Emmanouil Athanasakis

898 total citations
35 papers, 602 citations indexed

About

Emmanouil Athanasakis is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Emmanouil Athanasakis has authored 35 papers receiving a total of 602 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Genetics and 7 papers in Immunology. Recurrent topics in Emmanouil Athanasakis's work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Emmanouil Athanasakis is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomics and Rare Diseases (3 papers). Emmanouil Athanasakis collaborates with scholars based in Italy, United States and Spain. Emmanouil Athanasakis's co-authors include Paolo Gasparini, Sérgio Crovella, Pio D’Adamo, Ludovica Segat, Flavio Faletra, Rafael Lima Guimarães, Lucas André Cavalcanti Brandão, Alessandra Pontillo, Laura Esposito and Danilo Licastro and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Emmanouil Athanasakis

35 papers receiving 591 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emmanouil Athanasakis Italy 14 301 124 98 73 66 35 602
Seby Edassery United States 20 448 1.5× 87 0.7× 287 2.9× 104 1.4× 33 0.5× 45 1.1k
Stéphanie Leclerc‐Mercier France 14 221 0.7× 110 0.9× 127 1.3× 33 0.5× 23 0.3× 59 896
Keiko Danzaki Japan 12 251 0.8× 72 0.6× 350 3.6× 63 0.9× 29 0.4× 20 849
David P. Dimasi Australia 16 319 1.1× 90 0.7× 78 0.8× 26 0.4× 13 0.2× 26 893
Gail Coghlan Canada 15 316 1.0× 157 1.3× 60 0.6× 130 1.8× 21 0.3× 60 896
Stephen F. Murphy United States 14 163 0.5× 61 0.5× 137 1.4× 93 1.3× 10 0.2× 32 597
Sueshige Wakisaka Japan 17 370 1.2× 79 0.6× 170 1.7× 54 0.7× 8 0.1× 30 926
Yukiko Sakamoto Japan 13 315 1.0× 120 1.0× 167 1.7× 152 2.1× 9 0.1× 31 783
Chien‐Hao Huang Taiwan 16 240 0.8× 39 0.3× 123 1.3× 116 1.6× 97 1.5× 68 836
Ruijin Wu China 9 138 0.5× 101 0.8× 163 1.7× 69 0.9× 7 0.1× 13 465

Countries citing papers authored by Emmanouil Athanasakis

Since Specialization
Citations

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

Fields of papers citing papers by Emmanouil Athanasakis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanouil Athanasakis

