Emmanouil Kanavakis

735 total citations
23 papers, 451 citations indexed

About

Emmanouil Kanavakis is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Emmanouil Kanavakis has authored 23 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Physiology. Recurrent topics in Emmanouil Kanavakis's work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Genetic Syndromes and Imprinting (2 papers). Emmanouil Kanavakis is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Genetic Syndromes and Imprinting (2 papers). Emmanouil Kanavakis collaborates with scholars based in Greece, United States and Italy. Emmanouil Kanavakis's co-authors include Maria Tzetis, Ariadni Mavrou, Ανδρέας Παμπάνος, Helen Fryssira, Zoi Kanaki, Margaritis Avgeris, Gabriel E. Pantelias, Dimitris Karagiannis, Apostolos Klinakis and Θεόδωρος Ράμπιας and has published in prestigious journals such as Blood, Journal of Investigative Dermatology and EMBO Reports.

In The Last Decade

Emmanouil Kanavakis

22 papers receiving 440 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 Kanavakis Greece 12 167 129 75 67 64 23 451
Gülden Dınız Türkiye 12 193 1.2× 43 0.3× 62 0.8× 60 0.9× 64 1.0× 78 457
Lynelle K. Jones Australia 14 199 1.2× 91 0.7× 41 0.5× 63 0.9× 77 1.2× 19 522
Nerea Alonso United Kingdom 11 198 1.2× 52 0.4× 217 2.9× 40 0.6× 35 0.5× 28 583
Müge Sayitoğlu Türkiye 13 326 2.0× 76 0.6× 98 1.3× 30 0.4× 80 1.3× 49 605
Aizhen Zhao China 11 220 1.3× 122 0.9× 64 0.9× 41 0.6× 218 3.4× 19 485
Manuel Martín‐González Spain 14 193 1.2× 50 0.4× 144 1.9× 123 1.8× 16 0.3× 32 534
Michael Marble United States 13 370 2.2× 234 1.8× 28 0.4× 40 0.6× 62 1.0× 33 636
M. M. Brentani Brazil 13 116 0.7× 101 0.8× 100 1.3× 13 0.2× 20 0.3× 29 390
Walter Lisch Germany 17 258 1.5× 122 0.9× 17 0.2× 46 0.7× 32 0.5× 79 1.3k
J P Harpey France 9 232 1.4× 45 0.3× 84 1.1× 38 0.6× 24 0.4× 21 442

Countries citing papers authored by Emmanouil Kanavakis

Since Specialization
Citations

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

Fields of papers citing papers by Emmanouil Kanavakis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanouil Kanavakis

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanouil Kanavakis. A scholar is included among the top collaborators of Emmanouil Kanavakis 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 Kanavakis. Emmanouil Kanavakis 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.
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Palaiologou, Danai, et al.. (2022). Retrocollis as the cardinal feature in a de novo ITRP1 variant. Brain and Development. 44(5). 347–352. 1 indexed citations
3.
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Ράμπιας, Θεόδωρος, Dimitris Karagiannis, Margaritis Avgeris, et al.. (2019). The lysine‐specific methyltransferase KMT 2C/ MLL 3 regulates DNA repair components in cancer. EMBO Reports. 20(3). 96 indexed citations
5.
Soldatou, Alexandra, et al.. (2019). Diabetic neuropathy in children and adolescents with type 1 diabetes mellitus: Diagnosis, pathogenesis, and associated genetic markers. Diabetes/Metabolism Research and Reviews. 35(7). e3178–e3178. 35 indexed citations
6.
Batsali, Aristea, Elisavet Kouvidi, Athanasios Galanopoulos, et al.. (2017). The Effect of 5-Azacitidine Treatment on the Biologic Characteristics of Bone Marrow Mesenchymal Stem Cells in Patients with Myelodysplastic Syndromes. Blood. 130. 4242–4242. 1 indexed citations
7.
Tzetis, Maria, Κρινιώ Γιαννίκου, Maria Braoudaki, et al.. (2017). Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly. Pediatric Research. 82(2). 253–260. 2 indexed citations
8.
Lepetsos, Panagiotis, Ανδρέας Παμπάνος, Emmanouil Kanavakis, et al.. (2014). Association ofMMP-1-1607 1G/2G (rs1799750) polymorphism with primary knee osteoarthritis in the Greek population. Journal of Orthopaedic Research®. 32(9). 1155–1160. 22 indexed citations
9.
Lepetsos, Panagiotis, et al.. (2013). Association of NADPH oxidase p22phox gene C242T, A640G and −930A/G polymorphisms with primary knee osteoarthritis in the Greek population. Molecular Biology Reports. 40(9). 5491–5499. 7 indexed citations
10.
Kitsiou‐Tzeli, Sophia, Maria Tzetis, Christalena Sofocleous, et al.. (2010). De novo interstitial duplication of the 15q11.2‐q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature. American Journal of Medical Genetics Part A. 152A(8). 1925–1932. 29 indexed citations
11.
Kolialexi, A, et al.. (2009). Unilateral microtia in an infant with trisomy 18 mosaicism.. PubMed. 20(2). 181–7. 5 indexed citations
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Nicolaidou, Polyxeni, et al.. (2006). Steroid hormones polymorphisms and cholelithiasis in Greek population. Liver International. 27(1). 61–68. 5 indexed citations
14.
Stratigos, Alexander, Vasiliki Nikolaou, Myrto Poulou, et al.. (2006). Melanocortin Receptor-1 Gene Polymorphisms and the Risk of Cutaneous Melanoma in a Low-Risk Southern European Population. Journal of Investigative Dermatology. 126(8). 1842–1849. 70 indexed citations
15.
Fryssira, Helen, et al.. (2006). Clinical manifestations in 17 Greek patients with Goldenhar syndrome.. PubMed. 17(3). 359–70. 38 indexed citations
16.
Kolialexi, A, George Th. Tsangaris, Sofìa Kitsiou, Emmanouil Kanavakis, & Ariadni Mavrou. (2005). Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.. PubMed. 25(4). 2979–83. 11 indexed citations
17.
Kolialexi, A, et al.. (2005). Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.. PubMed. 18(5). 603–8. 34 indexed citations
18.
Stabouli, Stella, et al.. (2004). Severe hypertriglyceridaemia in diabetic ketoacidosis: clinical and genetic study. Diabetic Medicine. 21(4). 380–382. 19 indexed citations
19.
Tzetis, Maria, et al.. (2001). GILBERT SYNDROME ASSOCIATED WITH β-THALASSEMIA. Pediatric Hematology and Oncology. 18(8). 477–484. 14 indexed citations
20.
Kanavakis, Emmanouil, Joanne Traeger‐Synodinos, Ioannis Papasotiriou, et al.. (1996). The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H. British Journal of Haematology. 92(2). 332–335. 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.

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