Emmanouel Kanavakis

1.9k total citations
31 papers, 786 citations indexed

About

Emmanouel Kanavakis is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Emmanouel Kanavakis has authored 31 papers receiving a total of 786 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 8 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Emmanouel Kanavakis's work include Prenatal Screening and Diagnostics (6 papers), Hemoglobinopathies and Related Disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Emmanouel Kanavakis is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Hemoglobinopathies and Related Disorders (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Emmanouel Kanavakis collaborates with scholars based in Greece, United States and United Kingdom. Emmanouel Kanavakis's 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 and has published in prestigious journals such as Clinical Chemistry, Gene and Human Reproduction.

In The Last Decade

Emmanouel Kanavakis

31 papers receiving 766 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emmanouel Kanavakis Greece	17	253	220	165	128	104	31	786
Maria Soller Sweden	20	359 1.4×	84 0.4×	267 1.6×	106 0.8×	128 1.2×	46	884
Rivka Sukenik‐Halevy Israel	20	244 1.0×	493 2.2×	167 1.0×	52 0.4×	90 0.9×	59	966
Manuela Caruso‐Nicoletti Italy	12	259 1.0×	105 0.5×	257 1.6×	24 0.2×	257 2.5×	41	876
Jorge Román Corona‐Rivera Mexico	14	248 1.0×	88 0.4×	179 1.1×	37 0.3×	94 0.9×	81	636
Faith Pangilinan United States	22	500 2.0×	301 1.4×	267 1.6×	50 0.4×	263 2.5×	46	1.2k
Brian A. Kilburn United States	21	266 1.1×	529 2.4×	66 0.4×	102 0.8×	70 0.7×	39	1.3k
Brandon Holtrup United States	10	324 1.3×	42 0.2×	71 0.4×	137 1.1×	64 0.6×	11	1.1k
Zhoutao Chen Canada	11	399 1.6×	193 0.9×	123 0.7×	42 0.3×	223 2.1×	15	1.1k
Vincenzo Antona Italy	19	428 1.7×	145 0.7×	307 1.9×	33 0.3×	117 1.1×	57	821
Cynthia M. Bradley United States	13	277 1.1×	79 0.4×	283 1.7×	78 0.6×	296 2.8×	17	940

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

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20 of 20 papers shown

1.

Kouvidi, Elisavet, et al.. (2023). Chromosomal Abnormalities in Infertile Greek Men: A Single Institution’s Experience. 7(1). 1–17. 1 indexed citations

2.

Braoudaki, Maria, George Ι. Lambrou, Stavroula Papadodima, et al.. (2015). MicroRNA expression profiles in pediatric dysembryoplastic neuroepithelial tumors. Medical Oncology. 33(1). 5–5. 16 indexed citations

3.

Fragoulis, G., Aigli G. Vakrakou, Anna Papadopoulou, et al.. (2014). Impaired degradation and aberrant phagocytosis of necrotic cell debris in the peripheral blood of patients with primary Sjögren's syndrome. Journal of Autoimmunity. 56. 12–22. 18 indexed citations

4.

Dimitriadou, Eftychia, Γεώργιος Μαρκόπουλος, Joanne Traeger‐Synodinos, et al.. (2013). AbnormalDLK1/MEG3imprinting correlates with decreased HERV-K methylation after assisted reproduction and preimplantation genetic diagnosis. Stress. 16(6). 689–697. 14 indexed citations

5.

Dreesen, Jos, Aspasia Destouni, Georgia Kourlaba, et al.. (2013). Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study. European Journal of Human Genetics. 22(8). 1012–1018. 48 indexed citations

6.

Sofocleous, Christalena, Antonis Kattamis, Aggeliki Kοlialexi, et al.. (2013). Investigation of FANCA mutations in Greek patients.. PubMed. 33(8). 3369–74. 1 indexed citations

7.

Thomaidis, Loretta, Sophia Kitsiou‐Tzeli, Elena Critselis, et al.. (2012). Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation. World Journal of Pediatrics. 8(4). 309–316. 11 indexed citations

8.

Makrythanasis, Periklis, Maria Tzetis, Aggeliki Rapti, et al.. (2010). Cystic Fibrosis Conductance Regulator, Tumor Necrosis Factor, Interferon Alpha-10, Interferon Alpha-17, and Interferon Gamma Genotyping as Potential Risk Markers in Pulmonary Sarcoidosis Pathogenesis in Greek Patients. Genetic Testing and Molecular Biomarkers. 14(4). 577–584. 6 indexed citations

9.

Fatouros, Ioannis G., Athanasios Z. Jamurtas, Michalis G. Nikolaidis, et al.. (2010). Time of sampling is crucial for measurement of cell-free plasma DNA following acute aseptic inflammation induced by exercise. Clinical Biochemistry. 43(16-17). 1368–1370. 58 indexed citations

10.

Phylipsen, Marion, A. Amato, Joanne Traeger‐Synodinos, et al.. (2009). Two new -thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention. Haematologica. 94(9). 1289–1292. 9 indexed citations

11.

Sofocleous, Christalena, Sofìa Kitsiou, A Kolialexi, et al.. (2008). 10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.. PubMed. 22(4). 451–5. 9 indexed citations

12.

Sertedaki, Amalia, et al.. (2008). Conception and pregnancy outcome in a patient with 11-bp deletion of the steroidogenic acute regulatory protein gene. Fertility and Sterility. 91(3). 934.e15–934.e18. 22 indexed citations

13.

Kokkali, Georgia, Joanne Traeger‐Synodinos, Christina Vrettou, et al.. (2007). Blastocyst biopsy versus cleavage stage biopsy and blastocyst transfer for preimplantation genetic diagnosis of β-thalassaemia: a pilot study. Human Reproduction. 22(5). 1443–1449. 120 indexed citations

14.

Kekou, Kyriaki, et al.. (2007). Screening Human Genes for Small Alterations Performing an Enzymatic Cleavage Mismatched Analysis (ECMA) Protocol. Molecular Biotechnology. 37(3). 212–219. 9 indexed citations

15.

Kekou, Kyriaki, et al.. (2007). Screening Human Genes for Small Alterations Performing an Enzymatic Cleavage Mismatched Analysis (ECMA) Protocol. Molecular Biotechnology. 55(1). 1–9. 10 indexed citations

16.

Tzetis, Maria, Marios Kaliakatsos, Maria Fotoulaki, et al.. (2007). Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis. Clinical Genetics. 71(5). 451–457. 31 indexed citations

17.

Radivojevic, Danijela, et al.. (2005). [Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].. PubMed. 129 Suppl 1. 6–9. 1 indexed citations

18.

Kanavakis, Emmanouel, et al.. (1998). Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia. Molecular Human Reproduction. 4(4). 333–337. 46 indexed citations

19.

Traeger‐Synodinos, Joanne, Emmanouel Kanavakis, Steve E. Humphries, et al.. (1998). Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probands. Human Genetics. 102(3). 343–347. 24 indexed citations

20.

Traeger‐Synodinos, Joanne, et al.. (1994). Preliminary mutation analysis in the phenylanaline hydroxylase gene in Greek PKU and HPA patients. Human Genetics. 94(5). 573–5. 14 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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