Francesca Antonacci

8.4k citations

45 papers · 3.4k indexed · 2 hit papers · h-index 24

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 ⓘ

General Arts and Humanities 3
- Italian Literature and Culture 3
Genetics 28
- Genomic variations and chromosomal abnormalities 26
- Genomics and Rare Diseases 3

Co-authors: Evan E. Eichler (29 shared papers)Maika Malig (12 shared papers)Peter H. Sudmant (8 shared papers)Can Alkan (9 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)Nature Methods (2 papers)PLoS Genetics (2 papers)
Partner nations: United States Italy Spain

In The Last Decade

Francesca Antonacci

39 papers receiving 3.4k citations

Hit Papers

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Resolving the complexity of the human genome using single-molecule sequencing 2014 · 499 citations

Peers

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

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20 of 20 papers shown

Showing the 20 most-cited of 45 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 Nature Genetics ·Can Alkan, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, Gozde Aksay, Francesca Antonacci, Fereydoun Hormozdiari, Jacob O. Kitzman, Carl Baker, Maika Malig, Onur Mutlu, S. Cenk Şahinalp, Richard A. Gibbs, Evan E. Eichler Hit paper breakdown →	2009	505
2	Resolving the complexity of the human genome using single-molecule sequencing Nature ·Mark Chaisson, John Huddleston, Megan Y. Dennis, Peter H. Sudmant, Maika Malig, Fereydoun Hormozdiari, Francesca Antonacci, Urvashi Surti, Richard Sandstrom, Matthew Boitano, Jane M. Landolin, J Stamatoyannopoulos, Michael W. Hunkapiller, Jonas Korlach, Evan E. Eichler Hit paper breakdown →	2014	499
3	Diversity of Human Copy Number Variation and Multicopy Genes Science ·Peter H. Sudmant, Jacob O. Kitzman, Francesca Antonacci, Can Alkan, Maika Malig, Anya Tsalenko, Nick Sampas, Laurakay Bruhn, Jay Shendure, (unknown), (unknown)	2010	483
4	Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication Cell ·Megan Y. Dennis, Xander Nuttle, Peter H. Sudmant, Francesca Antonacci, Tina Graves, Mikhail Nefedov, Jill A. Rosenfeld, Saba Sajjadian, Maika Malig, Holland Kotkiewicz, Cynthia J. Curry, Susan Shafer, Lisa G. Shaffer, Pieter J. de Jong, Richard K. Wilson, Evan E. Eichler	2012	274
5	Reconstructing complex regions of genomes using long-read sequencing technology Genome Research ·John Huddleston, Swati Ranade, Maika Malig, Francesca Antonacci, Mark Chaisson, Lawrence Hon, Peter H. Sudmant, Tina Graves, Can Alkan, Megan Y. Dennis, Richard K. Wilson, Stephen W. Turner, Jonas Korlach, Evan E. Eichler	2014	179
6	Evolutionary toggling of the MAPT 17q21.31 inversion region Nature Genetics ·Michael C. Zody, Zhaoshi Jiang, Hon‐Chung Fung, Francesca Antonacci, LaDeana W. Hillier, Maria Francesca Cardone, Tina Graves, Jeffrey M. Kidd, Ze Cheng, Amr Abouelleil, Lin Chen, John Wallis, Jarret Glasscock, Richard K. Wilson, Amy Denise Reily, Jaime Duckworth, Mario Ventura, John Hardy, Wesley C. Warren, Evan E. Eichler	2008	133
7	Evolutionary Formation of New Centromeres in Macaque Science ·Mario Ventura, Francesca Antonacci, Maria Francesca Cardone, Roscoe Stanyon, Pietro D’Addabbo, Angelo Cellamare, Leslee Sprague, Evan E. Eichler, Nicoletta Archidiacono, Mariano Rocchi	2007	108
8	Programmed loss of millions of base pairs from a vertebrate genome Proceedings of the National Academy of Sciences ·Jeramiah J. Smith, Francesca Antonacci, Evan E. Eichler, Chris T. Amemiya	2009	106
9	Evolution and diversity of copy number variation in the great ape lineage Genome Research ·Peter H. Sudmant, John Huddleston, Claudia Rita Catacchio, Maika Malig, LaDeana W. Hillier, Carl Baker, Kiana Mohajeri, Ivanela Kondova, Ronald E. Bontrop, Stephan P. Persengiev, Francesca Antonacci, Mario Ventura, Javier Prado-Martinez, (unknown), Tomàs Marquès‐Bonet, Evan E. Eichler	2013	106
10	Characterization of missing human genome sequences and copy-number polymorphic insertions Nature Methods ·Jeffrey M. Kidd, Nick Sampas, Francesca Antonacci, Tina Graves, Robert S. Fulton, Hillary S. Hayden, Can Alkan, Maika Malig, Mario Ventura, Giuliana Giannuzzi, Joelle Kallicki, Paige Anderson, Anya Tsalenko, N. Alice Yamada, Peter Tsang, Rajinder Kaul, Richard K. Wilson, Laurakay Bruhn, Evan E. Eichler	2010	97
11	Characterization of six human disease-associated inversion polymorphisms Human Molecular Genetics ·Francesca Antonacci, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, Mario Ventura, Priscillia Siswara, Zhaoshi Jiang, Evan E. Eichler	2009	94
