Luigi Bisceglia

4.5k total citations
68 papers, 2.1k citations indexed

About

Luigi Bisceglia is a scholar working on Molecular Biology, Biochemistry and Rheumatology. According to data from OpenAlex, Luigi Bisceglia has authored 68 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 19 papers in Biochemistry and 18 papers in Rheumatology. Recurrent topics in Luigi Bisceglia's work include Amino Acid Enzymes and Metabolism (19 papers), Folate and B Vitamins Research (15 papers) and Metabolism and Genetic Disorders (11 papers). Luigi Bisceglia is often cited by papers focused on Amino Acid Enzymes and Metabolism (19 papers), Folate and B Vitamins Research (15 papers) and Metabolism and Genetic Disorders (11 papers). Luigi Bisceglia collaborates with scholars based in Italy, Spain and United States. Luigi Bisceglia's co-authors include Leopoldo Zelante, Paolo Gasparini, Patrizia De Bonis, Roberto Corrocher, Domenico Girelli, Oliviero Olivieri, Xavier Estivill, António Zorzano, Michele Gallucci and Virginia Nunes and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

In The Last Decade

Luigi Bisceglia

65 papers receiving 2.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Luigi Bisceglia Italy 25 660 401 368 317 307 68 2.1k
Per Flodby United States 27 1.3k 1.9× 91 0.2× 121 0.3× 42 0.1× 620 2.0× 46 2.5k
Toshiki Takenouchi Japan 20 689 1.0× 119 0.3× 158 0.4× 25 0.1× 175 0.6× 141 1.6k
Fangming Lin United States 21 1.8k 2.8× 41 0.1× 103 0.3× 58 0.2× 269 0.9× 36 3.1k
Alex Michotte Belgium 24 529 0.8× 58 0.1× 48 0.1× 465 1.5× 419 1.4× 86 2.1k
C. Ronald Scott United States 26 966 1.5× 38 0.1× 238 0.6× 26 0.1× 87 0.3× 75 2.5k
A E Broadus United States 21 1.5k 2.2× 30 0.1× 119 0.3× 88 0.3× 287 0.9× 24 2.7k
Nadia Sakati Saudi Arabia 22 819 1.2× 47 0.1× 123 0.3× 25 0.1× 111 0.4× 78 1.7k
Weston P. Miller United States 25 814 1.2× 47 0.1× 143 0.4× 29 0.1× 40 0.1× 72 1.7k
Sumita Gokhale United States 15 2.1k 3.1× 88 0.2× 43 0.1× 29 0.1× 136 0.4× 28 2.9k
W. Schachenmayr Germany 23 453 0.7× 25 0.1× 80 0.2× 106 0.3× 216 0.7× 80 1.8k

Countries citing papers authored by Luigi Bisceglia

Since Specialization
Citations

This map shows the geographic impact of Luigi Bisceglia'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 Luigi Bisceglia with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Luigi Bisceglia more than expected).

Fields of papers citing papers by Luigi Bisceglia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luigi Bisceglia. 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 Luigi Bisceglia. The network helps show where Luigi Bisceglia may publish in the future.

