S Cecchin

733 total citations
33 papers, 551 citations indexed

About

S Cecchin is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, S Cecchin has authored 33 papers receiving a total of 551 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in S Cecchin's work include Genomics and Rare Diseases (4 papers), Retinal Development and Disorders (4 papers) and Lymphatic System and Diseases (3 papers). S Cecchin is often cited by papers focused on Genomics and Rare Diseases (4 papers), Retinal Development and Disorders (4 papers) and Lymphatic System and Diseases (3 papers). S Cecchin collaborates with scholars based in Italy, United States and Türkiye. S Cecchin's co-authors include Matteo Bertelli, Paolo Enrico Maltese, Monia Zuntini, Daniela Tavian, Sara Missaglia, Barbara Paolini, G. Pompucci, Cristina Ciuoli, Massimo Pandolfo and Silvia Gallo and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Gene.

In The Last Decade

S Cecchin

31 papers receiving 542 citations

Peers

S Cecchin
Vlasta Korenková Czechia
Xueying Li China
G. Olivieri Italy
Juha‐Pekka Pursiheimo Finland
Jingbo Zhao United States
Debra A. Tokarz United States
Rui Cheng China
Johanna C. Craig United States
Yun Feng China
Vlasta Korenková Czechia
S Cecchin
Citations per year, relative to S Cecchin S Cecchin (= 1×) peers Vlasta Korenková

Countries citing papers authored by S Cecchin

Since Specialization
Citations

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

Fields of papers citing papers by S Cecchin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S Cecchin

This figure shows the co-authorship network connecting the top 25 collaborators of S Cecchin. A scholar is included among the top collaborators of S Cecchin 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 S Cecchin. S Cecchin 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.
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
3.
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
4.
Medori, Maria Chiara, K Dhuli, Cristian Micheletti, et al.. (2023). Serum proteomic profiling reveals potential inflammatory biomarkers in long-COVID patients: a comparative analysis with healthy controls.. PubMed. 27(6 Suppl). 1–12. 5 indexed citations
5.
Ceccarini, Maria Rachele, G Bonetti, Maria Chiara Medori, et al.. (2023). Autoantibodies in patients with post-COVID syndrome: a possible link with severity?. PubMed. 27(6 Suppl). 48–56. 8 indexed citations
6.
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
7.
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
8.
Tripathi, Yamini Bhusan, Priyanka Mishra, Preeti Tripathi, et al.. (2021). Effect of a dietary supplement on the reduction of lymphedema-progression in mouse tail-cut model. SHILAP Revista de lepidopterología. 4 indexed citations
9.
Naureen, Zakira, Astrit Dautaj, S Cecchin, et al.. (2020). Comparison between American and European legislation in the therapeutical and alimentary bacteriophage usage.. PubMed. 91(13-S). e2020023–e2020023. 24 indexed citations
10.
11.
D’Esposito, Fabiana, Gilda Cennamo, Giuseppe de Crecchio, et al.. (2018). Multimodal Imaging in Autosomal Dominant Cone-Rod Dystrophy Caused by Novel <b><i>CRX</i></b> Variant. Ophthalmic Research. 60(3). 169–175. 7 indexed citations
12.
Maltese, Paolo Enrico, A. Bonizzato, Natale Capodicasa, et al.. (2017). Genetic tests for low- and middle-income countries: a literature review. Genetics and Molecular Research. 16(1). 7 indexed citations
13.
Maltese, Paolo Enrico, Letizia Venturini, Matteo Bertelli, et al.. (2016). Genetic evaluation of AMPD1, CPT2, and PGYM metabolic enzymes in patients with chronic fatigue syndrome. Genetics and Molecular Research. 15(3). 5 indexed citations
14.
Paolini, Barbara, Paolo Enrico Maltese, Daniela Tavian, et al.. (2016). Prevalence of mutations in LEP, LEPR, and MC4R genes in individuals with severe obesity. Genetics and Molecular Research. 15(3). 282 indexed citations
15.
Pierrottet, Chiara O., Monia Zuntini, Maurizio Digiuni, et al.. (2014). Syndromic and non-syndromic forms of retinitis pigmentosa: a comprehensive Italian clinical and molecular study reveals new mutations. Genetics and Molecular Research. 13(4). 8815–8833. 29 indexed citations
16.
Maltese, Paolo Enrico, Matteo Bertelli, S Cecchin, et al.. (2013). Polymorphisms of alpha-actinin-3 and ciliary neurotrophic factor in national-level Italian athletes.. PubMed. 55(2). 217–24. 4 indexed citations
17.
Oldani, Marta, et al.. (2012). Clinical and molecular genetic study of 12 Italian families with autosomal recessive Stargardt disease. Genetics and Molecular Research. 11(4). 4342–4350. 6 indexed citations
18.
Bertelli, Matteo, Silvia Gallo, Andrea Buda, et al.. (2006). Novel mutations in the arylsulfatase A gene in eight Italian families with metachromatic leukodystrophy. Journal of Clinical Neuroscience. 13(4). 443–448. 7 indexed citations
19.
Bertelli, Matteo, S Cecchin, Daniela Danieli, et al.. (2006). Quantification of chloride channel 2 (CLCN2) gene isoforms in normal versus lesion- and epilepsy-associated brain tissue. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1772(1). 15–20. 11 indexed citations
20.
Bertelli, Matteo, S Cecchin, G. Jacomelli, et al.. (2006). Study of the adenosinergic system in the brain of HPRT knockout mouse (Lesch–Nyhan disease). Clinica Chimica Acta. 373(1-2). 104–107. 20 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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