Emanuele Agolini

2.9k total citations
82 papers, 989 citations indexed

About

Emanuele Agolini is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Emanuele Agolini has authored 82 papers receiving a total of 989 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 31 papers in Genetics and 19 papers in Genetics. Recurrent topics in Emanuele Agolini's work include Genomics and Rare Diseases (11 papers), Glioma Diagnosis and Treatment (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Emanuele Agolini is often cited by papers focused on Genomics and Rare Diseases (11 papers), Glioma Diagnosis and Treatment (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Emanuele Agolini collaborates with scholars based in Italy, United States and France. Emanuele Agolini's co-authors include Antonio Novelli, Bruno Dallapiccola, M. Cristina Digilio, Francesco Brancati, Angela Mastronuzzi, Andrea Carai, Antonella Cacchione, Martina Rinelli, Emanuele Bellacchio and Franco Locatelli and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Scientific Reports.

In The Last Decade

Emanuele Agolini

73 papers receiving 976 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emanuele Agolini Italy 16 479 327 122 110 102 82 989
Dorota Monies Saudi Arabia 22 579 1.2× 507 1.6× 188 1.5× 83 0.8× 106 1.0× 48 1.3k
Lifeng Tian United States 15 474 1.0× 366 1.1× 81 0.7× 57 0.5× 41 0.4× 47 900
Salma M. Wakil Saudi Arabia 19 517 1.1× 268 0.8× 154 1.3× 60 0.5× 102 1.0× 67 1.2k
Angela F. Brady United Kingdom 18 845 1.8× 593 1.8× 172 1.4× 51 0.5× 54 0.5× 43 1.6k
Güven Lüleci Türkiye 21 750 1.6× 808 2.5× 134 1.1× 99 0.9× 166 1.6× 110 1.7k
Sofia Grigoriadou United Kingdom 13 243 0.5× 356 1.1× 359 2.9× 84 0.8× 210 2.1× 29 1.0k
Karin E. M. Diderich Netherlands 21 822 1.7× 563 1.7× 52 0.4× 40 0.4× 54 0.5× 60 1.6k
Chela James United Kingdom 21 743 1.6× 378 1.2× 132 1.1× 106 1.0× 57 0.6× 39 1.4k
Andreas Ritter Germany 19 341 0.7× 90 0.3× 107 0.9× 33 0.3× 159 1.6× 32 902
Paolo Simi Italy 22 633 1.3× 571 1.7× 54 0.4× 201 1.8× 127 1.2× 82 1.4k

Countries citing papers authored by Emanuele Agolini

Since Specialization
Citations

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

Fields of papers citing papers by Emanuele Agolini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuele Agolini

