Emmanouel Kanavakis

1.9k citations
31 papers · 786 indexed · h-index 17
Topics
Prenatal Screening and Diagnostics (6 papers)Hemoglobinopathies and Related Disorders (5 papers)Genomic variations and chromosomal abnormalities (4 papers)

In The Last Decade

Emmanouel Kanavakis

31 papers receiving 766 citations

Peers

Emmanouel Kanavakis
Comparison fields: 5 of 73
  • Molecular Biology 253
  • Pediatrics, Perinatology and Child Health 220
  • Genetics 165
  • Cancer Research 128
  • Surgery 104
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Citations per year

Countries citing papers authored by Emmanouel Kanavakis

Since Specialization
Citations

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

Fields of papers citing papers by Emmanouel Kanavakis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanouel Kanavakis

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanouel Kanavakis. A scholar is included among the top collaborators of Emmanouel 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 Emmanouel Kanavakis. Emmanouel 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
#WorkIndexed citations
1 1
2 16
3 18
4 14
5 48
6
Investigation of FANCA mutations in Greek patients.
1
7 11
8 6
9 58
10 9
11
10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.
9
12 22
13 120
14 31
15 9
16 10
17
[Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].
1
18 46
19 24
20 14

About Emmanouel Kanavakis

Emmanouel Kanavakis is a scholar working on Genetics, Reproductive Medicine and Pediatrics, Perinatology and Child Health, having authored 31 papers that have together received 786 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Hemoglobinopathies and Related Disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (220 citations), Genetics (98 citations) and Cancer Research (128 citations). Emmanouel Kanavakis has collaborated with scholars based in Greece, United States and United Kingdom. Frequent co-authors include Christina Vrettou, Joanne Traeger‐Synodinos, Maria Tzetis, Aspasia Destouni, Ioannis Papassotiriou, Kiriakos Taxildaris, Athanasios Z. Jamurtas, Demetrios Kouretas, Ioannis G. Fatouros and Georgia Kokkali. Their work appears in journals such as Clinical Chemistry, Gene and Human Reproduction.

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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