Carmelo Piscopo

3.2k total citations
24 papers, 302 citations indexed

About

Carmelo Piscopo is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Carmelo Piscopo has authored 24 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Physiology. Recurrent topics in Carmelo Piscopo's work include Erythrocyte Function and Pathophysiology (6 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Carmelo Piscopo is often cited by papers focused on Erythrocyte Function and Pathophysiology (6 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Carmelo Piscopo collaborates with scholars based in Italy, France and Austria. Carmelo Piscopo's co-authors include Achille Iolascon, Maria Rosaria Esposito, Luigia De Falco, Clara Camaschella, Dagmar Pospı́šilová, G Tchernia, C. Beaumont, Silverio Perrotta, Franck Borgèse and Hélène Guizouarn and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and International Journal of Molecular Sciences.

In The Last Decade

Carmelo Piscopo

20 papers receiving 294 citations

Peers

Carmelo Piscopo
Roberta Marra Italy
Francisco J. Perea Mexico
Barbara Eleni Rosato Italy
S. Fattoum France
Prasanthi Chappa United States
Domenico Mattiucci Italy
Charlotta Böiers Sweden
Jessica Goodman United States
DL Rucknagel United States
Roberta Marra Italy
Carmelo Piscopo
Citations per year, relative to Carmelo Piscopo Carmelo Piscopo (= 1×) peers Roberta Marra

Countries citing papers authored by Carmelo Piscopo

Since Specialization
Citations

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

Fields of papers citing papers by Carmelo Piscopo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carmelo Piscopo

This figure shows the co-authorship network connecting the top 25 collaborators of Carmelo Piscopo. A scholar is included among the top collaborators of Carmelo Piscopo 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 Carmelo Piscopo. Carmelo Piscopo 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
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Falco, Alessandro De, Stefano Pagano, Rosanna Trovato, et al.. (2024). Exploring the Clinical Spectrum of HUWE1 ‐Related Neurodevelopmental Disorder: Five New Patients and Literature Review. American Journal of Medical Genetics Part A. 197(4). e63959–e63959.
3.
Ferrigno, Rosario, Immacolata Andolfo, Roberta Russo, et al.. (2024). Genotype–Phenotype Correlation of GNAS Gene: Review and Disease Management of a Hotspot Mutation. International Journal of Molecular Sciences. 25(20). 10913–10913.
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Falco, Alessandro De, Daniele De Brasi, Stefano Petrocchi, et al.. (2023). A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis. Genes. 14(1). 119–119. 2 indexed citations
7.
Falco, Alessandro De, Achille Iolascon, Flora Ascione, & Carmelo Piscopo. (2023). New Insights in 9q21.13 Microdeletion Syndrome: Genotype–Phenotype Correlation of 28 Patients. Genes. 14(5). 1116–1116.
8.
Terracciano, Antonio, Achille Iolascon, Matteo Della Monica, et al.. (2023). A New de novo Mosaic Mutation of PHEX Gene: A Case Report of a Boywith Hypophosphatemic Rickets. Endocrine Metabolic & Immune Disorders - Drug Targets. 23(9). 1235–1239. 2 indexed citations
9.
Siano, Maria, Ilaria Maggio, Roberta Petillo, et al.. (2022). De Novo Mutation in KMT2C Manifesting as Kleefstra Syndrome 2: Case Report and Literature Review. Pediatric Reports. 14(1). 131–139. 16 indexed citations
10.
Genovese, Silvia, Silvia Di Tommaso, Bruno Dallapiccola, et al.. (2022). Reciprocal Xp11.4p11.3 microdeletion/microduplication spanning USP9X, DDX3X, and CASK genes in two patients with syndromic intellectual disability. American Journal of Medical Genetics Part A. 188(6). 1836–1847. 5 indexed citations
11.
Torres, Bárbara, et al.. (2022). Case Report: A Novel Homozygous Missense Variant of FBN3 Supporting It Is a New Candidate Gene Causative of a Bardet–Biedl Syndrome–Like Phenotype. Frontiers in Genetics. 13. 924362–924362. 1 indexed citations
12.
Lonardo, Fortunato, M. Cristina Digilio, Daniela Rogaia, et al.. (2021). Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. American Journal of Medical Genetics Part A. 185(4). 1204–1210. 5 indexed citations
13.
Sparago, Angela, Flavia Cerrato, Laura Pignata, et al.. (2021). Variable Expressivity of the Beckwith-Wiedemann Syndrome in Four Pedigrees Segregating Loss-of-Function Variants of CDKN1C. Genes. 12(5). 706–706. 3 indexed citations
14.
Candia, Francesca Di, Paolo Fontana, Mariateresa Falco, et al.. (2021). Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literature. European Journal of Pediatrics. 181(1). 171–187. 14 indexed citations
15.
Falco, Luigia De, Antonella Nai, Alessia Pagani, et al.. (2010). Novel TMPRSS6 mutations associated with iron-refractory iron deficiency anemia (IRIDA). Human Mutation. 31(5). E1390–E1405. 52 indexed citations
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Iolascon, Achille, et al.. (2010). Hereditary spherocytosis. Transfusion Clinique et Biologique. 17(3). 138–142. 21 indexed citations
17.
Iolascon, Achille, Roberta Russo, Maria Rosaria Esposito, et al.. (2009). Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship. Haematologica. 95(5). 708–715. 45 indexed citations
18.
Iolascon, Achille, Luigia De Falco, Franck Borgèse, et al.. (2009). A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis. Haematologica. 94(8). 1049–1059. 52 indexed citations
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Iolascon, Achille, Clara Camaschella, Dagmar Pospı́šilová, et al.. (2007). Natural History of Recessive Inheritance of DMT1 Mutations. The Journal of Pediatrics. 152(1). 136–139. 34 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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