This map shows the geographic impact of T. Lukusa'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 T. Lukusa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Lukusa more than expected).
This network shows the impact of papers produced by T. Lukusa. 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 T. Lukusa. The network helps show where T. Lukusa may publish in the future.
Co-authorship network of co-authors of T. Lukusa
This figure shows the co-authorship network connecting the top 25 collaborators of T. Lukusa.
A scholar is included among the top collaborators of T. Lukusa 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 T. Lukusa. T. Lukusa is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Lukusa, T. & J. P. Fryns. (2010). Pure de novo 17q25.3 micro duplication characterized by micro array CGH in a dysmorphic infant with growth retardation, developmental delay and distal arthrogryposis.. PubMed. 21(1). 25–34.16 indexed citations
4.
Lumaka, Aimé, et al.. (2009). Werdnig-Hoffmann disease: report of the first case clinically identified and genetically confirmed in central Africa (Kinshasa-Congo).. PubMed. 20(4). 349–58.4 indexed citations
5.
Lukusa, T. & J. P. Fryns. (2007). WITHDRAWN: Human chromosome fragility. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression.1 indexed citations
6.
Lukusa, T. & J. P. Fryns. (2007). Human chromosome fragility. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1779(1). 3–16.151 indexed citations
7.
Lukusa, T., Joris Vermeesch, & J P Fryns. (2005). De novo deletion 7q36 resulting from a distal 7q/8q translocation: phenotypic expression and comparison to the literature.. PubMed. 16(1). 1–15.8 indexed citations
8.
Lukusa, T., et al.. (2001). Terminal 6q25.3 deletion and abnormal behaviour.. PubMed. 12(3). 213–21.5 indexed citations
Lukusa, T., Koenraad Devriendt, & J. P. Fryns. (1999). A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter).. PubMed. 42(2). 91–4.4 indexed citations
11.
Lukusa, T., L. Van Den Berghe, Eric Smeets, & J. P. Fryns. (1999). Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.. PubMed. 42(4). 215–20.3 indexed citations
Lukusa, T., et al.. (1991). Role of gonadal dysgenesis in gonadoblastoma induction in 46, XY individuals. The Leuven experience in 46, XY pure gonadal dysgenesis and testicular feminization syndromes.. PubMed. 2(1). 9–16.8 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.