This figure shows the co-authorship network connecting the top 25 collaborators of Emanuele Agolini. A scholar is included among the top collaborators of Emanuele Agolini 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 Emanuele Agolini. Emanuele Agolini 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.
Baldo, Giada Del, Andrea Carai, Antonella Cacchione, et al.. (2024). A second case report of medulloblastoma in a patient carrying biallelic pathogenic MUTYH germline variants. Neuropathology and Applied Neurobiology. 50(2). e12968–e12968.
2.
Carrozzo, Rosalba, Angela Di Giannatale, Isabella Giovannoni, et al.. (2024). Case report: A safeguard in the sea of variants of uncertain significance: a case study on child with high risk neuroblastoma and acute myeloid leukemia. Frontiers in Oncology. 13. 1324013–1324013. 2 indexed citations
3.
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.
4.
Cacchione, Antonella, Andrea Carai, Giovanna Stefania Colafati, et al.. (2023). Safety and Efficacy of Mek Inhibitors in the Treatment of Plexiform Neurofibromas: A Retrospective Study. Cancer Control. 30. 2905562978–2905562978. 7 indexed citations
5.
Capra, Anna Paola, et al.. (2023). Coexistence of Genetic Diseases Is a New Clinical Challenge: Three Unrelated Cases of Dual Diagnosis. Genes. 14(2). 484–484. 6 indexed citations
6.
Fusco, Carmela, Silvia Morlino, Lucia Micale, et al.. (2023). Nucleotide substitutions at the p.Gly117 and p.Thr180 mutational hot-spots of SKI alter molecular dynamics and may affect cell cycle. Journal of Human Genetics. 69(1). 53–58. 1 indexed citations
7.
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
8.
Sticht, Heinrich, François Lecoquierre, Alice Goldenberg, et al.. (2022). Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy. European Journal of Human Genetics. 31(3). 345–352. 4 indexed citations
9.
Agolini, Emanuele, Elena Botta, M. Cristina Digilio, et al.. (2021). Expansion of the clinical and molecular spectrum of an XPD ‐related disorder linked to biallelic mutations in ERCC2 gene. Clinical Genetics. 99(6). 842–848. 5 indexed citations
10.
Strocchio, Luisa, Daria Pagliara, Mattia Algeri, et al.. (2021). HLA-haploidentical TCRαβ+/CD19+-depleted stem cell transplantation in children and young adults with Fanconi anemia. Blood Advances. 5(5). 1333–1339. 15 indexed citations
11.
Pascolini, Giulia, Emanuele Agolini, Antonio Novelli, Silvia Majore, & Paola Grammatico. (2020). The p.Arg377Trp variant in ACTL6A underlines a recognizable BAF‐opathy phenotype. Clinical Genetics. 97(4). 672–674. 3 indexed citations
12.
Majore, Silvia, Emanuele Agolini, Lucia Micale, et al.. (2020). Clinical presentation and molecular characterization of a novel patient with variant POC1A ‐ related syndrome. Clinical Genetics. 99(4). 540–546. 9 indexed citations
13.
Latini, Andrea, Emanuele Agolini, Antonio Novelli, et al.. (2020). COVID-19 and Genetic Variants of Protein Involved in the SARS-CoV-2 Entry into the Host Cells. Genes. 11(9). 1010–1010. 84 indexed citations
14.
Martinelli, Diego, et al.. (2020). CUGC for lysinuric protein intolerance (LPI). European Journal of Human Genetics. 28(8). 1129–1134. 3 indexed citations
15.
Micale, Lucia, Silvia Morlino, Emanuele Agolini, et al.. (2020). Exon-Trapping Assay Improves Clinical Interpretation of COL11A1 and COL11A2 Intronic Variants in Stickler Syndrome Type 2 and Otospondylomegaepiphyseal Dysplasia. Genes. 11(12). 1513–1513. 9 indexed citations
16.
Cocciadiferro, Dario, Emanuele Agolini, M. Cristina Digilio, et al.. (2020). The splice c.1815G>A variant in KIAA0586 results in a phenotype bridging short-rib-polydactyly and oral-facial-digital syndrome. Medicine. 99(8). e19169–e19169. 6 indexed citations
17.
Agolini, Emanuele, Claudio Cherchi, Emanuele Bellacchio, et al.. (2019). Expanding the clinical and molecular spectrum of lethal congenital contracture syndrome 8 associated with biallelic variants of ADCY6. Clinical Genetics. 97(4). 649–654. 4 indexed citations
18.
Micale, Lucia, Vito Guarnieri, Bartolomeo Augello, et al.. (2019). Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome. Genes. 10(12). 967–967. 9 indexed citations
19.
Fortugno, Paola, Emmanuelle Josselin, Konstantinos Tsiakas, et al.. (2014). Nectin-4 Mutations Causing Ectodermal Dysplasia with Syndactyly Perturb the Rac1 Pathway and the Kinetics of Adherens Junction Formation. Journal of Investigative Dermatology. 134(8). 2146–2153. 27 indexed citations
20.
Dallapiccola, Bruno, et al.. (2009). A Nationwide Genetic Testing Survey in Italy, Year 2007. Genetic Testing and Molecular Biomarkers. 14(1). 17–22. 9 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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