Silvia Maitz
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 12
- Genomics and Rare Diseases 8
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 5
-
- Genomics and Chromatin Dynamics 6
- Epigenetics and DNA Methylation 4
- RNA modifications and cancer 4
- Co-authors
- Angelo Selicorni (21 shared papers)Lidia Larizza (7 shared papers)Anna Cereda (10 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)Genetics in Medicine (2 papers)Molecular Cytogenetics (2 papers)Epigenetics (2 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Silvia Maitz
38 papers receiving 612 citations
Peers
Comparison fields: 5 of 66
- Genetics 319
- Developmental Neuroscience 27
- Pediatrics, Perinatology and Child Health 123
- Obstetrics and Gynecology 43
- Molecular Biology 330
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 | 2010 | 38 | |
| 3 | 2007 | 38 | |
| 4 | 2010 | 34 | |
| 5 | 2017 | 32 | |
| 6 | 2013 | 31 | |
| 7 | 2009 | 30 | |
| 8 | 2019 | 30 | |
| 9 | 2019 | 28 | |
| 10 | 2019 | 25 | |
| 11 | 2020 | 24 | |
| 12 | 2018 | 24 | |
| 13 | 2011 | 22 | |
| 14 | 2021 | 22 | |
| 15 | 2020 | 19 | |
| 16 | 2020 | 18 | |
| 17 | 2016 | 18 | |
| 18 | 2021 | 16 | |
| 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 Surgery, having authored 40 papers that have together received 617 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genomics and Rare Diseases (8 papers), Genomics and Chromatin Dynamics (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Epigenetics and DNA Methylation (4 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Genetics (319 citations), Developmental Neuroscience (27 citations), Pediatrics, Perinatology and Child Health (123 citations), Obstetrics and Gynecology (43 citations) and Molecular Biology (330 citations). Silvia Maitz has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Angelo Selicorni, Lidia Larizza, Anna Cereda, Silvia Tabano, Monica Miozzo, Faustina Lalatta, Patrizia Colapietro, Donatella Milani, Silvia Maria Sirchia and Barbara Gentilin. Their work appears in journals such as European Journal of Medical Genetics, International Journal of Molecular Sciences, Genetics in Medicine, Molecular Cytogenetics and Epigenetics.
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.