Gianfranco Sebastio

5.0k total citations
82 papers, 3.4k citations indexed

About

Gianfranco Sebastio is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Gianfranco Sebastio has authored 82 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 29 papers in Clinical Biochemistry and 28 papers in Rheumatology. Recurrent topics in Gianfranco Sebastio's work include Metabolism and Genetic Disorders (29 papers), Amino Acid Enzymes and Metabolism (27 papers) and Folate and B Vitamins Research (20 papers). Gianfranco Sebastio is often cited by papers focused on Metabolism and Genetic Disorders (29 papers), Amino Acid Enzymes and Metabolism (27 papers) and Folate and B Vitamins Research (20 papers). Gianfranco Sebastio collaborates with scholars based in Italy, United Kingdom and United States. Gianfranco Sebastio's 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 and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Gianfranco Sebastio

80 papers receiving 3.3k citations

Peers

Gianfranco Sebastio

GENET

RHEUM

BIOCH

Vorasuk Shotelersuk Thailand

Luisa Bonafé Switzerland

Yoko Aoki Japan

Paige Kaplan United States

Ayelet Erez United States

Maja Di Rocco Italy

Lawrence Charnas United States

Masahide Yazaki Japan

Luigi Bisceglia Italy

Marc De Braekeleer France

Vorasuk Shotelersuk Thailand

Gianfranco Sebastio

1.6k ×1.0

1.1k ×1.1

GENET

617 ×0.8

RHEUM

391 ×0.5

BIOCH

193 ×0.3

Citations per year, relative to Gianfranco Sebastio Gianfranco Sebastio (= 1×) peers Vorasuk Shotelersuk

Countries citing papers authored by Gianfranco Sebastio

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Gianfranco Sebastio

This figure shows the co-authorship network connecting the top 25 collaborators of Gianfranco Sebastio. A scholar is included among the top collaborators of Gianfranco Sebastio based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gianfranco Sebastio. Gianfranco Sebastio is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sebastio, Gianfranco, Maria Pia Sperandeo, & Generoso Andria. (2011). Lysinuric protein intolerance: Reviewing concepts on a multisystem disease. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 157(1). 54–62. 75 indexed citations

Cerrato, Flavia, Angela Sparago, Gaetano Verde, et al.. (2008). Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour. Human Molecular Genetics. 17(10). 1427–1435. 66 indexed citations

Garavelli, Livia, Daniele De Brasi, Filomena Cariola, et al.. (2008). Holt–Oram syndrome associated with anomalies of the feet. American Journal of Medical Genetics Part A. 146A(9). 1185–1189. 11 indexed citations

Sperandeo, Maria Pia, Generoso Andria, & Gianfranco Sebastio. (2007). Lysinuric protein intolerance: update and extended mutation analysis of theSLC7A7 gene. Human Mutation. 29(1). 14–21. 62 indexed citations

Scala, Iris, Maria Sellitto, Serena Salomè, et al.. (2006). Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring. Genetics in Medicine. 8(7). 409–416. 103 indexed citations

Sperandeo, Maria Pia, Patrizia Annunziata, Virginia Ammendola, et al.. (2005). Lysinuric protein intolerance: identification and functional analysis of mutations of the SLC7A7 gene. Human Mutation. 25(4). 410–410. 22 indexed citations

Sperandeo, Maria Pia, Simona Paladino, Luigi Maiuri, et al.. (2005). A y+LAT-1 mutant protein interferes with y+LAT-2 activity: implications for the molecular pathogenesis of lysinuric protein intolerance. European Journal of Human Genetics. 13(5). 628–634. 21 indexed citations

Franchis, R. de, Lorenzo D. Botto, Gianfranco Sebastio, et al.. (2002). Spina bifida and folate-related genes: A study of gene-gene interactions. Genetics in Medicine. 4(3). 126–130. 17 indexed citations

Brasi, Daniele De, Elena Rossi, Sabrina Giglio, et al.. (2001). Inv dup del (1)(pter?q44::q44?q42:) with the classical phenotype of trisomy 1q42-qter. American Journal of Medical Genetics. 104(2). 127–130. 29 indexed citations

10.

Titomanlio, Luigi, Elena Rossi, Maria DʼArmiento, et al.. (2001). Case of Myhre syndrome with autism and peculiar skin histological findings. American Journal of Medical Genetics. 103(2). 163–165. 27 indexed citations

11.

Santamaria, Francesca, Giancarlo Parenti, Guido De Guidi, et al.. (1996). Early Detection of Lung Involvement in Lysinuric Protein Intolerance: Role of High-Resolution Computed Tomography and Radioisotopic Methods. American Journal of Respiratory and Critical Care Medicine. 153(2). 731–735. 34 indexed citations

12.

Sebastio, Gianfranco, Lucia Perone, Vito Guzzetta, et al.. (1996). Molecular and cytogenetic characterization of a recurrent unbalanced translocation (4;21) (p16.3;q22.1): Relevance to the Wolf-Hirschhorn and Down syndrome critical regions. American Journal of Medical Genetics. 63(2). 366–372. 2 indexed citations

13.

Chiurazzi, Pietro, Maurizio Genuardi, Libor Kozák, et al.. (1996). Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity. American Journal of Medical Genetics. 64(1). 209–215. 36 indexed citations

14.

Parenti, Giancarlo, Gianfranco Sebastio, Pietro Strisciuglio, et al.. (1995). Lysinuric protein intolerance characterized by bone marrow abnormalities and severe clinical course. The Journal of Pediatrics. 126(2). 246–251. 44 indexed citations

15.

Incerti, Barbara, Gianfranco Sebastio, & Giancarlo Parenti. (1994). The structure of the gene ATRC1 coding for a cationic amino acid transport system in man: Molecular studies in lysinuric protein intolerance. The American Journal of Human Genetics. 55. 1 indexed citations

16.

Sebastio, Gianfranco, Maria Pia Sperandeo, & Maria Panico. (1994). Molecular characterization of twelve patients affected by homocystinuria due to cystathionine beta-synthase deficiency: Report of two novel mutations. The American Journal of Human Genetics. 55. 1 indexed citations

17.

Sebastio, Gianfranco, et al.. (1990). The ΔF508 mutation in cystic fibrosis patients of Southern Italy. Human Genetics. 85(4). 430–431. 2 indexed citations

18.

Cross, Nicholas C.P., Timothy M. Cox, R. de Franchis, et al.. (1990). Molecular analysis of aldolase B genes in hereditary fructose intolerance. The Lancet. 335(8685). 306–309. 82 indexed citations

19.

Ballabio, Andrea, Giancarlo Parenti, Rosalba Carrozzo, et al.. (1987). Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.. Proceedings of the National Academy of Sciences. 84(13). 4519–4523. 115 indexed citations

20.

Mardon, Helen J., Gianfranco Sebastio, & Francisco E. Baralle. (1987). A role for exon sequences in alternative splicing of the human fibronection gene. Nucleic Acids Research. 15(19). 7725–7733. 132 indexed citations

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.

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