Francesca Mari
Impact in
- Immunology and Allergy top 1%
- Cell Adhesion Molecules Research
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 65
- Genetics and Neurodevelopmental Disorders 39
- Genomic variations and chromosomal abnormalities 26
- Genomics and Rare Diseases 10
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- Congenital heart defects research 11
- RNA modifications and cancer 8
- Renal and related cancers 6
- Co-authors
- Alessandra Renieri (96 shared papers)Francesca Ariani (51 shared papers)Ilaria Longo (33 shared papers)Ilaria Meloni (38 shared papers)Maria Antonietta Mencarelli (41 shared papers)Mirella Bruttini (22 shared papers)Chiara Pescucci (18 shared papers)Michele Zappella (12 shared papers)
- Journals
- European Journal of Medical Genetics (7 papers)European Journal of Human Genetics (7 papers)Clinical Genetics (6 papers)Human Mutation (6 papers)Brain and Development (4 papers)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Francesca Mari
102 papers receiving 3.8k citations
Peers
Comparison fields: 5 of 110
- Immunology and Allergy 458
- Genetics 2.1k
- Cognitive Neuroscience 646
- Nephrology 194
- Molecular Biology 1.9k
Countries citing papers authored by Francesca Mari
This map shows the geographic impact of Francesca Mari'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 Mari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francesca Mari more than expected).
Fields of papers citing papers by Francesca Mari
This network shows the impact of papers produced by Francesca Mari. 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 Mari. The network helps show where Francesca Mari may publish in the future.
Co-authors
The 25 scholars most cited alongside Francesca Mari, 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 105 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 343 | |
| 2 | 2008 | 300 | |
| 3 | 2005 | 253 | |
| 4 | 2000 | 181 | |
| 5 | 2002 | 158 | |
| 6 | 2015 | 109 | |
| 7 | 2004 | 101 | |
| 8 | 2018 | 88 | |
| 9 | 2004 | 83 | |
| 10 | 2009 | 74 | |
| 11 | 2011 | 71 | |
| 12 | 2008 | 71 | |
| 13 | 2003 | 64 | |
| 14 | 2011 | 64 | |
| 15 | 2003 | 62 | |
| 16 | 2006 | 61 | |
| 17 | 2009 | 60 | |
| 18 | 2011 | 58 | |
| 19 | 2014 | 57 | |
| 20 | Are behaviour and motor performances of rheumatoid arthritis patients influenced by subclinical cognitive impairments? A clinical and neuroimaging study. | 2003 | 56 |
About Francesca Mari
Francesca Mari is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Immunology and Allergy and Oncology, having authored 105 papers that have together received 3.9k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (39 papers), Genomic variations and chromosomal abnormalities (26 papers), Autism Spectrum Disorder Research (16 papers), Cell Adhesion Molecules Research (12 papers), Congenital heart defects research (11 papers), Genomics and Rare Diseases (10 papers), RNA modifications and cancer (8 papers) and Renal and related cancers (6 papers). The work is most often cited by research in Immunology and Allergy (458 citations), Genetics (2.1k citations), Cognitive Neuroscience (646 citations), Nephrology (194 citations) and Molecular Biology (1.9k citations). Francesca Mari has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Alessandra Renieri, Francesca Ariani, Ilaria Longo, Ilaria Meloni, Maria Antonietta Mencarelli, Mirella Bruttini, Chiara Pescucci, Michele Zappella, Rossella Caselli and Eduardo Magalhães Rego. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics, Human Mutation and Brain and Development.
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.