This map shows the geographic impact of D Soekarman'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 D Soekarman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D Soekarman more than expected).
This network shows the impact of papers produced by D Soekarman. 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 D Soekarman. The network helps show where D Soekarman may publish in the future.
Co-authorship network of co-authors of D Soekarman
This figure shows the co-authorship network connecting the top 25 collaborators of D Soekarman.
A scholar is included among the top collaborators of D Soekarman 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 D Soekarman. D Soekarman is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
Soekarman, D, et al.. (1997). On the nosology of the craniodigital syndromes: report of a family and review of the literature.. PubMed. 8(3). 217–22.1 indexed citations
4.
Soekarman, D, et al.. (1996). A form of non-specific mental retardation is probably caused by a microdeletion in a Belgian family. American Journal of Medical Genetics Part A. 64(1). 16.12 indexed citations
5.
Soekarman, D, et al.. (1996). Marden-Walker phenotype: a diagnostic dilemma.. PubMed. 7(1). 31–9.1 indexed citations
Fryns, J. P., et al.. (1993). The association of hemifacial microsomia, homolateral micro/anophthalmos, hemihypotrophy, dental anomalies, submucous cleft palate, CNS malformations and hypopigmented skin lesions following Blaschko's lines in two unrelated female patients. Further evidence for a lethal mutation surviving in mosaic form in "hypomelanosis of Ito".. PubMed. 4(1). 63–7.1 indexed citations
11.
Soekarman, D, et al.. (1993). Macrocephaly and mental retardation. The unique association with short stature, spastic paraplegia and CNS malformations.. PubMed. 4(1). 47–50.1 indexed citations
Soekarman, D, J. P. Fryns, & Herman Van den Berghe. (1992). Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child.. PubMed. 3(4). 217–20.8 indexed citations
Soekarman, D, J. P. Fryns, Paul Casaer, & Herman Van den Berghe. (1991). Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome.. PubMed. 2(3). 157–62.20 indexed citations
16.
Soekarman, D, et al.. (1991). bcr-abl mRNA lacking abl exon a2 detected by polymerase chain reaction in a chronic myelogeneous leukemia patient.. PubMed. 5(6). 457–61.34 indexed citations
17.
Soekarman, D, J van Denderen, L. H. Hoefsloot, et al.. (1990). A novel variant of the bcr-abl fusion product in Philadelphia chromosome-positive acute lymphoblastic leukemia.. PubMed. 4(6). 397–403.45 indexed citations
18.
Hagemeijer, A., et al.. (1990). The Philadelphia translocation in CML and ALL: recent investigations, new detection methods.. PubMed. 32(1). 83–6.2 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.