Roberto Cusano

4.2k total citations · 1 hit paper
69 papers, 1.9k citations indexed

About

Roberto Cusano is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Roberto Cusano has authored 69 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 19 papers in Genetics and 11 papers in Cancer Research. Recurrent topics in Roberto Cusano's work include Neuroblastoma Research and Treatments (7 papers), Cancer-related molecular mechanisms research (6 papers) and Gut microbiota and health (6 papers). Roberto Cusano is often cited by papers focused on Neuroblastoma Research and Treatments (7 papers), Cancer-related molecular mechanisms research (6 papers) and Gut microbiota and health (6 papers). Roberto Cusano collaborates with scholars based in Italy, United States and United Kingdom. Roberto Cusano's co-authors include Aldo Manzin, Vanessa Palmas, Silvia Pisanu, Paolo Uva, Sarah Vascellari, Veronica Madau, Roberto Ravazzolo, Marco Seri, Andrea Deledda and Andrea Loviselli and has published in prestigious journals such as Blood, Oncogene and Scientific Reports.

In The Last Decade

Roberto Cusano

69 papers receiving 1.8k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Gut microbiota markers associated with obesity and overweight in Italian adults

2021 258 citations Vanessa Palmas, Silvia Pisanu et al. Scientific Reports profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Roberto Cusano	1.1k	399	357	220	182	69	1.9k
Luca Massimino	1.2k 1.1×	408 1.0×	205 0.6×	151 0.7×	185 1.0×	73	2.1k
George Koike	894 0.8×	698 1.7×	353 1.0×	91 0.4×	86 0.5×	61	2.3k
Thomas P. Yang	1.5k 1.4×	750 1.9×	437 1.2×	101 0.5×	84 0.5×	59	3.3k
Irini Manoli	1.0k 1.0×	281 0.7×	346 1.0×	68 0.3×	116 0.6×	58	2.0k
Paola Carrera	936 0.9×	383 1.0×	169 0.5×	491 2.2×	74 0.4×	128	2.3k
Christophe Poirier	1.2k 1.1×	235 0.6×	454 1.3×	72 0.3×	86 0.5×	56	2.1k
John C. Fyfe	1.3k 1.2×	667 1.7×	373 1.0×	91 0.4×	92 0.5×	52	2.9k
Keitaro Yamanouchi	1.3k 1.2×	484 1.2×	535 1.5×	105 0.5×	41 0.2×	151	2.3k
Dong‐Ming Su	832 0.8×	222 0.6×	278 0.8×	129 0.6×	280 1.5×	49	2.3k
Vincent Laugel	1.7k 1.5×	475 1.2×	123 0.3×	84 0.4×	104 0.6×	88	2.3k

Countries citing papers authored by Roberto Cusano

Since Specialization

Citations

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

Fields of papers citing papers by Roberto Cusano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberto Cusano

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Simula, Elena Rita, Seyedesomaye Jasemi, Davide Cossu, et al.. (2024). The Genetic Landscape of Systemic Rheumatic Diseases: A Comprehensive Multigene-Panel Study Identifying Key Gene Polymorphisms. Pharmaceuticals. 17(4). 438–438. 1 indexed citations

Grossi, Alice, Marta Rusmini, Roberto Cusano, et al.. (2023). Whole genome sequencing in ROHHAD trios proved inconclusive: what’s beyond?. Frontiers in Genetics. 14. 1031074–1031074. 4 indexed citations

Scarpa, Fabio, Davide Cossu, Elena Rita Simula, et al.. (2023). A Multigene-Panel Study Identifies Single Nucleotide Polymorphisms Associated with Prostate Cancer Risk. International Journal of Molecular Sciences. 24(8). 7594–7594. 4 indexed citations

Dattilo, Alessia, Giovanni Ceccarini, Gaia Scabia, et al.. (2022). Circulating Levels of MiRNAs From 320 Family in Subjects With Lipodystrophy: Disclosing Novel Signatures of the Disease. Frontiers in Endocrinology. 13. 866679–866679. 1 indexed citations