Co-authorship network of co-authors of Luigi Bisceglia

This figure shows the co-authorship network connecting the top 25 collaborators of Luigi Bisceglia. A scholar is included among the top collaborators of Luigi Bisceglia 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 Luigi Bisceglia. Luigi Bisceglia is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Fransén, Erik, Manou Sommen, R. de Ridder, et al.. (2021). Resequencing of candidate genes for Keratoconus reveals a role for Ehlers–Danlos Syndrome genes. European Journal of Human Genetics. 29(12). 1745–1755. 12 indexed citations
3.
Krishnamurthy, Sriram, et al.. (2017). Cystinuria in a 13-month-old girl with absence of mutations in the SLC3A1 and SLC7A9 Genes. Indian Journal of Nephrology. 28(1). 84–84.
4.
Laborante, Antonio, et al.. (2013). Lattice Corneal Dystrophy-Variant: a report of three new cases due to p.V631D mutation in the TGFBI gene.. PubMed. 164(1). e41–3. 2 indexed citations
5.
Bonis, Patrizia De, Antonio Laborante, Raffaella Stallone, et al.. (2011). Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus.. PubMed. 17. 2482–94. 84 indexed citations
6.
Bisceglia, Luigi, et al.. (2010). Novel human pathological mutations. Human Genetics. 127(4). 463–490. 10 indexed citations
7.
Bisceglia, Luigi, Alessandra Torraco, Maria Rosaria Piemontese, et al.. (2010). A new locus on 3p23–p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H. European Journal of Human Genetics. 18(6). 636–641. 17 indexed citations
8.
Fischetti, Lucia, George Dedoussis, Helen Michelakakis, et al.. (2008). Twenty-Four Novel Mutations Identified in a Cohort of 85 Patients by Direct Sequencing of the SLC3A1 and SLC7A9 Cystinuria Genes. Genetic Testing. 12(3). 351–355. 11 indexed citations
9.
Schena, Francesca, Giuseppina Cerullo, Gianluigi Zaza, et al.. (2007). Searching for IgA Nephropathy Candidate Genes: Genetic Studies Combined with High Throughput Innovative Investigations. PubMed. 157. 80–89. 6 indexed citations
10.
Ghiggeri, Gian Marco, Filippo Aucella, Gianluca Caridi, et al.. (2006). Posttransplant Recurrence of Proteinuria in a Case of Focal Segmental Glomerulosclerosis Associated with WT1 Mutation. American Journal of Transplantation. 6(9). 2208–2211. 13 indexed citations
11.
Bisceglia, Luigi, Giuseppina Cerullo, Paola Forabosco, et al.. (2006). Genetic Heterogeneity in Italian Families with IgA Nephropathy: Suggestive Linkage for Two Novel IgA Nephropathy Loci. The American Journal of Human Genetics. 79(6). 1130–1134. 81 indexed citations
12.
Barbaro, V., Enzo Di Iorio, Stefano Ferrari, et al.. (2006). Expression ofVSX1in Human Corneal Keratocytes during Differentiation into Myofibroblasts in Response to Wound Healing. Investigative Ophthalmology & Visual Science. 47(12). 5243–5243. 45 indexed citations
13.
Savino, Michelangelo, et al.. (2005). Indirect CFTR Mutation Identification by PCR/OLA Anomalous Electropherograms. Genetic Testing. 9(4). 285–291. 1 indexed citations
14.
Martinelli, Marcella, Luca Scapoli, Furio Pezzetti, et al.. (2001). C677T variant form at the MTHFR gene and CL/P: A risk factor for mothers?. American Journal of Medical Genetics. 98(4). 357–360. 100 indexed citations
15.
Bisceglia, Luigi, Maria Rosaria Piemontese, Massimo Carella, et al.. (1998). Cellular Retinol Binding Protein 1 (RBP1): A frequent polymorphism, refined map position and exclusion as the Blepharophimosis Ptosis Epicanthus inversus Syndrome gene. Molecular and Cellular Probes. 12(4). 255–258. 1 indexed citations
16.
Palacı́n, Manuel, Conchi Mora, Juan J. Chillarón, et al.. (1996). The molecular basis of cystinuria: the role of the rBAT gene. Amino Acids. 11(2). 225–246. 10 indexed citations
17.
Bisceglia, Luigi, Marı́a Julia Calonge, Luca Dello Strologo, et al.. (1996). Molecular analysis of the cystinuria disease gene: identification of four new mutations, one large deletion, and one polymorphism. Human Genetics. 98(4). 447–451. 41 indexed citations
18.
Rinaldi, Monica, Paolo Gasparini, Davide Seripa, et al.. (1995). Stability and functional effectiveness of phosphorothioate modified duplex DNA and synthetic ‘mini-genes’. Nucleic Acids Research. 23(20). 4134–4142. 25 indexed citations
19.
Bonizzato, A., Elena Nicolis, G Borgo, et al.. (1995). Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from North-Eastern Italy: identification of 90% of the mutations. Human Genetics. 95(4). 397–402. 50 indexed citations
20.
Gasparini, Paolo, Marı́a Julia Calonge, Luigi Bisceglia, et al.. (1995). Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.. PubMed. 57(4). 781–8. 72 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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