Francesca Antonacci
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Molecular Biology top 5%
- Genomics and Phylogenetic Studies
- Genomics and Chromatin Dynamics
- RNA and protein synthesis mechanisms
- Congenital heart defects research
Papers in
-
- Genomics and Phylogenetic Studies 11
- Genomics and Chromatin Dynamics 9
- Genetics 28
- Genomic variations and chromosomal abnormalities 26
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Evan E. Eichler (29 shared papers)Maika Malig (12 shared papers)Can Alkan (9 shared papers)Peter H. Sudmant (8 shared papers)Jacob O. Kitzman (2 shared papers)Jeffrey M. Kidd (7 shared papers)Mario Ventura (18 shared papers)Tomàs Marquès‐Bonet (6 shared papers)
- Journals
- Genome Research (7 papers)Nature Genetics (6 papers)Science (3 papers)Genes (2 papers)PLoS Genetics (2 papers)
- Partner nations
- United StatesItalySpain
In The Last Decade
Francesca Antonacci
41 papers receiving 3.5k citations
Francesca Antonacci's Hit Papers
Peers
Comparison fields: 5 of 132
- Genetics 1.8k
- Molecular Biology 2.2k
- Plant Science 1.1k
- Cancer Research 285
- Developmental Neuroscience 66
Countries citing papers authored by Francesca Antonacci
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
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-authors
The 25 scholars most cited alongside Francesca Antonacci, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Personalized copy number and segmental duplication maps using next-generation sequencing Hit paper breakdown → | 2009 | 534 |
| 2 | Resolving the complexity of the human genome using single-molecule sequencing Hit paper breakdown → | 2014 | 533 |
| 3 | Diversity of Human Copy Number Variation and Multicopy Genes Hit paper breakdown → | 2010 | 508 |
| 4 | 2012 | 295 | |
| 5 | 2014 | 186 | |
| 6 | 2008 | 136 | |
| 7 | 2009 | 117 | |
| 8 | 2013 | 117 | |
| 9 | 2007 | 116 | |
| 10 | 2010 | 104 | |
| 11 | 2009 | 98 | |
| 12 | 2012 | 90 | |
| 13 | 2014 | 88 | |
| 14 | 2009 | 88 | |
| 15 | 2010 | 77 | |
| 16 | 2010 | 74 | |
| 17 | 2010 | 64 | |
| 18 | 2019 | 54 | |
| 19 | 2009 | 42 | |
| 20 | 2020 | 41 |
About Francesca Antonacci
Francesca Antonacci is a scholar working on Molecular Biology, Genetics, Plant Science, Education and General Arts and Humanities, having authored 46 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (26 papers), Chromosomal and Genetic Variations (24 papers), Genomics and Phylogenetic Studies (11 papers), Genomics and Chromatin Dynamics (9 papers), Educational and Social Studies (6 papers), Genomics and Rare Diseases (3 papers), Italian Literature and Culture (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (1.8k citations), Molecular Biology (2.2k citations), Plant Science (1.1k citations), Cancer Research (285 citations) and Developmental Neuroscience (66 citations). Francesca Antonacci has collaborated with scholars based in United States, Italy and Spain. Frequent co-authors include Evan E. Eichler, Maika Malig, Can Alkan, Peter H. Sudmant, Jacob O. Kitzman, Jeffrey M. Kidd, Mario Ventura, Tomàs Marquès‐Bonet, Fereydoun Hormozdiari and Megan Y. Dennis. Their work appears in journals such as Genome Research, Nature Genetics, Science, Genes and PLoS Genetics.
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.