Michela Malacarne
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 44
- Genomic variations and chromosomal abnormalities 28
- Genetics and Neurodevelopmental Disorders 15
- Genetic Syndromes and Imprinting 9
- Genomics and Rare Diseases 3
-
- Congenital heart defects research 12
- Epigenetics and DNA Methylation 4
- Co-authors
- Simona Cavani (17 shared papers)Mauro Pierluigi (16 shared papers)Maria Piccione (15 shared papers)Giovanni Corsello (12 shared papers)Federico Zara (8 shared papers)Domenico Coviello (23 shared papers)Francesca Faravelli (6 shared papers)Elena Di Gennaro (3 shared papers)
- Journals
- European Journal of Medical Genetics (6 papers)International Journal of Molecular Sciences (4 papers)Genes (3 papers)Stem Cell Research (3 papers)Epilepsia (2 papers)
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
Michela Malacarne
53 papers receiving 602 citations
Peers
Comparison fields: 5 of 58
- Genetics 376
- Pediatrics, Perinatology and Child Health 124
- Psychiatry and Mental health 93
- Genetics 40
- Molecular Biology 242
Countries citing papers authored by Michela Malacarne
This map shows the geographic impact of Michela Malacarne'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 Michela Malacarne with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michela Malacarne more than expected).
Fields of papers citing papers by Michela Malacarne
This network shows the impact of papers produced by Michela Malacarne. 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 Michela Malacarne. The network helps show where Michela Malacarne may publish in the future.
Co-authors
The 25 scholars most cited alongside Michela Malacarne, 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 56 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 68 | |
| 2 | 2013 | 42 | |
| 3 | 2006 | 40 | |
| 4 | 2006 | 36 | |
| 5 | 2000 | 34 | |
| 6 | 2012 | 31 | |
| 7 | 2012 | 31 | |
| 8 | 2013 | 27 | |
| 9 | 2017 | 24 | |
| 10 | 2020 | 22 | |
| 11 | 1999 | 19 | |
| 12 | 2005 | 18 | |
| 13 | 2010 | 18 | |
| 14 | 2011 | 17 | |
| 15 | 2010 | 17 | |
| 16 | 2012 | 16 | |
| 17 | 2015 | 16 | |
| 18 | 2011 | 15 | |
| 19 | 2021 | 13 | |
| 20 | 2003 | 10 |
About Michela Malacarne
Michela Malacarne is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 56 papers that have together received 664 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (28 papers), Genetics and Neurodevelopmental Disorders (15 papers), Congenital heart defects research (12 papers), Genetic Syndromes and Imprinting (9 papers), Chromosomal and Genetic Variations (5 papers), Prenatal Screening and Diagnostics (5 papers), Epigenetics and DNA Methylation (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (376 citations), Pediatrics, Perinatology and Child Health (124 citations), Psychiatry and Mental health (93 citations), Genetics (40 citations) and Molecular Biology (242 citations). Michela Malacarne has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Simona Cavani, Mauro Pierluigi, Maria Piccione, Giovanni Corsello, Federico Zara, Domenico Coviello, Francesca Faravelli, Elena Di Gennaro, M. Pierluigi and R. Gaggero. Their work appears in journals such as European Journal of Medical Genetics, International Journal of Molecular Sciences, Genes, Stem Cell Research and Epilepsia.
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.