This map shows the geographic impact of A Kleczkowska'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 A Kleczkowska with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Kleczkowska more than expected).
This network shows the impact of papers produced by A Kleczkowska. 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 A Kleczkowska. The network helps show where A Kleczkowska may publish in the future.
Co-authorship network of co-authors of A Kleczkowska
This figure shows the co-authorship network connecting the top 25 collaborators of A Kleczkowska.
A scholar is included among the top collaborators of A Kleczkowska 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 A Kleczkowska. A Kleczkowska 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.
Kleczkowska, A, et al.. (1991). Inverted distal duplication of the long arm of chromosome 8: borderline intelligence and discrete dysmorphic syndrome.. PubMed. 2(2). 109–13.1 indexed citations
Kleczkowska, A, et al.. (1990). Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989.. PubMed. 1(3-4). 227–33.20 indexed citations
Kleczkowska, A, et al.. (1990). Turner syndrome: II. Associated anomalies, mental performance and psychological problems in 218 patients diagnosed in Leuven in the period 1965-1989.. PubMed. 1(3-4). 241–9.1 indexed citations
Jp, Fryns, et al.. (1989). Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.. PubMed. 32(3). 177–9.5 indexed citations
9.
Fryns, J. P., A Kleczkowska, J. Jaeken, & Herman Van den Berghe. (1988). Ring chromosome 4 mosaicism and Potter sequence.. PubMed. 31(2). 120–2.6 indexed citations
10.
Kleczkowska, A, Jean‐Pierre Fryns, & Herman Van den Berghe. (1988). X-chromosome polysomy in the male. Human Genetics. 80(1). 16–22.80 indexed citations
Fryns, J P & A Kleczkowska. (1987). Ring chromosome 21 in the mother and 21/21 translocation in the fetus: karyotype: 45,XX,-21,-21,+t(21;21)(p11;q11).. PubMed. 30(2). 109–10.5 indexed citations
15.
Kleczkowska, A, et al.. (1987). Partial duplication 8p due to interstitial duplication: inv dup(8)(p21.1----p22). Further delineation of the phenotype from birth to adulthood.. PubMed. 30(1). 47–51.7 indexed citations
Jp, Fryns, et al.. (1982). Ring chromosome 14 syndrome.. PubMed. 25(3). 179–80.11 indexed citations
20.
Sokołowski, J, et al.. (1970). [Developmental anomalies in children with a ring chromosome in group E].. PubMed. 45(11). 1341–50.2 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.