Palmas, Vanessa, Silvia Pisanu, Veronica Madau, et al.. (2021). Gut microbiota markers associated with obesity and overweight in Italian adults. Scientific Reports. 11(1). 5532–5532. 258 indexed citations breakdown →

Marongiu, Mara, Manila Deiana, Andrea Sbardellati, et al.. (2016). Novel action of FOXL2 as mediator of Col1a2 gene autoregulation. Developmental Biology. 416(1). 200–211. 6 indexed citations

Reinier, Frédéric, Magdalena Żołędziewska, D. Hanna, et al.. (2015). Mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome in the context of inherited lipodystrophies. Metabolism. 64(11). 1530–1540. 22 indexed citations

Marconi, Caterina, Giovanni Badiali, Emanuela Caci, et al.. (2012). A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree. European Journal of Human Genetics. 21(6). 613–619. 47 indexed citations

Panza, Emanuele, Tommaso Pippucci, Roberto Cusano, et al.. (2008). Refinement of the SPG9 locus on chromosome 10q23.3‐24.2 and exclusion of candidate genes. European Journal of Neurology. 15(5). 520–524. 3 indexed citations

10.

Benedetti, Fabrizio De, Antonella Insalaco, Antonella Diamanti, et al.. (2006). Mechanistic Associations of a Mild Phenotype of Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome. Clinical Gastroenterology and Hepatology. 4(5). 653–659. 48 indexed citations

11.

Ghiorzo, Paola, Sara Gargiulo, Lorenza Pastorino, et al.. (2006). Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. Human Molecular Genetics. 15(18). 2682–2689. 28 indexed citations

12.

Pastorino, Lorenza, Roberto Cusano, Chiara Baldo, et al.. (2005). Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis. Child Care Health and Development. 31(3). 351–354. 8 indexed citations

13.

Giacopelli, Francesca, et al.. (2003). The First Intron of the Human Osteopontin Gene Contains a C/EBP-Beta-Responsive Enhancer. Gene Expression. 11(2). 95–104. 18 indexed citations

14.

Marini, Monica, Roberto Cusano, Pierangela De Biasio, et al.. (2003). Previously undescribed nonsense mutation in SHH caused autosomal dominant holoprosencephaly with wide intrafamilial variability. American Journal of Medical Genetics Part A. 117A(2). 112–115. 23 indexed citations

15.

Perri, Patrizia, Luca Longo, Roberto Cusano, et al.. (2002). Weak linkage at 4p16 to predisposition for human neuroblastoma. Oncogene. 21(54). 8356–8360. 27 indexed citations

16.

Meloni, Ilaria, Pietro Rubegni, G. De Aloe, et al.. (2001). Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11. Human Mutation. 18(1). 85–85. 37 indexed citations

17.

Cusano, Roberto, Simone Gangarossa, Paola Forabosco, et al.. (2000). Localisation of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11–q13. European Journal of Human Genetics. 8(11). 895–899. 7 indexed citations

18.

Seri, Marco, Roberto Cusano, Paola Forabosco, et al.. (1999). Genetic Mapping to 10q23.3-q24.2, in a Large Italian Pedigree, of a New Syndrome Showing Bilateral Cataracts, Gastroesophageal Reflux, and Spastic Paraparesis with Amyotrophy. The American Journal of Human Genetics. 64(2). 586–593. 65 indexed citations

19.

Fimiani, Michele, Marco Seri, Pietro Rubegni, et al.. (1999). Autosomal dominant aplasia cutis congenita: report of a large Italian family and no hint for candidate chromosomal regions. Archives of Dermatological Research. 291(12). 637–642. 6 indexed citations

20.

Iolascon, Achille, Crocifissa Lo Cunsolo, Lucia Giordani, et al.. (1998). Interstitial and large chromosome 1p deletion occurs in localized and disseminated neuroblastomas and predicts an unfavourable outcome. Cancer Letters. 130(1-2). 83–92. 18 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.

Explore authors with similar magnitude of impact