Ιoannis Kakkas

619 total citations
7 papers, 251 citations indexed

About

Ιoannis Kakkas is a scholar working on Genetics, Hematology and Immunology. According to data from OpenAlex, Ιoannis Kakkas has authored 7 papers receiving a total of 251 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Hematology and 3 papers in Immunology. Recurrent topics in Ιoannis Kakkas's work include Acute Myeloid Leukemia Research (3 papers), Blood disorders and treatments (3 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Ιoannis Kakkas is often cited by papers focused on Acute Myeloid Leukemia Research (3 papers), Blood disorders and treatments (3 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). Ιoannis Kakkas collaborates with scholars based in Greece, United Kingdom and United States. Ιoannis Kakkas's co-authors include Jude Fitzgibbon, Tim Lister, Dominique Bonnet, Claire Green, Alan K. Burnett, Rosemary E. Gale, Jane Stevens, Christopher Allen, Robert K. Hills and Hans G. Drexler and has published in prestigious journals such as Journal of Clinical Oncology, Blood and International Journal of Molecular Sciences.

In The Last Decade

Ιoannis Kakkas

6 papers receiving 249 citations

Peers

Ιoannis Kakkas

HEMAT

MB

PHEOH

GENET

CR

E. S. J. M. de Bont Netherlands

Torsten Haferlach Germany

Sally Jeffries United Kingdom

A Dufour Germany

Michael T. Zimmerman United States

Christina Schessl Germany

Zinia J. Kwidama Netherlands

Karolína Perglerová Germany

Karine Celli‐Lebras France

Elena Vendramini Italy

E. S. J. M. de Bont Netherlands

Ιoannis Kakkas

184 ×0.9

HEMAT

148 ×1.1

MB

72 ×0.8

PHEOH

30 ×0.5

GENET

45 ×1.0

CR

Citations per year, relative to Ιoannis Kakkas Ιoannis Kakkas (= 1×) peers E. S. J. M. de Bont

Countries citing papers authored by Ιoannis Kakkas

Since Specialization

Citations

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

Fields of papers citing papers by Ιoannis Kakkas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ιoannis Kakkas

This figure shows the co-authorship network connecting the top 25 collaborators of Ιoannis Kakkas. A scholar is included among the top collaborators of Ιoannis Kakkas 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 Ιoannis Kakkas. Ιoannis Kakkas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

1.

Sarrou, Styliani, Katerina Dadouli, Ιoannis Kakkas, et al.. (2024). Heterozygous SERPINA1 Defects and Their Impact on Clinical Manifestations of Patients with Predominantly Antibody Deficiencies. International Journal of Molecular Sciences. 25(10). 5382–5382.

2.

Vrettou, Charikleia S., Alice G. Vassiliou, Ιoannis Kakkas, et al.. (2021). Low Admission Immunoglobulin G Levels Predict Poor Outcome in Patients with Mild-to-Critical COVID-19: A Prospective, Single-Center Study. Journal of Epidemiology and Global Health. 11(4). 338–343. 2 indexed citations

3.

Kakkas, Ιoannis, Fani Kalala, Evangelia Farmaki, et al.. (2021). TACI Mutations in Primary Antibody Deficiencies: A Nationwide Study in Greece. Medicina. 57(8). 827–827. 9 indexed citations

4.

Raghavan, Manoj, Lan‐Lan Smith, Debra M. Lillington, et al.. (2008). Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia. Blood. 112(3). 814–821. 79 indexed citations

5.

Gale, Rosemary E., Robert K. Hills, Ιoannis Kakkas, et al.. (2008). Mutation of the Wilms’ Tumor 1 Gene Is a Poor Prognostic Factor Associated With Chemotherapy Resistance in Normal Karyotype Acute Myeloid Leukemia: The United Kingdom Medical Research Council Adult Leukaemia Working Party. Journal of Clinical Oncology. 26(33). 5429–5435. 146 indexed citations

6.

Livaditi, Olga, Evangelos J. Giamarellos‐Bourboulis, Ιoannis Kakkas, et al.. (2007). Grouping of patients with common variable immunodeficiency based on immunoglobulin biosynthesis: Comparison with a classification system on CD4-naïve cells. Immunology Letters. 114(2). 103–109. 8 indexed citations

7.

Gale, Rosemary E., Robert K. Hills, Ιoannis Kakkas, et al.. (2007). Mutation of the Wilms’ Tumor 1 Gene Is a Poor Prognostic Factor Associated with Chemoresistance in Normal Karyotype Acute Myeloid Leukemia.. Blood. 110(11). 361–361. 7 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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