Giuseppe Simoni
Impact in
-
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
- Assisted Reproductive Technology and Twin Pregnancy
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Prenatal Screening and Diagnostics 69
- Fetal and Pediatric Neurological Disorders 14
- Genetics 53
- Genomic variations and chromosomal abnormalities 30
- Genetic Syndromes and Imprinting 20
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Co-authors
- B. Brambati (17 shared papers)Francesca Romana Grati (42 shared papers)M. Fraccaro (9 shared papers)G. L. Terzoli (10 shared papers)Monica Miozzo (12 shared papers)Federico Maggi (29 shared papers)F. Rossella (15 shared papers)Cesare Danesino (6 shared papers)
- Journals
- Prenatal Diagnosis (26 papers)Human Genetics (13 papers)Journal of Medical Genetics (5 papers)Human Reproduction (4 papers)Placenta (3 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Giuseppe Simoni
112 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 100
- Pediatrics, Perinatology and Child Health 2.0k
- Genetics 1.5k
- Hepatology 202
- Obstetrics and Gynecology 193
- Reproductive Medicine 165
Countries citing papers authored by Giuseppe Simoni
This map shows the geographic impact of Giuseppe Simoni'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 Giuseppe Simoni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giuseppe Simoni more than expected).
Fields of papers citing papers by Giuseppe Simoni
This network shows the impact of papers produced by Giuseppe Simoni. 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 Giuseppe Simoni. The network helps show where Giuseppe Simoni may publish in the future.
Co-authors
The 25 scholars most cited alongside Giuseppe Simoni, 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 112 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1983 | 346 | |
| 2 | 2004 | 207 | |
| 3 | 2005 | 144 | |
| 4 | 2014 | 144 | |
| 5 | 2015 | 134 | |
| 6 | 1987 | 91 | |
| 7 | 1992 | 88 | |
| 8 | 2002 | 79 | |
| 9 | 1984 | 78 | |
| 10 | 2005 | 76 | |
| 11 | 2018 | 72 | |
| 12 | 2019 | 64 | |
| 13 | 2015 | 64 | |
| 14 | 1985 | 63 | |
| 15 | 1992 | 61 | |
| 16 | 2006 | 61 | |
| 17 | 1986 | 61 | |
| 18 | 2019 | 59 | |
| 19 | 2000 | 50 | |
| 20 | 1983 | 50 |
About Giuseppe Simoni
Giuseppe Simoni is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Surgery and Plant Science, having authored 112 papers that have together received 3.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (69 papers), Genomic variations and chromosomal abnormalities (30 papers), Congenital Anomalies and Fetal Surgery (21 papers), Genetic Syndromes and Imprinting (20 papers), Fetal and Pediatric Neurological Disorders (14 papers), Chromosomal and Genetic Variations (12 papers), Gestational Trophoblastic Disease Studies (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (2.0k citations), Genetics (1.5k citations), Hepatology (202 citations), Obstetrics and Gynecology (193 citations) and Reproductive Medicine (165 citations). Giuseppe Simoni has collaborated with scholars based in Italy, United States and France. Frequent co-authors include B. Brambati, Francesca Romana Grati, M. Fraccaro, G. L. Terzoli, Monica Miozzo, Federico Maggi, F. Rossella, Cesare Danesino, Beatrice Grimi and Maurizio Ferrari. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Journal of Medical Genetics, Human Reproduction and Placenta.
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.