Giuseppe Marceddu

782 total citations
40 papers, 456 citations indexed

About

Giuseppe Marceddu is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Giuseppe Marceddu has authored 40 papers receiving a total of 456 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Cancer Research. Recurrent topics in Giuseppe Marceddu's work include Genomics and Rare Diseases (7 papers), Cancer Genomics and Diagnostics (5 papers) and Lymphatic System and Diseases (4 papers). Giuseppe Marceddu is often cited by papers focused on Genomics and Rare Diseases (7 papers), Cancer Genomics and Diagnostics (5 papers) and Lymphatic System and Diseases (4 papers). Giuseppe Marceddu collaborates with scholars based in Italy, United States and Slovakia. Giuseppe Marceddu's co-authors include Matteo Bertelli, Marina Marcet‐Houben, Toni Gabaldón, Chiara Napoli, Emmanuelle Morin, Claude Murat, Paola Bonfante, Antonietta Mello, Paolo Enrico Maltese and Tommaso Beccari and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Gene.

In The Last Decade

Giuseppe Marceddu

36 papers receiving 449 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giuseppe Marceddu Italy 13 166 107 78 68 47 40 456
Isabel Matas Spain 14 72 0.4× 322 3.0× 124 1.6× 51 0.8× 26 0.6× 32 558
Katalin Molnár Hungary 13 113 0.7× 292 2.7× 91 1.2× 39 0.6× 10 0.2× 38 801
Yanyan Feng China 15 245 1.5× 18 0.2× 55 0.7× 106 1.6× 34 0.7× 55 611
Ralf Moser Australia 12 282 1.7× 27 0.3× 65 0.8× 53 0.8× 29 0.6× 19 617
Joseph R. Dobosy United States 9 479 2.9× 124 1.2× 16 0.2× 98 1.4× 30 0.6× 9 629
Claire Joly France 10 342 2.1× 23 0.2× 82 1.1× 103 1.5× 41 0.9× 15 572
Sandra Fourré France 9 737 4.4× 41 0.4× 23 0.3× 77 1.1× 50 1.1× 9 1.1k
Shuang-Li Hao China 11 252 1.5× 25 0.2× 48 0.6× 108 1.6× 29 0.6× 24 531
RB Wallace United States 11 142 0.9× 43 0.4× 17 0.2× 85 1.3× 44 0.9× 14 685

Countries citing papers authored by Giuseppe Marceddu

Since Specialization
Citations

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

Fields of papers citing papers by Giuseppe Marceddu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuseppe Marceddu

