Michele Traversa
Impact in
- Genetics top 10%
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Dermatological and Skeletal Disorders
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
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- Congenital heart defects research
Papers in
- Genetics 10
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 3
- Connective tissue disorders research 2
- Genetic Associations and Epidemiology 2
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- Congenital heart defects research 2
- Co-authors
- Chiara Magri (7 shared papers)Massimo Gennarelli (4 shared papers)Paolo Valsecchi (3 shared papers)Emilio Sacchetti (3 shared papers)Alessandra Minelli (3 shared papers)Sergio Barlati (3 shared papers)Marina Colombi (2 shared papers)Chiara Dordoni (2 shared papers)
- Journals
- PLoS ONE (2 papers)Molecular Genetics and Genomics (1 paper)Cancers (1 paper)Orphanet Journal of Rare Diseases (1 paper)The Pharmacogenomics Journal (1 paper)
- Partner nations
- ItalyUnited StatesIsrael
In The Last Decade
Michele Traversa
16 papers receiving 391 citations
Peers
Comparison fields: 5 of 62
- Genetics 232
- Molecular Biology 183
- Biological Psychiatry 6
- Pediatrics, Perinatology and Child Health 45
- Psychiatry and Mental health 33
Countries citing papers authored by Michele Traversa
This map shows the geographic impact of Michele Traversa'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 Michele Traversa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michele Traversa more than expected).
Fields of papers citing papers by Michele Traversa
This network shows the impact of papers produced by Michele Traversa. 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 Michele Traversa. The network helps show where Michele Traversa may publish in the future.
Co-authors
The 25 scholars most cited alongside Michele Traversa, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 93 | |
| 2 | 2010 | 70 | |
| 3 | 2013 | 40 | |
| 4 | 2016 | 32 | |
| 5 | 2014 | 30 | |
| 6 | 2017 | 23 | |
| 7 | 2014 | 20 | |
| 8 | 2019 | 19 | |
| 9 | 2011 | 15 | |
| 10 | 2017 | 15 | |
| 11 | 2010 | 11 | |
| 12 | 2014 | 10 | |
| 13 | 2015 | 5 | |
| 14 | 2015 | 5 | |
| 15 | 2018 | 3 | |
| 16 | 2019 | 2 |
About Michele Traversa
Michele Traversa is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Rheumatology and Plant Science, having authored 16 papers that have together received 393 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Chromosomal and Genetic Variations (3 papers), Genomics and Rare Diseases (3 papers), Connective tissue disorders research (2 papers), Sarcoma Diagnosis and Treatment (2 papers), Genetic Associations and Epidemiology (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (232 citations), Molecular Biology (183 citations), Biological Psychiatry (6 citations), Pediatrics, Perinatology and Child Health (45 citations) and Psychiatry and Mental health (33 citations). Michele Traversa has collaborated with scholars based in Italy, United States and Israel. Frequent co-authors include Chiara Magri, Massimo Gennarelli, Paolo Valsecchi, Emilio Sacchetti, Alessandra Minelli, Sergio Barlati, Marina Colombi, Chiara Dordoni, Nicola Chiarelli and Nicoletta Zoppi. Their work appears in journals such as PLoS ONE, Molecular Genetics and Genomics, Cancers, Orphanet Journal of Rare Diseases and The Pharmacogenomics Journal.
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.