Francesca Antonacci

7.9k citations
42 papers · 5.3k · 7 hit papers · h-index 29

Impact in

  • Genetics top 0.5%
    • Genomic variations and chromosomal abnormalities
    • Genetic Associations and Epidemiology
    • Genomics and Rare Diseases
    • Genome Rearrangement Algorithms
    • Genetics and Neurodevelopmental Disorders
    • Neurogenesis and neuroplasticity mechanisms

Papers in

    • Genomic variations and chromosomal abnormalities 32
    • Genome Rearrangement Algorithms 5
    • Chromosomal and Genetic Variations 11

Francesca Antonacci

40 papers receiving 5.2k citations

Francesca Antonacci's Hit Papers

Complete sequencing of ape genomes 2025 · 65 citations
650+6+12Years since publication250500750

Peers

Francesca Antonacci
Comparison fields: 5 of 130
  • Genetics 3.1k
  • Developmental Neuroscience 171
  • Molecular Biology 1.5k
  • Plant Science 782
  • Cancer Research 141
Replace James M. Sikela with:
James M. Sikela United States
Belén Lorente-Galdós United States
Megan Y. Dennis United States
Mario Ventura Italy
Zev N. Kronenberg United States
David Juan Spain
Mario Cáceres Spain
Craig B. Lowe United States
Kendra Hoekzema United States
Ingrid Plajzer-Frick United States
Francesca Antonacci relative to James M. Sikela United States James M. Sikela's profile →
Citations per field
00.5×2×3.0×
James M. Sikela · 1×
Citations per year

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-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.

Border = papers with Francesca Antonacci Line = papers co-authored together Francesca Antonacci links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mapping and sequencing of structural variation from eight human genomes
Hit paper breakdown →
2008827
2
Resolving the complexity of the human genome using single-molecule sequencing
Hit paper breakdown →
2014557
3
Personalized copy number and segmental duplication maps using next-generation sequencing
Hit paper breakdown →
2009547
4
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Hit paper breakdown →
2010523
5
Diversity of Human Copy Number Variation and Multicopy Genes
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2010522
6 2012308
7 2008156
8 2009124
9 2020117
10 2017112
11 2012110
12 2007109
13 2010109
14 200999
15 201696
16 201494
17 202294
18 200991
19 201079
20 201069

About Francesca Antonacci

Francesca Antonacci is a scholar working on Genetics, Plant Science, Molecular Biology, Neurology and Sensory Systems, having authored 42 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (32 papers), Chromosomal and Genetic Variations (11 papers), Genomics and Phylogenetic Studies (6 papers), Genome Rearrangement Algorithms (5 papers), Neuroblastoma Research and Treatments (2 papers), Vestibular and auditory disorders (1 paper), Pleistocene-Era Hominins and Archaeology (1 paper) and Genomics and Chromatin Dynamics (1 paper). The work is most often cited by research in Genetics (3.1k citations), Developmental Neuroscience (171 citations), Molecular Biology (1.5k citations), Plant Science (782 citations) and Cancer Research (141 citations). Francesca Antonacci has collaborated with scholars based in United States, Italy and Germany. Frequent co-authors include Evan E. Eichler, Maika Malig, Peter H. Sudmant, Can Alkan, Jacob Otto Kitzman, Jeffrey M. Kidd, Fereydoun Hormozdiari, Tomàs Marquès‐Bonet, Mario Ventura and Megan Y. Dennis. Their work appears in journals such as Nature, Nature Genetics, Science, Genes and Nature Methods.

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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