This figure shows the co-authorship network connecting the top 25 collaborators of Giuseppe Marceddu. A scholar is included among the top collaborators of Giuseppe Marceddu 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 Giuseppe Marceddu. Giuseppe Marceddu 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.
Cristofoli, Francesca, Sabrina Benedetti, G Bonetti, et al.. (2024). Assessing the efficacy of an innovative diagnostic method for identifying 5 % variants in somatic ctDNA. Gene. 928. 148771–148771.
2.
Cannarella, Rossella, Rosita A. Condorelli, Andrea Bernini, et al.. (2023). Genetic Analysis of Patients with Congenital Hypogonadotropic Hypogonadism: A Case Series. International Journal of Molecular Sciences. 24(8). 7428–7428. 3 indexed citations
3.
Bonetti, G, Giuseppe Marceddu, K Dhuli, et al.. (2023). AKR1C1 and hormone metabolism in lipedema pathogenesis: a computational biology approach.. PubMed. 27(6 Suppl). 137–147. 3 indexed citations
4.
Cristofoli, Francesca, Paolo Enrico Maltese, G Bonetti, et al.. (2023). MAGI-ACMG: Algorithm for the Classification of Variants According to ACMG and ACGS Recommendations. Genes. 14(8). 1600–1600. 7 indexed citations
5.
Cecchin, S, Paolo Gisondi, Sandro Michelini, et al.. (2023). Optimization of long-range PCR protocol to prepare filaggrin exon 3 libraries for PacBio long-read sequencing. Molecular Biology Reports. 50(4). 3119–3127. 1 indexed citations
6.
Michelini, Sandro, Karen L. Herbst, Vincenza Precone, et al.. (2022). A Multi-Gene Panel to Identify Lipedema-Predisposing Genetic Variants by a Next-Generation Sequencing Strategy. Journal of Personalized Medicine. 12(2). 268–268. 16 indexed citations
7.
Falsini, Benedetto, Pietro Chiurazzi, Angelo Maria Minnella, et al.. (2022). Genetic characteristics of 234 Italian patients with macular and cone/cone-rod dystrophy. Scientific Reports. 12(1). 3774–3774. 13 indexed citations
8.
Cecchin, S, Stefano Paolacci, Ján Miertuš, et al.. (2022). PacMAGI: A pipeline including accurate indel detection for the analysis of PacBio sequencing data applied to RPE65. Gene. 832. 146554–146554. 3 indexed citations
9.
Cristofoli, Francesca, Giulia Guerri, Roberta Maia de Castro Romanelli, et al.. (2021). Variant Selection and Interpretation: An Example of Modified VarSome Classifier of ACMG Guidelines in the Diagnostic Setting. Genes. 12(12). 1885–1885. 9 indexed citations
10.
Precone, Vincenza, Rossella Cannarella, Stefano Paolacci, et al.. (2021). Male Infertility Diagnosis: Improvement of Genetic Analysis Performance by the Introduction of Pre-Diagnostic Genes in a Next-Generation Sequencing Custom-Made Panel. Frontiers in Endocrinology. 11. 605237–605237. 18 indexed citations
11.
Ceccarini, Maria Rachele, Vincenza Precone, Elena Manara, et al.. (2021). A next generation sequencing gene panel for use in the diagnosis of anorexia nervosa. Eating and Weight Disorders - Studies on Anorexia Bulimia and Obesity. 27(5). 1869–1880. 12 indexed citations
12.
Cristofoli, Francesca, et al.. (2021). Integration of VarSome API in an existing bioinformatic pipeline for automated ACMG interpretation of clinical variants.. PubMed. 25(1 Suppl). 1–6. 6 indexed citations
13.
Maltese, Paolo Enrico, Paolo Fogagnolo, Marco Castori, et al.. (2021). Spectral-Domain Optical Coherence Tomography Analysis in Syndromic and Nonsyndromic Forms of Retinitis Pigmentosa due to <b><i>USH2A</i></b> Genetic Variants. Ophthalmic Research. 65(2). 180–195. 12 indexed citations
14.
Compagna, Rita, Bruno Amato, Syed Hussain Basha, et al.. (2020). Mutations in the ARAP3 Gene in Three Families with Primary Lymphedema Negative for Mutations in Known Lymphedema-Associated Genes. International Journal of Genomics. 2020. 1–9.
15.
Paolacci, Stefano, Raúl Mattassi, Giuseppe Marceddu, et al.. (2020). Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations. Journal of Clinical Medicine. 9(11). 3387–3387. 7 indexed citations
16.
Guerri, Giulia, Sandro Gerli, Gian Carlo Di Renzo, et al.. (2019). Non-syndromic monogenic female infertility.. PubMed. 90(10-S). 62–67. 28 indexed citations
17.
Noia, Giuseppe, Paolo Enrico Maltese, Giuseppe Zampino, et al.. (2018). Cystic Hygroma: A Preliminary Genetic Study and a Short Review from the Literature. Lymphatic Research and Biology. 17(1). 30–39. 13 indexed citations
18.
Marceddu, Giuseppe, et al.. (2017). Non-invasive prenatal diagnosis of beta-thalassemia by semiconductor sequencing: a feasibility study in the sardinian population. European Journal of Human Genetics. 25(5). 600–607. 23 indexed citations
19.
Origa, Raffaella, Giuseppe Marceddu, Fabrice Danjou, et al.. (2015). IFNL3 polymorphisms and HCV infection in patients with beta thalassemia. Annals of Hepatology. 14(3). 389–395. 5 indexed citations
20.
Marcet‐Houben, Marina, Giuseppe Marceddu, & Toni Gabaldón. (2009). Phylogenomics of the oxidative phosphorylation in fungi reveals extensive gene duplication followed by functional divergence. BMC Evolutionary Biology. 9(1). 295–295. 56 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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