Gianfranco Sebastio
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders 29
- Biochemistry top 0.5%
- Amino Acid Enzymes and Metabolism 27
- Rheumatology top 1%
- Folate and B Vitamins Research 20
- Genetics top 2%
- Genomic variations and chromosomal abnormalities 6
- Genetic Syndromes and Imprinting 5
- Molecular Biology top 5%
- Epigenetics and DNA Methylation 9
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- Prenatal Screening and Diagnostics 7
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- Biomedical Research and Pathophysiology 5
- Co-authors
- Generoso AndriaMaria Pia SperandeoAndrea BallabioR. de FranchisAndrea RiccioHelen J. MardonFrancisco E. BaralleGiancarlo Parenti
- Journals
- Journal of Medical Genetics (7 papers)European Journal of Human Genetics (5 papers)Journal of Inherited Metabolic Disease (5 papers)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Gianfranco Sebastio
80 papers receiving 3.3k citations
Peers
Comparison fields: 5 of 110
- Clinical Biochemistry 711
- Biochemistry 754
- Rheumatology 756
- Genetics 1.0k
- Molecular Biology 1.6k
Countries citing papers authored by Gianfranco Sebastio
This map shows the geographic impact of Gianfranco Sebastio'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 Gianfranco Sebastio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gianfranco Sebastio more than expected).
Fields of papers citing papers by Gianfranco Sebastio
This network shows the impact of papers produced by Gianfranco Sebastio. 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 Gianfranco Sebastio. The network helps show where Gianfranco Sebastio may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Gianfranco Sebastio, 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 | 2011 | 75 | |
| 2 | 2008 | 66 | |
| 3 | 2008 | 11 | |
| 4 | 2007 | 62 | |
| 5 | 2006 | 103 | |
| 6 | 2005 | 22 | |
| 7 | 2005 | 21 | |
| 8 | 2002 | 17 | |
| 9 | 2001 | 29 | |
| 10 | 2001 | 27 | |
| 11 | 1996 | 34 | |
| 12 | 1996 | 2 | |
| 13 | 1996 | 36 | |
| 14 | 1995 | 44 | |
| 15 | The structure of the gene ATRC1 coding for a cationic amino acid transport system in man: Molecular studies in lysinuric protein intolerance | 1994 | 1 |
| 16 | Molecular characterization of twelve patients affected by homocystinuria due to cystathionine beta-synthase deficiency: Report of two novel mutations | 1994 | 1 |
| 17 | 1990 | 2 | |
| 18 | 1990 | 82 | |
| 19 | 1987 | 115 | |
| 20 | 1987 | 132 |
About Gianfranco Sebastio
Gianfranco Sebastio is a scholar working on Clinical Biochemistry, Biochemistry and Rheumatology, having authored 82 papers that have together received 3.4k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (29 papers), Amino Acid Enzymes and Metabolism (27 papers), Folate and B Vitamins Research (20 papers), Epigenetics and DNA Methylation (9 papers), Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Genetic Syndromes and Imprinting (5 papers) and Biomedical Research and Pathophysiology (5 papers). The work is most often cited by research in Clinical Biochemistry (711 citations), Biochemistry (754 citations) and Rheumatology (756 citations). Gianfranco Sebastio has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Generoso Andria, Maria Pia Sperandeo, Andrea Ballabio, R. de Franchis, Andrea Riccio, Helen J. Mardon, Francisco E. Baralle, Giancarlo Parenti, Jan P. Kraus and Ian Craig. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Journal of Inherited Metabolic Disease, Human Genetics and Human Mutation.
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.