12	Structural diversity and African origin of the 17q21.31 inversion polymorphism Nature Genetics ·Karyn Meltz Steinberg, Francesca Antonacci, Peter H. Sudmant, Jeffrey M. Kidd, Colin Campbell, Laura Vives, Maika Malig, Laura Scheinfeldt, William Beggs, Muntaser E. Ibrahim, Godfrey Lema, Thomas Nyambo, Sabah A. Omar, Jean-Marie Bodo, Alain Froment, Michael P. Donnelly, Kenneth K. Kídd, Sarah A. Tishkoff, Evan E. Eichler	2012	88
13	Palindromic GOLGA8 core duplicons promote chromosome 15q13.3 microdeletion and evolutionary instability Nature Genetics ·Francesca Antonacci, Megan Y. Dennis, John Huddleston, Peter H. Sudmant, Karyn Meltz Steinberg, Jill A. Rosenfeld, Mattia Miroballo, Tina Graves, Laura Vives, Maika Malig, Laura Denman, Archana N. Raja, Andrew B. Stuart, Joyce Tang, Brenton P. Munson, Lisa G. Shaffer, Chris T. Amemiya, Richard K. Wilson, Evan E. Eichler	2014	86
14	Death and Resurrection of the Human IRGM Gene PLoS Genetics ·Cemalettin Bekpen, Tomàs Marquès‐Bonet, Can Alkan, Francesca Antonacci, Maria Bruna Leogrande, Mario Ventura, Jeffrey M. Kidd, Priscillia Siswara, Jonathan C. Howard, Evan E. Eichler	2009	82
15	A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk Nature Genetics ·Francesca Antonacci, Jeffrey M. Kidd, Tomàs Marquès‐Bonet, Brian Teague, Mario Ventura, Santhosh Girirajan, Can Alkan, Colin Campbell, Laura Vives, Maika Malig, Jill A. Rosenfeld, Blake C. Ballif, Lisa G. Shaffer, Tina Graves, Richard K. Wilson, David C. Schwartz, Evan E. Eichler	2010	73
16	Genome-wide characterization of centromeric satellites from multiple mammalian genomes Genome Research ·Can Alkan, Maria Francesca Cardone, Claudia Rita Catacchio, Francesca Antonacci, Stephen J. O’Brien, Oliver A. Ryder, Stefania Purgato, Monica Zoli, Giuliano Della Valle, Evan E. Eichler, Mario Ventura	2010	69
17	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 ·Heather C Mefford, Neil Shafer, Francesca Antonacci, Jesse Tsai, Sarah S. Park, Anne Hing, Mark J. Rieder, Matthew D. Smyth, Matthew L. Speltz, Evan E. Eichler, Michael L. Cunningham	2010	59
18	Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes Science ·PingHsun Hsieh, Mitchell R. Vollger, Vy Dang, David Porubský, Carl Baker, Stuart Cantsilieris, Kendra Hoekzema, Alexandra P. Lewis, Katherine M. Munson, Melanie Sorensen, Zev Kronenberg, Shwetha C. Murali, Bradley J. Nelson, Giorgia Chiatante, Flavia Angela Maria Maggiolini, Hélène Blanché, Jason G. Underwood, Francesca Antonacci, Jean‐François Deleuze, Evan E. Eichler	2019	51
19	New Insights into Centromere Organization and Evolution from the White-Cheeked Gibbon and Marmoset Molecular Biology and Evolution ·Angelo Cellamare, Claudia Rita Catacchio, Can Alkan, Giuliana Giannuzzi, Francesca Antonacci, Maria Francesca Cardone, Giuliano Della Valle, Maika Malig, Mariano Rocchi, Evan E. Eichler, Mario Ventura	2009	41
20	Recurrent inversion toggling and great ape genome evolution Nature Genetics ·David Porubský, Ashley D. Sanders, Wolfram Höps, PingHsun Hsieh, Arvis Sulovari, Ruiyang Li, Ludovica Mercuri, Melanie Sorensen, Shwetha C. Murali, David Gordon, Stuart Cantsilieris, Alex A. Pollen, Mario Ventura, Francesca Antonacci, Tobias Marschall, Jan O. Korbel, Evan E. Eichler	2020	37

About Francesca Antonacci

Francesca Antonacci is a scholar working on General Arts and Humanities, Genetics, Plant Science, Neuropsychology and Physiological Psychology and Molecular Biology, having authored 45 papers that have together received 3.4k indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (26 papers), Genomic variations and chromosomal abnormalities (26 papers), Genomics and Phylogenetic Studies (11 papers), Genomics and Chromatin Dynamics (10 papers), Educational and Social Studies (6 papers), Italian Literature and Culture (3 papers), Genomics and Rare Diseases (3 papers) and Neuroblastoma Research and Treatments (2 papers). The work is most often cited by research in Genetics (1.9k citations), Molecular Biology (2.3k citations), Plant Science (1.3k citations), Cancer Research (315 citations) and Developmental Neuroscience (64 citations). Francesca Antonacci has collaborated with scholars based in United States, Italy and Spain. Frequent 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. Their work appears in journals such as Genome Research, Nature Genetics, Science, Nature Methods 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.

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