G Fioretti
- Genetics top 5%
- Hemoglobinopathies and Related Disorders 11
- Genomic variations and chromosomal abnormalities 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genomics and Rare Diseases 2
- Hematology top 10%
- Iron Metabolism and Disorders 5
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- Hemoglobinopathies and Related Disorders 11
- Genomic variations and chromosomal abnormalities 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genomics and Rare Diseases 2
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- Prenatal Screening and Diagnostics 3
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- Testicular diseases and treatments 2
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- Epigenetics and DNA Methylation 2
- Co-authors
- Livio PaganoClementina CarestiaMaria De AngiolettiGiuseppina LacerraEstrella GuarinoPiero PucciGiuseppe MaglioneLaura Camardella
- Partner nations
- ItalySwitzerlandGermany
In The Last Decade
G Fioretti
28 papers receiving 373 citations
Peers
Comparison fields: 5 of 56
- Genetics 188
- Hematology 133
- Developmental Biology 14
- Genetics 128
- Pediatrics, Perinatology and Child Health 73
Countries citing papers authored by G Fioretti
This map shows the geographic impact of G Fioretti'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 G Fioretti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G Fioretti more than expected).
Fields of papers citing papers by G Fioretti
This network shows the impact of papers produced by G Fioretti. 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 G Fioretti. The network helps show where G Fioretti may publish in the future.
Co-authorship network
The 25 scholars most cited alongside G Fioretti, 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 | 2015 | 22 | |
| 2 | 2013 | 19 | |
| 3 | 2013 | 20 | |
| 4 | 2007 | 7 | |
| 5 | 2000 | 11 | |
| 6 | 1998 | 1 | |
| 7 | 1997 | 8 | |
| 8 | 1995 | 3 | |
| 9 | 1993 | 2 | |
| 10 | 1993 | 25 | |
| 11 | 1992 | 4 | |
| 12 | Origin heterogeneity of Hb Lepore-Boston gene in Italy. | 1992 | 20 |
| 13 | 1991 | 6 | |
| 14 | 1991 | 25 | |
| 15 | 1987 | 17 | |
| 16 | 1985 | 57 | |
| 17 | Clinical features of monosomy 10qter. | 1983 | 21 |
| 18 | [Partial trisomy 10q24 leads to 10qter due to familial translocation (9;10) (p24;q24) recurring in 3 generations]. | 1983 | 1 |
| 19 | Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter. | 1980 | 4 |
| 20 | Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter. | 1980 | 2 |
About G Fioretti
G Fioretti is a scholar working on Genetics, Developmental Biology, Hematology, Genetics and Reproductive Medicine, having authored 28 papers that have together received 402 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (11 papers), Genomic variations and chromosomal abnormalities (7 papers), Iron Metabolism and Disorders (5 papers), Prenatal Screening and Diagnostics (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genomics and Rare Diseases (2 papers), Testicular diseases and treatments (2 papers) and Epigenetics and DNA Methylation (2 papers). The work is most often cited by research in Genetics (188 citations), Hematology (133 citations), Developmental Biology (14 citations), Genetics (128 citations) and Pediatrics, Perinatology and Child Health (73 citations). G Fioretti has collaborated with scholars based in Italy, Switzerland and Germany. Frequent co-authors include Livio Pagano, Clementina Carestia, Maria De Angioletti, Giuseppina Lacerra, Estrella Guarino, Piero Pucci, Giuseppe Maglione, Laura Camardella, Maria Luigia Cavaliere and Lucio Nitsch. Their work appears in journals such as Blood, The Journal of Urology, Molecular Cytogenetics, Clinical Genetics and British Journal of Haematology.
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.