008). Evolutionary toggling of the MAPT 17q21.31 inversion region. Nature Genetics. 40(9). 1076–1083. 133 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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