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanouil Athanasakis. A scholar is included among the top collaborators of Emmanouil Athanasakis 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 Emmanouil Athanasakis. Emmanouil Athanasakis 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.
Moura, Ronald, et al.. (2024). Genomic instability in congenital lung malformations in children. Pediatric Surgery International. 40(1). 248–248. 2 indexed citations
2.
Girardelli, Martina, Erica Valencic, Alessandra Tesser, et al.. (2021). Genetic and immunologic findings in children with recurrent aphthous stomatitis with systemic inflammation. Pediatric Rheumatology. 19(1). 70–70. 12 indexed citations
3.
Stazio, Mariateresa Di, et al.. (2021). Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique. PLoS ONE. 16(3). e0247603–e0247603. 24 indexed citations
4.
Brumatti, Liza Vecchi, Valentina Rosolen, Marika Mariuz, et al.. (2020). Impact of Methylmercury and Other Heavy Metals Exposure on Neurocognitive Function in Children Aged 7 Years: Study Protocol of the Follow-up. Journal of Epidemiology. 31(2). 157–163. 10 indexed citations
5.
Faletra, Flavio, Pio D’Adamo, Anna Monica Bianco, et al.. (2020). Could the MED13 mutations manifest as a Kabuki‐like syndrome?. American Journal of Medical Genetics Part A. 185(2). 584–590. 7 indexed citations
6.
Rizzardi, Clara, Emmanouil Athanasakis, Simeone Dal Monego, et al.. (2017). Puzzling Results from BAP1 Germline Mutations Analysis in a Group of Asbestos-Exposed Patients in a High-risk Area of Northeast Italy. Anticancer Research. 37(6). 3073–3083. 1 indexed citations
7.
Licastro, Danilo, Luciana Caenazzo, Valentina Torboli, et al.. (2016). A technical application of quantitative next generation sequencing for chimerism evaluation. Molecular Medicine Reports. 14(4). 2967–2974. 28 indexed citations
8.
Franca, Raffaella, Paola Rebora, Emmanouil Athanasakis, et al.. (2014). TNF- α SNP rs1800629 and Risk of Relapse in Childhood Acute Lymphoblastic Leukemia: Relation to Immunophenotype. Pharmacogenomics. 15(5). 619–627. 1 indexed citations
9.
Athanasakis, Emmanouil, Danilo Licastro, Flavio Faletra, et al.. (2013). Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection. American Journal of Medical Genetics Part A. 164(1). 170–176. 31 indexed citations
10.
Athanasakis, Emmanouil, Sophie Dahoun, Ambroise Wonkam, et al.. (2013). Complex rearrangement of the exon 6 genomic region among Opitz G/BBB Syndrome MID1 alterations. European Journal of Medical Genetics. 56(8). 404–410. 7 indexed citations
11.
Faletra, Flavio, Emmanouil Athanasakis, Anna Morgan, et al.. (2013). Congenital hyperinsulinism: Clinical and molecular analysis of a large Italian cohort. Gene. 521(1). 160–165. 23 indexed citations
12.
Athanasakis, Emmanouil, Xevi Biarnés, Maria Teresa Bonati, Paolo Gasparini, & Flavio Faletra. (2012). Identification of a New Mutation (L46P) in the Human <b><i>NOG</i></b> Gene in an Italian Patient with Symphalangism Syndrome. Molecular Syndromology. 3(1). 21–24. 6 indexed citations
13.
Licastro, Danilo, Margherita Mutarelli, Ivana Peluso, et al.. (2012). Molecular Diagnosis of Usher Syndrome: Application of Two Different Next Generation Sequencing-Based Procedures. PLoS ONE. 7(8). e43799–e43799. 24 indexed citations
14.
Athanasakis, Emmanouil, et al.. (2012). Two Novel <b><i>COH1</i></b> Mutations in an Italian Patient with Cohen Syndrome. Molecular Syndromology. 3(1). 30–33. 2 indexed citations
15.
Pirastu, Nicola, Antonietta Robino, Carmela Lanzara, et al.. (2012). Genetics of Food Preferences: A First View from Silk Road Populations. Journal of Food Science. 77(12). S413–8. 42 indexed citations
16.
Sorice, Rossella, Silvia Bione, Sheila Ulivi, et al.. (2011). Association of a variant in the CHRNA5-A3-B4 gene cluster region to heavy smoking in the Italian population. European Journal of Human Genetics. 19(5). 593–596. 13 indexed citations
17.
Pontillo, Alessandra, Lucas André Cavalcanti Brandão, Rafael Lima Guimarães, et al.. (2010). A 3′UTR SNP in NLRP3 Gene is Associated With Susceptibility to HIV-1 Infection. JAIDS Journal of Acquired Immune Deficiency Syndromes. 54(3). 236–240. 79 indexed citations
18.
Segat, Ludovica, Lucas André Cavalcanti Brandão, Rafael Lima Guimarães, et al.. (2010). Polymorphisms in innate immunity genes and patients response to dendritic cell-based HIV immuno-treatment. Vaccine. 28(10). 2201–2206. 11 indexed citations
19.
Faletra, Flavio, Nicola Pirastu, Emmanouil Athanasakis, et al.. (2010). A novel mutation in the vWFA2 domain of the COCH gene in an Italian DFNA9 family. Audiological Medicine. 9(1). 4–7. 3 indexed citations
20.
Segat, Ludovica, Marcello Morgutti, Emmanouil Athanasakis, et al.. (2010). Analysis of DEFB1 regulatory SNPs in cystic fibrosis patients from North‐Eastern Italy. International Journal of Immunogenetics. 37(3). 169–175. 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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