G Fioretti
Impact in
- Genetics top 5%
- Hemoglobinopathies and Related Disorders
- Genomic variations and chromosomal abnormalities
- Hematology top 10%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 13
- Hemoglobinopathies and Related Disorders 11
- Genomic variations and chromosomal abnormalities 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Congenital Ear and Nasal Anomalies 2
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- Sexual Differentiation and Disorders 2
- Co-authors
- Livio Pagano (20 shared papers)Clementina Carestia (6 shared papers)Giuseppina Lacerra (9 shared papers)Maria De Angioletti (9 shared papers)Piero Pucci (4 shared papers)Estrella Guarino (5 shared papers)Giuseppe Maglione (5 shared papers)Laura Camardella (2 shared papers)
- Journals
- Blood (4 papers)The Journal of Urology (2 papers)Clinical Genetics (2 papers)Molecular Cytogenetics (2 papers)Gene (1 paper)
- Partner nations
- ItalyGermanySwitzerland
In The Last Decade
G Fioretti
28 papers receiving 385 citations
Peers
Comparison fields: 5 of 55
- Genetics 195
- Hematology 117
- Developmental Biology 14
- Genetics 123
- Pediatrics, Perinatology and Child Health 64
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-authors
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
Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 60 | |
| 2 | 1991 | 31 | |
| 3 | 1991 | 26 | |
| 4 | 1991 | 26 | |
| 5 | 1991 | 26 | |
| 6 | 1993 | 25 | |
| 7 | 1998 | 24 | |
| 8 | 2015 | 23 | |
| 9 | Clinical features of monosomy 10qter. | 1983 | 21 |
| 10 | 2013 | 20 | |
| 11 | 2013 | 20 | |
| 12 | Origin heterogeneity of Hb Lepore-Boston gene in Italy. | 1992 | 20 |
| 13 | 1987 | 17 | |
| 14 | 1980 | 14 | |
| 15 | 2000 | 12 | |
| 16 | A case of Edward's syndrome with pseudodicentric isochromosome 18: 46,XY,i dic(18) (p11::p11). | 1982 | 11 |
| 17 | 1997 | 8 | |
| 18 | 2007 | 7 | |
| 19 | 1991 | 7 | |
| 20 | 1992 | 5 |
About G Fioretti
G Fioretti is a scholar working on Genetics, Genetics, Molecular Biology, Hematology and Surgery, having authored 28 papers that have together received 420 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), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Prenatal Screening and Diagnostics (3 papers), Blood groups and transfusion (2 papers), Sexual Differentiation and Disorders (2 papers) and Congenital Ear and Nasal Anomalies (2 papers). The work is most often cited by research in Genetics (195 citations), Hematology (117 citations), Developmental Biology (14 citations), Genetics (123 citations) and Pediatrics, Perinatology and Child Health (64 citations). G Fioretti has collaborated with scholars based in Italy, Germany and Switzerland. Frequent co-authors include Livio Pagano, Clementina Carestia, Giuseppina Lacerra, Maria De Angioletti, Piero Pucci, Estrella Guarino, Giuseppe Maglione, Laura Camardella, Maria Luigia Cavaliere and A. Conti. Their work appears in journals such as Blood, The Journal of Urology, Clinical Genetics, Molecular Cytogenetics and Gene.
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.