Silvia Maitz
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 4
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- Genomics and Chromatin Dynamics 6
- Congenital heart defects research 4
- Epigenetics and DNA Methylation 4
- Co-authors
- Angelo Selicorni (21 shared papers)Anna Cereda (11 shared papers)Lidia Larizza (7 shared papers)Silvia Tabano (6 shared papers)Monica Miozzo (6 shared papers)Faustina Lalatta (5 shared papers)Patrizia Colapietro (3 shared papers)Donatella Milani (6 shared papers)
- Journals
- European Journal of Medical Genetics (5 papers)International Journal of Molecular Sciences (3 papers)Epigenetics (2 papers)Molecular Cytogenetics (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Silvia Maitz
39 papers receiving 624 citations
Peers
Comparison fields: 5 of 63
- Genetics 299
- Developmental Neuroscience 27
- Obstetrics and Gynecology 42
- Pediatrics, Perinatology and Child Health 92
- Molecular Biology 275
Countries citing papers authored by Silvia Maitz
This map shows the geographic impact of Silvia Maitz'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 Silvia Maitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Silvia Maitz more than expected).
Fields of papers citing papers by Silvia Maitz
This network shows the impact of papers produced by Silvia Maitz. 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 Silvia Maitz. The network helps show where Silvia Maitz may publish in the future.
Co-authors
The 25 scholars most cited alongside Silvia Maitz, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 55 | |
| 2 | 2007 | 38 | |
| 3 | 2010 | 38 | |
| 4 | 2010 | 34 | |
| 5 | 2017 | 32 | |
| 6 | 2013 | 31 | |
| 7 | 2019 | 30 | |
| 8 | 2009 | 30 | |
| 9 | 2019 | 29 | |
| 10 | 2019 | 25 | |
| 11 | 2018 | 25 | |
| 12 | 2020 | 25 | |
| 13 | 2021 | 23 | |
| 14 | 2011 | 22 | |
| 15 | 2020 | 19 | |
| 16 | 2020 | 18 | |
| 17 | 2016 | 18 | |
| 18 | 2021 | 18 | |
| 19 | 2020 | 12 | |
| 20 | 2020 | 12 |
About Silvia Maitz
Silvia Maitz is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Oncology and Cognitive Neuroscience, having authored 40 papers that have together received 629 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (6 papers), Genomics and Chromatin Dynamics (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital heart defects research (4 papers), Genetic Syndromes and Imprinting (4 papers) and Epigenetics and DNA Methylation (4 papers). The work is most often cited by research in Genetics (299 citations), Developmental Neuroscience (27 citations), Obstetrics and Gynecology (42 citations), Pediatrics, Perinatology and Child Health (92 citations) and Molecular Biology (275 citations). Silvia Maitz has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Angelo Selicorni, Anna Cereda, Lidia Larizza, Silvia Tabano, Monica Miozzo, Faustina Lalatta, Patrizia Colapietro, Donatella Milani, Silvia Maria Sirchia and Cristina Gervasini. Their work appears in journals such as European Journal of Medical Genetics, International Journal of Molecular Sciences, Epigenetics, Molecular Cytogenetics and Genetics in Medicine.
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.